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Research 31–60 of 1000+
- Trichoscopy in Hair Shaft Disorders
- Expression of Hex during feather bud development
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- Connexin mutations in human disease
- Generalized Hair-Follicle Hamartoma
- Investigating the roles of cellular senescence in embryogenesis and aging
- Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations.
- Exploiting the Keratin 17 Gene Promoter To Visualize Live Cells in Epithelial Appendages of Mice
- New-Onset Gastrointestinal Polyposis
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Morpho-Regulation of Ectodermal Organs
- Transcriptome and proteome characterization of surface ectoderm cells differentiated from human iPSCs
- Functional ectodermal organ regeneration as the next generation of organ replacement therapy
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern