Search
for
Sort by
Research 31–60 of 1000+
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Isolation and characterization of a sheep cysteine-rich cuticle keratin pseudogene
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biology
- Association analysis of polymorphisms in six keratin genes with wool traits in sheep
- Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice
- Influence of TRPV3 mutation on hair growth cycle in mice
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
- Characterization of Human Keratin-Associated Protein 1 Family Members
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- In vivo Alteration of the Keratin 17 Gene in Hair Follicles by Oligonucleotide-directed Gene Targeting
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- A Small Deletion Hotspot in the Type II Keratin Gene<i>mK6irs1/Krt2-6g</i>on Mouse Chromosome 15, a Candidate for Causing the Wavy Hair of the Caracul (<i>Ca</i>) Mutation
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Genetically separable determinants of hair keratin gene expression
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Clinical Snippets
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Molecular Genetics of Alopecias