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Research 661–690 of 1000+
- Corticotropin releasing hormone and the skin
- Targeted Inactivation of Gh/Tissue Transglutaminase II
- ERG induces androgen receptor-mediated regulation of SOX9 in prostate cancer
- Activation of β-catenin signaling programs embryonic epidermis to hair follicle fate
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- The role of VEGF and thrombospondins in skin angiogenesis
- Zeb2 recruits HDAC–NuRD to inhibit Notch and controls Schwann cell differentiation and remyelination
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Identification of reptilian genes encoding hair keratin-like proteins suggests a new scenario for the evolutionary origin of hair
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- The Krüppel-like Factor Epiprofin Is Expressed by Epithelium of Developing Teeth, Hair Follicles, and Limb Buds and Promotes Cell Proliferation
- m6A Methylation Analysis of Differentially Expressed Genes in Skin Tissues of Coarse and Fine Type Liaoning Cashmere Goats
- Novel Type I Hair Keratins K39 and K40 Are the Last to be Expressed in Differentiation of the Hair: Completion of the Human Hair Keratin Catalog
- Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation
- FLCN, a novel autophagy component, interacts with GABARAP and is regulated by ULK1 phosphorylation
- Gsdma3 Mutation Causes Bulge Stem Cell Depletion and Alopecia Mediated by Skin Inflammation
- Characterization of Human KAP24.1, A Cuticular Hair Keratin-Associated Protein with Unusual Amino-Acid Composition and Repeat Structure
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- 17 beta-hydroxysteroid dehydrogenase 3 deficiency in the Mediterranean population.
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Neural Wiskott-Aldrich syndrome protein modulates Wnt signaling and is required for hair follicle cycling in mice
- Intermittent treatment with farnesyltransferase inhibitor and sulforaphane improves cellular homeostasis in Hutchinson-Gilford progeria fibroblasts
- Comparative genome analyses reveal the unique genetic composition and selection signals underlying the phenotypic characteristics of three Chinese domestic goat breeds
- Keratinocyte-derived follistatin regulates epidermal homeostasis and wound repair
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- Integrated analysis of lncRNAs and mRNAs by RNA-Seq in secondary hair follicle development and cycling (anagen, catagen and telogen) of Jiangnan cashmere goat (Capra hircus)
- Characterisation of an Ovine Keratin Associated Protein (KAP) Gene, Which Would Produce a Protein Rich in Glycine and Tyrosine, but Lacking in Cysteine
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions