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Research 541–570 of 1000+
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Skin diseases associated with atopic dermatitis
- Conversion of the Nipple to Hair-Bearing Epithelia by Lowering Bone Morphogenetic Protein Pathway Activity at the Dermal-Epidermal Interface
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- The Functional Relevance of the Type 1 Cytokines IFN-γ and IL-2 in Alopecia Areata of C3H/HeJ Mice
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Prolactin Signaling Influences the Timing Mechanism of the Hair Follicle: Analysis of Hair Growth Cycles in Prolactin Receptor Knockout Mice
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Cell Polarization Defects in Early Heart Development
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets
- A newborn presenting with congenital blistering
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Genetic Susceptibility to Alopecia
- Identification of a Novel MPL Loss of Function Mutation in a Patient with Cyclic Thrombocytopenia and Characterization of This Syndrome
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Homologous recombination induced by doxazosin mesylate and saw palmetto in the <i>Drosophila</i> wing‐spot test
- Highly Conserved Keratin-Associated Protein 7-1 Gene in Yak, Taurine and Zebu Cattle
- Spatial Gene Profiling in the Ischemic Heart
- Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia
- Jojoba (Simmondsia chinensis (Link) Schneider): An important Medicinal Plant- The Gold of the Desert
- Unravelling the threads of central centrifugal cicatricial alopecia
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- Glutathione S-transferase gene polymorphism, total antioxidant status, and blood pressure changes in androgenic alopecia
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report