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Research 661–690 of 1000+
- Mice with a null mutation of the TGFα gene have abnormal skin architecture, wavy hair, and curly whiskers and often develop corneal inflammation
- WNT Signaling in the Control of Hair Growth and Structure
- Update on detection, morphology and fragility in pili annulati in three kindreds
- Culture and Differentiation of Human Hair Follicle Dermal Papilla Cells in a Soft 3D Self-Assembling Peptide Scaffold
- Transgenic rescue of desmoglein 3 null mice with desmoglein 1 to develop a syngeneic mouse model for pemphigus vulgaris
- Vitamin D receptor ablation alters skin architecture and homeostasis of dendritic epidermal T cells
- Anti-Müllerian hormone gene polymorphism is associated with androgen levels in Chinese polycystic ovary syndrome patients with insulin resistance
- Growth retardation and hair loss in transgenic mice overexpressing human H-ferritin gene
- Hutchinson-gilford progeria syndrome and its relevance to cardiovascular diseases and normal aging.
- PO:17:252 | The choice between belimumab and anifrolumab: analysis of a monocentric cohort
- An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
- THE PATTERN OF SILVER-RUSSELL SYNDROME: OWN OBSERVATION
- An Unusual Cause of Primary Amenorrhea
- Effects of the bovine slick mutation on heat stress responses and hair growth in mice
- Transgneic Endothelin 3 Regulates Murine Pigment Production and Coat Color
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration
- Clinical characteristics of polycystic ovary syndrome: investigating differences in White and South Asian women
- Prenatal diagnosis of a fetus harboring an intermediate load of the A3243G mtDNA mutation in a maternal carrier diagnosed with MELAS syndrome
- Pigmentary mosaicism: An update
- Proteomics Characterization of Primary Human Oral Epithelial Cells Using a Novel Culture Technique for Use in Tissue Regeneration
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- The keratins and their disorders
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- Remodeling of Root Growth Under Combined Arsenic and Hypoxia Stress Is Linked to Nutrient Deprivation
- Distinct mechanisms underlie pattern formation in the skin and skin appendages
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart