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Research 751–780 of 803
- Betaine supplementation is less effective than methionine restriction in correcting phenotypes of CBS deficient mice
- Identification of Drug-Disease Associations Using Information of Molecular Structures and Clinical Symptoms via Deep Convolutional Neural Network
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Hairless Plays a Role in Formation of Inner Root Sheath via Regulation of Dlx3 Gene
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Hairless down-regulates expression of Msx2 and its related target genes in hair follicles
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Hair follicle stem cell progeny heal blisters while pausing skin development
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Ontogeny of Skin Stem Cells and Molecular Underpinnings
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Nutritional Disorders of the Hair and Their Management
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Desmogleins: Hair perspective
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- The incidental pore: Ca<sub>V</sub>1.2 and stem cell activation in quiescent hair follicles
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Immunostaining study of cytokeratins in human hair follicle development
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