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Research 631–660 of 1000+
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Dickkopf-1 Expression in Androgenetic Alopecia and Alopecia Areata in Male Patients
- Epigenetic regulation of 5α reductase-1 underlies adaptive plasticity of reproductive function and pubertal timing
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Spectrum of Phenotypes Associated with Human MC1R Variations
- Increasing GSH-Px Activity and Activating Wnt Pathway Promote Fine Wool Growth in FGF5-Edited Sheep
- Are STK11 polymorphisms a predictor of the response to metformin in polycystic ovarian syndrome?
- Induction of basal cell carcinomas and trichoepitheliomas in mice overexpressing GLI-1
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Intelligent nanotherapeutic strategies for the delivery of CRISPR system
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury
- Alkaline Ceramidase 1 Protects Mice from Premature Hair Loss by Maintaining the Homeostasis of Hair Follicle Stem Cells
- Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- The RpoS Gatekeeper in Borrelia burgdorferi: An Invariant Regulatory Scheme That Promotes Spirochete Persistence in Reservoir Hosts and Niche Diversity
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Thyroxine Differentially Modulates the Peripheral Clock: Lessons from the Human Hair Follicle
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Profibrotic Molecules Are Reduced in CRISPR-Edited Emery–Dreifuss Muscular Dystrophy Fibroblasts
- Decision letter: Human biallelic MFN2 mutations induce mitochondrial dysfunction, upper body adipose hyperplasia, and suppression of leptin expression
- Characterization of DNA Methylation and Screening of Epigenetic Markers in Polycystic Ovary Syndrome
- A symphony of signals: the intricate role of lncRNAs in dermatological disorders
- Identification of Potential miRNA–mRNA Regulatory Network Associated with Growth and Development of Hair Follicles in Forest Musk Deer