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Research 151–180 of 1000+
- Skin Development and Disease: A Molecular Perspective
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- A New Case of Isolated Trichothiodystrophy
- New-Onset Gastrointestinal Polyposis
- Hair Shaft Dysplasias
- Morpho-Regulation of Ectodermal Organs
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- Identification of dkk4 as a target of Eda-A1/Edar pathway reveals an unexpected role of ectodysplasin as inhibitor of Wnt signalling in ectodermal placodes
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- The Wnt inhibitor, Dickkopf 4, is induced by canonical Wnt signaling during ectodermal appendage morphogenesis
- Epidermal Dysplasia and Abnormal Hair Follicles in Transgenic Mice Overexpressing Homeobox Gene MSX-2
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Expression of Hex during feather bud development
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- 1435 Dynamic morphogen-p63 chromatin interactions that guide epigenetic changes and p63 activity in surface ectoderm commitment
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Connexin mutations in human disease
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Hair shaft disorders in children – An update
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Molecular biology of hair morphogenesis: Development and cycling
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome