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Research 211–240 of 1000+
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Structural and epistatic regulatory variants cause hallmark white spotting in cattle
- Genetic association of wool quality characteristics in United States Rambouillet sheep
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Establishment of an in vitro hairless guinea pig dermal model
- Proteomic Analysis of Two Stem Cell Secretomes Used in Combination in a Topical Skin Care Product That Has Demonstrated Efficacy in a Double-Blinded, Vehicle-Controlled Clinical Trial
- Resequencing Analyses Revealed Genetic Diversity and Selection Signatures during Rabbit Breeding and Improvement
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Editor's evaluation: Plant Trans-Golgi Network/Early Endosome pH regulation requires Cation Chloride Cotransporter (CCC1)
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Role of the Wnt signaling pathway in keratoacanthoma
- 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies
- 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation
- 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis
- Morpho-Regulation of Ectodermal Organs
- Cellular senescence in tissue repair: every cloud has a silver lining
- Computational derivation of a molecular framework for hair follicle biology from disease genes
- 9 Role of 5α-reductase in health and disease
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Inherited Disorders of the Hair
- Prediction of male-pattern baldness from genotypes
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Unravelling the link between insulin resistance and androgen excess
- Cartilage to bone transformation during fracture healing is coordinated by the invading vasculature and induction of the core pluripotency genes
- Trans‐species hair growth induction by human hair follicle dermal papillae
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- LRIG1 is a positive prognostic marker in Merkel cell carcinoma and Merkel cell carcinoma expresses epithelial stem cell markers