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Research 211–240 of 1000+
- The metabolic syndrome- associated small G protein ARL15 plays a role in adipocyte differentiation and adiponectin secretion
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Congenital adrenal hyperplasia
- Australasian Society for Dermatology Research Meeting, May 2006
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Morphological Approach to Hair Disorders
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Inherited Disorders of the Hair
- Genetic Defects of Female Sexual Differentiation
- Syndromes of Severe Insulin Resistance (SSIRs)
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Biology and Genetics of Hair
- How to diagnose a lipodystrophy syndrome
- Dermatopathology and molecular genetics
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- Current Genetics in Hair Diseases
- FGF5 is a crucial regulator of hair length in humans
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- 5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
- Clinical features and genetic analysis of acrodermatitis enteropathica in an ethnic minority infant from Western China: a case report and literature review
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Recently Identified Forms of Epidermolysis Bullosa
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Genetically separable determinants of hair keratin gene expression