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Research 601–630 of 1000+
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- Development of a mouse model for Hutchinson-Gilford progeria syndrome reveal defects in adult stem cell maintenance
- Structural Stability of Wild Type and Mutated α-Keratin Fragments: Molecular Dynamics and Free Energy Calculations
- Histological and dermatoscopic description of sphynx cat skin
- Matriptase-2, A Novel Suppressor of Hepcidin.
- Molecular Mechanisms Regulating Hair Follicle Development
- Wnt/β-catenin signalling: function, biological mechanisms, and therapeutic opportunities
- Roles for Msx and Dlx homeoproteins in vertebrate development
- Induction of the hair growth phase in postnatal mice by localized transient expression of Sonic hedgehog
- Physical and Functional Interaction between the Vitamin D Receptor and Hairless Corepressor, Two Proteins Required for Hair Cycling
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Epithelial Wnt Ligand Secretion Is Required for Adult Hair Follicle Growth and Regeneration
- Genetic Disorders and Defects in Vitamin D Action
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Shh maintains dermal papilla identity and hair morphogenesis via a Noggin–Shh regulatory loop
- Agouti and Agouti-related Protein: Analogies and Contrasts
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Pax9 is required for filiform papilla development and suppresses skin-specific differentiation of the mammalian tongue epithelium
- Post-transcriptional Regulation of Keratinocyte Progenitor Cell Expansion, Differentiation and Hair Follicle Regression by miR-22