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Research 121–150 of 1000+
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- A Synonymous Polymorphism of APCDD1 Affects Translation Efficacy and is Associated with Androgenic Alopecia
- Transient agonism of the sonic hedgehog pathway triggers a permanent transition of skin appendage fate in the chicken embryo
- Molecular characterization of caprine<i>KRTAP13-3</i>in Liaoning cashmere goat in China
- Regional Differences in Dorsal Skin Determine the Rate of Adhesive Material-Induced Hair Regeneration
- Hormonal regulation of hair follicles exhibits a biological paradox
- Hunting the genes in male‐pattern alopecia: how important are they, how close are we and what will they tell us?
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Skin transcriptome reveals the dynamic changes in the Wnt pathway during integument morphogenesis of chick embryos
- Development and Maintenance of Epidermal Stem Cells in Skin Adnexa
- Genetic and hormonal influence on SARS-CoV-2-infection susceptibility
- Research progress on mechanisms of skin aging and anti-aging strategies
- Integration Analysis of Hair Follicle Transcriptome and Proteome Reveals the Mechanisms Regulating Wool Fiber Diameter in Angora Rabbits
- Ancient Genomes Reveal the Evolutionary History and Origin of Cashmere-Producing Goats in China
- Exploring differentially expressed genes between anagen and telogen secondary hair follicle stem cells from the Cashmere goat (Capra hircus) by RNA-Seq
- Developmental genetics of color pattern establishment in cats
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Developmental origin of polycystic ovary syndrome - a hypothesis
- Enhanced ectodysplasin-A receptor (EDAR) signaling alters multiple fiber characteristics to produce the East Asian hair form
- Chapter 3 Expression and Modification of Keratins During Terminal Differentiation of Mammalian Epidermis
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Cost-effectively dissecting the genetic architecture of complex wool traits in rabbits by low-coverage sequencing
- The potential of androgenic alopecia management from plant derivatives
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- A global analysis of CNVs in Chinese indigenous fine-wool sheep populations using whole-genome resequencing
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü