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Results: 1-23 |
Results: 23
MICE LACKING SARCOGLYCAN EXHIBIT APOPTOSIS AND SARCOLEMMAL INSTABILITY WITH NORMAL DYSTROPHIN
Authors: HACK AA LY CT JIANG F CLENDENIN CJ SIGRIST KS WOLLMAN RL MCNALLY EM
Citation: Aa. Hack et al., MICE LACKING SARCOGLYCAN EXHIBIT APOPTOSIS AND SARCOLEMMAL INSTABILITY WITH NORMAL DYSTROPHIN, Molecular biology of the cell, 9, 1998, pp. 151-151
CAVEOLIN-3 IN MUSCULAR-DYSTROPHY
Authors: MCNALLY EM MOREIRA ED DUGGAN DJ LISANTI MP LIDOV HGW VAINZOF M BONNEMANN CG PASSOSBUENO MR HOFFMAN EP ZATZ M KUNKEL LM
Citation: Em. Mcnally et al., CAVEOLIN-3 IN MUSCULAR-DYSTROPHY, Human molecular genetics, 7(5), 1998, pp. 871-877
GAMMA-SARCOGLYCAN DEFICIENCY LEADS TO MUSCLE MEMBRANE DEFECTS AND APOPTOSIS INDEPENDENT OF DYSTROPHIN
Authors: HACK AA LY CT JIANG F CLENDENIN CJ SIGRIST KS WOLLMANN RL MCNALLY EM
Citation: Aa. Hack et al., GAMMA-SARCOGLYCAN DEFICIENCY LEADS TO MUSCLE MEMBRANE DEFECTS AND APOPTOSIS INDEPENDENT OF DYSTROPHIN, The Journal of cell biology, 142(5), 1998, pp. 1279-1287
HUMAN EPSILON-SARCOGLYCAN IS HIGHLY RELATED TO ALPHA-SARCOGLYCAN (ADHALIN), THE LIMB-GIRDLE MUSCULAR-DYSTROPHY 2D GENE
Authors: MCNALLY EM LY CT KUNKEL LM
Citation: Em. Mcnally et al., HUMAN EPSILON-SARCOGLYCAN IS HIGHLY RELATED TO ALPHA-SARCOGLYCAN (ADHALIN), THE LIMB-GIRDLE MUSCULAR-DYSTROPHY 2D GENE, FEBS letters, 422(1), 1998, pp. 27-32
GENETIC AND PHYSICA MAPPING OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT AND MUSCULAR-DYSTROPHY (FDC-CDM)
Authors: ZHU X LY CT MESSINA DN MCNALLY EM
Citation: X. Zhu et al., GENETIC AND PHYSICA MAPPING OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT AND MUSCULAR-DYSTROPHY (FDC-CDM), Circulation, 98(17), 1998, pp. 3127-3127
GENETIC-LINKAGE OF AUTOSOMAL-DOMINANT DILATED CARDIOMYOPATHY AND LIMB-GIRDLE MUSCULAR-DYSTROPHY
Authors: MCNALLY EM SPEER MC PERICAKVANCE MA MESSINA DN
Citation: Em. Mcnally et al., GENETIC-LINKAGE OF AUTOSOMAL-DOMINANT DILATED CARDIOMYOPATHY AND LIMB-GIRDLE MUSCULAR-DYSTROPHY, American journal of human genetics, 61(4), 1997, pp. 145-145
PHYSICAL MAPPING AND DISTANCE REFINEMENT OF A MARKER (D13S232) IN COMPLETE LINKAGE DISEQUILIBRIUM WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C)
Authors: ROCHELLE JM BENOTHMANE K HENTATI F BARKER J PERICAKVANCE MA MCNALLY EM KUNKEL L VANCE JM
Citation: Jm. Rochelle et al., PHYSICAL MAPPING AND DISTANCE REFINEMENT OF A MARKER (D13S232) IN COMPLETE LINKAGE DISEQUILIBRIUM WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2C (LGMD2C), American journal of human genetics, 61(4), 1997, pp. 2295-2295
LINKAGE OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT ANDMUSCULAR-DYSTROPHY TO CHROMOSOME 6Q23
Authors: MESSINA DN SPEER MC PERICAKVANCE MA MCNALLY EM
Citation: Dn. Messina et al., LINKAGE OF FAMILIAL DILATED CARDIOMYOPATHY WITH CONDUCTION DEFECT ANDMUSCULAR-DYSTROPHY TO CHROMOSOME 6Q23, American journal of human genetics, 61(4), 1997, pp. 909-917
GENETIC LOCALIZATION OF A NEWLY RECOGNIZED AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIAC INVOLVEMENT (LGMD1B) TO CHROMOSOME 1Q11-21
Authors: VANDERKOOI AJ VANMEEGEN M LEDDERHOF TM MCNALLY EM DEVISSER M BOLHUIS PA
Citation: Aj. Vanderkooi et al., GENETIC LOCALIZATION OF A NEWLY RECOGNIZED AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIAC INVOLVEMENT (LGMD1B) TO CHROMOSOME 1Q11-21, American journal of human genetics, 60(4), 1997, pp. 891-895
INTERACTION OF ARIA, A NEUREGULIN, WITH THE DYSTROGLYCAN SARCOGLYCAN COMPLEX IN SKELETAL-MUSCLE/
Authors: KHURANA TS BONNEMANN CG MCNALLY EM KUNKEL LM FISCHBACH GD
Citation: Ts. Khurana et al., INTERACTION OF ARIA, A NEUREGULIN, WITH THE DYSTROGLYCAN SARCOGLYCAN COMPLEX IN SKELETAL-MUSCLE/, Molecular biology of the cell, 7, 1996, pp. 1826-1826
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
THE SARCOGLYCAN COMPLEX IN THE 6 AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES
Authors: VAINZOF M PASSOSBUENO MR CANOVAS M MOREIRA ES PAVANELLO RCM MARIE SK ANDERSON LVB BONNEMANN CG MCNALLY EM NIGRO V KUNKEL LM ZATZ M
Citation: M. Vainzof et al., THE SARCOGLYCAN COMPLEX IN THE 6 AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES, Human molecular genetics, 5(12), 1996, pp. 1963-1969
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
DEFICIENCY OF ADHALIN IN A PATIENT WITH MUSCULAR-DYSTROPHY AND CARDIOMYOPATHY
Authors: MCNALLY EM BONNEMANN CG KUNKEL LM BHATTACHARYA SK
Citation: Em. Mcnally et al., DEFICIENCY OF ADHALIN IN A PATIENT WITH MUSCULAR-DYSTROPHY AND CARDIOMYOPATHY, The New England journal of medicine, 334(24), 1996, pp. 1610-1611
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
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
IGG BUT NOT OTHER CLASSES OF ANTI-[(H2A-H2B)-DNA] IS AN EARLY SIGN OFPROCAINAMIDE-INDUCED LUPUS
Authors: RUBIN RL BURLINGAME RW ARNOTT JE TOTORITIS MC MCNALLY EM JOHNSON AD
Citation: Rl. Rubin et al., IGG BUT NOT OTHER CLASSES OF ANTI-[(H2A-H2B)-DNA] IS AN EARLY SIGN OFPROCAINAMIDE-INDUCED LUPUS, The Journal of immunology, 154(5), 1995, pp. 2483-2493
NOVEL ACTIN CROSS-LINKER SUPERFAMILY MEMBER IDENTIFIED BY A 2-STEP DEGENERATE PCR PROCEDURE
Authors: BYERS TJ BEGGS AH MCNALLY EM KUNKEL LM
Citation: Tj. Byers et al., NOVEL ACTIN CROSS-LINKER SUPERFAMILY MEMBER IDENTIFIED BY A 2-STEP DEGENERATE PCR PROCEDURE, FEBS letters, 368(3), 1995, pp. 500-504
THE 43 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN A3B IS MUTATED IN AN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY
Authors: BONNEMANN CG MODI R NOGUCHI S YOSHIDA M GUSSONI E MCNALLY EM DUGGAN DJ ANGELINI C HOFFMAN EP OZAWA E KUNKEL LM
Citation: Cg. Bonnemann et al., THE 43 KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN A3B IS MUTATED IN AN AUTOSOMAL RECESSIVE MUSCULAR-DYSTROPHY, American journal of human genetics, 57(4), 1995, pp. 102-102
AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIOMYOPATHY- A GENETICALLY DISTINCT DISORDER
Authors: MCNALLY EM LIDOV HGW KUNKEL LM
Citation: Em. Mcnally et al., AUTOSOMAL-DOMINANT LIMB-GIRDLE MUSCULAR-DYSTROPHY WITH CARDIOMYOPATHY- A GENETICALLY DISTINCT DISORDER, American journal of human genetics, 57(4), 1995, pp. 283-283
HUMAN ADHALIN IS ALTERNATIVELY SPLICED AND THE GENE IS LOCATED ON CHROMOSOME 17Q21
Authors: MCNALLY EM YOSHIDA M MIZUNO Y OZAWA E KUNKEL LM
Citation: Em. Mcnally et al., HUMAN ADHALIN IS ALTERNATIVELY SPLICED AND THE GENE IS LOCATED ON CHROMOSOME 17Q21, Proceedings of the National Academy of Sciences of the United Statesof America, 91(21), 1994, pp. 9690-9694
CHARACTERIZATION OF THE GENE ENCODING ADHALIN, THE 50 KD DYSTROPHIN-ASSOCIATED PROTEIN - A CANDIDATE GENE FOR CARDIOMYOPATHY
Authors: MCNALLY EM KUNKEL LM
Citation: Em. Mcnally et Lm. Kunkel, CHARACTERIZATION OF THE GENE ENCODING ADHALIN, THE 50 KD DYSTROPHIN-ASSOCIATED PROTEIN - A CANDIDATE GENE FOR CARDIOMYOPATHY, Circulation, 90(4), 1994, pp. 319-319
CHARACTERIZATION OF THE GENE ENCODING ADHALIN, THE 50 KD DYSTROPHIN-ASSOCIATED PROTEIN - A CANDIDATE GENE FOR CARDIOMYOPATHY
Authors: MCNALLY EM KUNKEL LM
Citation: Em. Mcnally et Lm. Kunkel, CHARACTERIZATION OF THE GENE ENCODING ADHALIN, THE 50 KD DYSTROPHIN-ASSOCIATED PROTEIN - A CANDIDATE GENE FOR CARDIOMYOPATHY, Circulation, 90(4), 1994, pp. 319-319
Risultati: 1-23 |