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Results: 1-15 |
Results: 15

Authors: MEZEY E DEHEJIA AM HARTA G SUCHY SF NUSSBAUM RL BROWNSTEIN MJ POLYMEROPOULOS MH
Citation: E. Mezey et al., ALPHA-SYNUCLEIN IS PRESENT IN LEWY BODIES IN SPORADIC PARKINSONS-DISEASE, Molecular psychiatry, 3(6), 1998, pp. 493-499

Authors: LIN T ORRISON BM SUCHY SF LEWIS RA NUSSBAUM RL
Citation: T. Lin et al., MUTATIONS ARE NOT UNIFORMLY DISTRIBUTED THROUGHOUT THE OCRL1 GENE IN LOWE-SYNDROME PATIENTS, MOLECULAR GENETICS AND METABOLISM, 64(1), 1998, pp. 58-61

Authors: SUCHY SF NUSSBAUM RL
Citation: Sf. Suchy et Rl. Nussbaum, SUBCELLULAR-LOCALIZATION OF THE LOWE-SYNDROME PROTEIN (OCRL1) BY DIFFERENTIAL CENTRIFUGATION - COMPARISON OF ITS DISTRIBUTION TO GOLGI-ASSOCIATED PROTEINS, Molecular biology of the cell, 9, 1998, pp. 582-582

Authors: SUCHY SF LIN T HORWITZ JA OBRIEN WE NUSSBAUM RL
Citation: Sf. Suchy et al., FIRST REPORT OF PRENATAL BIOCHEMICAL-DIAGNOSIS OF LOWE-SYNDROME, Prenatal diagnosis, 18(11), 1998, pp. 1117-1121

Authors: SRINIVASAN S SEAMAN M NEMOTO Y DANIELL L SUCHY SF EMR S DECAMILLI P NUSSBAUM R
Citation: S. Srinivasan et al., DISRUPTION OF 3 PHOSPHATIDYLINOSITOL-POLYPHOSPHATE 5-PHOSPHATASE GENES FROM SACCHAROMYCES-CEREVISIAE RESULTS IN PLEIOTROPIC ABNORMALITIES OF VACUOLE MORPHOLOGY, CELL-SHAPE, AND OSMOHOMEOSTASIS (VOL 74, PG 350,1997), European journal of cell biology, 75(3), 1998, pp. 246-246

Authors: JANNE PA SUCHY SF BERNARD D MACDONALD M CRAWLEY J GRINBERG A WYNSHAWBORIS A WESTPHAL H NUSSBAUM RL
Citation: Pa. Janne et al., FUNCTIONAL OVERLAP BETWEEN MURINE INPP5B AND OCRL1 MAY EXPLAIN WHY DEFICIENCY OF THE MURINE ORTHOLOG FOR OCRL1 DOES NOT CAUSE LOWE-SYNDROMEIN MICE, The Journal of clinical investigation, 101(10), 1998, pp. 2042-2053

Authors: SRINIVASAN S SEAMAN M NEMOTO Y DANIELL L SUCHY SF EMR S DECAMILLI P NUSSBAUM R
Citation: S. Srinivasan et al., DISRUPTION OF 3 PHOSPHATIDYLINOSITOL-POLYPHOSPHATE 5-PHOSPHOTOSE GENES FROM SACCHAROMYCES-CEREVISIAE RESULTS IN PLEIOTROPIC ABNORMALITIES OF VACUOLE MORPHOLOGY, CELL-SHAPE, AND OSMOHOMEOSTASIS, European journal of cell biology, 74(4), 1997, pp. 350-360

Authors: HELLSTEN EO JANNE PA BERNARD DJ ECKHAUS M OWENS J SUCHY SF PEARLINE RV NUSSBAUM RL
Citation: Eo. Hellsten et al., MICE DEFICIENT IN INPP5B, AN AUTOSOMAL PHOSPHATIDYLINOSITOL BISPHOSPHATE 5-PHOSPHATASE HOMOLOGOUS TO THE LOWE-SYNDROME PROTEIN, American journal of human genetics, 61(4), 1997, pp. 140-140

Authors: LIN T ORRISON BM LEAHEY AM SUCHY SF BERNARD DJ LEWIS RA NUSSBAUM RL
Citation: T. Lin et al., SPECTRUM OF MUTATIONS IN THE OCRL1 GENE IN THE LOWE OCULOCEREBRORENALSYNDROME, American journal of human genetics, 60(6), 1997, pp. 1384-1388

Authors: SUCHY SF NUSSBAUM RL
Citation: Sf. Suchy et Rl. Nussbaum, A DEFECTIVE PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE 5-PHOSPHATASE IS RESPONSIBLE FOR THE OCULOCEREBRORENAL SYNDROME OF LOWE, Journal of neurochemistry, 66, 1996, pp. 45-45

Authors: SUCHY SF OLIVOSGLANDER IM NUSSBAUM RL
Citation: Sf. Suchy et al., LOWE-SYNDROME, A DEFICIENCY OF A PHOSPHATIDYL-INOSITOL 4,5-BISPHOSPHATE 5-PHOSPHATASE IN THE GOLGI-APPARATUS, Human molecular genetics, 4(12), 1995, pp. 2245-2250

Authors: JANNE PA BERNARD D CANNA C WYNSHAWBORIS A GRIMES P MCDONALD M CRAWLEY J OLIVOSGLANDER IM SUCHY SF NUSSBAUM RL
Citation: Pa. Janne et al., PRODUCTION OF MICE DEFICIENT IN THE LOWE SYNDROME GENE (OCRL-1) AND ITS HIGHLY RELATED HOMOLOG, INOSITOL POLYPHOSPHATE 5-PHOSPHATASE (INPP5B), American journal of human genetics, 57(4), 1995, pp. 57-57

Authors: SUCHY SF OLIVOSGLANDER IM NUSSBAUM RL
Citation: Sf. Suchy et al., LOWE SYNDROME GENE ENCODES A PHOSPHATIDYLINOSITOL 4,5-BISPHOSPHATE 5-PHOSPHATASE EXPRESSED IN THE GOLGI-APPARATUS, American journal of human genetics, 57(4), 1995, pp. 187-187

Authors: CUALING H SIEGEL R SCHWARTING GA SUCHY SF MCCLUER RH BERNAL S
Citation: H. Cualing et al., THE EXPRESSION OF H-LIKE BLOOD-GROUP GLYCOLIPIDS IN SMALL-CELL CARCINOMA OF THE LUNG, Hybridoma, 12(3), 1993, pp. 239-247

Authors: SUCHY SF YEAGER MT
Citation: Sf. Suchy et Mt. Yeager, FALSE-POSITIVE AMNIOTIC-FLUID ACETYLCHOLINESTERASE ANALYSIS IN THE 3RD TRIMESTER, Prenatal diagnosis, 13(5), 1993, pp. 363-369
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