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Research 31–60 of 1000+
- Genetic Analysis of Androgen Receptors in Development and Disease
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- 197 A novel splice site mutation in LIPH identified in a Japanese patient with autosomal recessive woolly hair
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic
- Management of a Refractory EIF3E-RSPO2 Fusion Positive Pilomatrical Cancer Patient with Encyclopedic Tumor Analysis Guided Treatment
- Stem cell identification-<i>in vivo</i> lineage analysis versus <i>in vitro</i> isolation and clonal expansion
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
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- Evolution of hard proteins in the sauropsid integument in relation to the cornification of skin derivatives in amniotes
- Gsdma3 is required for hair follicle differentiation in mice
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Brief study of hypertrichosis
- Molecular genetics of androgen insensitivity
- Skin diseases associated with atopic dermatitis
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- At the Root: Cutaneous Langerhans Cell Histiocytosis