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Research 121–150 of 1000+
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Role of polymorphism of the androgen receptor gene andnon-random x chromosome inactivation in the pathogenesisof androgenic alopecia
- Cloning, computational analysis and expression profiling of steroid 5 alpha-reductase 1 (SRD5A1) gene during reproductive phases and ovatide stimulation in endangered catfish, Clarias magur
- Effects of Short-Term Finasteride on Apoptotic Factors and Androgen Receptors in Prostate Cancer Cells
- Administration of Nrf-2-Modified Hair-Follicle MSCs Ameliorates DSS-Induced Ulcerative Colitis in Rats
- Virilism and Ectopic Expression of HSD17B5 in Mature Cystic Teratoma
- Comparative analysis of stemness between dermal papilla cells and human dermalstem/progenitor cells
- Seasonal Gene Expression Profile Responsible for Hair Follicle Development in Angora Goats
- History and physical examination of polycystic ovary syndrome: Detecting too much or too little
- The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- Recommendations for treatment of nonclassic congenital adrenal hyperplasia (NCCAH): An update
- Nonclassic adrenal hyperplasia
- Prediction of male-pattern baldness from genotypes
- Congenital adrenal hyperplasia
- Sex-limited chromosomes and non-reproductive traits
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- SARS-CoV-2 Infection and Alpha-Synucleinopathies: Potential Links and Underlying Mechanisms
- A Tale of Two Haplotypes: The EDA2R/AR Intergenic Region is the Most Divergent Genomic Segment between Africans and East Asians in the Human Genome
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Mister XX
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Ovine KRTAP36-2: A New Keratin-Associated Protein Gene Related to Variation in Wool Yield
- Genetics and Pathophysiology of Congenital Adrenal Hyperplasia
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential