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Results: 1-20 |
Results: 20
Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectors
Authors: Ye, XH Zimmer, KP Brown, R Pabin, C Batshaw, ML Wilson, JM Robinson, MB
Citation: Xh. Ye et al., Differences in the human and mouse amino-terminal leader peptides of ornithine transcarbamylase affect mitochondrial import and efficacy of adenoviral vectors, HUM GENE TH, 12(9), 2001, pp. 1035-1046
Surfactant protein A and lipid are internalized via the coated-pit pathwayby type II pneumocytes
Authors: Stevens, PA Wissel, H Zastrow, S Sieger, D Zimmer, KP
Citation: Pa. Stevens et al., Surfactant protein A and lipid are internalized via the coated-pit pathwayby type II pneumocytes, AM J P-LUNG, 280(1), 2001, pp. L141-L151
Body complaints and neuroticism in pediatric rheumatic disease.
Authors: Weber, P Niesse, G Ganser, G Zimmer, KP
Citation: P. Weber et al., Body complaints and neuroticism in pediatric rheumatic disease., KLIN PADIAT, 213(1), 2001, pp. 17-20
Placental alkaline phosphatase expression at the apical and basal plasma membrane in term villous trophoblasts
Authors: Leitner, K Szlauer, R Ellinger, I Ellinger, A Zimmer, KP Fuchs, R
Citation: K. Leitner et al., Placental alkaline phosphatase expression at the apical and basal plasma membrane in term villous trophoblasts, J HIST CYTO, 49(9), 2001, pp. 1155-1164
Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder
Authors: Spodsberg, N Jacob, R Alfalah, M Zimmer, KP Naim, HY
Citation: N. Spodsberg et al., Molecular basis of aberrant apical protein transport in an intestinal enzyme disorder, J BIOL CHEM, 276(26), 2001, pp. 23506-23510
Twenty-four hour intraesophageal pH monitoring in children and adolescentswith scleroderma and mixed connective tissue disease
Authors: Weber, P Ganser, G Frosch, M Roth, J Hulskamp, G Zimmer, KP
Citation: P. Weber et al., Twenty-four hour intraesophageal pH monitoring in children and adolescentswith scleroderma and mixed connective tissue disease, J RHEUMATOL, 27(11), 2000, pp. 2692-2695
Arthrogryposis, renal tubular dysfunction, cholestasis (ARC)-syndrome: Case report and review of the literature
Authors: Denecke, J Zimmer, KP Kleta, R Koch, HG Rabe, H August, C Harms, E
Citation: J. Denecke et al., Arthrogryposis, renal tubular dysfunction, cholestasis (ARC)-syndrome: Case report and review of the literature, KLIN PADIAT, 212(2), 2000, pp. 77-80
Retinitis pigmentosa, renal insufficiency and Caroli syndrome: new association in a patient with Opitz trigonocephaly syndrome
Authors: Weber, P Kuwertz-Broking, E Majewski, F Zimmer, KP Bulla, M
Citation: P. Weber et al., Retinitis pigmentosa, renal insufficiency and Caroli syndrome: new association in a patient with Opitz trigonocephaly syndrome, KLIN PADIAT, 212(1), 2000, pp. 31-34
Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme
Authors: Jacob, R Zimmer, KP Schmitz, J Naim, HY
Citation: R. Jacob et al., Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme, J CLIN INV, 106(2), 2000, pp. 281-287
Modulation of antigen trafficking to MHC class II-positive late endosomes of enterocytes
Authors: Zimmer, KP Buning, J Weber, P Kaiserlian, D Strobel, S
Citation: Kp. Zimmer et al., Modulation of antigen trafficking to MHC class II-positive late endosomes of enterocytes, GASTROENTY, 118(1), 2000, pp. 128-137
Is gliadin mispresented to the immune system in coeliac disease? A hypothesis
Authors: Biagi, F Zimmer, KP Thomas, PD Ellis, HJ Ciclitira, PJ
Citation: F. Biagi et al., Is gliadin mispresented to the immune system in coeliac disease? A hypothesis, QJM-MON J A, 92(2), 1999, pp. 119-122
Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency
Authors: Zimmer, KP Bendiks, M Mori, M Kominami, E Robinson, MB Ye, XH Wilson, JM
Citation: Kp. Zimmer et al., Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency, MOL MED, 5(4), 1999, pp. 244-253
O-linked glycans mediate apical sorting of human intestinal sucrase-isomaltase through association with lipid rafts
Authors: Alfalah, M Jacob, R Preuss, U Zimmer, KP Naim, H Naim, HY
Citation: M. Alfalah et al., O-linked glycans mediate apical sorting of human intestinal sucrase-isomaltase through association with lipid rafts, CURR BIOL, 9(11), 1999, pp. 593-596
Coagulation and fibrinolysis in children, adolescents, and young adults with inflammatory bowel disease
Authors: Weber, P Husemann, S Vielhaber, H Zimmer, KP Nowak-Gottl, U
Citation: P. Weber et al., Coagulation and fibrinolysis in children, adolescents, and young adults with inflammatory bowel disease, J PED GASTR, 28(4), 1999, pp. 418-422
Transepithelial transport processes at the intestinal mucosa in inflammatory bowel disease
Authors: Schurmann, G Bruwer, M Klotz, A Schmid, KW Senninger, N Zimmer, KP
Citation: G. Schurmann et al., Transepithelial transport processes at the intestinal mucosa in inflammatory bowel disease, INT J COL R, 14(1), 1999, pp. 41-46
Esophageal motility disorders in progressive systemic sclerosis and MorbusSharp
Authors: Weber, P Ganser, G Zimmer, KP
Citation: P. Weber et al., Esophageal motility disorders in progressive systemic sclerosis and MorbusSharp, MONATS KIND, 147(3), 1999, pp. 279-282
Celiac disease
Authors: Zimmer, KP
Citation: Kp. Zimmer, Celiac disease, MONATS KIND, 147(1), 1999, pp. 60-72
Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism
Authors: Marquardt, T Brune, T Luhn, K Zimmer, KP Korner, C Fabritz, L van der Werft, N Vormoor, J Freeze, HH Louwen, F Biermann, B Harms, E von Figura, K Vestweber, D Koch, HG
Citation: T. Marquardt et al., Leukocyte adhesion deficiency II syndrome, a generalized defect in fucose metabolism, J PEDIAT, 134(6), 1999, pp. 681-688
Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation)
Authors: Zimmer, KP Le Coutre, P Aerts, HMFG Harzer, K Fukuda, M O'Brien, JS Naim, HY
Citation: Kp. Zimmer et al., Intracellular transport of acid beta-glucosidase and lysosome-associated membrane proteins is affected in Gaucher's disease (G202R mutation), J PATHOLOGY, 188(4), 1999, pp. 407-414
Hereditary pancreatitis and mutation of the trypsinogen gene
Authors: Weber, P Keim, V Zimmer, KP
Citation: P. Weber et al., Hereditary pancreatitis and mutation of the trypsinogen gene, ARCH DIS CH, 80(5), 1999, pp. 473-474
Risultati: 1-20 |