Search
for
Sort by
Research 481–510 of 1000+
- How to diagnose a lipodystrophy syndrome
- Analysis of the FGF gene family provides insights into aquatic adaptation in cetaceans
- Dermatopathology and molecular genetics
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Combined hormonal contraception and venous thromboembolism
- 5-Alpha reductase deficiency
- Morphological Approach to Hair Disorders
- The hair shaft: normality, abnormality, and genetics
- Cardiac biopsy in myocarditis
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Premature aging syndromes: From patients to mechanism
- 14-3-3σ Is Required for Club Hair Retention
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Piecing together the pigment-type switching puzzle
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- CRISPR/Cas9-mediated Generation of<i>COL7A1</i>-deficient Keratinocyte Model of Recessive Dystrophic Epidermolysis Bullosa
- An unusual presentation of X-linked adrenoleukodystrophy
- FOXN1 deficient nude severe combined immunodeficiency
- An unexpected role for keratin 10 end domains in susceptibility to skin cancer
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- The disruption of Sox21-mediated hair shaft cuticle differentiation causes cyclic alopecia in mice
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Converging physiological roles of the anthrax toxin receptors