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Research 481–510 of 1000+
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- In vivo function of VDR in gene expression-VDR knock-out mice
- Genetically separable determinants of hair keratin gene expression
- An X-Linked Gene Involved in Androgenetic Alopecia: A Lesson to Be Learned from Adrenoleukodystrophy
- Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- Current Genetics in Hair Diseases
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Research Snippets
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Defective control of growth rate and cell diameter in tip-growing root hairs of the<i>rhd4</i>mutant of<i>Arabidopsis thaliana</i>
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Transcriptome Meta-Analysis Confirms the Hidradenitis Suppurativa Pathogenic Triad: Upregulated Inflammation, Altered Epithelial Organization, and Dysregulated Metabolic Signaling
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Editors' Picks
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Immune deficiency–related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiency
- Expanding the Phenotypic Spectrum of Olmsted Syndrome
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Deimination in epidermal barrier and hair formation
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes