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Research 631–660 of 1000+
- 1440 DNA dioxygenases Tet2/3 regulate gene promoter accessibility and chromatin topology in lineage-specific loci to control keratinocyte differentiation and hair growth
- Deletion of the Developmentally Essential Gene ATR in Adult Mice Leads to Age-Related Phenotypes and Stem Cell Loss
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Clinical Snippets
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Decay of Skin-Specific Gene Modules in Pangolins
- Systematic analysis of somatic mutations driving cancer: uncovering functional protein regions in disease development
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- A Ca <sup>2+</sup> /calmodulin-dependent protein kinase required for symbiotic nodule development: Gene identification by transcript-based cloning
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- The <i>IRE</i> gene encodes a protein kinase homologue and modulates root hair growth in <i>Arabidopsis</i>
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- A variant of the glucocorticoid receptor gene is not associated with adrenal androgen excess in women with polycystic ovary syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Correlation Analysis of BLTP1 (KIAA1109) and KIF27 Gene Polymorphisms with Wool Traits in Subo Merino Sheep
- Correlation analysis of four KRTAP gene polymorphisms and cashmere fiber diameters in two cashmere goat breeds
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Study on the zona pellucida 4 (ZP4) gene sequence and its expression in the ovaries of patients with polycystic ovary syndrome
- The heme-responsive PrrH sRNA regulates <i>Pseudomonas aeruginosa</i> pyochelin gene expression
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Convergent Decay of Skin-specific Gene Modules in Pangolins