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Research 481–510 of 1000+
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Lactate dehydrogenase activity drives hair follicle stem cell activation
- Genetic Basis of Male Pattern Baldness
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Epithelial Integrity Is Maintained by a Matriptase-Dependent Proteolytic Pathway
- Congenital Adrenal Hyperplasia
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Characterization of hairless (Hr) and FGF5genes provides insights into the molecular basis of hair loss in cetaceans
- Lysophospholipid Mediators in Health and Disease
- Peripheral Skin Temperature and Circadian Biological Clock in Shift Nurses after a Day off
- CD34 defines melanocyte stem cell subpopulations with distinct regenerative properties
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Differences in reproductive toxicology between alopecia drugs: an analysis on adverse events among female and male cases
- Minoxidil may suppress androgen receptor-related functions
- Development of Autoimmune Hair Loss Disease Alopecia Areata Is Associated with Cardiac Dysfunction in C3H/HeJ Mice
- Androgen Receptor Copy Number Variation and Androgenetic Alopecia: A Case-Control Study
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Androgen receptor CAG repeat length is associated with ovarian reserve but not with ovarian response
- Examination of epigenetic inhibitor zebularine in treatment of skin wounds in healthy and diabetic mice
- Bald thigh syndrome in sighthounds—Revisiting the cause of a well-known disease
- Assessment of hair and cashmere properties and their genetic background of several goat breeds in Southwest China
- Skin regional specification and higher-order <i>HoxC</i> regulation
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Combined Systemic and Cutaneous Ovalbumin–Aluminum Sensitization Triggers Thermal Hyperalgesia, Spinal Gliosis, and Nociceptive Nerve Fibers Sprouting in Mice
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies