Search
for
Sort by
Research 721–750 of 1000+
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Whole-Genome Resequencing Reveals Selection Signal Related to Sheep Wool Fineness
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- LPA3, a unique G protein-coupled receptor for lysophosphatidic acid
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Androgenetic alopecia: An update
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Familial scarring alopecia associated with scalp psoriasis
- Genomic Regions Associated with Wool, Growth and Reproduction Traits in Uruguayan Merino Sheep
- Partial Reversal of Canities in a 22-Year-Old Normal Chinese Male
- Hepatitis C virus: host, environmental and viral factors promoting spontaneous clearance
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Genomics
- Identification of Candidate Genes for Min Pig Villi Hair Traits by Genome-Wide Association of Copy Number Variation
- Comparing Current Therapeutic Modalities of Androgenic Alopecia: A Literature Review of Clinical Trials
- Mendelian Randomization Identifies CD25+ CD4+ Tregs and Plasma Proteins in Androgenetic Alopecia Pathogenesis
- RNA-seq analysis identifies key genes enhancing hoof strength to withstand barefoot racing in Standardbred trotters
- Erosive Lichen Planus of the Scalp and Hepatitis C Infection
- Evolution of long scalp hair in humans
- ST Premature Graying Hair in Seven Years Old Children
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Androgenetic alopecia
- Genome-Wide Association Studies for Immunoglobulin Concentrations in Colostrum and Serum in Chinese Holstein
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Supplementary Material for: Polymorphic CAG Repeat Numbers in the Androgen Receptor Gene of Female Pattern Hair Loss in a Han Chinese Population
- Widespread Dystrophic-Anagen Alopecia and Drug Eruption due to Usage of PEG-IFN ?-2a /Ribavirin Combination Therapy
- Senescent alopecia (“senile alopecia” or “senescent balding”)
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Selenoproteins Are Essential for Proper Keratinocyte Function and Skin Development