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Research 301–330 of 1000+
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Distinct Phenotypic and Genomic Signatures Underlie Contrasting Pathogenic Potential of Staphylococcus epidermidis Clonal Lineages
- The Female Pattern Hair Loss: Review of Etiopathogenesis and Diagnosis
- Divergent neuroactive steroid responses to stress and ethanol in rat and mouse strains: relevance for human studies
- A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients
- High-coverage genome of the Tyrolean Iceman reveals unusually high Anatolian farmer ancestry
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Elevated Dehydroepiandrosterone Sulfate Levels as the Reproductive Phenotype in the Brothers of Women with Polycystic Ovary Syndrome
- What causes acne inversa (or hidradenitis suppurativa)? – the debate continues
- A Comprehensive Review of Mammalian Pigmentation: Paving the Way for Innovative Hair Colour-Changing Cosmetics
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- The mouse hairy ears mutation exhibits an extended growth (anagen) phase in hair follicles and altered <i>Hoxc</i> gene expression in the ears
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- What causes acne inversa (or hidradenitis suppurativa)? – The debate continues
- How Our Microbiome Influences the Pathogenesis of Alopecia Areata
- A new tool for conditional gene manipulation in a subset of keratin‐expressing epithelia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Sequence Variation in Caprine KRTAP6-2 Affects Cashmere Fiber Diameter
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- Obesity in Adults: Position Statement of Polish Association for the Study on Obesity, Polish Association of Endocrinology, Polish Association of Cardiodiabetology, Polish Psychiatric Association, Section of Metabolic and Bariatric Surgery of the Association of Polish Surgeons, and the College of Family Physicians in Poland
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Evaluation of Susceptibility Genes/Loci Associated with Male Androgenetic Alopecia (MAGA) for Female-Pattern Hair Loss in a Chinese Han Population and a Brief Literature Review