|1.||Moore, Steven A: 2 articles (12/2015 - 07/2013)|
|2.||Campbell, Kevin P: 2 articles (12/2015 - 07/2013)|
|3.||Willer, Tobias: 2 articles (12/2015 - 07/2013)|
|4.||Barth, Carina: 2 articles (05/2011 - 01/2010)|
|5.||Winder, Thomas L: 1 article (12/2015)|
|6.||Mathews, Katherine D: 1 article (12/2015)|
|7.||Jensen, Braden S: 1 article (12/2015)|
|8.||Scavina, Mena: 1 article (12/2015)|
|9.||Mozaffar, Tahseen: 1 article (12/2015)|
|10.||Cox, Mary O: 1 article (12/2015)|
11/25/2008 - "Here, we report that mutations in the Arabidopsis gene encoding GDP-mannose pyrophosphorylase (GMPase) essential for synthesizing GDP-mannose confer hypersensitivity to NH(4)(+). "
05/01/2011 - "The ascorbic acid (AA)-deficient Arabidopsis thaliana mutant vtc1-1, which is defective in GDP-mannose pyrophosphorylase (GMPase), exhibits conditional hypersensitivity to ammonium (NH(4) (+) ), a phenomenon that is independent of AA deficiency. "
01/01/2010 - "A mutation in GDP-mannose pyrophosphorylase causes conditional hypersensitivity to ammonium, resulting in Arabidopsis root growth inhibition, altered ammonium metabolism, and hormone homeostasis."
|2.||Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
01/01/2015 - "Limb Girdle Muscular Dystrophy (LGMD), caused by defective α-dystroglycan (α-DG) glycosylation, was recently associated with mutations in Isoprenoid synthase domain-containing (ISPD) and GDP-mannose pyrophosphorylase B (GMPPB) genes. "
07/11/2013 - "Mutations in GDP-mannose pyrophosphorylase B cause congenital and limb-girdle muscular dystrophies associated with hypoglycosylation of α-dystroglycan."
|3.||Muscular Dystrophies (Muscular Dystrophy)
07/11/2013 - "Using a combination of exome and Sanger sequencing in eight unrelated individuals, we present evidence that mutations in guanosine diphosphate mannose (GDP-mannose) pyrophosphorylase B (GMPPB) can result in muscular dystrophy variants with hypoglycosylated α-DG. "
12/01/2015 - "Mutations in GDP-mannose pyrophosphorylase B (GMPPB), a catalyst for the formation of the sugar donor GDP-mannose, were recently identified as a cause of muscular dystrophy resulting from abnormal glycosylation of α-dystroglycan. "
|4.||Cystic Fibrosis (Mucoviscidosis)
10/01/2008 - "The bceA(J) gene from the cystic fibrosis isolate Burkholderia cenocepacia J2315 encodes a 56-kDa bifunctional protein, with phosphomannose isomerase (PMI) and guanosine diphosphate (GDP)-mannose pyrophosphorylase (GMP) activities, a new member of the poorly characterised type II PMI class of proteins. "
07/01/1987 - "The specific activities of phosphomannose isomerase (PMI), phosphomannomutase (PMM), GDP-mannose pyrophosphorylase (GMP), and GDP-mannose dehydrogenase (GMD) were compared in a mucoid cystic fibrosis isolate of Pseudomonas aeruginosa and in two spontaneous nonmucoid revertants. "
|5.||Esophageal Achalasia (Megaesophagus)
|1.||Guanosine Diphosphate Mannose (GDP Mannose)
|3.||Mannose-6-Phosphate Isomerase (Mannose 6 Phosphate Isomerase)
|4.||5'-Guanylic Acid (GMP)
|5.||Guanosine Diphosphate (GDP)
|6.||Quaternary Ammonium Compounds (Ammonium)
|7.||Guanidine (Guanidine Nitrate)
|8.||Nonsense Codon (Nonsense Mutation)
|9.||Proteins (Proteins, Gene)