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Research 391–420 of 1000+
- Complex Changes in the Apoptotic and Cell Differentiation Programs during Initiation of the Hair Follicle Response to Chemotherapy
- The Mechanisms of Fur Development and Color Formation in American Mink Revealed Using Comparative Transcriptomics
- In That Issue: Proceedings From the Third Intercontinental Meeting of Hair Research Societies
- Influence of TRPV3 mutation on hair growth cycle in mice
- Multi-potentiality of a new immortalized epithelial stem cell line derived from human hair follicles
- The formulation and in‐vitro evaluation of WS Biotin, a novel encapsulated form of D‐Biotin with improved water solubility for hair and skin treatment applications
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Cylindroma as Tumor of Hair Follicle Origin
- A nonsense variant in <i>KRT31</i> is associated with autosomal-dominant monilethrix
- 874 Chromatin architectural protein CTCF controls epidermal barrier formation, hair follicle fate maintenance and suppresses inflammatory responses in the skin epithelium
- Construction and Verification of Recombinant Follicle-specific Expression Vector
- Generation of folliculogenic human epithelial stem cells from induced pluripotent stem cells
- Biomarkers of alopecia areata disease activity and response to corticosteroid treatment
- Office Diagnosis of Hair Shaft Defects
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- An interview Drs. Felix Brockschmidt and Markus Nöthen about the genetics of androgenetic alopecia
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The keratins and their disorders
- Characterization of Hair Follicle Antigens Targeted by the Anti-Hair Follicle Immune Response
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Faculty Opinions recommendation of Identification of novel hair-growth inducers by means of connectivity mapping.
- Multiple roles for activated LEF/TCF transcription complexes during hair follicle development and differentiation
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Assembly of Hair Keratins in Transfected Epithelial Cells
- Monilethrix: Beaded hair and hypotrichosis in a child
- Effect of Oral Minoxidil on Monilethrix
- Discovery of a novel murine keratin 6 (K6) isoform explains the absence of hair and nail defects in mice deficient for K6a and K6b
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Keratin 71 Mutations: From Water Dogs to Woolly Hair