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Research 91–120 of 1000+
- Studies on changes in the concentration of serum adrenal androgens in pubertal twins
- Lack of concordance and linkage disequilibrium among brothers for androgenetic alopecia and CAG/GGC haplotypes of the androgen receptor gene in Mexican families
- Single nucleotide polymorphisms in the KRT82 promoter region modulate irregular thickening and patchiness in the dorsal skin of New Zealand rabbits
- Abstracts
- Interleukins gene polymorphism in alopecia areata patients: a systematic review
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- THE RELATION BETWEEN VITILIGO AND OTHER AUTOIMMUNE DISORDERS
- Mult-trait analysis of GWAS - Perceived youtfulness - UKBB
- Sirtuins pathways and redox homeostasis: a pilot study on young and old monozygotic twins
- The effect of DNMTs and MBPs on hypomethylation in systemic lupus erythematosus
- Abstracts of 42nd National Conference of Association of Clinical Biochemists of India (ACBICON 2015)
- Nonclassic congenital adrenal hyperplasia
- Genome-wide association study for cashmere traits in Inner Mongolia cashmere goat population reveals new candidate genes and haplotypes
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Personalized Medicine in the Field of Inflammatory Skin Disorders
- Prevalence Of Male Balding Pattern In Patient From Saveetha Dental College- Retrospective Comparative Evaluation Study
- Vitamin D-dependent rickets type II. Defective induction of 25-hydroxyvitamin D3-24-hydroxylase by 1,25-dihydroxyvitamin D3 in cultured skin fibroblasts.
- Skin diseases associated with atopic dermatitis
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- 268 Male-pattern baldness and its association with coronary heart disease
- HAIR LOSS IN WOMEN
- Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report
- Erosive Lichen Planus of the Scalp and Hepatitis C Infection
- Correction: Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Evaluation of androgen receptor gene as a candidate gene in female androgenetic alopecia
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study