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Research 481–510 of 1000+
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Regulation of feather follicle development and Msx2 gene SNP degradation in Hungarian white goose
- A computationally inferred regulatory heart aging model including post-transcriptional regulations
- SPT6 maintains epidermal homeostasis by inhibiting an NF-κB-positive feedback loop to prevent excessive inflammation
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- The Impact of Vitamin D Receptor Gene Polymorphisms (FokI, ApaI, TaqI) in Correlation with Oxidative Stress and Hormonal and Dermatologic Manifestations in Polycystic Ovary Syndrome
- Investigating the role of obesity, circadian disturbances and lifestyle factors in people with schizophrenia and bipolar disorder: Study protocol for the SOMBER trial
- Is polymorphism of the STK11 gene a predictor of response to metformin in polycystic ovarian syndrome?
- Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Alopecia areata susceptibility variant identified by MHC risk haplotype sequencing reproduces symptomatic patched hair loss in mice
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Australasian Society for Dermatology Research Meeting, May 2006
- Genetic basis of polycystic ovary syndrome
- Association between <i>VEGF</i> gene polymorphisms (11 sites) and polycystic ovary syndrome risk
- Effect of the FA2H Gene on cashmere fineness of Jiangnan cashmere goats based on transcriptome sequencing
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- An Update of Congenital Adrenal Hyperplasia
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Calcitonin gene‐related peptide (CGRP) may award relative protection from interferon‐γ‐induced collapse of human hair follicle immune privilege
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Aromatase deficiency in a male patient - Case report and review of the literature.
- Identification of the keratin-associated protein 13-3 (KAP13-3) gene in sheep