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Results: 1-25 | 26-27
Results: 1-25/27
MUTATION IN THE EXON-10 (R173W) OF THE HYDROXYMETHYLBILANE SYNTHASE GENE IN 2 UNRELATED JAPANESE FAMILIES WITH ACUTE INTERMITTENT PORPHYRIA
Authors: TOMIE Y HORIE Y TAJIMA F KITAOKA S NANBA E YUASA I KAWASAKI H
Citation: Y. Tomie et al., MUTATION IN THE EXON-10 (R173W) OF THE HYDROXYMETHYLBILANE SYNTHASE GENE IN 2 UNRELATED JAPANESE FAMILIES WITH ACUTE INTERMITTENT PORPHYRIA, Research communications in molecular pathology and pharmacology, 99(1), 1998, pp. 5-15
SERUM-SOLUBLE C-KIT RECEPTOR AND EXPRESSION OF C-KIT PROTEIN AND MESSENGER-RNA IN ACUTE MYELOID-LEUKEMIA
Authors: TAJIMA F KAWATANI T ISHIGA K NANBA E KAWASAKI H
Citation: F. Tajima et al., SERUM-SOLUBLE C-KIT RECEPTOR AND EXPRESSION OF C-KIT PROTEIN AND MESSENGER-RNA IN ACUTE MYELOID-LEUKEMIA, European journal of haematology, 60(5), 1998, pp. 289-296
UNPROVOKED SEIZURES AND EPILEPSIES IN KURAYOSHI, JAPAN
Authors: KIMURA M YOSHINO K NANBA E IESHIMA A NARAI S TAKESHITA K
Citation: M. Kimura et al., UNPROVOKED SEIZURES AND EPILEPSIES IN KURAYOSHI, JAPAN, Journal of epilepsy, 11(3), 1998, pp. 162-167
INCREASED EXPRESSION OF BETA-HEXOSAMINIDASE ALPHA-CHAIN IN CULTURED SKIN FIBROBLASTS FROM PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEINSYNDROME TYPE-I
Authors: ICHISAKA S OHNO K YUASA I NANBA E SAKURABA H SUZUKI Y
Citation: S. Ichisaka et al., INCREASED EXPRESSION OF BETA-HEXOSAMINIDASE ALPHA-CHAIN IN CULTURED SKIN FIBROBLASTS FROM PATIENTS WITH CARBOHYDRATE-DEFICIENT GLYCOPROTEINSYNDROME TYPE-I, Brain & development, 20(5), 1998, pp. 302-306
JIMPY(MSD) MOUSE MUTATION AND CONNATAL PELIZAEUS-MERZBACHER-DISEASE
Authors: YAMAMOTO T NANBA E ZHANG HD SASAKI M KOMAKI H TAKESHITA K
Citation: T. Yamamoto et al., JIMPY(MSD) MOUSE MUTATION AND CONNATAL PELIZAEUS-MERZBACHER-DISEASE, American journal of medical genetics, 75(4), 1998, pp. 439-440
ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY - NOVEL POINT MUTATIONS WITHIN AND ADJACENT TO THE PHOSPHATIDYLINOSITOL 3-KINASE-LIKE DOMAIN
Authors: TOYOSHIMA M HARA T ZHANG HD YAMAMOTO T AKABOSHI S NANBA E OHNO K HORI N SATO K TAKESHITA K
Citation: M. Toyoshima et al., ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY - NOVEL POINT MUTATIONS WITHIN AND ADJACENT TO THE PHOSPHATIDYLINOSITOL 3-KINASE-LIKE DOMAIN, American journal of medical genetics, 75(2), 1998, pp. 141-144
NEUROPATHOLOGICAL CHARACTERIZATION OF ASTROCYTIC HYALINE INCLUSIONS IN FAMILIAR AMYOTROPHIC SCLEROSIS
Authors: KATO S HAYASHI H MIYATA H TANAKA S NAKASHIMA K KATO M NANBA E HIRANO A NAKANO I ASAYAMA K OHAMA E
Citation: S. Kato et al., NEUROPATHOLOGICAL CHARACTERIZATION OF ASTROCYTIC HYALINE INCLUSIONS IN FAMILIAR AMYOTROPHIC SCLEROSIS, Brain pathology, 7(4), 1997, pp. 1074-1074
ABNORMAL EXPANSION OF PERIPHERAL GAMMA-DELTA T-CELLS IN PATIENTS WITHNEUROLOGIC DISORDERS
Authors: YAMAMOTO T HARA T NANBA E OHASHI S SUZUKI N YOSHINO K TAKESHITA K
Citation: T. Yamamoto et al., ABNORMAL EXPANSION OF PERIPHERAL GAMMA-DELTA T-CELLS IN PATIENTS WITHNEUROLOGIC DISORDERS, Brain, behavior, and immunity, 11(3), 1997, pp. 157-166
HUMAN OROSOMUCOID POLYMORPHISM - MOLECULAR-BASIS OF THE 3 COMMON ORM1ALLELES, ORMI(ASTERISK)F1, ORM1(ASTERISK)F2, AND ORM1(ASTERISK)S
Authors: YUASA I UMETSU K VOGT U NAKAMURA H NANBA E TAMAKI N IRIZAWA Y
Citation: I. Yuasa et al., HUMAN OROSOMUCOID POLYMORPHISM - MOLECULAR-BASIS OF THE 3 COMMON ORM1ALLELES, ORMI(ASTERISK)F1, ORM1(ASTERISK)F2, AND ORM1(ASTERISK)S, Human genetics, 99(3), 1997, pp. 393-398
INSTABILITY OF EXPRESSED CU ZN SUPEROXIDE-DISMUTASE WITH 2 BP DELETION FOUND IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS/
Authors: WATANABE Y KONO Y NANBA E OHAMA E NAKASHIMA K
Citation: Y. Watanabe et al., INSTABILITY OF EXPRESSED CU ZN SUPEROXIDE-DISMUTASE WITH 2 BP DELETION FOUND IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS/, FEBS letters, 400(1), 1997, pp. 108-112
ESTABLISHMENT AND CHARACTERISTICS OF A PRACTICAL AND USEFUL ASTROCYTECELL-LINE TRANSFORMED BY A TEMPERATURE-SENSITIVE MUTANT OF SIMIAN-VIRUS-40
Authors: KITAMURA Y MICHIKAWA M TANIGAWA T KATSUMOTO T MORITA T NANBA E OHAMA E TERADA T
Citation: Y. Kitamura et al., ESTABLISHMENT AND CHARACTERISTICS OF A PRACTICAL AND USEFUL ASTROCYTECELL-LINE TRANSFORMED BY A TEMPERATURE-SENSITIVE MUTANT OF SIMIAN-VIRUS-40, Brain research, 759(2), 1997, pp. 295-300
HYPOXIA-INDUCED ABR CHANGE AND HEAT-SHOCK-PROTEIN EXPRESSION IN THE PONTINE AUDITORY PATHWAY OF YOUNG-RABBITS
Authors: INAGAKI M KAGA M ISUMI H HIRANO S TAKASHIMA S NANBA E
Citation: M. Inagaki et al., HYPOXIA-INDUCED ABR CHANGE AND HEAT-SHOCK-PROTEIN EXPRESSION IN THE PONTINE AUDITORY PATHWAY OF YOUNG-RABBITS, Brain research, 757(1), 1997, pp. 111-118
PATHOLOGICAL CHARACTERIZATION OF ASTROCYTIC HYALINE INCLUSIONS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS
Authors: KATO S HAYASHI H NAKASHIMA K NANBA E KATO M HIRANO A NAKANO I ASAYAMA K OHAMA E
Citation: S. Kato et al., PATHOLOGICAL CHARACTERIZATION OF ASTROCYTIC HYALINE INCLUSIONS IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, The American journal of pathology, 151(2), 1997, pp. 611-620
ABSENCE OF THE MUTANT SOD1 IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS (FALS) WITH 2 BASE-PAIR DELETION IN THE SOD1 GENE
Authors: WATANABE Y KUNO N KONO Y NANBA E OHAMA E NAKASHIMA K TAKAHASHI K
Citation: Y. Watanabe et al., ABSENCE OF THE MUTANT SOD1 IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS (FALS) WITH 2 BASE-PAIR DELETION IN THE SOD1 GENE, Acta neurologica Scandinavica, 95(3), 1997, pp. 167-172
PRENATAL-DIAGNOSIS OF CONGENITAL MYOTONIC-DYSTROPHY IN 2 JAPANESE FAMILIES - DIRECT MUTATION ANALYSIS BY A NON-RADIOISOTOPE PCR METHOD AND HAPLOTYPE ANALYSIS WITH FLANKING DNA MARKERS
Authors: NANBA E ITO T KADOWAKI K MAKIO A NAKAGAWA M YAMAMOTO T YUASA I TAKESHITA K
Citation: E. Nanba et al., PRENATAL-DIAGNOSIS OF CONGENITAL MYOTONIC-DYSTROPHY IN 2 JAPANESE FAMILIES - DIRECT MUTATION ANALYSIS BY A NON-RADIOISOTOPE PCR METHOD AND HAPLOTYPE ANALYSIS WITH FLANKING DNA MARKERS, Brain & development, 18(2), 1996, pp. 122-126
EPIDEMIOLOGIC AND GENETIC-STUDIES OF HUNTINGTONS-DISEASE IN THE SAN-IN AREA OF JAPAN
Authors: NAKASHIMA K WATANABE Y KUSUMI M NANBA E MAEOKA Y NAKAGAWA M IGO M IRIE H ISHINO H FUJIMOTO A GOTO J TAKAHASHI K
Citation: K. Nakashima et al., EPIDEMIOLOGIC AND GENETIC-STUDIES OF HUNTINGTONS-DISEASE IN THE SAN-IN AREA OF JAPAN, Neuroepidemiology, 15(3), 1996, pp. 126-131
DIAGNOSIS OF LYMPHOMA IN PARAFFIN WAX SECTIONS BY NESTED PCR AND IMMUNOHISTOCHEMISTRY
Authors: KITAMURA Y NANBA E INUI S TANIGAWA T ICHIHARA K
Citation: Y. Kitamura et al., DIAGNOSIS OF LYMPHOMA IN PARAFFIN WAX SECTIONS BY NESTED PCR AND IMMUNOHISTOCHEMISTRY, Journal of Clinical Pathology, 49(4), 1996, pp. 333-337
A NEW-TYPE OF FAMILIAL CENTRAL DIABETES-INSIPIDUS CAUSED BY A SINGLE-BASE SUBSTITUTION IN THE NEUROPHYSIN-II CODING REGION OF THE VASOPRESSIN GENE
Authors: UETA Y TANIGUCHI S YOSHIDA A MURAKAMI I MITANI Y HISATOME I MANABE I SATO R TSUBOI M OHTAHARA A NANBA E SHIGEMASA C
Citation: Y. Ueta et al., A NEW-TYPE OF FAMILIAL CENTRAL DIABETES-INSIPIDUS CAUSED BY A SINGLE-BASE SUBSTITUTION IN THE NEUROPHYSIN-II CODING REGION OF THE VASOPRESSIN GENE, The Journal of clinical endocrinology and metabolism, 81(5), 1996, pp. 1787-1790
FLUSH INDUCED BY FLUOROQUINOLONES IN CANINE SKIN
Authors: KURATA M KASUGA Y NANBA E NAKAMURA H ASANO T HARUTA K
Citation: M. Kurata et al., FLUSH INDUCED BY FLUOROQUINOLONES IN CANINE SKIN, Inflammation research, 44(11), 1995, pp. 461-465
HEREDITARY NONPROGRESSIVE TORSION DYSTONIA WITH INTELLECTUAL DISTURBANCE
Authors: NAKASHIMA K SHIMODA M SATO K NANBA E
Citation: K. Nakashima et al., HEREDITARY NONPROGRESSIVE TORSION DYSTONIA WITH INTELLECTUAL DISTURBANCE, Internal medicine, 34(9), 1995, pp. 843-846
NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES
Authors: NANBA E KOHNO Y MATSUDA A YANO M SATO C HASHIMOTO K KOEDA T YOSHINO K KIMURA M MAEOKA Y YAMAMOTO T MAEGAKI Y EDA I TAKESHITA K
Citation: E. Nanba et al., NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES, Brain & development, 17(5), 1995, pp. 317-321
ABNORMALITY OF CU ZN SUPEROXIDE-DISMUTASE (SOD1) ACTIVITY IN JAPANESEFAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS WITH 2 BASE-PAIR DELETION IN THE SOD1 GENE/
Authors: NAKASHIMA K WATANABE Y KUNO N NANBA E TAKAHASHI K
Citation: K. Nakashima et al., ABNORMALITY OF CU ZN SUPEROXIDE-DISMUTASE (SOD1) ACTIVITY IN JAPANESEFAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS WITH 2 BASE-PAIR DELETION IN THE SOD1 GENE/, Neurology, 45(5), 1995, pp. 1019-1020
CLINICAL USEFULNESS OF CIMETIDINE TREATMENT FOR ACUTE RELAPSE IN INTERMITTENT PORPHYRIA
Authors: HORIE Y NORIMOTO M TAJIMA F SASAKI H NANBA E KAWASAKI H
Citation: Y. Horie et al., CLINICAL USEFULNESS OF CIMETIDINE TREATMENT FOR ACUTE RELAPSE IN INTERMITTENT PORPHYRIA, Clinica chimica acta, 234(1-2), 1995, pp. 171-175
ANTISENSE OLIGONUCLEOTIDE INHIBITS THE EXPRESSION OF PROCOLLAGEN TYPE-III GENE IN MOUSE FIBROBLASTS
Authors: KITAMURA Y TANIGAWA T NANBA E UENO E FUKUMOTO S ICHIHARA K
Citation: Y. Kitamura et al., ANTISENSE OLIGONUCLEOTIDE INHIBITS THE EXPRESSION OF PROCOLLAGEN TYPE-III GENE IN MOUSE FIBROBLASTS, Biochemical and biophysical research communications, 215(3), 1995, pp. 849-854
A 2-BASEPAIR DELETION IN THE SOD-1 GENE CAUSES FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS
Authors: PRAMATAROVA A GOTO J NANBA E NAKASHIMA K TAKAHASHI K TAKAGI A KANAZAWA I FIGLEWICZ DA ROULEAU GA
Citation: A. Pramatarova et al., A 2-BASEPAIR DELETION IN THE SOD-1 GENE CAUSES FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS, Human molecular genetics, 3(11), 1994, pp. 2061-2062
Risultati: 1-25 | 26-27