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Research 421–450 of 1000+
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- 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
- Where WNT the Hair
- 257 Is EBF1 a negative regulator of WNT10A in the development of androgenetic alopecia?
- A splice variant in KRT71 is associated with curly coat phenotype of Selkirk Rex cats
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Caractérisation d’une modification «bigarré» de la couleur du pelage chez le chat domestique
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- MLO-mediated Ca<sup>2+</sup>influx regulates root hair tip growth in Arabidopsis
- Biomedical applications of Janus membrane
- Natural Compound Isoliensinine Inhibits Stress-Induced Hair Greying by Blocking β2-Adrenoceptor
- Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- Effect of Inositol upon Rat Alopecia.
- Generation of Tβ4 knock-in Cashmere goat using CRISPR/Cas9
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene 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.
- Pinkie, the First Viable Germline Hypomorph Allele of Retinoid X Receptor Alpha, Reveals an Important Role for RXRa in Th2 Development.
- IRF2BP2 genes provide new insights into coat type and fiber composition variation in sheep
- Genetics of blond hair
- Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Genome-wide association study in frontal fibrosing alopecia identifies four susceptibility loci including HLA-B*07:02
- Organization and Expression of Hair Follicle Genes.
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- Prevalence of CYP21 mutations and IRS1 variant among women with polycystic ovary syndrome and adrenal androgen excess
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- Validation and casework testing of the BioPlex-11 for STR typing of telogen hair roots