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Research 811–840 of 1000+
- Wound Healing Impairment in Type 2 Diabetes Model of Leptin-Deficient Mice—A Mechanistic Systematic Review
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- The Hairless Phenotype of the Hirosaki Hairless Rat Is Due to the Deletion of an 80-kb Genomic DNA Containing Five Basic Keratin Genes
- Difficult and rare forms of acne
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: “D-CHRAMPS syndrome”
- PNKP is required for maintaining the integrity of progenitor cell populations in adult mice
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Molecular mechanism of ligand recognition and activation of lysophosphatidic acid receptor LPAR6
- Unusual symptoms of iron deficiency anemia (2 clinical observations)
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Navaratnas in Dermatology
- Effects of Androgen Treatment on Growth in Patients with 5-α-Reductase Type 2 Deficiency
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Skin-specific regulation of SREBP processing and lipid biosynthesis by glycerol kinase 5
- A rare case of woolly hair with unusual associations
- Discovery of Four New<em> FGF5</em> Variants Causing Long Hair in the Dog
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Trichoscopy in genetic hair shaft abnormalities
- WNT10A promotes an invasive and self-renewing phenotype in esophageal squamous cell carcinoma
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle