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Research 61–90 of 1000+
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Acne
- CAG polymorphism in the androgen receptor gene in women may be associated with nodulocystic acne
- Prediction of male-pattern baldness from genotypes
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Significance of the polyglutamine tract polymorphism in the androgen receptor
- The ITGB6 gene: its role in experimental and clinical biology
- Identification and characterization of an antisense RNA transcript (gfg) from the human basic fibroblast growth factor gene.
- Analysis of lncRNAs Expression Profiles in Hair Follicle of Hu Sheep Lambskin
- Medical Treatment of Alopecia
- Combination of Transcriptomics and Proteomics Reveals Differentially Expressed Genes and Proteins in the Skin of EDAR Gene-Targeted and Wildtype Cashmere Goats
- Clinicopathologic and molecular characterization of a series of sporadic trichoblastic neoplasms
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Large-Scale, Multicenter, Prospective Registry Study of Ripretinib in Advanced GIST: A Real-World Study from China
- No improvement in male-pattern hair loss using laser hair-comb therapy: a 6-month, half-head, assessor-blinded investigation in two men
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Androgen Receptor Polymorphism-Dependent Variation in Prostate-Specific Antigen Concentrations of European Men
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- What does acne genetics teach us about disease pathogenesis?
- CYP21A2 Mutations in Women with Polycystic Ovary Syndrome (PCOS)
- 192 MicroRNAs and their regulatory interactions in the human hair follicle