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Research 91–120 of 1000+
- Combinatorial expression of cell cycle regulators is more suitable for immortalization than oncogenic methods in dermal papilla cells
- Case Report: Disorder of Sexual Development in a Chinese Crested Dog With XX/XY Leukocyte Chimerism and Mixed Cell Testicular Tumors
- Imprinted Dlk1-Gtl2 cluster miRNAs are potential epigenetic regulators of lamb fur quality
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Human Adipose-derived Mesenchymal Stromal Cells Exhibit High HLA-DR Levels and Altered Cellular Characteristics under a Xeno-free and Serum-free Condition
- Author response: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Decision letter: Deletion of the MAD2L1 spindle assembly checkpoint gene is tolerated in mouse models of acute T-cell lymphoma and hepatocellular carcinoma
- Androgenetic alopecia: Identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiology
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia
- Male-pattern baldness susceptibility locus at 20p11
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- A mutation in the hair matrix and cuticle keratin KRTHB5 gene causes ectodermal dysplasia of hair and nail type
- A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Size Polymorphisms in the Human Ultrahigh Sulfur Hair Keratin-Associated Protein 4, KAP4, Gene Family
- Polycystic ovary syndrome (PCOS) trilogy: a translational and clinical review
- The sheep KAP8-2 gene, a new KAP8 family member that is absent in humans
- Treatment of alopecia areata: “What is new on the horizon?”
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Hair of the Dog: Identification of a Cis-Regulatory Module Predicted to Influence Canine Coat Composition
- Potential Role of the Epidermal Differentiation Complex in the Pathogenesis of Psoriasis