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Research 391–420 of 1000+
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- Genes for intermediate filament proteins and the draft sequence of the human genome
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Toxicological Studies on Procyanidin B-2 for Extern?al Application as a Hair Growing Agent
- Damage of hair follicle stem cells and alteration of keratin expression in external radiation-induced acute alopecia
- Validation of Replacement of the Synthetic Food Dye 'Sunset Yellow'-Induced Hepatotoxicity and Genotoxicity with the Nutraceutical 'Curcumin' in Mice
- Acromegaloid Facial Appearance: Case Report and Literature Review
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test
- Primary Amenorrhoea
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- The genetics of androgenetic alopecia
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- Prediction of male-pattern baldness from genotypes
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- Genetic and molecular aspects of androgenetic alopecia
- Polymorphism of CAG and GGN repeats of androgen receptor gene in women with polycystic ovary syndrome
- Induced pluripotent stem cell line MUSIi006-A derived from hair follicle keratinocytes as a non-invasive somatic cell source
- Psoriasis y alopecia areata con traquioniquia concurrente en una paciente pediátrica con síndrome de Turner
- 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
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Treatment-resistant Schizophrenia and Global Cortical Atrophy in a Patient with Turner Syndrome
- Coexistence of psoriasis, and alopecia areata with trachyonychia in a pediatric patient with Turner Syndrome
- The Roles of EDA2R in Ageing and Disease
- It’s X-Related: Biological Bases of Increased COVID-19 Morbidity and Mortality in Men
- Uncovering the genetic architecture and evolutionary roots of androgenetic alopecia in African men
- Unusual Presentation of Childhood Leukemia With Vaginal Bleeding: A Case Report