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202,410 Newest Publications
rss23-10-2013 | Ata Abbas, William Patterson III, Philippe T. Georgel, Biochemistry and Cell Biology, 2013
Le cancer de la prostate est une maladie grandement affectée par le style de vie, particulièrement la diète, et il est plus fréquent aux États-Unis et dans les pays européens comparativement à l'Asie de sud et de l'est. Parmi les nombreuses causes et facteurs de risques connus, la nutrition ...
01-07-2013 | Hilda Tateossian; Susan Morse; Andrew Parker; Philomena Mburu; Nick Warr; Abraham Acevedo-Arozena; Michael Cheeseman ..., Human Molecular Genetics, 2013
Otitis media with effusion (OME) is the most common cause of hearing loss in children and tympanostomy to alleviate the condition remains the commonest surgical intervention in children in the developed world. Chronic and recurrent forms of OM are known to have a very significant genetic ...
01-07-2013 | Swagatika Sahoo; Ines Thiele, Human Molecular Genetics, 2013
Small intestinal epithelial cells (sIECs) have a significant share in whole body metabolism as they perform enzymatic digestion and absorption of nutrients. Furthermore, the diet plays a key role in a number of complex diseases including obesity and diabetes. The impact of diet and altered ...
01-07-2013 | Jhuma Ganguly; Lieh Y Low; Nazia Kamal; Elke Saile; L Scott Forsberg; Gerardo Gutierrez-Sanchez; Alex R Hoffmaster; ..., Glycobiology , 2013
Endolysins are bacteriophage enzymes that lyse their bacterial host for phage progeny release. They commonly contain an N-terminal catalytic domain that hydrolyzes bacterial peptidoglycan (PG) and a C-terminal cell wall-binding domain (CBD) that confers enzyme localization to the PG ...
01-07-2013 | Dwight Stambolian; Robert Wojciechowski; Konrad Oexle; Mario Pirastu; Xiaohui Li; Leslie J. Raffel; Mary Frances Cot ..., Human Molecular Genetics, 2013
Visual refractive errors (REs) are complex genetic traits with a largely unknown etiology. To date, genome-wide association studies (GWASs) of moderate size have identified several novel risk markers for RE, measured here as mean spherical equivalent (MSE). We performed a GWAS using a total ...
01-07-2013 | Ping K. Chan; Raul Torres; Cihangir Yandim; Pui P. Law; Sanjay Khadayate; Marta Mauri; Crina Grosan; Nadine Chapman- ..., Human Molecular Genetics, 2013
Large intronic expansions of the triplet-repeat sequence (GAA.TTC) cause transcriptional repression of the Frataxin gene (FXN) leading to Friedreich's ataxia (FRDA). We previously found that GAA-triplet expansions stimulate heterochromatinization in vivo in transgenic mice. We report here ...
01-07-2013 | Derek P. Narendra; Chunxin Wang; Richard J. Youle; John E. Walker, Human Molecular Genetics, 2013
Mutations in Parkin or PINK1 are the most common cause of recessively inherited parkinsonism. Parkin and PINK1 function in a conserved mitochondrial quality control pathway, in which PINK1, a putative mitochondrial kinase, directs Parkin, a cytosolic E3 ubiquitin ligase, selectively to ...
01-07-2013 | Msano Mandalasi; Nelum Dorabawila; David F Smith; Jamie Heimburg-Molinaro; Richard D Cummings; A Kwame Nyame, Glycobiology , 2013
The parasitic blood fluke Schistosoma mansoni synthesizes immunogenic glycans containing the human Lewis x antigen (Lex; Galactose-β1-4(Fucα1-3)N-acetylglucosamine-β-R, also called CD15), but the biological role(s) of this antigen in the parasites and in humans is poorly understood. To ...
01-07-2013 | Paul L DeAngelis; Jian Liu; Robert J Linhardt, Glycobiology , 2013
Glycosaminoglycans (GAGs) are complex polysaccharides composed of hexosamine-containing disaccharide repeating units. The three most studied classes of GAGs, heparin/heparan sulfate, hyaluronan and chondroitin/dermatan sulfate, are essential macromolecules. GAGs isolated from animal and ...
01-07-2013 | Nalinda B. Wasala; Brian Bostick; Yongping Yue; Dongsheng Duan, Human Molecular Genetics, 2013
Duchenne muscular dystrophy (DMD) is characterized by severe degeneration and necrosis of both skeletal and cardiac muscle. While many experimental therapies have shown great promise in treating skeletal muscle disease, an effective therapy for Duchenne cardiomyopathy remains a challenge in ...
