IndraLab

Statements


USP41 affects SNAI1
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USP41 binds SNAI1.
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"USP41 Interacts with and Deubiquitinates Snail."

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"Since DUBs regulate various cellular processes by interacting with target proteins [28], we examined the interaction between USP41 and Snail."

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"USP41 interacts with Snail and stabilizes Snail via deubiquitination."

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"In mechanisms, USP41 bound to Snail, a master regulator of EMT, and induced Snail deubiquitination, thereby increasing the stabilization of Snail."

sparser
"Since DUBs regulate various cellular processes by interacting with target proteins [ xref ], we examined the interaction between USP41 and Snail."

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"Therefore, these results indicated that USP41 interacts with Snail resulting in the induction of Snail destabilization."

sparser
"USP41 interacts with Snail and stabilizes Snail via deubiquitination."

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"In mechanisms, USP41 bound to Snail, a master regulator of EMT, and induced Snail deubiquitination, thereby increasing the stabilization of Snail."
USP41 ubiquitinates SNAI1.
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USP41 leads to the ubiquitination of SNAI1. 3 / 3
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"Moreover, siRNA-mediated USP41 downregulation increased the ubiquitination of Snail in both breast cancer cells (Figure 5B), whereas overexpression of USP41 decreased Snail ubiquitination (Figure 5C)."

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"Collectively, these results suggest that Snail ubiquitination is modulated by the expression levels of USP41 and TRIM21."

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"Therefore, we supposed that the balance of USP41 and TRIM21 may modulate the ubiquitination and stabilization of Snail."
USP41 deubiquitinates SNAI1.
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USP41 deubiquitinates SNAI1. 3 / 3
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"Moreover, siRNA-mediated USP41 downregulation increased the ubiquitination of Snail in both breast cancer cells (Figure 5B), whereas overexpression of USP41 decreased Snail ubiquitination (Figure 5C)."

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"Furthermore, USP41 interacted with and inhibited ubiquitination of Snail, resulting in the increase in Snail stabilization."

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"USP41 Interacts with and Deubiquitinates Snail."
USP41 activates SNAI1.
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USP41 activates SNAI1. 2 / 2
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"USP41-mediated Snail stabilization plays a critical role in EMT and metastasis, and provides a crucial target against breast cancer therapy."

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"Next, we investigated the USP41-mediated Snail protein stability using cycloheximide (CHX; protein synthesis inhibitor)."
USP41 bound to SNAI1 activates SNAI1. 1 / 1
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"In mechanisms, USP41 bound to Snail, a master regulator of EMT, and induced Snail deubiquitination, thereby increasing the stabilization of Snail."
USP41 inhibits SNAI1.
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USP41 inhibits SNAI1. 2 / 2
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"As shown in Figure 4F, MG132 inhibited USP41 siRNA-induced Snail downregulation in MDA-MB-231 and MDA-MB-361 cells."

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"Knockdown of TRIM21 markedly rescued Snail downregulation by USP41 siRNA in both breast cancer cells."
USP41 increases the amount of SNAI1.
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USP41 increases the amount of SNAI1. 2 / 2
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"In addition, depletion of USP41 downregulated Snail protein expression, an epithelial-mesenchymal transition marker, but not mRNA expression."

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"In addition, ectopic expression of USP41 upregulated Snail protein expression (Figure 4C)."
USP41 decreases the amount of SNAI1.
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USP41 decreases the amount of SNAI1. 2 / 2
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"Downregulation of USP41 only decreased the protein level of Snail (Figure 4A,B), as a transcription repressor in the EMT process, whereas other EMT-related proteins (E-cadherin, Vimentin and Slug) were not altered (Figure 4A)."

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"In our study, knockdown or overexpression of USP41 induced the downregulation or upregulation of Snail protein expression in breast cancer cells, respectively (Figure 4A–C)."

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"As shown in Figure 3, knockdown of USP41 suppressed the proliferation of MCF-7 and MDA-MB-231 cells (Figure 3A,3C)."

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"Our study suggested that USP41 knockdown inhibits proliferation and invasive ability of breast cancer cells."

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"It has been reported that USP41 promotes proliferation of lung cancer cells , as well as in other cancerous cell lines, through regulating the deubiquitination of the receptor for activated C kinase 1 (RACK1) and the epithelial-mesenchymal transition transcription factor (EMT-TF) Snail ."

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"In contrast, the overexpression of USP41 significantly enhanced the proliferation of MCF-7 cells and MDA-MB-231 cells (Figure 3B,3D)."

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"Likewise, the ectopic expression of Snail prevented the USP41 siRNA-mediated reduction of cancer cell proliferation, while knockdown of Snail inhibits proliferation by USP41 overexpression (Figure 6G,H)."

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"Overexpression of USP41 greatly enhanced BC colony-forming ability, proliferation, and migration."

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"In vitro experiments further revealed that the knockdown of ABHD12 and USP41 significantly inhibit the proliferation, invasion and migration of breast cancer cells."

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"Other study revealed that USP41 knockdown inhibited cell proliferation, cell migration, and increased cell apoptosis in lung cancer (Ji et al. 2021)."

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"In contrast, USP41 knockdown significantly inhibited BC colony-forming ability, proliferation, and migration."

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"Knockdown of USP41 Inhibits Migration and Proliferation of Breast Cancer Cells."

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"Interestingly, drug sensitivity analysis with IC50 further suggested that docetaxel, epirubicin and inhibitors of PI3K/AKT/mTOR signaling pathway (afuresertib, buparlisib, ipatasertib and dactolisib) are more beneficial to patients in the low-risk group, whereas tyrosine kinase inhibitors (ibrutinib, lapatinib and sapitinib) may better benefit patients in the high-risk group ( Supplementary Figure S6 ).3.9 Sponging ABHD12 and USP41 significantly inhibited the proliferation, invasion and migration of breast cancer cells."
USP41 affects NPPA
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"An in vitro disintegration test was performed following the general disintegration testing procedure as per USP41-NF36."

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"The drug content of the prepared lornoxicam DT was found to be within the pharmacopoeial guidelines (USP41-NF36) requirement."

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"The X-SSG is available in different types and grades, differing in their degrees of substitution, sodium content, pH value, crosslink density, and swelling capacity ( JRS, 2019; Shah and Augsburger, 2[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"The friability testing was performed on 6.5 g equivalent number of randomly picked tablets (USP41-NF36)."

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"This might be attributed to the lower sodium glycolate content of this grade (2.0–3.4%) compared to the regular and CLV grades (2.8–4.2%) ( USP41-NF36, 2019a )."

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"Sodium starch glycolate may contain up to 7.0% sodium chloride ( USP41-NF36, 2019a )."

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"Explotab® Low pH has a lower percentage of sodium (2.0–3.4% versus 2.8–4.2%), exhibiting a lower pH value (3.0–5.0 versus 5.5–7.5) ( USP41-NF36, 2019a )."

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"The results of % drug available in the dissolution media ( Table 6 ) showed values within the USP acceptance criteria, as per different monographs of opioid drugs ( USP41-NF36, 2019c, 2019d, 2019e, 20[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"

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"The results were within the USP limits specified for different opioid drug products ( USP41-NF36, 2019b, 2019c, 2019d, 2019e, 2019f )."

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"The following solutions were prepared and used in this study: 0.1 N hydrochloric acid (8.3 mL of HCl 37% adjusted to 1 L with distilled water), pH 3 solution (distilled water adjusted to pH 3 with HCl[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
SNAI1 affects USP41
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SNAI1 binds USP41.
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"USP41 Interacts with and Deubiquitinates Snail."

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"Since DUBs regulate various cellular processes by interacting with target proteins [28], we examined the interaction between USP41 and Snail."

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"USP41 interacts with Snail and stabilizes Snail via deubiquitination."

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"In mechanisms, USP41 bound to Snail, a master regulator of EMT, and induced Snail deubiquitination, thereby increasing the stabilization of Snail."

sparser
"Since DUBs regulate various cellular processes by interacting with target proteins [ xref ], we examined the interaction between USP41 and Snail."

sparser
"Therefore, these results indicated that USP41 interacts with Snail resulting in the induction of Snail destabilization."

sparser
"USP41 interacts with Snail and stabilizes Snail via deubiquitination."

sparser
"In mechanisms, USP41 bound to Snail, a master regulator of EMT, and induced Snail deubiquitination, thereby increasing the stabilization of Snail."
SNAI1 activates USP41.
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SNAI1 activates USP41. 1 / 1
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"Likewise, the ectopic expression of Snail prevented the USP41 siRNA-mediated reduction of cancer cell proliferation, while knockdown of Snail inhibits proliferation by USP41 overexpression (Figure 6G,H)."
USP41 affects RACK1
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USP41 binds RACK1.
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"The Co-IP results indicated that USP41 could interact with RACK1 ( xref )."

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"USP41 interacted with RACK1 in BC cells."

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"Moreover, Co-Immunoprecipitation mass spectrometry results indicated that USP41 could interact with RACK1 ."
USP41 activates RACK1.
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USP41 activates RACK1. 3 / 3
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"Thus, USP41 promoted BC function through upregulating RACK1."

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"Since function of RACK1 is diverse and extensive in breast cancer, they mentioned that the investigation of the roles of USP41-mediated RACK1 in cancer cell migration are necessary."

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"Previously, Huang et al. identified the RACK1 as a novel protein interacting with USP41 through CoIP-MS analysis and indicated the promotion of migration via USP41-induced RACK1 upregulation [25]."
USP41 increases the amount of RACK1.
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USP41 increases the amount of RACK1. 2 / 2
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"Immunoblotting results showed that USP41 promoted the protein expression of RACK1 (Figure 6B)."

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"USP41 promoted the protein expression of RACK1."
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"We found that USP41 upregulation enhanced the growth, proliferation, and invasion of BC cells."

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"Meanwhile, the overexpression of USP41 enhanced cell invasion in MCF-7 cells (Figure 4C)."

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"In vitro experiments further revealed that the knockdown of ABHD12 and USP41 significantly inhibit the proliferation, invasion and migration of breast cancer cells."

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"Ectopic expression of USP41 promoted cell migration and invasion in MDA-MB-231 and MDA-MB-361 cells (Figure 3B,C)."

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"Together, these data suggest that USP41 overexpression could enhance the growth and invasion of breast cancer cells."

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"Interestingly, drug sensitivity analysis with IC50 further suggested that docetaxel, epirubicin and inhibitors of PI3K/AKT/mTOR signaling pathway (afuresertib, buparlisib, ipatasertib and dactolisib) are more beneficial to patients in the low-risk group, whereas tyrosine kinase inhibitors (ibrutinib, lapatinib and sapitinib) may better benefit patients in the high-risk group ( Supplementary Figure S6 ).3.9 Sponging ABHD12 and USP41 significantly inhibited the proliferation, invasion and migration of breast cancer cells."
USP41P affects USP18
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No evidence text available

No evidence text available

sparser
"Here, we show that USP18 interacts with its paralog USP41, whose catalytic domain shares 97% identity with USP18."

No evidence text available

No evidence text available

eidos
"USP41 knockdown inhibits cell proliferation and migration and induces cell apoptosis of lung cancer ."

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"Deubiquitinating enzyme USP41 promotes lung cancer cell proliferation and migration."

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"MTT, EdU, flow cytometry, and transwell assays further determined that USP41 enhanced the proliferation and migration of lung cancer cells."

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"USP41 knockdown inhibits cell proliferation and migration and induces cell apoptosis of lung cancer."
USP41 affects UBD
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USP41 inhibits UBD.
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USP41 inhibits UBD. 2 / 2
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"Finally, we propose that USP41 antagonizes conjugation of the understudied ubiquitin-like protein FAT10 (HLA-F adjacent transcript 10) from substrates in a catalytic-independent manner."

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"Based on our data and the AlphaFold prediction, it is tempting to speculate that USP41 might be sequestering FAT10 away from its conjugation machinery, leading to decreased levels of FAT10 conjugation, but this will require additional investigation.Finally, it is notable that over the course of our study, USP41 went from being annotated as a protein-coding gene in databases to now being a pseudogene."
USP41 binds UBD.
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"We first assessed binding between USP41 and FAT10 by co-immunoprecipitation experiment."

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"Again, we took advantage of AlphaFold to generate the structure of USP41 bound to FAT10, where we highlighted the catalytic triad of the DUB as well as FAT10 Gly165, which gets conjugated to substrates (Figure 6C)."
RACK1 affects USP41
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RACK1 binds USP41.
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"The Co-IP results indicated that USP41 could interact with RACK1 ( xref )."

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"USP41 interacted with RACK1 in BC cells."

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"Moreover, Co-Immunoprecipitation mass spectrometry results indicated that USP41 could interact with RACK1 ."
RACK1 inhibits USP41.
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RACK1 inhibits USP41. 1 / 1
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"Knockdown of RACK1 inhibited cell growth and migration, and reversed the oncogenic function of USP41 in BC cells."
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"Ectopic expression of USP41 promoted cell migration and invasion in MDA-MB-231 and MDA-MB-361 cells (Figure 3B,C)."

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"Identically, USP41 overexpression promoted cell migration in MDA-MB-231 cell line (Figure 4D)."

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"Other study revealed that USP41 knockdown inhibited cell proliferation, cell migration, and increased cell apoptosis in lung cancer (Ji et al. 2021)."
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Indometacin increases the amount of USP41P.
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Indometacin increases the amount of USP41P. 1 / 1
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No evidence text available
Indometacin decreases the amount of USP41P.
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Indometacin decreases the amount of USP41P. 1 / 1
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No evidence text available
Hsa-miR-628-3p affects USP41
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Hsa-miR-628-3p inhibits USP41. 2 / 2
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"We also selected TLR3 and MDA5, receptors of double-stranded RNA as same as RIG-I, and TNFSF13B, AIM2, USP41, STAP1, GBP4, CCL8, and IFI27 that had been reported to be down-regulated by the hsa-miR-628-3p mimic (Ueta et al., 2021b)."

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"TNFSF13B, AIM2, USP41, STAP1, GBP4, CCL8, and IFI27, reportedly down-regulated by the hsa-miR-628-3p mimic, were also significantly up-regulated in the transfected cells."
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Dexamethasone increases the amount of USP41P.
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Dexamethasone increases the amount of USP41P. 1 / 1
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No evidence text available
Dexamethasone decreases the amount of USP41P.
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Dexamethasone decreases the amount of USP41P. 1 / 1
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No evidence text available
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Bisphenol A increases the amount of USP41P. 2 / 2
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No evidence text available

No evidence text available
USP41P affects migration
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USP41P activates migration. 2 / 2
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"USP41 knockdown inhibits cell proliferation and migration and induces cell apoptosis of lung cancer ."

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"In contrast , USP41 knockdown significantly inhibited BC colony-forming ability , proliferation , and migration ."

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"USP41 knockdown inhibits cell proliferation and migration and induces cell apoptosis of lung cancer."

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"USP41 knockdown promotes lung cancer cell apoptosis."
USP41P affects RACK1
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No evidence text available

No evidence text available

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"To verify the involvement of Snail in USP41-mediated EMT regulation, we executed the overexpression of Snail in USP41-depleted cells."

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"USP41 Enhances Epithelial-Mesenchymal Transition of Breast Cancer Cells through Snail Stabilization."
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"As shown in Figure 5A,5B, knockdown of USP41 enhanced cell apoptosis in MCF-7 and MDA-MB-231 cells."
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"Other study revealed that USP41 knockdown inhibited cell proliferation, cell migration, and increased cell apoptosis in lung cancer (Ji et al. 2021)."
USP41 affects USP18
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USP41 binds USP18.
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"USP41 bound to USP18, and importantly, this binding occurs through their respective USP domains (Figure 1G and Supplementary Figure 1D)."
USP41 activates USP18.
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USP41 activates USP18. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects TRIM21
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"Moreover, we found the interaction of USP41 and TRIM21 through Snail IP assay using USP41 antibody ( xref E)."

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"Moreover, we found the interaction of USP41 and TRIM21 through Snail IP assay using USP41 antibody (Figure 5E)."
USP41 affects ISG15
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"While both databases reported several identical ISG15-interacting proteins such as UBA7, the E1 for ISG15, or several members of the IFNA family of proteins (such as IFNA1, IFNA2, INFA8, IFNA10, IFNA14), neither database reported an interaction between ISG15 and USP41."

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"Finally, we examined whether USP41 could bind ISG15, since USP18 non-covalently interacts with ISG15."
USP18 affects USP41
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USP18 binds USP41.
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"USP41 bound to USP18, and importantly, this binding occurs through their respective USP domains (Figure 1G and Supplementary Figure 1D)."
USP18 activates USP41.
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USP18 activates USP41. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
UBD affects USP41
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"We first assessed binding between USP41 and FAT10 by co-immunoprecipitation experiment."

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"Again, we took advantage of AlphaFold to generate the structure of USP41 bound to FAT10, where we highlighted the catalytic triad of the DUB as well as FAT10 Gly165, which gets conjugated to substrates (Figure 6C)."
TRIM21 affects USP41
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"Moreover, we found the interaction of USP41 and TRIM21 through Snail IP assay using USP41 antibody ( xref E)."

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"Moreover, we found the interaction of USP41 and TRIM21 through Snail IP assay using USP41 antibody (Figure 5E)."
RACK1 affects USP41P
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No evidence text available

No evidence text available
OGT affects USP41
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OGT binds USP41.
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"Mechanically, USP41 interacted with OGT in MDA-MB-231 cells."
OGT activates USP41.
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OGT activates USP41. 1 / 1
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"Overexpression of OGT enhanced the protein stability of USP41."
ISG15 affects USP41
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"While both databases reported several identical ISG15-interacting proteins such as UBA7, the E1 for ISG15, or several members of the IFNA family of proteins (such as IFNA1, IFNA2, INFA8, IFNA10, IFNA14), neither database reported an interaction between ISG15 and USP41."

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"Finally, we examined whether USP41 could bind ISG15, since USP18 non-covalently interacts with ISG15."
3-isobutyl-1-methyl-7H-xanthine increases the amount of USP41P.
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No evidence text available
3-isobutyl-1-methyl-7H-xanthine decreases the amount of USP41P.
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No evidence text available
Urethane affects USP41P
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Urethane decreases the amount of USP41P. 1 / 1
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No evidence text available

No evidence text available
Transferase affects USP41
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"The interaction between USP41 and O-linked N-acetylglucosamine transferase (OGT) was evaluated by co-immunoprecipitation assay."

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"An independent cohort confirmed LPS induction of USP41 and IL10 genes."
Let-7a-5p affects USP41
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Let-7a-5p activates USP41. 1 / 1
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"Elsewhere , we reported that let-7a-5p could positively regulate STAP1, IFI44L, CXCL11, TNFSF10, AIM2, RSAD2, IFITM1, CXCL10, CCL8, TRIM22, HERC5, IFI27, IFIT2, GBP4, IFIT1, TNFSF13B, and USP41; genes that were negatively regulated by the miR-628-3p mimic."
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Doxorubicin decreases the amount of USP41P. 1 / 1
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No evidence text available
Bis(2-ethylhexyl) phthalate increases the amount of USP41P. 1 / 1
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No evidence text available
ZBTB16 affects USP41
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ZBTB16 activates USP41. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41P affects protein RACK1
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USP41P activates protein RACK1. 1 / 1
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"USP41 promoted the protein expression of RACK1 ."
USP41P affects migration A549 H1299 cells
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USP41P inhibits migration A549 H1299 cells. 1 / 1
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"Transwell assay further demonstrated that USP41 knockdown increased the migration rate of A549 and H1299 cells ."
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"In addition , depletion of USP41 downregulated Snail protein expression , an epithelial-mesenchymal transition marker , but not mRNA expression ."

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"We knocked down E-cadherin in lung cancer cell lines using siRNA, and demonstrated that E-Cadherin knockout offseted the effect of inhibition of USP41 on cell migration, and inhibition of USP41 may reverse EMT of lung cancer cells."
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"These results indicated that USP41 promoted lung cancer cell migration."
USP41P affects cell apoptosis lung cancer
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USP41P inhibits cell apoptosis lung cancer. 1 / 1
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"USP41 knockdown inhibits cell proliferation and migration and induces cell apoptosis of lung cancer ."
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"Overexpression of the Ubiquitin Specific Proteases USP43, USP41, USP27x and USP6 in Osteosarcoma Cell Lines: Inhibition of Osteosarcoma Tumor Growth and Lung Metastasis Development by the USP Antagonist PR619."
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"USP41 promotes breast cancer via regulating RACK1 ."
USP41P affects BC colony-forming
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USP41P activates BC colony-forming. 1 / 1
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"In contrast , USP41 knockdown significantly inhibited BC colony-forming ability , proliferation , and migration ."
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"Knockdown of USP41 suppressed wound healing activity and migration in two breast cancer cells (Figure 2B,C)."
USP41 affects transferase
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"The interaction between USP41 and O-linked N-acetylglucosamine transferase (OGT) was evaluated by co-immunoprecipitation assay."

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"USP41 contributes to invasion, apoptosis and drug resistance in breast and lung cancer cells."
USP41 affects conjugation
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"Finally, we propose that USP41 antagonizes conjugation of the understudied ubiquitin-like protein FAT10 (HLA-F adjacent transcript 10) from substrates in a catalytic-independent manner."
USP41 affects cell growth
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"Knockdown of USP41 inhibited migration and growth of breast cancer cells, whereas overexpression of USP41 increased cell growth and migration."
USP41 affects ZBTB16
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USP41 activates ZBTB16. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects UBASH3B
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USP41 activates UBASH3B. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects STAG3
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USP41 activates STAG3. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects SPATS2L
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USP41 activates SPATS2L. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects RSAD2
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USP41 activates RSAD2. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects RGS13
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USP41 activates RGS13. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects OGT
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"Mechanically, USP41 interacted with OGT in MDA-MB-231 cells."
USP41 affects OAS3
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USP41 activates OAS3. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects ILI27
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USP41 activates ILI27. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects IL1R2
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USP41 activates IL1R2. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects IFI44L
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USP41 activates IFI44L. 1 / 1
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"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects FKBP5
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USP41 activates FKBP5. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects FERIL14
| 1
USP41 activates FERIL14. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41 affects CDH1
| 1
USP41 activates CDH1. 1 / 1
| 1

reach
"Previously, Ji et al. reported that shRNA-mediated USP41 knockout suppresses migration via E-cadherin upregulation in lung adenocarcinoma [26]."
USP41 affects BC
| 1
USP41 activates BC. 1 / 1
| 1

reach
"Overexpression of USP41 greatly enhanced BC colony-forming ability, proliferation, and migration."

reach
"Previously, Ji et al. reported that shRNA-mediated USP41 knockout suppresses migration via E-cadherin upregulation in lung adenocarcinoma [26]."
UBASH3B affects USP41
| 1
UBASH3B activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
STAG3 affects USP41
| 1
STAG3 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
SPATS2L affects USP41
| 1
SPATS2L activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
RSAD2 affects USP41
| 1
RSAD2 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
RGS13 affects USP41
| 1
RGS13 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
PM affects USP41
| 1
PM inhibits USP41. 1 / 1
| 1

reach
"In summary, PM inhibited cell viability, proliferation, and migration of BC by regulating the O-GlcNAcylation of USP41."
OAS3 affects USP41
| 1
OAS3 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
USP41P is modified
| 1
USP41P is deubiquitinated. 1 / 1
| 1

trips
"Deubiquitinating enzyme USP41 promotes lung cancer cell proliferation and migration."
Neoplasms affects USP41
| 1
Neoplasms increases the amount of USP41. 1 / 1
| 1

reach
"Tumor tissues of breast cancer patients were overexpressed USP41 expression and had shorter survival time than patients with low expression of USP41 (Figure 1C,D)."
ILI27 affects USP41
| 1
ILI27 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
IL1R2 affects USP41
| 1
IL1R2 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
IFNA affects USP41P
1 |
IFNA increases the amount of USP41P. 1 / 1
1 |

"Table 3. Genes on chromosome 22 exhibiting IFN-sensitive expression changes"
IFI44L affects USP41
| 1
IFI44L activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
FKBP5 affects USP41
| 1
FKBP5 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
FERIL14 affects USP41
| 1
FERIL14 activates USP41. 1 / 1
| 1

reach
"OAS3, RGS13, STAG3, IFI44L, STS-1, FERIL14, ZBTB16, USP18, USP41, RSAD2, FKBP5, IL1R2, DNAPTP6 and ILI27, which top 14 significantly upregulated mRNAs in SLE patients compared with Healthy donors, sho[MISSING/INVALID CREDENTIALS: limited to 200 char for Elsevier]"
4,4'-sulfonyldiphenol decreases the amount of USP41P. 1 / 1
1 |

No evidence text available