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Research 361–390 of 1000+
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Dysfunction of keratinocyte adhesion
- MICRO-MORPHOMETRIC STUDY OF SKIN IN DEVELOPING HUMAN FETUSES AND ITS CLINICAL RELEVANCE
- Current Genetics in Hair Diseases
- 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
- 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
- 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
- Clinical report of a Holstein's calf with ichthyosis.
- The Naked (N) Mutation, Chromosome 15
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Index
- Hypotrichosis and Alopecia
- Congenital and Hereditary Skin Diseases
- Mutant Cx43 in Skin Differentiation and Disease
- A clinician's approach to canine alopecia
- El teorema del 0,7 o el otro teorema de Pitágoras
- FC‐10 Adult‐onset hair loss in Chesapeake Bay retrievers: a clinical and histological study
- N02. Hair and Nails
- Displasia folicular en un Doberman adulto de capa negra : un caso clínico