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Results: 1-9 |
Results: 9
MUTATIONS IN THE DELTA(1)-PYRROLINE 5-CARBOXYLATE DEHYDROGENASE GENE CAUSE TYPE-II HYPERPROLINEMIA
Authors: GERAGHTY MT VAUGHN D NICHOLSON AJ LIN WW JIMENEZSANCHEZ G OBIE C FLYNN MP VALLE D HU CAA
Citation: Mt. Geraghty et al., MUTATIONS IN THE DELTA(1)-PYRROLINE 5-CARBOXYLATE DEHYDROGENASE GENE CAUSE TYPE-II HYPERPROLINEMIA, Human molecular genetics (Print), 7(9), 1998, pp. 1411-1415
RESTORATION OF PEX2 PEROXISOME ASSEMBLY DEFECTS BY OVEREXPRESSION OF PMP70
Authors: GARTNER J BROSIUS U OBIE C WATKINS PA VALLE D
Citation: J. Gartner et al., RESTORATION OF PEX2 PEROXISOME ASSEMBLY DEFECTS BY OVEREXPRESSION OF PMP70, European journal of cell biology, 76(4), 1998, pp. 237-245
EXPRESSION OF PEX11-BETA MEDIATES PEROXISOME PROLIFERATION IN THE ABSENCE OF EXTRACELLULAR STIMULI
Authors: SCHRADER M REUBER BE MORRELL JC JIMENEZSANCHEZ G OBIE C STROH TA VALLE D SCHROER TA GOULD SJ
Citation: M. Schrader et al., EXPRESSION OF PEX11-BETA MEDIATES PEROXISOME PROLIFERATION IN THE ABSENCE OF EXTRACELLULAR STIMULI, The Journal of biological chemistry, 273(45), 1998, pp. 29607-29614
HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA
Authors: BRAVERMAN N STEEL G OBIE C MOSER A MOSER H GOULD SJ VALLE D
Citation: N. Braverman et al., HUMAN PEX7 ENCODES THE PEROXISOMAL PTS2 RECEPTOR AND IS RESPONSIBLE FOR RHIZOMELIC CHONDRODYSPLASIA PUNCTATA, Nature genetics, 15(4), 1997, pp. 369-376
NVL - A NEW MEMBER OF THE AAA FAMILY OF ATPASES LOCALIZED TO THE NUCLEUS
Authors: GERMAINLEE EL OBIE C DAVID V
Citation: El. Germainlee et al., NVL - A NEW MEMBER OF THE AAA FAMILY OF ATPASES LOCALIZED TO THE NUCLEUS, Genomics, 44(1), 1997, pp. 22-34
HUMAN AND MURINE GENOMES CONTAIN 2 PROLINE OXIDASE HOMOLOGS, ONE OF WHICH MAPS TO DIGEORGE VCFS REGION AND IS DEFICIENT IN THE PRO/RE/
Authors: LIN WW HU CA STEEL G OBIE C STEEL J LUND J REEVES R RUTBERG J GERAGHTY M VALLE D
Citation: Ww. Lin et al., HUMAN AND MURINE GENOMES CONTAIN 2 PROLINE OXIDASE HOMOLOGS, ONE OF WHICH MAPS TO DIGEORGE VCFS REGION AND IS DEFICIENT IN THE PRO/RE/, American journal of human genetics, 61(4), 1997, pp. 1492-1492
PYRIDOXINE-RESPONSIVE GYRATE ATROPHY OF THE CHOROID AND RETINA - CLINICAL AND BIOCHEMICAL CORRELATES OF THE MUTATION A226V
Authors: MICHAUD J THOMPSON GN BRODY LC STEEL G OBIE C FONTAINE G SCHAPPERT K KEITH CG VALLE D MITCHELL GA
Citation: J. Michaud et al., PYRIDOXINE-RESPONSIVE GYRATE ATROPHY OF THE CHOROID AND RETINA - CLINICAL AND BIOCHEMICAL CORRELATES OF THE MUTATION A226V, American journal of human genetics, 56(3), 1995, pp. 616-622
RESTORATION OF PEROXISOME BIOGENESIS IN A PEROXISOME-DEFICIENT MAMMALIAN-CELL LINE BY EXPRESSION OF EITHER THE 35-KDA OR THE 70-KDA PEROXISOMAL MEMBRANE-PROTEINS
Authors: GARTNER J OBIE C WATKINS P VALLE D
Citation: J. Gartner et al., RESTORATION OF PEROXISOME BIOGENESIS IN A PEROXISOME-DEFICIENT MAMMALIAN-CELL LINE BY EXPRESSION OF EITHER THE 35-KDA OR THE 70-KDA PEROXISOMAL MEMBRANE-PROTEINS, Journal of inherited metabolic disease, 17(3), 1994, pp. 327-329
RESTORATION OF PEROXISOME ASSEMBLY IN A PEROXISOME-DEFICIENT MAMMALIAN-CELL LINE BY EXPRESSION OF EITHER THE 70 KD (PMP70) OR THE 35 KD (PMP35) PEROXISOMAL MEMBRANE-PROTEIN
Authors: GARTNER J OBIE C WATKINS P VALLE D
Citation: J. Gartner et al., RESTORATION OF PEROXISOME ASSEMBLY IN A PEROXISOME-DEFICIENT MAMMALIAN-CELL LINE BY EXPRESSION OF EITHER THE 70 KD (PMP70) OR THE 35 KD (PMP35) PEROXISOMAL MEMBRANE-PROTEIN, American journal of human genetics, 53(3), 1993, pp. 108-108
Risultati: 1-9 |