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Research 61–90 of 1000+
- Adult Onset Isolated Hypogonadotropic Hypogonadism- a Cause of Secondary Amenorrhea
- The polygenic architecture of hidradenitis suppurativa reveals signaling mechanisms that implicate epithelial remodeling
- Fortnightly review: Male pattern androgenetic alopecia
- Alopecia Areata: a Comprehensive Review of Pathogenesis and Management
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- The endocrinology of baldness
- Research Progress on External Treatment of Hashimoto Thyroiditis with Traditional Chinese Medicine
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- 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
- Hair Diseases (Alopecia Areata and Androgenetic Alopecia)
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- Data from Synergistic Function of Smad4 and PTEN in Suppressing Forestomach Squamous Cell Carcinoma in the Mouse
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Faculty Opinions recommendation of Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.
- Female Androgenetic (?) Alopecia
- Melanocytes: The new Black
- PSEUDOPELADE: AN INHERITED ALOPECIA
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Trichothiodystrophy in a child with occult learning disorder
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- Androgenetic alopecia
- Discreet monilethrix: De novo mutation on the example of polish families
- Loose Anagen Hair Syndrome in an Indian Child with Trichoscopic Features
- Identification of Genes Related to Hair Follicle Cycle Development in Inner Mongolia Cashmere Goat by WGCNA
- Investigation of the male pattern baldness major genetic susceptibility loci AR/EDA2R and 20p11 in female pattern hair loss
- Identification of Potential Hub Genes in Alopecia Areata
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals