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Research 361–390 of 1000+
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Immunopharmacological potential of Arctium lappa L. in immune-mediated skin diseases: A critical review of experimental and clinical evidence
- Pediatric adrenocortical carcinoma complicated by uric acid nephrolithiasis: a unique case report
- Deep Hair Phenomics: Implications in Endocrinology, Development, and Aging
- Effects of Biomaterials Derived from Germinated Hemp Seeds on Stressed Hair Stem Cells and Immune Cells
- Differences in Demographic and Clinical Characteristics Among Subtypes of Female Pattern Hair Loss
- Acne Vulgaris
- Hair Sciences: The hair cycle discussed with Dr. Gilliam Westgate
- Women’s hair loss: pathophysiological, diagnostic and therapeutic aspects
- Androgenic alopecia and dutasteride in hair mesotherapy: A short review
- New approach to the understanding of keloid: psychoneuroimmune–endocrine aspects
- Prevalence and characteristics of polycystic ovary syndrome in Brazilian women: protocol for a nation-wide case–control study
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- Hair follicle culture—a historical perspective
- Synthetically programmed antioxidant delivery by a domesticated skin commensal
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Skin transcriptomic and selection signature analyses identify ASIP as a key gene in cattle coat color determination
- Melanocytes: The new Black
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- A single-cell transcriptomic atlas elucidates the hair cycle and apoptosis mechanisms in goat hair follicles
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Congenital adrenal hyperplasia
- sc-eQTL unveil immunogenetic architecture of polycystic ovary syndrome
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness