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Research 541–570 of 1000+
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Depression from a physical symptom.
- Signaling pathways in hair aging
- More than one way to skin . . .
- Keratin 17 modulates hair follicle cycling in a TN<i>Fα</i>-dependent fashion
- 9 Pilosebaceous physiology in relation to hirsutism and acne
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Le gène<i>hairless</i>de la souris
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Woolly Antics between the Sheaths
- ARHGEF3 Regulates Hair Follicle Morphogenesis
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Role of skin enzymes in metabolism of topical drugs
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- 376 Tsc2 disruption in mesenchymal progenitors regulates hair follicles and TGF beta signaling
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Uterus Hyperplasia and Increased Carcinogen-Induced Tumorigenesis in Mice Carrying a Targeted Mutation of the Chk2 Phosphorylation Site in Brca1
- Genetically modified laboratory mice with sebaceous glands abnormalities
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Multiple cell types guided by neurocytes orchestrate horn bud initiation in dairy goats
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Keratin disorders: from gene to therapy
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Disturbed Keratinocyte Differentiation in Transgenic Mice and Organotypic Keratinocyte Cultures as a Result of Spermidine/Spermine N1-Acetyltransferase Overexpression
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load