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Research 211–240 of 1000+
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Tooth, hair and claw: Comparing epithelial stem cell niches of ectodermal appendages
- Altered skin development and impaired proliferative and inflammatory responses in transgenic mice overexpressing the glucocorticoid receptor
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Trichoscopy in Hair Shaft Disorders
- Atrichia With Papular Lesions
- <i>WNT10A</i> , dermatology and dentistry
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Genetic Hair Disorders: A Review
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair and Nail Relationship
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Congenital atrichia and hypotrichosis
- Hair loss among a group of Egyptian children
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- The fundamentals of WNT10A
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Analogs of human genetic skin disease in domesticated animals
- Dysfunction of keratinocyte adhesion
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India