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Unknown
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Genomics
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Homo sapiens
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Illumina HumanCNV370, Illumina HumanHap 300 v2 Duo, Taqman and sequencing, Illumina Human660W-Quad
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Niclosamide induces miR-148a to inhibit PXR and sensitize colon cancer stem cells to chemotherapy.
Not available
S-EPMC9023769
|
biostudies-literature
Cite
Screening Mammography and Breast Cancer: Variation in Risk with Rare Deleterious or Predicted Deleterious Variants in DNA Repair Genes.
Not available
S-EPMC11987804
|
biostudies-literature
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A randomized, placebo-controlled phase 2 study of paclitaxel in combination with reparixin compared to paclitaxel alone as front-line therapy for metastatic triple-negative breast cancer (fRida).
Not available
S-EPMC8558154
|
biostudies-literature
Cite
Naturally Occurring Resistance-Associated Variants of Hepatitis C Virus Protease Inhibitors in Poor Responders to Pegylated Interferon-Ribavirin.
Not available
S-EPMC4473242
|
biostudies-literature
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Gene- and pathway-level analyses of iCOGS variants highlight novel signaling pathways underlying familial breast cancer susceptibility.
Not available
S-EPMC9290690
|
biostudies-literature
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Diagnostic chest X-rays and breast cancer risk among women with a hereditary predisposition to breast cancer unexplained by a BRCA1 or BRCA2 mutation.
Not available
S-EPMC8336294
|
biostudies-literature
Cite
MELARISK_SNP_MITF_geno
Genotypes at MITF E318K variant
EGAD00000000122
|
EGA
Cite
MELARISK_MITF_geno
Genotypes at MITF E318K variant
EGAD00000000121
|
EGA
Cite
A MITF germline mutation predisposes to melanoma and renal cell carcinoma
Study EGAS00000000048
EGAS00000000048
|
EGA
Cite
MELARISK Data Access Committee
Access to data generated by the MELARISK is available by emailing application to the data access committee and will be granted to qualified investigators for appropriate use.
EGAC00000000016
|
EGA
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