Diabetes Mellitus, Non-Insulin-Dependent
|
0.900 |
Biomarker
|
disease |
HPO |
|
|
|
Diabetes Mellitus, Non-Insulin-Dependent
|
0.900 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Insulin Resistance
|
0.400 |
Biomarker
|
phenotype |
HPO |
|
|
|
CORONARY ARTERY DISEASE, SUSCEPTIBILITY TO
|
0.100 |
SusceptibilityMutation
|
disease |
CLINVAR |
|
|
|
INSULIN RESISTANCE, SUSCEPTIBILITY TO
|
0.100 |
SusceptibilityMutation
|
disease |
CLINVAR |
|
|
|
Decreased waist to hip ratio
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Polycystic Ovary Syndrome
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Polycystic ovary syndrome patient and healthy control genotypes, with the CYP21 and IRS1 variants.
|
15705377 |
2005 |
Hyperinsulinism
|
0.400 |
Biomarker
|
disease |
BEFREE |
Insulin increased insulin receptor substrate 1 (IRS-1) tyrosine phosphorylation, IRS-1-associated phosphatidylinositol (PI) 3-kinase activity, and phosphorylation of Akt Ser473 and AS160, a newly described Akt substrate that plays a role in GLUT4 exocytosis, approximately 2.3 fold before treatment.
|
15855334 |
2005 |
Obesity
|
0.600 |
Biomarker
|
disease |
CTD_human |
Obese mouse ovaries had decreased Irs1, Foxo3a, Cyp2e1, MiR-103, and MiR-21 but increased Kitlg, Akt1, and miR-184 levels relative to lean littermates.
|
23954404 |
2013 |
Polycystic Ovary Syndrome
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
PCOS was associated with lower expression of GLUT4 and IRS1 and a higher level of oxidative stress in VAT, which was strongly correlated with WC and HOMA-IR.
|
25064406 |
2014 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
Tumor suppressors miR-143 and miR-145 and predicted target proteins API5, ERK5, K-RAS, and IRS-1 are differentially expressed in proximal and distal colon.
|
25477374 |
2015 |
Hyperglycemia
|
0.100 |
PosttranslationalModification
|
disease |
BEFREE |
Hyperglycemia (25 mM glucose) and TNF-alpha showed analogous (> 50% inhibition) effects on tyrosine phosphorylation of insulin receptor substrate-1, Shc, p60, and p44, whereas opposite effects were observed for tyrosine phosphorylation of FAK125, which is dephosphorylated after insulin stimulation.
|
8617880 |
1996 |
Liver Cirrhosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
IRS-1 was significantly increased in cirrhosis compared to normal liver (1.61 +/- 0.31 vs 0.86 +/- 0.21; P < 0.05).
|
10210639 |
1999 |
Cirrhosis
|
0.010 |
Biomarker
|
disease |
BEFREE |
IRS-1 was significantly increased in cirrhosis compared to normal liver (1.61 +/- 0.31 vs 0.86 +/- 0.21; P < 0.05).
|
10210639 |
1999 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
IRS-1 was expressed at high levels in estrogen-dependent growth of MCF-7 xenografts, but withdrawal of estrogen, which decreased tumor growth, resulted in a dramatic decrease in IRS-1 expression.
|
10319328 |
1999 |
Carcinoma
|
0.030 |
AlteredExpression
|
group |
BEFREE |
IRS-1 and IGF-IR were expressed at high levels in control tissues and in well and moderately differentiated carcinomas but at low levels in poorly differentiated breast cancers.
|
11102895 |
2000 |
Breast Carcinoma
|
0.100 |
Biomarker
|
disease |
BEFREE |
Insulin receptor substrate-1 (IRS-1) is a key protein in the IGF signaling pathway in the estrogen-dependent MCF-7 breast carcinoma cell line.
|
12960057 |
2003 |
Diabetes Mellitus
|
0.400 |
Biomarker
|
group |
BEFREE |
Insulin receptor substrate-1 and -2 (IRS-1 and IRS-2), two major downstream molecules of IGF-1R, are known to be important in the genesis of diabetes.
|
14604996 |
2004 |
Diabetes
|
0.100 |
Biomarker
|
disease |
BEFREE |
Insulin receptor substrate-1 and -2 (IRS-1 and IRS-2), two major downstream molecules of IGF-1R, are known to be important in the genesis of diabetes.
|
14604996 |
2004 |
Gestational Diabetes
|
0.100 |
GeneticVariation
|
phenotype |
BEFREE |
IRS-1 G972R was associated with the baseline characteristics of the patients with GDM, and might be related to insulin resistance that is seen in obese patients with GDM.
|
16522427 |
2006 |
Neoplasms
|
0.100 |
AlteredExpression
|
group |
BEFREE |
IRS-1 and IRS-2 are expressed in normal mammary epithelial cells and in breast carcinoma cells, where they have been implicated in mediating signals to promote tumor cell survival, growth and motility.
|
17361103 |
2007 |
estrogen receptor-negative breast cancer
|
0.020 |
Biomarker
|
disease |
BEFREE |
Insulin receptor substrate 1 knockdown in human MCF7 ER+ breast cancer cells by nuclease-resistant IRS1 siRNA conjugated to a disulfide-bridged D-peptide analogue of insulin-like growth factor 1.
|
17922544 |
2008 |
Malignant neoplasm of breast
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
IRS-1 may serve as an alternative target to overexpressed IGF1R in breast cancer.
|
17922544 |
2008 |
Breast Carcinoma
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
IRS-1 may serve as an alternative target to overexpressed IGF1R in breast cancer.
|
17922544 |
2008 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.900 |
GeneticVariation
|
disease |
BEFREE |
IRS1 G972R polymorphism and type 2 diabetes: a paradigm for the difficult ascertainment of the contribution to disease susceptibility of 'low-frequency-low-risk' variants.
|
19557384 |
2009 |