Search
for
Sort by
Research 30 of 63
- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- The E6/E7 oncogenes of human papilloma virus and estradiol regulate hedgehog signaling activity in a murine model of cervical cancer
- In vitro skin models to study epithelial regeneration from the hair follicle
- The human keratins: biology and pathology
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Keratin disorders: from gene to therapy
- Differentiation of Mouse Induced Pluripotent Stem Cells into a Multipotent Keratinocyte Lineage
- Control of pelage hair follicle development and cycling by complex interactions between follistatin and activin
- Beyond Expectations
- Convergent Evolution of Cysteine-Rich Keratins in Hard Skin Appendages of Terrestrial Vertebrates
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- UNCONVENTIONAL PROTEIN SECRETION OF KERATIN 75 BY AMELOBLASTS IN VIVO
- Adenomatous Polyposis Coli (APC) Is Required for Normal Development of Skin and Thymus
- Modulation of Hair Growth with Small Molecule Agonists of the Hedgehog Signaling Pathway
- Thymosin β<sub>4</sub>increases hair growth by activation of hair follicle stem cells
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Characterization of a 300 kbp Region of Human DNA Containing the Type II Hair Keratin Gene Domain
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- Transcriptional regulation analysis and the potential transcription regulator site in the extended KAP6.1 promoter in sheep
- Building Models for Keratin Disorders
- Keratins of the Human Hair Follicle
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia