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Research 691–720 of 1000+
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Melanocytes: The new Black
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Senescence-accelerated Mouse (SAM): With Special Reference to Development and Pathobiological Phenotypes
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Exome-wide age-of-onset analysis reveals exonic variants in ERN1 and SPPL2C associated with Alzheimer’s disease
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Phenotypic, transcriptomic, and genomic analyses reveal the spatiotemporal patterns and associated genes of coarse hair density in goats
- Hair Follicle-Related MicroRNA-34a Serum Expression and rs2666433A/G Variant in Patients with Alopecia: A Cross-Sectional Analysis
- Male androgenetic alopecia
- 1301 STIM1, but not STIM2, is the calcium sensor critical for sweat secretion
- Cyberspace Chat
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- A clinical case of CNOT3 syndrome in a 10-year-old girl
- Primary Follicular Dystrophy With Scarring Dermatitis in C57BL/6 Mouse Substrains Resembles Central Centrifugal Cicatricial Alopecia in Humans
- Variation in human hair ultrastructure among three biogeographic populations
- The possible implication of the S250C variant of the autoimmune regulator protein in a patient with autoimmunity and immunodeficiency: in silico analysis suggests a molecular pathogenic mechanism for the variant
- High‐Sulfur Protein Gene Expression in a Transgenic Mouse
- Association of estrogen receptor gene variants (ESR1 and ESR2) with polycystic ovary syndrome in Tunisia
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- Drivers of plateau adaptability in cashmere goats revealed by genomic and transcriptomic analyses
- Acne Tarda and Male-Pattern Baldness Unmasking Primary Ovarian Insufficiency: A Case and Review
- REVIEW ON PREMATURELY GREYING OF HAIR IN CHILDREN: CLINICAL ASPECTS, ETIOPATHOGENESIS AND HOMOEOPATHIC MANAGEMENT
- Integrative mRNA and lncRNA Transcriptome Analysis of Skin Tissues with Different Coat Types in Cashmere Goats Across Stages of Hair Follicle Development
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Supplementary Material for: Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping