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Research 901–930 of 1000+
- Hutchinson-Gilford Progeria Syndrome: Premature Aging
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Bachmann–Bupp syndrome and treatment
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics
- Functional redundancy of <i>Frizzled 3</i> and <i>Frizzled 6</i> in planar cell polarity control of mouse hair follicles
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches
- An LRH-RSL4 feedback regulatory loop controls the determinate growth of root hairs in Arabidopsis
- Genome wide association analysis of root hair traits in rice reveals novel genomic regions controlling epidermal cell differentiation
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Nucleocytoplasmic Communication in Progeria
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Strontium ranelate promotes chondrogenesis through inhibition of the Wnt/β-catenin pathway
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- The 1,25-dihydroxyvitamin D3-independent actions of the vitamin D receptor in skin
- EGFR Controls Hair Shaft Differentiation in a p53-Independent Manner
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”