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Research 211–240 of 1000+
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Diagnostic approach to low‐renin hypertension
- CAG Repeat Testing of Androgen Receptor Polymorphism: Is This Necessary for the Best Clinical Management of Hypogonadism?
- Identification and dissection of an enhancer controlling epithelial gene expression in skin
- The VEGF +405 G>C 5' untranslated region polymorphism and risk of PCOS: a study in the South Indian Women
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Genetic basis of polycystic ovary syndrome
- Basal Cell Carcinoma, Hedgehog Signaling, and Targeted Therapeutics: The Long and Winding Road
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- The hair shaft: normality, abnormality, and genetics
- The relationship among androgens, insulin resistanceand ghrelin polymorphisms in post-adolescent malepatients with severe acne vulgaris
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Candidate Gene Analysis Of Alopecia Areata In Jordanian Population Of Arab Descent: A Case–Control Study
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Deletions in the <i>KAP6-1</i> gene are associated with fiber traits in cashmere-producing goats
- The potential of androgenic alopecia management from plant derivatives
- The Telomerase Reverse Transcriptase (TERT) Gene Molecular Characterization in Sheep and the Association of Its Variation with Wool Traits
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- RORA Regulates Autophagy in Hair Follicle Stem Cells by Upregulating the Expression Level of the Sqstm1 Gene
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Molecular mechanisms of Y chromosome loss and <i>UTY</i> gene activity
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- The Relation of the SHBG Gene Polymorphism (rs1799941) with PCOS in a Group of Iraqi Women
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Inherited Epidermolysis Bullosa: A Clinical Case