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Research 151–180 of 1000+
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Noninflammatory, Nonpruritic Alopecia of Horses
- Forme létale de syndrome de Netherton au sein d’une famille multiplex consanguine
- Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- [Sodium valproate-induced kinky hair].
- 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
- MmuPV1-Induced Cutaneous Squamous Cell Carcinoma Arises Preferentially from Lgr5+ Epithelial Progenitor Cells
- Dysfunction of keratinocyte adhesion
- ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Current Genetics in Hair Diseases
- What was your diagnosis?
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- p63 in skin homeostasis and disease: molecular mechanisms and therapeutic potentials
- Approach to Alopecia in Dogs in Clinical Practice
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Polarized microscopy in genetic hair disorders: case series
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- Short anagen hair syndrome is caused by mutations in the <i>WNT10A</i> gene and has a genetic overlap with male pattern hair loss
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Congenital Atrichia: A Case Report
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- Molecular Basis of Hereditary Hair Diseases
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Coat Problems
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations