-
1
-
-
0030070055
-
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption
-
Martin MG, Turk E, Lostao MP, Kerner C, Wright EM. Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption. Nat Genet 1996;12:216-220.
-
(1996)
Nat Genet
, vol.12
, pp. 216-220
-
-
Martin, M.G.1
Turk, E.2
Lostao, M.P.3
Kerner, C.4
Wright, E.M.5
-
2
-
-
0031034371
-
Regulation of intestinal sugar transport
-
Ferraris RP, Diamond J. Regulation of intestinal sugar transport. Physiol Rev 1997;77:257-302.
-
(1997)
Physiol Rev
, vol.77
, pp. 257-302
-
-
Ferraris, R.P.1
Diamond, J.2
-
3
-
-
0026510354
-
Human intestinal glucose transporter expression and localization of GLUT5
-
Davidson NO, Hausman AM, Ifkovits CA, Buse JB. Gould GW, Burant CF, Bell GI. Human intestinal glucose transporter expression and localization of GLUT5. Am J Physiol 1992;262:C795-800.
-
(1992)
Am J Physiol
, vol.262
-
-
Davidson, N.O.1
Hausman, A.M.2
Ifkovits, C.A.3
Buse, J.B.4
Gould, G.W.5
Burant, C.F.6
Bell, G.I.7
-
4
-
-
0025886960
-
Expression of human glucose transporters in Xenopus oocytes: Kinetic characterization and substrate specificities of the erythrocyte, liver, brain isoforms
-
Gould GW, Thomas HM, Jess TJ, Bell GI. Expression of human glucose transporters in Xenopus oocytes: Kinetic characterization and substrate specificities of the erythrocyte, liver, brain isoforms. Biochemistry 1991;30:5139-5145.
-
(1991)
Biochemistry
, vol.30
, pp. 5139-5145
-
-
Gould, G.W.1
Thomas, H.M.2
Jess, T.J.3
Bell, G.I.4
-
5
-
-
0035949597
-
Normal kinetics of intestinal glucose absorption in the absence of GLUT2: Evidence for a transport pathway requiring glucose phosphorylation and transfer into the endoplasmic reticulum
-
Stümpel F, Burcelin R, Jungermann K, Thorens B. Normal kinetics of intestinal glucose absorption in the absence of GLUT2: Evidence for a transport pathway requiring glucose phosphorylation and transfer into the endoplasmic reticulum. Proc Natl Acad Sci U S A 2001;98:11330-11335.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 11330-11335
-
-
Stümpel, F.1
Burcelin, R.2
Jungermann, K.3
Thorens, B.4
-
6
-
-
0030667885
-
Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome
-
Santer R, Schneppenheim R, Dombrowski A, Götze H, Steinmann B, Schaub J. Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndrome. Nat Genet 1997;17:324-326.
-
(1997)
Nat Genet
, vol.17
, pp. 324-326
-
-
Santer, R.1
Schneppenheim, R.2
Dombrowski, A.3
Götze, H.4
Steinmann, B.5
Schaub, J.6
-
7
-
-
0030750018
-
Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia
-
Müller D, Santer R, Krawinkel M, Christiansen B, Schaub J. Fanconi-Bickel syndrome presenting in neonatal screening for galactosaemia. J Inherit Metab Dis 1997;20:607-608.
-
(1997)
J Inherit Metab Dis
, vol.20
, pp. 607-608
-
-
Müller, D.1
Santer, R.2
Krawinkel, M.3
Christiansen, B.4
Schaub, J.5
-
8
-
-
0031705401
-
Fanconi-Bickel syndrome - The original patient and his natural history, historical steps leading to the primary defect, and a review of the literature
-
Santer R, Schneppenheim R, Suter D, Schaub J, Steinmann B. Fanconi-Bickel syndrome - The original patient and his natural history, historical steps leading to the primary defect, and a review of the literature. Eur J Pediatr 1998;157:783-797.
-
(1998)
Eur J Pediatr
, vol.157
, pp. 783-797
-
-
Santer, R.1
Schneppenheim, R.2
Suter, D.3
Schaub, J.4
Steinmann, B.5
-
9
-
-
0036461262
-
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome
-
Santer R, Groth S, Kinner M, Dombrowski A, Berry GT, Brodehl J, Leonard JV, Moses S, Norgren S, Skovby F, Schneppenheim R, Steinmann B, Schaub J. The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome. Hum Genet 2002;110:21-29.
-
(2002)
Hum Genet
, vol.110
, pp. 21-29
-
-
Santer, R.1
Groth, S.2
Kinner, M.3
Dombrowski, A.4
Berry, G.T.5
Brodehl, J.6
Leonard, J.V.7
Moses, S.8
Norgren, S.9
Skovby, F.10
Schneppenheim, R.11
Steinmann, B.12
Schaub, J.13
-
10
-
-
0020514295
-
Impaired metabolic function of polymorphonuclear leukocytes in glycogen storage disease lb
-
Gahr M, Heyne K. Impaired metabolic function of polymorphonuclear leukocytes in glycogen storage disease lb. Eur J Pediatr 1983;140:329-330.
-
(1983)
Eur J Pediatr
, vol.140
, pp. 329-330
-
-
Gahr, M.1
Heyne, K.2
-
11
-
-
0034243484
-
Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients
-
Santer R, Rischewski J, Block G, Kinner M, Wendel U, Schaub J, Schneppenheim R. Molecular analysis in glycogen storage disease 1 non-A: DHPLC detection of the highly prevalent exon 8 mutations of the G6PT1 gene in German patients. Hum Mutat 2000;16:177.
-
(2000)
Hum Mutat
, vol.16
, pp. 177
-
-
Santer, R.1
Rischewski, J.2
Block, G.3
Kinner, M.4
Wendel, U.5
Schaub, J.6
Schneppenheim, R.7
-
12
-
-
0019402978
-
Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings
-
Aperia A, Bergqvist G, Linne T, Zetterstrom R. Familial Fanconi syndrome with malabsorption and galactose intolerance, normal kinase and transferase activity. A report on two siblings. Acta Paediatr Scand 1981;70:527-533.
-
(1981)
Acta Paediatr Scand
, vol.70
, pp. 527-533
-
-
Aperia, A.1
Bergqvist, G.2
Linne, T.3
Zetterstrom, R.4
-
13
-
-
0035685698
-
The extended GLUT-family of sugar/polyol transport facilitators: Nomenclature, sequence characteristics, and potential function of its novel members
-
Joost HG, Thorens B. The extended GLUT-family of sugar/polyol transport facilitators: Nomenclature, sequence characteristics, and potential function of its novel members. Mol Membr Biol 2001;18:247-256.
-
(2001)
Mol Membr Biol
, vol.18
, pp. 247-256
-
-
Joost, H.G.1
Thorens, B.2
-
14
-
-
0032514612
-
Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes
-
Guillam MT, Burcelin R, Thorens B. Normal hepatic glucose production in the absence of GLUT2 reveals an alternative pathway for glucose release from hepatocytes. Proc Natl Acad Sci U S A 1998;95:12317-12321.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 12317-12321
-
-
Guillam, M.T.1
Burcelin, R.2
Thorens, B.3
-
15
-
-
0038831257
-
Liver hyperplasia and paradoxical regulation of glycogen metabolism and glucose-sensitive gene expression in GLUT2-null hepatocytes. Further evidence for the existence of a membrane-based glucose release pathway
-
Burcelin R, del Carmen Munoz M, Guillam MT, Thorens B. Liver hyperplasia and paradoxical regulation of glycogen metabolism and glucose-sensitive gene expression in GLUT2-null hepatocytes. Further evidence for the existence of a membrane-based glucose release pathway. J Biol Chem 2000;275:10930-10936.
-
(2000)
J Biol Chem
, vol.275
, pp. 10930-10936
-
-
Burcelin, R.1
Del Carmen Munoz, M.2
Guillam, M.T.3
Thorens, B.4
-
16
-
-
0036081139
-
Glucose release from GLUT2-null hepatocytes: Characterization of a major and a minor pathway
-
Hosokawa M, Thorens B. Glucose release from GLUT2-null hepatocytes: Characterization of a major and a minor pathway. Am J Physiol Endocrinol Metab 2002;282:E794-801.
-
(2002)
Am J Physiol Endocrinol Metab
, vol.282
-
-
Hosokawa, M.1
Thorens, B.2
-
17
-
-
0018051209
-
Disordered intestinal function in glycogen storage disease
-
Milla PJ, Atherton DA, Leonard JV, Wolff OH, Lake BD. Disordered intestinal function in glycogen storage disease. J Inherit Metab Dis 1978;1:155-157.
-
(1978)
J Inherit Metab Dis
, vol.1
, pp. 155-157
-
-
Milla, P.J.1
Atherton, D.A.2
Leonard, J.V.3
Wolff, O.H.4
Lake, B.D.5
-
18
-
-
0033797364
-
Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells
-
Ihara K, Nomura A, Hikino S, Takada H, Hara T. Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells. J Inherit Metab Dis 2000;23:583-592.
-
(2000)
J Inherit Metab Dis
, vol.23
, pp. 583-592
-
-
Ihara, K.1
Nomura, A.2
Hikino, S.3
Takada, H.4
Hara, T.5
-
19
-
-
0033060638
-
The glucose-6 phosphatase gene is expressed in human and rat small intestine: Regulation of expression in fasted and diabetic rats
-
Rajas F, Bruni N, Montano S, Zitoun C, Mithieux G. The glucose-6 phosphatase gene is expressed in human and rat small intestine: Regulation of expression in fasted and diabetic rats. Gastroenterology 1999;117:132-139.
-
(1999)
Gastroenterology
, vol.117
, pp. 132-139
-
-
Rajas, F.1
Bruni, N.2
Montano, S.3
Zitoun, C.4
Mithieux, G.5
-
20
-
-
0027928905
-
Quantitative aspects of glucose and glutamine metabolism by intestinal cells
-
Newsholme EA, Carrie AL. Quantitative aspects of glucose and glutamine metabolism by intestinal cells. Gut 1994;35(1 Suppl): S13-17.
-
(1994)
Gut
, vol.5
, Issue.1 SUPPL.
-
-
Newsholme, E.A.1
Carrie, A.L.2
-
21
-
-
0025286236
-
Gut exchange of glucose and lactate in basal state and after oral glucose ingestion in postoperative patients
-
Bjorkman O, Eriksson LS, Nyberg B, Wahren J. Gut exchange of glucose and lactate in basal state and after oral glucose ingestion in postoperative patients. Diabetes 1990;39:747-751.
-
(1990)
Diabetes
, vol.39
, pp. 747-751
-
-
Bjorkman, O.1
Eriksson, L.S.2
Nyberg, B.3
Wahren, J.4
-
22
-
-
0001175173
-
Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid and purine abnormalities
-
Howell RR, Ashton DM, Wyngaarden JB. Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid and purine abnormalities. Pediatrics 1962;29:553-565.
-
(1962)
Pediatrics
, vol.29
, pp. 553-565
-
-
Howell, R.R.1
Ashton, D.M.2
Wyngaarden, J.B.3
-
23
-
-
0014594057
-
Intestinal absorption in type I glycogen storage disease
-
Fine RN, Kogut MD, Donnell GN. Intestinal absorption in type I glycogen storage disease. J Pediatr 1969;75:632-635.
-
(1969)
J Pediatr
, vol.75
, pp. 632-635
-
-
Fine, R.N.1
Kogut, M.D.2
Donnell, G.N.3
-
24
-
-
0036690864
-
Intestinal function in glycogen storage disease type I
-
Visser G, Rake JP, Kokke FTM, Nikkels PGJ, Sauer PJJ, Smit GPA. Intestinal function in glycogen storage disease type I. J Inherit Metab Dis 2002;25:261-267.
-
(2002)
J Inherit Metab Dis
, vol.25
, pp. 261-267
-
-
Visser, G.1
Rake, J.P.2
Kokke, F.T.M.3
Nikkels, P.G.J.4
Sauer, P.J.J.5
Smit, G.P.A.6
-
25
-
-
0021709836
-
Fasting breath hydrogen concentration: Normal values and clinical application
-
Perman JA, Modler S, Barr RG, Rosenthal P. Fasting breath hydrogen concentration: Normal values and clinical application. Gastroenterology 1984;87:1358-1363.
-
(1984)
Gastroenterology
, vol.87
, pp. 1358-1363
-
-
Perman, J.A.1
Modler, S.2
Barr, R.G.3
Rosenthal, P.4
|