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Research 511–540 of 1000+
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- The Naked (N) Mutation, Chromosome 15
- Strange cutaneous abnormalities and polyposis in an Asiatic man
- Hair Loss in Children, Etiologies, and Treatment
- El teorema del 0,7 o el otro teorema de Pitágoras
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- Onset of Keratin 17 Expression Coincides with the Definition of Major Epithelial Lineages during Skin Development
- Hair structure anatomy and comparative anatomy1 1Dedicated to the memory of the late Dr. R. E. Rivett whose untimely death prevented his role in co-authorship.
- Expression of COUP-TF-interacting protein 2 (CTIP2) in mouse skin during development and in adulthood
- Expression Profiling Reveals Genes Involved in the Regulation of Wool Follicle Bulb Regression and Regeneration in Sheep
- HOXC8 initiates an ectopic mammary program by regulating Fgf10 and Tbx3 expression, and Wnt/β-catenin signaling
- Integumentary System
- Effects of Collagen Peptides on Gene Expression Related to Hair Cycle Activation in the Skin
- Edar Signaling in the Control of Hair Follicle Development
- 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
- Expression of Hex during feather bud development
- Suppression of hair follicle development inhibits induction of sonic hedgehog, patched, and patched-2 in hair germs in mice
- Store-operated calcium channels in skin
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Investigating the roles of cellular senescence in embryogenesis and aging
- 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
- A new type of pachyonychia congenita.
- Ugreelig hår