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Research 61–90 of 1000+
- THE PATHOGENESIS OF ALOPECIA AREATA
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The Changing Landscape of Alopecia Areata: The Translational Landscape
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- The hair shaft: normality, abnormality, and genetics
- Disease causing homozygous variants in the human hairless gene
- Marie-unna hereditary hypotrichosis
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- ANDROGENIC ALOPECIA: PATHOGENETIC MECHANISMS AND THERAPEUTIC APPROACHES
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Role of polymorphism of the androgen receptor gene and non-random X chromosome inactivation in the genesis of androgenic alopecia in women of childbearing potential
- Caída capilar: nuevos factores causales y nuevos principios activos para un abordaje más integral con complementos alimenticios
- The X Factor in Immunity: Sex Differences Shaped by the X Chromosome
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Krtap16, Characterization of a New Hair Keratin-associated Protein (KAP) Gene Complex on Mouse Chromosome 16 and Evidence for Regulation by Hoxc13
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Alopecia con patrón femenino. Su importancia en medicina y cirugía estética
- Alopecia con patrón femenino. Su importancia en medicina y cirugía estética
- Pallister-Killian Syndrome
- Biological Function of Long Non-coding RNA (LncRNA) Xist
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Identification of seven new prostate cancer susceptibility loci through a genome-wide association study
- Social selection favours offspring prone to the development of androgenetic alopecia.
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability