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Research 31–60 of 1000+
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- Genome-Wide Associations with Body and Fleece Weight in United States Sheep
- Characterization of the Human Hair Shaft Cuticle–Specific Keratin-Associated Protein 10 Family
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Treatment of alopecia areata: “What is new on the horizon?”
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Genome-Wide Association Study of Fiber Diameter in Alpacas
- Depression from a physical symptom.
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Improving human forensics through advances in genetics, genomics and molecular biology
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- The slick hair coat locus maps to chromosome 20 in Senepol-derived cattle
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Health and fertility in World Health Organization group 2 anovulatory women
- Oxidative Activity of the Type 2 Isozyme of 17β-Hydroxysteroid Dehydrogenase (17β-HSD) Predominates in Human Sebaceous Glands
- Gene expression of type 2 17β hydroxysteroid dehydrogenase in scalp hairs of hirsute women
- Intraovarian vascular enhancement via stromal injection of platelet-derived growth factors: Exploring subsequent oocyte chromosomal status and in vitro fertilization outcomes
- Serum IL-21 Level and Its Relation to Activity and Severity of Alopecia Areata
- Purple corn extract improves benign prostatic hyperplasia by inhibiting 5 alpha-reductase type 2 and inflammation in testosterone propionate-induced rats
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Gomez?Lopez?Hernandez syndrome: another consideration in focal congenital alopecia
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Analysis of genetic polymorphisms of steroid 5α-reductase type 1 and 2 genes in Korean men with androgenetic alopecia