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Research 451–480 of 1000+
- Autologous Platelet Concentrates in Periodontology : Science, Concept, Protocols and Clinical Applications
- Clinical analysis of 78 patients with non-classical 21-hydroxylase deficiency
- Association of eNOS and STAT6 Gene Polymorphisms with the Susceptibility of Polycystic Ovary Syndrome in South Indian Women
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- AKT2 Gene Polymorphisms, sRANKL/OPG and Hormone Measurements in Polycystic Ovarian Syndrome (PCOS) Women
- Gonads
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Epithelial Skin Biology
- Nonclassic adrenal hyperplasia
- Functional identification of the phosphorylation sites of Arabidopsis PIN-FORMED3 for its subcellular localization and biological role
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Differentiation of Adipose Derived Stem Cells by Stimulating with Extracellular Vesicles Secreted from Dermal Papilla Cells Activated with Osteogenic and Adipogenic Inducers
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Effects of the bovine slick mutation on heat stress responses and hair growth in mice
- Reduced plakoglobin increases the risk of sodium current defects and atrial conduction abnormalities in response to androgenic anabolic steroid abuse
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Birt-Hogg-Dube Syndrome with a Novel Mutation in the <i>FLCN</i> Gene
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis