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Research 211–240 of 1000+
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Faculty Opinions recommendation of Androgen receptor gene polymorphisms and risk for androgenetic alopecia: a meta-analysis.
- Association between Polymorphisms of OCT1 and Metabolic Response to Metformin in Women with Polycystic Ovary Syndrome
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Genotypic and Phenotypic Study of PDCD4 gene Concerning micro RNA-21 and micro RNA-449b Polymorphism in Breast Cancer
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Regulatory pathway analysis of coat color genes in Mongolian horses
- 40 PRLR and PCCA variants associated with hair length in Brangus heifers
- Enhanced ectodysplasin-A receptor (EDAR) signaling alters multiple fiber characteristics to produce the East Asian hair form
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- The androgen receptor gene polyglycine repeat polymorphism is associated with memory performance in healthy Chinese individuals
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Why were Sardinians the shortest Europeans? A journey through genes, infections, nutrition, and sex
- Androgens and hair: a biological paradox
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Genome-Wide Association Studies for Immunoglobulins in Colostrum and Serum in Chinese Holstein
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- How the leopard gets its spots: a transmembrane peptidase specifies feline pigmentation patterns
- From bedside to bench: regulation of host factors in SARS-CoV-2 infection
- Gray Hair: From Preventive to Treatment
- SEXUAL DIMORPHISM IN MAMMALS
- Gender aspects in skin diseases
- Gene expression of FOXA1 and CCL2 in different phenotypes of infertile women with polycystic ovarian syndrome
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Sparse haplotype-based fine-scale local ancestry inference at scale reveals recent selection on immune responses