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Research 181–210 of 1000+
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Toxicity assessment of the green Dunaliella salina microalgae
- Telomere Dynamics and Telomerase in the Biology of Hair Follicles and their Stem Cells as a Model for Aging Research
- Congenital atrichia associated with situs inversus and mesocardia
- Dyslipidaemia in women with polycystic ovary syndrome referred to a teaching hospital in Cape Town, South Africa
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Nutritional roles of selenium in cellular and mouse aging
- This Month in the Journal
- Recurrent implantation failure: A comprehensive summary from etiology to treatment
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Impaired wound healing in transgenic mice overexpressing the activin antagonist follistatin in the epidermis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Lymphotoxin-β regulates periderm differentiation during embryonic skin development
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Serum anti-Müllerian hormone as a predictor of polycystic ovarian syndrome among women of reproductive age
- The genetics of autism and steroid-related traits in prenatal and postnatal life
- Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome
- Hair Sciences: An interview with Dr. Rodney Sinclair on female pattern hair loss
- The Use of Adipose-Derived Stem Cells in Selected Skin Diseases (Vitiligo, Alopecia, and Nonhealing Wounds)
- Collagen-Heparin-FGF2-VEGF Scaffolds Induce a Regenerative Gene Expression Profile in a Fetal Sheep Wound Model
- The PDGF/PDGFR pathway as a drug target