Reporte Demo

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk

Nature Communications·2017

Genetic prediction of male pattern baldness

PLOS Genetics·2017

Male-pattern baldness susceptibility locus at 20p11

Nature Genetics·2008

Six novel susceptibility loci for early-onset androgenetic alopecia

PLOS Genetics·2012

EDA2R is associated with androgenetic alopecia

Journal of Investigative Dermatology·2008

A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features

Nature Communications·2016

GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk

Nature Communications·2017

FGF5 is a crucial regulator of hair length in humans

PNAS·2014

A common 936 C/T mutation in the gene for vascular endothelial growth factor is associated with vascular endothelial growth factor plasma levels

Journal of Vascular Research·2000

Contribution of VEGF polymorphisms to variation in VEGF serum levels in a healthy population

European Cytokine Network·2011

Minoxidil sulfotransferase enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss

Journal of the European Academy of Dermatology and Venereology·2021

Buhl et al., 1990 — farmacocinética/prodroga del minoxidil tópico *

—·1990

Novel enzymatic assay predicts minoxidil response in the treatment of androgenetic alopecia

Dermatologic Therapy·2014

Sulfotransferase activity in plucked hair follicles predicts response to topical minoxidil in the treatment of female androgenetic alopecia

Dermatologic Therapy·2014

Functional Genetic Variants in the 3′-Untranslated Region of Sulfotransferase Isoform 1A1 (SULT1A1) and Their Effect on Enzymatic Activity

Toxicological Sciences·2010

Sanchez-Spitman et al., 2018 — rs1042157 reduce actividad SULT1A1 *

—·2018

Pilot study: Genetic distribution of AR, FGF5, SULT1A1 and CYP3A5 polymorphisms in male Mexican population with androgenetic alopecia

International Journal of Molecular Epidemiology and Genetics·2022

A population pharmacokinetic model for individualized regimens of finasteride according to CYP3A5 genotype and liver function

Journal of Pharmaceutical Investigation·2023

Finasteride concentrations and prostate cancer risk: Results from the Prostate Cancer Prevention Trial

PLOS ONE·2015

Genome-wide association study of circulating vitamin D levels

Human Molecular Genetics·2010

Rivera-Paredez et al., 2020 — haplotipo GC en mujeres mexicanas *

—·2020

The role of TMPRSS6 gene polymorphism in iron resistance iron deficiency anaemia (IRIDA): A systematic review

Annals of Hematology·2024

TMPRSS6 rs855791 modulates hepcidin transcription in vitro and serum hepcidin levels in normal individuals

Blood·2011

High incidence of partial biotinidase deficiency in the first 3 years of a regional newborn screening program

International Journal of Environmental Research and Public Health·2022

Genome-wide association study of selenium concentrations

Human Molecular Genetics·2015

Selenoproteins are essential for proper keratinocyte function and skin development

PLOS ONE·2010

Oxidative stress-associated senescence in dermal papilla cells of men with androgenetic alopecia

Journal of Investigative Dermatology·2015

Genotype–activity relationship for Mn-superoxide dismutase, glutathione peroxidase 1 and catalase in humans

Pharmacogenetics and Genomics·2006

Jablonska et al., 2009 — relación genotipo-actividad de GPX1 *

—·2009

The Ala16Val genetic dimorphism modulates the import of human manganese superoxide dismutase into rat liver mitochondria

Pharmacogenetics·2003

Superoxide imbalance triggered by Val16Ala-SOD2 polymorphism increases the risk of depression and self-reported psychological stress in free-living elderly people

Molecular Genetics & Genomic Medicine·2020

Examination of androgenetic alopecia with serum biomarkers

Journal of Cosmetic Dermatology·2021

Effects of a polymorphism in the human tumor necrosis factor α promoter on transcriptional activation

PNAS·1997