|1.||Campbell, Kevin P: 2 articles (12/2015 - 07/2013)|
|2.||Moore, Steven A: 2 articles (12/2015 - 07/2013)|
|3.||Willer, Tobias: 2 articles (12/2015 - 07/2013)|
|4.||Mathews, Katherine D: 1 article (12/2015)|
|5.||Jensen, Braden S: 1 article (12/2015)|
|6.||Winder, Thomas L: 1 article (12/2015)|
|7.||Mozaffar, Tahseen: 1 article (12/2015)|
|8.||Scavina, Mena: 1 article (12/2015)|
|9.||Saade, Dimah N: 1 article (12/2015)|
|10.||Stefans, Vikki A: 1 article (12/2015)|
|1.||Congenital Disorders of Glycosylation
11/01/2010 - "Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations."
08/01/2000 - "Mannose supplementation corrects GDP-mannose deficiency in cultured fibroblasts from some patients with Congenital Disorders of Glycosylation (CDG)."
02/01/1998 - "In fibroblasts from five patients with carbohydrate-deficient glycoprotein syndrome type 1, the incorporation of [2-3H] mannose into mannose phosphates, GDP-mannose, GDP-fucose, dolichol-P-mannose, lipid-linked oligosaccharides, and glycoprotein fraction was determined. "
|2.||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. "
09/01/1986 - "However, both mutants were known to be reverted to lectin sensitivity by growth in L-fucose, making them similar to the mouse lymphoma mutant, PLR1.3, which is defective in the conversion of GDP-mannose to GPD-fucose [M. "
03/15/1986 - "Class E Thy-1-negative mutant mouse lymphoma cell membranes, which are defective in dolichyl phosphate mannose synthesis, also fail to transfer mannose from GDP-mannose to exogenous phosphatidic acid or retinyl phosphate. "
|4.||Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
|3.||mannose 1-phosphate guanylyltransferase
|7.||Guanidine (Guanidine Nitrate)
|8.||Citric Acid (Citrate)
|9.||Vitamin A (Retinol)
|10.||Uridine Diphosphate (UDP)