Search
for
Sort by
Research 31–60 of 1000+
- Keratinization and its Disorders
- Disorders of Keratinization
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Analysis of Sequences Controlling Tissue-Specific and Hyperproliferation-Related Keratin 6 Gene Expression in Transgenic Mice
- System support in the forming and growth of hair in alopecias and the disorders of hair shaft
- Extraction and Formulation of hydrolyzed-wool keratin solution for hair growth
- Molecular Evolution of The Keratin‐associated Protein Gene Family
- Forkhead/winged-helix transcription factor whn regulates hair keratin gene expression: Molecular analysis of theNude skin phenotype
- Angora Mouse Mutation: Altered Hair Cycle, Follicular Dystrophy, Phenotypic Maintenance of Skin Grafts, and Changes in Keratin Expression
- Genetics of Structural Hair Disorders
- A 5'-upstream region of a bovine keratin 6 gene confers tissue-specific expression and hyperproliferation-related induction in transgenic mice.
- Congenital hair loss disorders: Rare, but not too rare
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Mutation detection of type II hair cortex keratin gene KRT86 in a Chinese Han family with congenital monilethrix
- Identification of human hair follicle antigens targeted in the presumptive autoimmune hair follicle disorder alopecia areata and their potential functional relevance in vitro : methods development for isolation and identification of alopecia areata-relevant human hair follicle antigens using a proteomics approach and their functional assessment using an ex vivo hair follicle organ culture model
- Beyond Expectations
- Molecular Genetics of Alopecias
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Comparative Anatomy of Mouse and Human Nail Units
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Does collapse of immune privilege in the hair-follicle bulge play a role in the pathogenesis of primary cicatricial alopecia?
- Early Dengue Virus Infection in Human Skin: A Cycle of Inflammation and Infectivity
- Unexpected Autocrine Role of Vascular Endothelial Growth Factor in Squamous Cell Carcinoma
- Pachyonychia congenita: Sporadic onset with mutation analysis