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Research 361–390 of 1000+
- Montagna Symposium 2014—Skin Aging: Molecular Mechanisms and Tissue Consequences
- Seasonal Variability in Transcript Expression of Type I and Type II Keratins in Wool Follicles of Lustrous Fleece-Producing Magra Sheep
- Comprehensive Genomic Profiling of Cutaneous Adnexal Carcinomas: A Genomic Landscape Study
- Molecular Mechanisms Regulating Hair Follicle Development
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Activator Protein-1 Activity Regulates Epithelial Tumor Cell Identity
- Targeted Disruption of Stat3 Reveals a Major Role for Follicular Stem Cells in Skin Tumor Initiation
- Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment
- β1 Integrins with Individually Disrupted Cytoplasmic NPxY Motifs Are Embryonic Lethal but Partially Active in the Epidermis
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- PCSK9: From Nature’s Loss to Patient’s Gain
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Identification of the Keratin-Associated Protein 22-2 Gene in the Capra hircus and Association of Its Variation with Cashmere Traits
- Rare and Underappreciated Causes of Polycystic Ovarian Syndrome
- K25 (K25irs1), K26 (K25irs2), K27 (K25irs3), and K28 (K25irs4) Represent the Type I Inner Root Sheath Keratins of the Human Hair Follicle
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- 312 CRISPR/Cas9-based targeted genome editing for correction of recessive dystrophic epidermolysis bullosa using iPS cells
- Chrousos syndrome: from molecular pathogenesis to therapeutic management