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Cancer-Causative Mutations Occurring in Early Embryogenesis.
Not available
S-EPMC8983494
|
biostudies-literature
Cite
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.
Not available
S-EPMC5556360
|
biostudies-literature
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Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy.
Not available
S-EPMC7818383
|
biostudies-literature
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Acceleration of the loss of the first-phase insulin response during the progression to type 1 diabetes in diabetes prevention trial-type 1 participants.
Not available
S-EPMC3837047
|
biostudies-literature
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Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.
Not available
S-EPMC5364411
|
biostudies-literature
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SARS-CoV-2 evolution during treatment of chronic infection.
Not available
S-EPMC7610568
|
biostudies-literature
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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Not available
S-EPMC10932913
|
biostudies-literature
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GWAS meta-analysis of intrahepatic cholestasis of pregnancy implicates multiple hepatic genes and regulatory elements.
Not available
S-EPMC9385867
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biostudies-literature
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Plasma AR Alterations and Timing of Intensified Hormone Treatment for Prostate Cancer: the STAMPEDE Phase 3 Randomized Clinical Trial.
Not available
S-EPMC11869088
|
biostudies-literature
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Metformin for patients with metastatic prostate cancer starting androgen deprivation therapy: a randomised phase 3 trial of the STAMPEDE platform protocol.
Not available
S-EPMC12303861
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biostudies-literature
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