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Research 511–540 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
- 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
- Approach to Alopecia in Dogs in Clinical Practice
- 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
- Molecular Basis of Hereditary Hair Diseases
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- The Naked (N) Mutation, Chromosome 15
- Index
- El teorema del 0,7 o el otro teorema de Pitágoras
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Disorders of the Hair and Scalp in Children
- Dermatological diseases from a genetic perspective
- Ectodysplasin research—Where to next?
- Identification of Ectodysplasin Target Genes Reveals the Involvement of Chemokines in Hair Development
- Expression of <i>Foxi3</i> is regulated by ectodysplasin in skin appendage placodes
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- Clinical Snippets
- Clouston syndrome associated with eccrine syringofibroadenoma
- Role of the Autoimmune Regulator (<i>AIRE</i>) gene in alopecia areata: Strong association of a potentially functional <i>AIRE</i> polymorphism with alopecia universalis
- XEDAR activates the non-canonical NF-κB pathway
- Ugreelig hår
- Research Snippets
- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil