نتایج جستجو برای: msud

تعداد نتایج: 148  

2013
Armando Reyes-Palomares Rocío Rodríguez-López Juan A. G. Ranea Francisca Sánchez Jiménez Miguel Angel Medina

The molecular complexity of genetic diseases requires novel approaches to break it down into coherent biological modules. For this purpose, many disease network models have been created and analyzed. We highlight two of them, "the human diseases networks" (HDN) and "the orphan disease networks" (ODN). However, in these models, each single node represents one disease or an ambiguous group of dis...

Journal: :Genetics 2009
André Fleissner Spencer Diamond N Louise Glass

Cell-cell fusion is essential for a variety of developmental steps in many eukaryotic organisms, during both fertilization and vegetative cell growth. Although the molecular mechanisms associated with intracellular membrane fusion are well characterized, the molecular mechanisms of plasma membrane merger between cells are poorly understood. In the filamentous fungus Neurospora crassa, cell fusi...

Journal: :Iranian biomedical journal 2007
Hamid Shahbaz Mohammadi Eskander Omidinia Abbas Lotfi Sahebghadam Reza Saghiri

BACKGROUND Amino acid dehydrogenases (L-amino acid: oxidoreductase deaminating; EC 1.4.1.X) are members of the wider superfamily of oxidoreductases that catalyze the reversible oxidative deamination of an amino acid to its keto acid and ammonia with the concomitant reduction of either NAD+, NADP+ or FAD. These enzymes have been received much attention as biocatalysts for use in biosensors or...

Journal: :iranian journal of child neurology 0
mahmoud reza ashrafi professor of pediatric neurology- children’s medical center, tehran university of medical sciences,tehran,iran alireza tavasoli fellow of pediatric neurology- children’s medical center tehran university of medical sciences,tehran, iran

clinical differential diagnosisthe organic acidemias are important in the differential diagnosis of metabolic and neurologic derangement in the neonate and of new-onset neurologic signs in the older child. a-organic aciduriaseveral disorders, not classified as primary disorders of organic acid metabolism, have a characteristic urinary organic acid profile that suggests the appropriate diagnosis...

Journal: :iranian biomedical journal 0
حمید شهباز محمدی hamid shahbaz mohammadi اسکندر امیدی نیا eskander omidinia عباس صاحبقدم لطفی abbas sahebghadam lotfi رضا صغیری reza saghiri

amino acid dehydrogenases (l-amino acid: oxidoreductase deaminating ec 1.4.1.x) are members of the wider superfamily of oxidoreductases that catalyze the reversible oxidative deamination of an amino acid to its keto acid and ammonia with the concomitant reduction of either nad+, nadp+ or fad. these enzymes have been received much attention as biocatalysts for use in biosensors or diagnostic kit...

2008
AM Murphy C Halling SA Lynch AA Monavari S Harty E Crushell EP Treacy H Crawford SA McKee J Chukwu A Taha Fiona J Stewart Anthony W Ryan David Hughes Thomas Ryan Ross McManus Mark Stoneking Colm Ó'Dúshláine Ciara Dolan Alice Stanton David Croke Reetta Kalviainen Samuel Berkovic Terry O'Brien Sanjay Sisodiya David Goldstein Derek Morris Norman Delanty Gianpiero Cavalleri William P. Gilks Emma Allott Gary Donohoe John L. Waddington Michael Gill Aiden P. Corvin Derek W. Morris D McGibbon C Benson G Meenagh G Wright M Doherty A Hughes Seona McErlean Natalie Scott Jenny Worthington Gillian Brown Adriana Falchi Daniel Berrar Anthony J Bjourson Andrew McLellan Freda Wynne Melanie Ball Tom Moore David E. Barton Ros J. Hastings Sarah Berwouts Christine Brady Philippe Corbisier Anniek Corveleyn Rob Elles Brian Fowler David Gancberg Piotr Litynski Milan Macek Ute Malburg Gert Matthijs Michael Morris Clemens Mueller Nick Nagels Bettina Quellhorst-Pawley Alexandra Stambergova Jan Vermeesch Kate Vickers Elisabeth Dequeker Alex Magee Sally Ann Lynch Amaka Offiah J Walsh D Lambert DM Baldridge R Morello D Eyre B Lee AJ Green Kirsty O'Brien Anne Parle-McDermott A Langseth E Doherty T Nestor T Lynch F Asmus MD Mary Arun Kumar Mankan Jacqueline Daly Emma Caraher Dermot Kelleher Brónagh Ó hIcí Edith Gould Elaine Kenny Carlos Pinto Aiden Corvin Katherine Schouest Avril Coghlan Charles Spillane DP Dash s George G Silvestri J Jackson D Frazer AE Hughes C Willoughby Deirdre Donnelly Shane McKee Emma H. Allott Kevin J. Mitchell EB Skehan M Abdulrahim NP Parfrey CK Hand G Colleran A Rowan N Miller E Sawyer C Curran M Kerin I Tomlinson GJ McKay N Orr U Chakravarthy Helen Fitzpatrick Gillian Clarke Aidan Doherty CW Shepherd S McKee PJ Morrison Johanna Kelly Eibhlin Conneally Elizabeth Vandenburgh Karen Meaney KG Hegarty M Daly F Shanahan MG Molloy Mary E Laing Patrick Dicker Wen Lyn Ho Fergal J Moloney Gillian M Murphy Peter Conlon Alexander S Whitehead Denis C Shields Rosie O'Shea Eileen Treacy Anne Marie Murphy Deborah Lambert N Carroll S Cahill K O'Brien JM Scott A Parle-McDermott Tabib Dabir Brian McCrossan A Sands L Sweeney A Magee Alistair N Graham Trudi McDevitt Caitriona King Melissa Rogers Solvig Roring Shirley McQuaid David E Barton G Smith D McManus V McConnell VEF Crowley K Lim C Darby C Collison A Balfe S Heggarty Vivion EF Crowley Cindy Darby Sharon Whatley Mike Badminton W Meng CC Patterson C Belton MS Kamaruddin PG Horan F Kee PP McKeown F Cassidy C Zhao J Badger C Delaney L Mooney S Roche P McKeon SE Dobrin Aileen Butler David McManus June Jones Moya Clarkson

Keynote address: " Sweet dreams: using genome wide association methods to find genes for diabetes and obesity " Irish Travellers are a nomadic people in whom early marriage, frequent child bearing and consanguinity are cultural norms. They number 22,445, <0.5% of the Irish population, 9.6% of the 1465 patients listed at NCIMD on January 1 st 2007 were Travellers. To date 21 different inherited ...

2014
Nina A Zeltner Martina Huemer Matthias R Baumgartner Markus A Landolt

BACKGROUND In recent decades, considerable progress in diagnosis and treatment of patients with intoxication-type inborn errors of metabolism (IT-IEM) such as urea cycle disorders (UCD), organic acidurias (OA), maple syrup urine disease (MSUD), or tyrosinemia type 1 (TYR 1) has resulted in a growing group of long-term survivors. However, IT-IEM still require intense patient and caregiver effort...

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