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Research 121–150 of 1000+
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Androgenetic alopecia: a case report and family survey
- The 5 Alpha-Reductase Isozyme Family: A Review of Basic Biology and Their Role in Human Diseases
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Azithromycin and Roxithromycin define a new family of “senolytic” drugs that target senescent human fibroblasts
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- The human type I keratin gene family: Characterization of new hair follicle specific members and evaluation of the chromosome 17q21.2 gene domain
- A small multigene hydroxyproline-O-galactosyltransferase family functions in arabinogalactan-protein glycosylation, growth and development in Arabidopsis
- Tumor Mapping in 2 Large Multigenerational Families With CYLD Mutations
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Keratosis follicularis spinulosa decalvans in a family
- Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Inhibition of CCAAT/Enhancer Binding Protein Family DNA Binding in Mouse Epidermis Prevents and Regresses Papillomas
- Cloning of the human phenol sulfotransferase gene family: three genes implicated in the metabolism of catecholamines, thyroid hormones and drugs
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Prevalence of metabolic syndrome in the family members of women with polycystic ovary syndrome from North India
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Benign prostatic hyperplasia and male lower urinary symptoms: A guide for family physicians
- Potential use of the Asteraceae family as a cure for diabetes: A review of ethnopharmacology to modern day drug and nutraceuticals developments
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Identification and Analysis of MYB Gene Family for Discovering Potential Regulators Responding to Abiotic Stresses in Curcuma wenyujin
- Deficiency in Nucleotide Excision Repair Family Gene Activity, Especially ERCC3, Is Associated with Non-Pigmented Hair Fiber Growth
- Recurrent E413K Mutation of hHb6 in a Japanese Family with Monilethrix