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Results: 1-14 |
Results: 14
TARGETING OF GLIADIN PEPTIDES, CD8, ALPHA BETA-TCR, AND GAMMA/DELTA-TCR TO GOLGI COMPLEXES AND VACUOLES WITHIN CELIAC-DISEASE ENTEROCYTES/
Authors: ZIMMER KP NAIM H WEBER P ELLIS HJ CICLITIRA PJ
Citation: Kp. Zimmer et al., TARGETING OF GLIADIN PEPTIDES, CD8, ALPHA BETA-TCR, AND GAMMA/DELTA-TCR TO GOLGI COMPLEXES AND VACUOLES WITHIN CELIAC-DISEASE ENTEROCYTES/, The FASEB journal, 12(13), 1998, pp. 1349-1357
CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE IB - PHOSPHOMANNOSEISOMERASE DEFICIENCY AND MANNOSE THERAPY
Authors: NIEHUES R HASILIK M ALTON G KORNER C SCHIEBESUKUMAR M KOCH HG ZIMMER KP WU RR HARMS E REITER K VONFIGURA K FREEZE HH HARMS HK MARQUARDT T
Citation: R. Niehues et al., CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME TYPE IB - PHOSPHOMANNOSEISOMERASE DEFICIENCY AND MANNOSE THERAPY, The Journal of clinical investigation, 101(7), 1998, pp. 1414-1420
FALSE-POSITIVE GLIADIN AND ENDOMYSIUM ANTIBODIES AND EXOCRINE PANCREATIC INSUFFICIENCY AS PITFALLS IN THE DIFFERENTIAL-DIAGNOSIS OF DUODENAL CROHNS VERSUS CELIAC-DISEASE
Authors: WEBER P ZIMMER KP HUSEMANN S HARMS E
Citation: P. Weber et al., FALSE-POSITIVE GLIADIN AND ENDOMYSIUM ANTIBODIES AND EXOCRINE PANCREATIC INSUFFICIENCY AS PITFALLS IN THE DIFFERENTIAL-DIAGNOSIS OF DUODENAL CROHNS VERSUS CELIAC-DISEASE, The American journal of gastroenterology, 93(7), 1998, pp. 1177-1179
ULTRASTRUCTURAL-LOCALIZATION OF IGG AND TPO IN AUTOIMMUNE THYROCYTES REFERRING TO THE TRANSCYTOSIS OF IGG AND THE ANTIGEN PRESENTATION OF TPO
Authors: ZIMMER KP SCHEUMANN GFW BRAMSWIG J BOCKER W HARMS E SCHMID KW
Citation: Kp. Zimmer et al., ULTRASTRUCTURAL-LOCALIZATION OF IGG AND TPO IN AUTOIMMUNE THYROCYTES REFERRING TO THE TRANSCYTOSIS OF IGG AND THE ANTIGEN PRESENTATION OF TPO, HISTOCHEM C, 107(2), 1997, pp. 115-120
INTERNAL ABDOMINAL-HERNIAS IN CHILDHOOD
Authors: WEBER P VONLENGERKE HJ OLESZCZUKRASCKE K SCHLEEF J ZIMMER KP
Citation: P. Weber et al., INTERNAL ABDOMINAL-HERNIAS IN CHILDHOOD, Journal of pediatric gastroenterology and nutrition, 25(3), 1997, pp. 358-362
THE APICAL SORTING OF LACTASE-PHLORHIZIN HYDROLASE IMPLICATES SORTINGSEQUENCES FOUND IN THE MATURE DOMAIN
Authors: JACOB R ZIMMER KP NAIM H NAIM HY
Citation: R. Jacob et al., THE APICAL SORTING OF LACTASE-PHLORHIZIN HYDROLASE IMPLICATES SORTINGSEQUENCES FOUND IN THE MATURE DOMAIN, European journal of cell biology, 72(1), 1997, pp. 54-60
PRIMARY SCLEROSING CHOLANGITIS AND COLITI S ULCEROSA IN CHILDREN
Authors: WEBER P ZIMMER KP HARMS E
Citation: P. Weber et al., PRIMARY SCLEROSING CHOLANGITIS AND COLITI S ULCEROSA IN CHILDREN, Monatsschrift fur Kinderheilkunde, 144(4), 1996, pp. 370-373
CROHNS-DISEASE AND DRUG CONSUMPTION
Authors: WEBER P ZIMMER KP
Citation: P. Weber et Kp. Zimmer, CROHNS-DISEASE AND DRUG CONSUMPTION, Deutsche Medizinische Wochenschrift, 120(37), 1995, pp. 1261-1262
ULTRASTRUCTURAL, IMMUNOCYTOCHEMICAL AND STEREOLOGICAL INVESTIGATION OF HEPATOCYTES IN A PATIENT WITH THE MUTATION OF THE ORNITHINE TRANSCARBAMYLASE GENE
Authors: ZIMMER KP MATSUDA I MATSUURA T MORI M COLOMBO JP FAHIMI HD KOCH HG ULLRICH K HARMS E
Citation: Kp. Zimmer et al., ULTRASTRUCTURAL, IMMUNOCYTOCHEMICAL AND STEREOLOGICAL INVESTIGATION OF HEPATOCYTES IN A PATIENT WITH THE MUTATION OF THE ORNITHINE TRANSCARBAMYLASE GENE, European journal of cell biology, 67(1), 1995, pp. 73-83
A NOVEL POINT MUTATION AT CODON-269 OF THE ORNITHINE TRANSCARBAMYLASE(OTC) GENE CAUSING NEONATAL ONSET OF OTC DEFICIENCY
Authors: ZIMMER KP MATSUURA T COLOMBO JP KOCH HG ULLRICH K DEUFEL T HARMS E MATSUDA I
Citation: Kp. Zimmer et al., A NOVEL POINT MUTATION AT CODON-269 OF THE ORNITHINE TRANSCARBAMYLASE(OTC) GENE CAUSING NEONATAL ONSET OF OTC DEFICIENCY, Journal of inherited metabolic disease, 18(3), 1995, pp. 356-357
SURVIVAL AFTER EARLY TREATMENT FOR CARBAMYL-PHOSPHATE SYNTHETASE (CPS)-I DEFICIENCY ASSOCIATED WITH INCREASE OF INTRAMITOCHONDRIAL CPS-I
Authors: ZIMMER KP NAIM HY KOCH HG COLOMBO JP ROSSI R SCHMID KW DEUFEL T ULLRICH K HARMS E
Citation: Kp. Zimmer et al., SURVIVAL AFTER EARLY TREATMENT FOR CARBAMYL-PHOSPHATE SYNTHETASE (CPS)-I DEFICIENCY ASSOCIATED WITH INCREASE OF INTRAMITOCHONDRIAL CPS-I, Lancet, 346(8989), 1995, pp. 1530-1531
INCREASED INTRAMITOCHONDRIAL AMOUNT OF MUTANT CARBAMYLPHOSPHATE SYNTHETASE (CPS) IN THE LIVER OF A SIBLING WITH MILD COURSE OF CPS DEFICIENCY IN COMPARISON TO HER SISTER WITH LETHAL OUTCOME
Authors: ZIMMER KP NAIM H KOCH HG COLOMBO JP DEUFEL T ULRICH K HARMS E
Citation: Kp. Zimmer et al., INCREASED INTRAMITOCHONDRIAL AMOUNT OF MUTANT CARBAMYLPHOSPHATE SYNTHETASE (CPS) IN THE LIVER OF A SIBLING WITH MILD COURSE OF CPS DEFICIENCY IN COMPARISON TO HER SISTER WITH LETHAL OUTCOME, Pediatric research, 38(3), 1995, pp. 462-462
TRANSLOCATION OF GLIADIN INTO HLA-DR ANTIGEN CONTAINING LYSOSOMES IN CELIAC-DISEASE ENTEROCYTES
Authors: ZIMMER KP POREMBA C WEBER P CICLITIRA PJ HARMS E
Citation: Kp. Zimmer et al., TRANSLOCATION OF GLIADIN INTO HLA-DR ANTIGEN CONTAINING LYSOSOMES IN CELIAC-DISEASE ENTEROCYTES, Gut, 36(5), 1995, pp. 703-709
AN ALTERNATIVELY SPLICED FORM OF THE HUMAN LYSOSOME-ASSOCIATED MEMBRANE PROTEIN-2 GENE IS EXPRESSED IN A TISSUE-SPECIFIC MANNER
Authors: KONECKI DS FOETISCH K ZIMMER KP SCHLOTTER M KONECKI UL
Citation: Ds. Konecki et al., AN ALTERNATIVELY SPLICED FORM OF THE HUMAN LYSOSOME-ASSOCIATED MEMBRANE PROTEIN-2 GENE IS EXPRESSED IN A TISSUE-SPECIFIC MANNER, Biochemical and biophysical research communications, 215(2), 1995, pp. 757-767
Risultati: 1-14 |