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Research 751–780 of 1000+
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Skin and hair: models for exploring organ regeneration
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- GRHL3 binding and enhancers rearrange as epidermal keratinocytes transition between functional states
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Syndecan-1 Is Required to Maintain Intradermal Fat and Prevent Cold Stress
- Integrated single-cell chromatin and transcriptomic analyses of human scalp identify gene-regulatory programs and critical cell types for hair and skin diseases
- Integrated Analysis of Methylome and Transcriptome Changes Reveals the Underlying Regulatory Signatures Driving Curly Wool Transformation in Chinese Zhongwei Goats
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Telomere dysfunction impairs epidermal stem cell specification and differentiation by disrupting BMP/pSmad/P63 signaling
- Polycomb repressive complex 2 in adult hair follicle stem cells is dispensable for hair regeneration
- Short-term Efficacy of Tofacitinib, a JAK Inhibitor, in IFIH1-related Aicardi-Goutières Syndrome
- BAC-mediated gene-dosage analysis reveals a role for Zipro1 (Ru49/Zfp38) in progenitor cell proliferation in cerebellum and skin
- Identification of skin-expressed genes possibly associated with wool growth regulation of Aohan fine wool sheep
- Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics
- The retarded hair growth ( rhg ) mutation in mice is an allele of ornithine aminotransferase ( Oat )
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature
- Age-Related Changes in Hair Shaft Protein Profiling and Genetically Variant Peptides
- Stretching the limits: from homeostasis to stem cell plasticity in wound healing and cancer
- Physical and mechanical cues affecting biomaterial-mediated plasmid DNA delivery: insights into non-viral delivery systems
- Analysis of Genome DNA Methylation at Inherited Coat Color Dilutions of Rex Rabbits
- Recent advances in Forensic DNA Phenotyping of appearance, ancestry and age
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Optimal processing for proteomic genotyping of single human hairs
- Assessing protein sequencing in human single hair shafts of decreasing lengths
- Identification of the key proteins associated with different hair types in sheep and goats
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies