Zobrazeno 1 - 10
of 377
pro vyhledávání: '"R Potashnik"'
Publikováno v:
Diabetologia; May2003, Vol. 46 Issue 5, p639-648, 10p
Publikováno v:
Journal of Inherited Metabolic Disease. 17:16-22
Decreased 2-deoxyglucose (2-DOG) uptake is well described in the neutrophils of patients with glycogen storage disease type 1b (GSD 1b). We report a patient with GSD 1b who presented with a normal antenatal and perinatal 2-deoxyglucose uptake that sh
Publikováno v:
American Journal of Physiology-Cell Physiology. 263:C516-C520
Cystinosis is an inherited metabolic disease characterized by accumulation of lysosomal cystine and renal impairment. In an attempt to better understand the link between cystine accumulation and renal functions, we studied the effects of cystine load
Publikováno v:
Cellular Physiology and Biochemistry. 1:294-304
We studied the effect of lysosomal loading with cystine (by incubation with cystine dimethyl ester, CDME) on the functions of renal epithelial cells in culture (LLC-PK1). The concentrating
Autor:
William B. Guggino, Diane Markakis, Hans-Jürgen Westphale, N. Bashan, Rainer Greger, M. Granitzer, Wolfram Nagel, Hans Oberleithner, Luo Lu, Christof Schäfer, Arie Moran, J. Crabbé, B. Lyoussi, F. Hollunder-Reese, Markus Bleich, R. Nitschke, Jens Leipziger, A. Ben-Nun, M. Mohrmann, R. Potashnik
Publikováno v:
Cellular Physiology and Biochemistry. 1:I-IV
Publikováno v:
The Journal of biological chemistry. 274(15)
In a recent study we have demonstrated that 3T3-L1 adipocytes exposed to low micromolar H2O2 concentrations display impaired insulin stimulated GLUT4 translocation from internal membrane pools to the plasma membrane (Rudich, A., Tirosh, A., Potashnik
Publikováno v:
Journal of Inherited Metabolic Disease. 13:252-254
Publikováno v:
The American journal of physiology. 265(6 Pt 2)
To better understand the link between lysosomal cystine accumulation and the renal impairment seen in cystinosis, we have studied the effect of cystine loading in vivo, on renal function of rats, and in brush-border membrane vesicles (BBMV) prepared
Publikováno v:
European journal of pediatrics. 152
Patients with glycogen storage disease (GSD) 1b suffer from recurrent bacterial infections related to neutropenia and impairment of neutrophil functions. One of these functions is the oxidative burst activity which is initiated by NADPH oxidase and d
Publikováno v:
Pediatric research. 28(1)
Neutrophil functions and glucose metabolism are known to be impaired in glycogen storage disease (GSD) Ib patients. The uptake of nonmetabolizing glucose analogues into polymorphonuclear leukocytes (PMN) of GSD Ib patients was studied. 2-Deoxyglucose