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Results: 1-25 | 26-49
Results: 1-25/49
MUTATIONS IN THE INTEGRIN ALPHA-7 GENE CAUSE CONGENITAL MYOPATHY
Authors: HAYASHI YK CHOU FL ENGVALL E OGAWA M MATSUDA C HIRABAYASHI S YOKOCHI K ZIOBER BL KRAMER RH KAUFMAN SJ OZAWA E GOTO Y NONAKA I TSUKAHARA T WANG JZ HOFFMAN EP ARAHATA K
Citation: Yk. Hayashi et al., MUTATIONS IN THE INTEGRIN ALPHA-7 GENE CAUSE CONGENITAL MYOPATHY, Nature genetics, 19(1), 1998, pp. 94-97
INVITED REVIEW - FROM DYSTROPHINOPATHY TO SARCOGLYCANOPATHY - EVOLUTION OF A CONCEPT OF MUSCULAR-DYSTROPHY
Authors: OZAWA E NOGUCHI S MIZUNO Y HAGIWARA Y YOSHIDA M
Citation: E. Ozawa et al., INVITED REVIEW - FROM DYSTROPHINOPATHY TO SARCOGLYCANOPATHY - EVOLUTION OF A CONCEPT OF MUSCULAR-DYSTROPHY, Muscle & nerve, 21(4), 1998, pp. 421-438
DIFFERENTIAL EXPRESSION OF DYSTROPHIN ISOFORMS AND UTROPHIN DURING DIBUTYRYL-CAMP-INDUCED MORPHOLOGICAL-DIFFERENTIATION OF RAT-BRAIN ASTROCYTES
Authors: IMAMURA M OZAWA E
Citation: M. Imamura et E. Ozawa, DIFFERENTIAL EXPRESSION OF DYSTROPHIN ISOFORMS AND UTROPHIN DURING DIBUTYRYL-CAMP-INDUCED MORPHOLOGICAL-DIFFERENTIATION OF RAT-BRAIN ASTROCYTES, Proceedings of the National Academy of Sciences of the United Statesof America, 95(11), 1998, pp. 6139-6144
QUANTIZATION OF GL(1,R) GENERALIZED CHERN-SIMONS THEORY IN 1-DIMENSIONS(1)
Authors: KAWAMOTO N OZAWA E SUEHIRO K
Citation: N. Kawamoto et al., QUANTIZATION OF GL(1,R) GENERALIZED CHERN-SIMONS THEORY IN 1-DIMENSIONS(1), Modern physics letters A, 12(4), 1997, pp. 219-231
MUTATIONS IN THE SARCOGLYCAN GENES IN PATIENTS WITH MYOPATHY
Authors: DUGGAN DJ GOROSPE JR FANIN M HOFFMAN EP ANGELINI C PEGORARO E NOGUCHI S OZAWA E PENDLEBURY W WACLAWIK AJ DUENAS DA HAUSMANOWAPETRUSEWICZ I FIDZIANSKA A BEAN SC HALLER JS BODENSTEINER J GRECO CM PESTRONK A BERARDINELLI A GELINAS DF ABRAM H KUNEL RW
Citation: Dj. Duggan et al., MUTATIONS IN THE SARCOGLYCAN GENES IN PATIENTS WITH MYOPATHY, The New England journal of medicine, 336(9), 1997, pp. 618-624
THE 4TH COMPONENT OF THE SARCOGLYCAN COMPLEX
Authors: YOSHIDA M NOGUCHI S WAKABAYASHI E PILUSO G BELSITO A NIGRO V OZAWA E
Citation: M. Yoshida et al., THE 4TH COMPONENT OF THE SARCOGLYCAN COMPLEX, FEBS letters, 403(2), 1997, pp. 143-148
BETA-SARCOGLYCAN (A3B) MUTATIONS CAUSE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH LOSS OF THE SARCOGLYCAN COMPLEX (VOL 11, PG 266, 1995)
Authors: BONNEMAN CG MODI R NOGUCHI S MIZUNO Y YOSHIDA M GUSSONI E MCNALLEY EN DUGGAN DJ ANGELINI C HOFFMAN EP OZAWA E KUNKEL LM
Citation: Cg. Bonneman et al., BETA-SARCOGLYCAN (A3B) MUTATIONS CAUSE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH LOSS OF THE SARCOGLYCAN COMPLEX (VOL 11, PG 266, 1995), Nature genetics, 12(1), 1996, pp. 110-110
GENOMIC SCREENING FOR BETA-SARCOGLYCAN GENE-MUTATIONS - MISSENSE MUTATIONS MAY CAUSE SEVERE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2E (LGMD 2E)
Authors: BONNEMANN CG PASSOSBUENO MR MCNALLY EM VAINZOF M MOREIRA ED MARIE SK PAVANELLO RCM NOGUCHI S OZAWA E ZATZ M KUNKEL LM
Citation: Cg. Bonnemann et al., GENOMIC SCREENING FOR BETA-SARCOGLYCAN GENE-MUTATIONS - MISSENSE MUTATIONS MAY CAUSE SEVERE LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2E (LGMD 2E), Human molecular genetics, 5(12), 1996, pp. 1953-1961
MUTATIONS THAT DISRUPT THE CARBOXYL-TERMINUS OF GAMMA-SARCOGLYCAN CAUSE MUSCULAR-DYSTROPHY
Authors: MCNALLY EM DUGGAN D GOROSPE JR BONNEMANN CG FANIN M PEGORARO E LIDOV HGW NOGUCHI S OZAWA E FINKEL RS CRUSE RP ANGELINI C KUNKEL LM HOFFMAN EP
Citation: Em. Mcnally et al., MUTATIONS THAT DISRUPT THE CARBOXYL-TERMINUS OF GAMMA-SARCOGLYCAN CAUSE MUSCULAR-DYSTROPHY, Human molecular genetics, 5(11), 1996, pp. 1841-1847
ABNORMALITIES IN ALPHA-SARCOGLYCAN, BETA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN IN PATIENTS WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: SEWRY CA TAYLOR J ANDERSON LVB OZAWA E POGUE R PICCOLO F BUSHBY K DUBOWITZ V MUNTONI F
Citation: Ca. Sewry et al., ABNORMALITIES IN ALPHA-SARCOGLYCAN, BETA-SARCOGLYCAN AND GAMMA-SARCOGLYCAN IN PATIENTS WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY, Neuromuscular disorders, 6(6), 1996, pp. 467-474
NEUROSENSORY HEARING-LOSS IN SECONDARY ADHALINOPATHY
Authors: OEXLE K HERRMANN R DODE C LETURCQ F HUBNER C KAPLAN JC MIZUNO Y OZAWA E CAMPBELL KP VOIT T
Citation: K. Oexle et al., NEUROSENSORY HEARING-LOSS IN SECONDARY ADHALINOPATHY, Neuropediatrics, 27(1), 1996, pp. 32-36
CONGENITAL MUSCULAR-DYSTROPHY - CLINICAL AND PATHOLOGICAL-STUDY OF 50PATIENTS WITH THE CLASSICAL (OCCIDENTAL) MEROSIN-POSITIVE FORM
Authors: KOBAYASHI O HAYASHI Y ARAHATA K OZAWA E NONAKA I
Citation: O. Kobayashi et al., CONGENITAL MUSCULAR-DYSTROPHY - CLINICAL AND PATHOLOGICAL-STUDY OF 50PATIENTS WITH THE CLASSICAL (OCCIDENTAL) MEROSIN-POSITIVE FORM, Neurology, 46(3), 1996, pp. 815-818
SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY EXHIBITS HETEROGENEITY AT PROTEIN AND DNA LEVEL
Authors: KYRIAKIDES T CHRISTODOULOU K SODIEONO O OZAWA E ALDIN ASM VANCE J MIDDLETON L
Citation: T. Kyriakides et al., SEVERE CHILDHOOD AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY EXHIBITS HETEROGENEITY AT PROTEIN AND DNA LEVEL, Neurology, 46(2), 1996, pp. 4082-4082
MOLECULAR AND CLINICAL-FEATURES OF BETA-SARCOGLYCAN DEFICIENCY
Authors: HOFFMAN EP DUGGAN D GOROSPE JRM PEGORARO E BONNEMANN CG KUNKEL LM NOGUCHI S OZAWA E
Citation: Ep. Hoffman et al., MOLECULAR AND CLINICAL-FEATURES OF BETA-SARCOGLYCAN DEFICIENCY, Neurology, 46(2), 1996, pp. 12003-12003
THE 3 HUMAN SYNTROPHIN GENES ARE EXPRESSED IN DIVERSE TISSUES, HAVE DISTINCT CHROMOSOMAL LOCATIONS, AND EACH BIND TO DYSTROPHIN AND ITS RELATIVES
Authors: AHN AH FREENER CA GUSSONI E YOSHIDA M OZAWA E KUNKEL LM
Citation: Ah. Ahn et al., THE 3 HUMAN SYNTROPHIN GENES ARE EXPRESSED IN DIVERSE TISSUES, HAVE DISTINCT CHROMOSOMAL LOCATIONS, AND EACH BIND TO DYSTROPHIN AND ITS RELATIVES, The Journal of biological chemistry, 271(5), 1996, pp. 2724-2730
ON THE CHILDS ACQUISITION OF DIMENSIONAL TERMS
Authors: OZAWA E YOSHIMURA H
Citation: E. Ozawa et H. Yoshimura, ON THE CHILDS ACQUISITION OF DIMENSIONAL TERMS, International journal of psychology, 31(3-4), 1996, pp. 2247-2247
GRAMMATICAL CHARACTERISTICS OF MOTHERESE IN JAPANESE
Authors: SHIBAMURA K OZAWA E OHMORI A
Citation: K. Shibamura et al., GRAMMATICAL CHARACTERISTICS OF MOTHERESE IN JAPANESE, International journal of psychology, 31(3-4), 1996, pp. 28474-28474
AN ANALYSIS OF YOUNG CHILDRENS GESTURE IN SPEAKING
Authors: OHMORI A OZAWA E SHIBAMURA K
Citation: A. Ohmori et al., AN ANALYSIS OF YOUNG CHILDRENS GESTURE IN SPEAKING, International journal of psychology, 31(3-4), 1996, pp. 28499-28499
BETA-SARCOGLYCAN (A3B) MUTATIONS CAUSE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH LOSS OF THE SARCOGLYCAN COMPLEX
Authors: BONNEMANN CG MODI R NOGUCHI S MIZUNO Y YOSHIDA M GUSSONI E MCNALLY EM DUGGAN DJ ANGELINI C HOFFMAN EP OZAWA E KUNKEL LM
Citation: Cg. Bonnemann et al., BETA-SARCOGLYCAN (A3B) MUTATIONS CAUSE AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY WITH LOSS OF THE SARCOGLYCAN COMPLEX, Nature genetics, 11(3), 1995, pp. 266-273
DYSTROPHIN-ASSOCIATED PROTEINS IN MUSCULAR-DYSTROPHY
Authors: OZAWA E YOSHIDA M SUZUKI A MIZUNO Y HAGIWARA Y NOGUCHI S
Citation: E. Ozawa et al., DYSTROPHIN-ASSOCIATED PROTEINS IN MUSCULAR-DYSTROPHY, Human molecular genetics, 4, 1995, pp. 1711-1716
SARCOLEMMAL INDENTATION IN CARDIOMYOPATHY WITH MENTAL-RETARDATION ANDVACUOLAR MYOPATHY
Authors: MURAKAMI N GOTO Y ITOH M KATSUMI Y WADA T OZAWA E NONAKA I
Citation: N. Murakami et al., SARCOLEMMAL INDENTATION IN CARDIOMYOPATHY WITH MENTAL-RETARDATION ANDVACUOLAR MYOPATHY, Neuromuscular disorders, 5(2), 1995, pp. 149-155
MYOGENIC CELL-MIGRATION FROM SOMITES IS INDUCED BY TISSUE CONTACT WITH MEDIAL REGION OF THE PRESUMPTIVE LIMB MESODERM IN CHICK-EMBRYOS
Authors: HAYASHI K OZAWA E
Citation: K. Hayashi et E. Ozawa, MYOGENIC CELL-MIGRATION FROM SOMITES IS INDUCED BY TISSUE CONTACT WITH MEDIAL REGION OF THE PRESUMPTIVE LIMB MESODERM IN CHICK-EMBRYOS, Development, 121(3), 1995, pp. 661-669
MUTATIONS IN THE DYSTROPHIN-ASSOCIATED PROTEIN GAMMA-SARCOGLYCAN IN CHROMOSOME-13 MUSCULAR-DYSTROPHY
Authors: NOGUCHI S MCNALLY EM BENOTHMANE K HAGIWARA Y MIZUNO Y YOSHIDA M YAMAMOTO H BONNEMANN CG GUSSONI E DENTON PH KYRIAKIDES T MIDDLETON L HENTATI F BENHAMIDA M NONAKA I VANCE JM KUNKEL LM OZAWA E
Citation: S. Noguchi et al., MUTATIONS IN THE DYSTROPHIN-ASSOCIATED PROTEIN GAMMA-SARCOGLYCAN IN CHROMOSOME-13 MUSCULAR-DYSTROPHY, Science, 270(5237), 1995, pp. 819-822
THE FREQUENCY OF PATIENTS WITH 50-KD DYSTROPHIN-ASSOCIATED GLYCOPROTEIN (50DAG OR ADHALIN) DEFICIENCY IN A MUSCULAR-DYSTROPHY PATIENT POPULATION IN JAPAN - IMMUNOCYTOCHEMICAL ANALYSIS OF 50DAG, 43DAG, DYSTROPHIN, AND UTROPHIN
Authors: HAYASHI YK MIZUNO Y YOSHIDA M NONAKA I OZAWA E ARAHATA K
Citation: Yk. Hayashi et al., THE FREQUENCY OF PATIENTS WITH 50-KD DYSTROPHIN-ASSOCIATED GLYCOPROTEIN (50DAG OR ADHALIN) DEFICIENCY IN A MUSCULAR-DYSTROPHY PATIENT POPULATION IN JAPAN - IMMUNOCYTOCHEMICAL ANALYSIS OF 50DAG, 43DAG, DYSTROPHIN, AND UTROPHIN, Neurology, 45(3), 1995, pp. 551-554
LIMB-GIRDLE MUSCULAR-DYSTROPHY - CLINICAL AND PATHOLOGICAL REEVALUATION
Authors: YAMANOUCHI Y ARIKAWA E ARAHATA K OZAWA E NONAKA I
Citation: Y. Yamanouchi et al., LIMB-GIRDLE MUSCULAR-DYSTROPHY - CLINICAL AND PATHOLOGICAL REEVALUATION, Journal of the neurological sciences, 129(1), 1995, pp. 15-20
Risultati: 1-25 | 26-49