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Research 541–570 of 1000+
- Prolactin Signaling Influences the Timing Mechanism of the Hair Follicle: Analysis of Hair Growth Cycles in Prolactin Receptor Knockout Mice
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Cell Polarization Defects in Early Heart Development
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.
- A newborn presenting with congenital blistering
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- 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
- Investigation of the association of the MLPH gene with seasonal canine flank alopecia in Rhodesian Ridgeback dogs
- 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
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Glutathione S-transferase gene polymorphism, total antioxidant status, and blood pressure changes in androgenic alopecia
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Male sex hormone and reduced plakoglobin jointly impair atrial conduction and cardiac sodium currents
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- A Neonate with Blisters
- A direct link between<i>Prss53</i>, hair curvature, and skeletal dysplasia