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Results: 1-25 | 26-50 | 51-75 | 76-82
Results: 1-25/82
A CYTOPLASMIC AAA FAMILY PEROXIN, PEX1P, INTERACTS WITH PEX6P
Authors: TAMURA S SHIMOZAWA N SUZUKI Y TSUKAMOTO T OSUMI T FUJIKI Y
Citation: S. Tamura et al., A CYTOPLASMIC AAA FAMILY PEROXIN, PEX1P, INTERACTS WITH PEX6P, Biochemical and biophysical research communications, 245(3), 1998, pp. 883-886
15 POLYMORPHISMS IN THE N-ACETYLGALACTOSAMINE-6-SULFATE SULFATASE (GALNS) GENE - DIAGNOSTIC IMPLICATIONS IN MORQUIO-DISEASE
Authors: TOMATSU SJ FUKUDA S COOPER A WRAITH JE YAMAGISHI A KATO Z YAMADA N ISOGAI K SUKEGAWA K SUZUKI Y SHIMOZAWA N KONDO N ORII T
Citation: Sj. Tomatsu et al., 15 POLYMORPHISMS IN THE N-ACETYLGALACTOSAMINE-6-SULFATE SULFATASE (GALNS) GENE - DIAGNOSTIC IMPLICATIONS IN MORQUIO-DISEASE, Human mutation, 1998, pp. 42-46
A NOVEL MUTATION, R125X IN PEROXISOME ASSEMBLY FACTOR-I RESPONSIBLE FOR ZELLWEGER-SYNDROME
Authors: SHIMOZAWA N SUZUKI Y TOMATSU S NAKAMURA H KONO T TAKADA H TSUKAMOTO T FUJIKI Y ORII T KONDO N
Citation: N. Shimozawa et al., A NOVEL MUTATION, R125X IN PEROXISOME ASSEMBLY FACTOR-I RESPONSIBLE FOR ZELLWEGER-SYNDROME, Human mutation, 1998, pp. 134-136
MUTATIONS IN PEX10 IS THE CAUSE OF ZELLWEGER PEROXISOME DEFICIENCY SYNDROME OF COMPLEMENTATION GROUP-B
Authors: OKUMOTO K ITOH R SHIMOZAWA N SUZUKI Y TAMURA S KONDO N FUJIKI Y
Citation: K. Okumoto et al., MUTATIONS IN PEX10 IS THE CAUSE OF ZELLWEGER PEROXISOME DEFICIENCY SYNDROME OF COMPLEMENTATION GROUP-B, Human molecular genetics (Print), 7(9), 1998, pp. 1399-1405
MULTIPLE CARCINOIDS OF THE DUODENUM ACCOMPANIED BY TYPE-I FAMILIAL MULTIPLE ENDOCRINE NEOPLASIA
Authors: YAZAWA K KURODA T WATANABE H SHIMOZAWA N NIMURA Y NAKATA S FUJIMORI Y KOIDE N KOIKE S KAJIKAWA S ADACHI W KOBAYASHI S ISHII K AMANO J
Citation: K. Yazawa et al., MULTIPLE CARCINOIDS OF THE DUODENUM ACCOMPANIED BY TYPE-I FAMILIAL MULTIPLE ENDOCRINE NEOPLASIA, SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY, 28(6), 1998, pp. 636-639
ATAXIA-TELANGIECTASIA ASSOCIATED WITH B-CELL LYMPHOMA - THE EFFECT OFA HALF-DOSE OF THE DRUGS ADMINISTERED ACCORDING TO THE ACUTE LYMPHOBLASTIC-LEUKEMIA STANDARD RISK PROTOCOL
Authors: YAMADA Y INOUE R FUKAO T KANEKO H ISOGAI K FUKUDA S SHIMOZAWA N SUZUKI Y KONDO N AZUMA E SAKURAI M
Citation: Y. Yamada et al., ATAXIA-TELANGIECTASIA ASSOCIATED WITH B-CELL LYMPHOMA - THE EFFECT OFA HALF-DOSE OF THE DRUGS ADMINISTERED ACCORDING TO THE ACUTE LYMPHOBLASTIC-LEUKEMIA STANDARD RISK PROTOCOL, Pediatric hematology and oncology, 15(5), 1998, pp. 425-429
MAGNETIC-RESONANCE-IMAGING OF ACUTE CEREBELLAR-ATAXIA - REPORT OF A CASE WITH GADOLINIUM ENHANCEMENT AND REVIEW OF THE LITERATURE
Authors: KATO Z SHIMOZAWA N KOKUZAWA J IWAMURA M HIRATA T YAMAGISHI A HAYASHI T MOTOYOSHI T KONDO N
Citation: Z. Kato et al., MAGNETIC-RESONANCE-IMAGING OF ACUTE CEREBELLAR-ATAXIA - REPORT OF A CASE WITH GADOLINIUM ENHANCEMENT AND REVIEW OF THE LITERATURE, Acta Paediatrica Japonica Overseas Edition, 40(2), 1998, pp. 138-142
PEX12, THE PATHOGENIC GENE OF GROUP-III ZELLWEGER-SYNDROME - CDNA CLONING BY FUNCTIONAL COMPLEMENTATION ON A CHO CELL MUTANT, PATIENT ANALYSIS, AND CHARACTERIZATION OF PEX12P
Authors: OKUMOTO K SHIMOZAWA N KAWAI A TAMURA S TSUKAMOTO T OSUMI T MOSER H WANDERS RJA SUZUKI Y KONDO N FUJIKI Y
Citation: K. Okumoto et al., PEX12, THE PATHOGENIC GENE OF GROUP-III ZELLWEGER-SYNDROME - CDNA CLONING BY FUNCTIONAL COMPLEMENTATION ON A CHO CELL MUTANT, PATIENT ANALYSIS, AND CHARACTERIZATION OF PEX12P, Molecular and cellular biology, 18(7), 1998, pp. 4324-4336
MIXED HEPATOCELLULAR-CARCINOMA AND CHOLANGIOCARCINOMA TREATED BY EXTENDED LEFT HEPATIC LOBECTOMY WITH RESECTION OF THE RIGHT HEPATIC VEIN AND PRESERVATION OF THE INFERIOR RIGHT HEPATIC VEIN AFTER HEPATIC ARTERIAL INFUSION CHEMOTHERAPY
Authors: HANAZAKI K FUJIMORI Y KAJIKAWA S NAKATA S SHIMOZAWA N ADACHI W AMANO J
Citation: K. Hanazaki et al., MIXED HEPATOCELLULAR-CARCINOMA AND CHOLANGIOCARCINOMA TREATED BY EXTENDED LEFT HEPATIC LOBECTOMY WITH RESECTION OF THE RIGHT HEPATIC VEIN AND PRESERVATION OF THE INFERIOR RIGHT HEPATIC VEIN AFTER HEPATIC ARTERIAL INFUSION CHEMOTHERAPY, Hepato-gastroenterology, 45(21), 1998, pp. 812-815
AMINO-ACID AND NUCLEOTIDE-SEQUENCES OF HUMAN PEROXISOMAL ENOYL-COA HYDRATASE - 3-HYDROXYACYL-COA DEHYDROGENASE CDNA
Authors: FUKUDA S SUZUKI Y SHIMOZAWA N ZHANG Z ORII T AOYAMA T HASHIMOTO T KONDO N
Citation: S. Fukuda et al., AMINO-ACID AND NUCLEOTIDE-SEQUENCES OF HUMAN PEROXISOMAL ENOYL-COA HYDRATASE - 3-HYDROXYACYL-COA DEHYDROGENASE CDNA, Journal of inherited metabolic disease, 21(1), 1998, pp. 23-28
ADRENOLEUKODYSTROPHY PROTEIN TRANSPORTS VERY LONG-CHAIN ACYL-COA SYNTHETASE INTO THE PEROXISOME
Authors: YAMADA T SHINNOH N UCHIYAMA A SHIMOZAWA N SUZUKI Y KIRA J
Citation: T. Yamada et al., ADRENOLEUKODYSTROPHY PROTEIN TRANSPORTS VERY LONG-CHAIN ACYL-COA SYNTHETASE INTO THE PEROXISOME, Neurology, 50(4), 1998, pp. 3004-3004
HUMAN PEX1 CLONED BY FUNCTIONAL COMPLEMENTATION ON A CHO CELL MUTANT IS RESPONSIBLE FOR PEROXISOME-DEFICIENT ZELLWEGER-SYNDROME OF COMPLEMENTATION GROUP-I
Authors: TAMURA S OKUMOTO K TOYAMA R SHIMOZAWA N TSUKAMOTO T SUZUKI Y OSUMI T KONDO N FUJIKI Y
Citation: S. Tamura et al., HUMAN PEX1 CLONED BY FUNCTIONAL COMPLEMENTATION ON A CHO CELL MUTANT IS RESPONSIBLE FOR PEROXISOME-DEFICIENT ZELLWEGER-SYNDROME OF COMPLEMENTATION GROUP-I, Proceedings of the National Academy of Sciences of the United Statesof America, 95(8), 1998, pp. 4350-4355
NEWLY IDENTIFIED CHINESE-HAMSTER OVARY CELL MUTANTS ARE DEFECTIVE IN BIOGENESIS OF PEROXISOMAL MEMBRANE-VESICLES (PEROXISOMAL GHOSTS), REPRESENTING A NOVEL COMPLEMENTATION GROUP IN MAMMALS
Authors: KINOSHITA N GHAEDI K SHIMOZAWA N WANDERS RJA MATSUZONO Y IMANAKA T OKUMOTO K SUZUKI Y KONDO N FUJIKI Y
Citation: N. Kinoshita et al., NEWLY IDENTIFIED CHINESE-HAMSTER OVARY CELL MUTANTS ARE DEFECTIVE IN BIOGENESIS OF PEROXISOMAL MEMBRANE-VESICLES (PEROXISOMAL GHOSTS), REPRESENTING A NOVEL COMPLEMENTATION GROUP IN MAMMALS, The Journal of biological chemistry, 273(37), 1998, pp. 24122-24130
PEROXISOME BIOGENESIS DISORDERS - IDENTIFICATION OF A NEW COMPLEMENTATION GROUP DISTINCT FROM PEROXISOME-DEFICIENT CHO MUTANTS AND NOT COMPLEMENTED BY HUMAN PEX-13
Authors: SHIMOZAWA N SUZUKI Y ZHANG ZY IMAMURA A TSUKAMOTO T OSUMI T TATEISHI K OKUMOTO K FUJIKI Y ORII T BARTH PG WANDERS RJA KONDO N
Citation: N. Shimozawa et al., PEROXISOME BIOGENESIS DISORDERS - IDENTIFICATION OF A NEW COMPLEMENTATION GROUP DISTINCT FROM PEROXISOME-DEFICIENT CHO MUTANTS AND NOT COMPLEMENTED BY HUMAN PEX-13, Biochemical and biophysical research communications, 243(2), 1998, pp. 368-371
TEMPERATURE-SENSITIVE PHENOTYPES OF PEROXISOME-ASSEMBLY PROCESSES REPRESENT THE MILDER FORMS OF HUMAN PEROXISOME-BIOGENESIS DISORDERS
Authors: IMAMURA A TSUKAMOTO T SHIMOZAWA N SUZUKI Y ZHANG ZH IMANAKA T FUJIKI Y ORII T KONDO N OSUMI T
Citation: A. Imamura et al., TEMPERATURE-SENSITIVE PHENOTYPES OF PEROXISOME-ASSEMBLY PROCESSES REPRESENT THE MILDER FORMS OF HUMAN PEROXISOME-BIOGENESIS DISORDERS, American journal of human genetics, 62(6), 1998, pp. 1539-1543
THEOPHYLLINE-ASSOCIATED STATUS EPILEPTICUS RESULTING IN QUADRIPLEGIA
Authors: KATO Z YASUDA K SHIMOZAWA N KONDO N
Citation: Z. Kato et al., THEOPHYLLINE-ASSOCIATED STATUS EPILEPTICUS RESULTING IN QUADRIPLEGIA, Annals of allergy, asthma, & immunology, 78(3), 1997, pp. 332-332
HUNTER-DISEASE IN A GIRL CAUSED BY R468Q MUTATION IN THE IDURONATE-2-SULFATASE GENE AND SKEWED INACTIVATION OF THE X-CHROMOSOME CARRYING THE NORMAL ALLELE
Authors: SUKEGAWA K SONG XQ MASUNO M FUKAO T SHIMOZAWA N FUKUDA S ISOGAI K NISHIO H MATSUO M TOMATSU S KONDO N ORII T
Citation: K. Sukegawa et al., HUNTER-DISEASE IN A GIRL CAUSED BY R468Q MUTATION IN THE IDURONATE-2-SULFATASE GENE AND SKEWED INACTIVATION OF THE X-CHROMOSOME CARRYING THE NORMAL ALLELE, Human mutation, 10(5), 1997, pp. 361-367
14 NOVEL MUCOPOLYSACCHARIDOSIS IVA PRODUCING MUTATIONS IN GALNS GENE
Authors: TOMATSU S FUKUDA S COOPER A WRAITH JE FERREIRA P DINATALE P TORTORA P FUJIMOTO A KATO Z YAMADA N ISOGAI K YAMAGISHI A SUKEGAWA K SUZUKI Y SHIMOZAWA N KONDO N SLY WS ORII T
Citation: S. Tomatsu et al., 14 NOVEL MUCOPOLYSACCHARIDOSIS IVA PRODUCING MUTATIONS IN GALNS GENE, Human mutation, 10(5), 1997, pp. 368-375
BIOCHEMICAL AND IMMUNOCYTOCHEMICAL PROPERTIES OF PEROXISOMES AND MITOCHONDRIA IN BOVINE CHROMAFFIN CELLS
Authors: SUZUKI Y LEE K SHIMOZAWA N ORII T KONDO N
Citation: Y. Suzuki et al., BIOCHEMICAL AND IMMUNOCYTOCHEMICAL PROPERTIES OF PEROXISOMES AND MITOCHONDRIA IN BOVINE CHROMAFFIN CELLS, Cell structure and function, 22(6), 1997, pp. 615-619
USE OF BUCCAL SMEARS FOR RAPID DETECTION OF PEROXISOMES
Authors: SUZUKI Y ZHANG Z SHIMOZAWA N ORII T KONDO N
Citation: Y. Suzuki et al., USE OF BUCCAL SMEARS FOR RAPID DETECTION OF PEROXISOMES, European journal of pediatrics, 156(3), 1997, pp. 250-250
NEWLY IDENTIFIED CHINESE-HAMSTER OVARY CELL MUTANTS DEFECTIVE IN PEROXISOME BIOGENESIS REPRESENT 2 NOVEL COMPLEMENTATION GROUPS IN MAMMALS
Authors: TATEISHI K OKUMOTO K SHIMOZAWA N TSUKAMOTO T OSUMI T SUZUKI Y KONDO N OKANO I FUJIKI Y
Citation: K. Tateishi et al., NEWLY IDENTIFIED CHINESE-HAMSTER OVARY CELL MUTANTS DEFECTIVE IN PEROXISOME BIOGENESIS REPRESENT 2 NOVEL COMPLEMENTATION GROUPS IN MAMMALS, European journal of cell biology, 73(4), 1997, pp. 352-359
ISOLATION AND CHARACTERIZATION OF PEROXISOME-DEFICIENT CHINESE-HAMSTER OVARY CELL MUTANTS REPRESENTING HUMAN COMPLEMENTATION GROUP-III
Authors: OKUMOTO K BOGAKI A TATEISHI K TSUKAMOTO T OSUMI T SHIMOZAWA N SUZUKI Y ORII T FUJIKI Y
Citation: K. Okumoto et al., ISOLATION AND CHARACTERIZATION OF PEROXISOME-DEFICIENT CHINESE-HAMSTER OVARY CELL MUTANTS REPRESENTING HUMAN COMPLEMENTATION GROUP-III, Experimental cell research, 233(1), 1997, pp. 11-20
EPILEPSY IN PEROXISOMAL DISEASES
Authors: TAKAHASHI Y SUZUKI Y KUMAZAKI K TANABE Y AKABOSHI S MIURA K SHIMOZAWA N KONDO N NISHIGUCHI T TERADA K ORII T
Citation: Y. Takahashi et al., EPILEPSY IN PEROXISOMAL DISEASES, Epilepsia, 38(2), 1997, pp. 182-188
2 NOVEL MISSENSE MUTATIONS IN THE ATP-BINDING DOMAIN OF THE ADRENOLEUKODYSTROPHY GENE - IMMUNOBLOTTING AND IMMUNOCYTOLOGICAL STUDY OF 2 PATIENTS
Authors: IMAMURA A SUZUKI Y SONG XQ FUKAO T UCHIYAMA A SHIMOZAWA N KAMIJO K HASHIMOTO T ORII T KONDO N
Citation: A. Imamura et al., 2 NOVEL MISSENSE MUTATIONS IN THE ATP-BINDING DOMAIN OF THE ADRENOLEUKODYSTROPHY GENE - IMMUNOBLOTTING AND IMMUNOCYTOLOGICAL STUDY OF 2 PATIENTS, Clinical genetics, 51(5), 1997, pp. 322-325
MARINESCO-SJOGREN-SYNDROME ASSOCIATED WITH ACUTE MYELOBLASTIC-LEUKEMIA
Authors: FUKUDA S YAMADA Y NISHIMURA M ISOGAI K TERADA T IWATA M SHIMOZAWA N SUZUKI Y KONDO N
Citation: S. Fukuda et al., MARINESCO-SJOGREN-SYNDROME ASSOCIATED WITH ACUTE MYELOBLASTIC-LEUKEMIA, Clinical genetics, 51(4), 1997, pp. 278-280
Risultati: 1-25 | 26-50 | 51-75 | 76-82