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Research 631–660 of 1000+
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- 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
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Alopecia Areata is associated with MICA and an extended HLA haplotype
- Natural variation in trichome density and biochemistry in Antirrhinum
- A mouse with bad hair and poor taste
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Genetics of blond hair
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- A Mutation in the Serum and Glucocorticoid-Inducible Kinase-Like Kinase (Sgkl) Gene is Associated with Defective Hair Growth in Mice
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss
- Vesicle Formation and Follicular Root Sheath Separation in Mice Homozygous for Deleterious Alleles at the Balding (bal) Locus
- Organization and Expression of Hair Follicle Genes.
- 921 Generation of a new rodent model of scleroderma
- Genetics of Diabetes in Childhood
- Hair Keratin Associated Proteins: Characterization of a Second High Sulfur KAP Gene Domain on Human Chromosome 2111In fond memory of Dr Peter Steinert.
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Characterization of a First Domain of Human High Glycine-Tyrosine and High Sulfur Keratin-associated Protein (KAP) Genes on Chromosome 21q22.1
- Do Changes in Chromosomes Cause Aging?
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations