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Research 541–570 of 1000+
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Reshaped DNA methylation cooperating with homoeolog‐divergent expression promotes improved root traits in synthesized tetraploid wheat
- Skin-infiltrating CD4+ lymphoma cells depend on hair follicle-derived IL-7
- Mutations in Sterol O-Acyltransferase 1 (Soat1) Result in Hair Interior Defects in AKR/J Mice
- Loss of PIKFyve Kinase Function Driven by Platelet Factor 4 Promoter Results in Platelet Lysosomal Storage Defects and Infiltration of Multiple Organs with Vacuolated Macrophages
- Novel insights into cardiocutaneous syndromes
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Functional histopathology of keloid disease.
- Transdifferentiation of corneal epithelium into epidermis occurs by means of a multistep process triggered by dermal developmental signals
- Tissue regenerative delays and synthetic lethality in adult mice after combined deletion of Atr and Trp53
- Hair Defects and Pup Loss in Mice with Targeted Deletion of the First Cut Repeat Domain of theCux/CDPHomeoprotein Gene
- Alkaline ceramidase 1 is essential for mammalian skin homeostasis and regulating whole‐body energy expenditure
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- A Splice Site Mutation in the Gene of the Human Type I Hair Keratin hHa1 Results in the Expression of a Tailless Keratin Isoform
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Effect of body mass index (BMI) on phenotypic features of polycystic ovary syndrome (PCOS) in Singapore women: a prospective cross-sectional study
- Physical inactivity is a disease synonymous for a non-permissive brain disorder
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- Assessment of anogenital distance as a diagnostic tool in polycystic ovary syndrome
- Electrophoretic variability in human head hair: Polyacrylamide gel electrophoresis of hair proteins in the presence of sodium dodecyl sulfate and urea
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Gonadal Dysgenesis: Associations between Clinical Features and Sex of Rearing.
- Progranulin, a secreted tumorigenesis and dementia-related factor, regulates mouse hair growth
- A Comprehensive Approach in Diagnosing the Polycystic Ovary Syndrome
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- The Use of Stem Cell Differentiation Stage Factors (SCDSFs) Taken from Zebrafish Embryos during Organogenesis and Their Role in Regulating the Gene Expression of Normal and Pathological (Stem) Cells
- A new in vitro culture system to produce a fully differentiated epidermis from human hair follicle outer root sheath cells
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele