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Research 181–210 of 1000+
- A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease
- P56 Azathioprine-induced alopecia totalis and knuckle hyperpigmentation in a child with uveitis: test before you leap!
- LB1007 Systemic treatment with a KLK5 inhibitor shows efficacy in a murine model of Netherton syndrome
- The Naked (N) Mutation, Chromosome 15
- 190 Deficiency of the Human Cysteine Protease Inhibitor Cystatin M/E Causes Hypotrichosis and Dry Skin
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia
- Claudin tight junctionwhat's your function? The role of Claudin 6 in epidermal and hair follicle differentiation
- Neurochemical and Immunocytochemical Studies of Catecholamine System in the Brindled Mouse
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- 921 Generation of a new rodent model of scleroderma
- Abstract C4: Sp2: A regulator of stem cell differentiation and tumorigenesis
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- HSD3B1 Genotypes Conferring Adrenal-Restrictive and Adrenal-Permissive Phenotypes in Prostate Cancer and Beyond
- The ITGB6 gene: its role in experimental and clinical biology
- Genetically separable determinants of hair keratin gene expression
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Adam10 haploinsufficiency causes freckle-like macules in Hairless mice
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- Association of Gly972Arg variant of insulin receptor subtrate-1 and Gly1057Asp variant of insulin receptor subtrate-2 with polycystic ovary syndrome in the Chinese population
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- [Hirsutism and hypertrichosis in adults: investigations and treatment].