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Research 541–570 of 1000+
- Lack of the Vitamin D Receptor is Associated with Reduced Epidermal Differentiation and Hair Follicle Growth
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- Conditional Activin Receptor Type 1B (Acvr1b) Knockout Mice Reveal Hair Loss Abnormality
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Bone vs. fat: Embryonic origin of progenitors determines response to androgen in adipocytes and osteoblasts
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Chronic overlapping pain conditions and nociplastic pain
- Tabby pattern genetics – a whole new breed of cat
- Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Two mutations at KRT74 and EDAR synergistically drive the fine-wool production in Chinese sheep
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Differential Expression and Analysis of TBX3 Gene in Skin Tissues of Dun Mongolian Horses with and Without Bider Markings
- Understanding the Intricate Pathophysiology of Psoriasis and Related Skin Disorders
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Author response: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- Decision letter: Loss of Dnmt3a and Dnmt3b does not affect epidermal homeostasis but promotes squamous transformation through PPAR-γ
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Genetically separable determinants of hair keratin gene expression
- Association of single nucleotide polymorphisms in the <i>RAB5B</i> gene 3′UTR region with polycystic ovary syndrome in Chinese Han women
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Frizzled Receptors in Development and Disease
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Rare and common genetic determinants of metabolic individuality and their effects on human health
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Genetic Prediction of Eye, Hair, and Skin Color: Forensic Applications and Challenges in Latin American Populations
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree