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Research 91–120 of 1000+
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- From structural resilience to cell specification — Intermediate filaments as regulators of cell fate
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Human iPS Cell-Derived Cell Aggregates Exhibited Dermal Papilla Cell Properties in in vitro Three-Dimensional Assemblage Mimicking Hair Follicle Structures
- Disorders of hair
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Protein and amino acid composition of hair from mice carrying the naked (<i>N</i>) gene
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- Self‐organizing hair peg‐like structures from dissociated skin progenitor cells: New insights for human hair follicle organoid engineering and Turing patterning in an asymmetric morphogenetic field
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Dynamic expression of Runx1 in skin affects hair structure
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations
- Development, Structure, and Keratin Expression in <i>C57BL/6J</i> Mouse Eccrine Glands
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Sox21 Regulates Anapc10 Expression and Determines the Fate of Ectodermal Organ
- Hair Keratin: Composition, Structure and Biogenesis
- Recent Tissue Engineering Approaches to Mimicking the Extracellular Matrix Structure for Skin Regeneration
- iPSC-based approach for human hair follicle regeneration
- Prenatal hair development: Implications for drug exposure determination
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Genetic Hair Disorders: A Review
- Neural Potential of a Stem Cell Population in the Hair Follicle
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatological diseases from a genetic perspective
- Dysfunction of keratinocyte adhesion
- Myodegeneration in EDA-A2 Transgenic Mice Is Prevented by XEDAR Deficiency
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument