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Results: 1-20 |
Results: 20
UTROPHIN MESSENGER-RNA EXPRESSION IN MUSCLE IS NOT RESTRICTED TO THE NEUROMUSCULAR-JUNCTION
Authors: VATER R YOUNG C ANDERSON LVB LINDSAY S BLAKE DJ DAVIES KE ZUELLIG R SLATER CR
Citation: R. Vater et al., UTROPHIN MESSENGER-RNA EXPRESSION IN MUSCLE IS NOT RESTRICTED TO THE NEUROMUSCULAR-JUNCTION, Molecular and cellular neurosciences, 10(5-6), 1998, pp. 229-242
ALTERNATIVE DYSTROPHIN GENE TRANSCRIPTS IN GOLDEN RETRIEVER MUSCULAR-DYSTROPHY
Authors: SCHATZBERG SJ ANDERSON LVB WILTON SD KORNEGAY JN MANN CJ SOLOMON GG SHARP NJH
Citation: Sj. Schatzberg et al., ALTERNATIVE DYSTROPHIN GENE TRANSCRIPTS IN GOLDEN RETRIEVER MUSCULAR-DYSTROPHY, Muscle & nerve, 21(8), 1998, pp. 991-998
ABNORMAL MEROSIN IN ADULTS - A NEW FORM OF LATE-ONSET MUSCULAR-DYSTROPHY NOT LINKED TO CHROMOSOME 6Q2
Authors: BUSHBY K ANDERSON LVB POLLITT C NAOM I MUNTONI F BINDOFF L
Citation: K. Bushby et al., ABNORMAL MEROSIN IN ADULTS - A NEW FORM OF LATE-ONSET MUSCULAR-DYSTROPHY NOT LINKED TO CHROMOSOME 6Q2, Brain, 121, 1998, pp. 581-588
CHARACTERIZATION OF MONOCLONAL-ANTIBODIES TO CALPAIN-3 AND PROTEIN EXPRESSION IN MUSCLE FROM PATIENTS WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A
Authors: ANDERSON LVB DAVISON K MOSS JA RICHARD I FARDEAU M TOME FMS HUBNER C LASA A COLOMER J BECKMANN JS
Citation: Lvb. Anderson et al., CHARACTERIZATION OF MONOCLONAL-ANTIBODIES TO CALPAIN-3 AND PROTEIN EXPRESSION IN MUSCLE FROM PATIENTS WITH LIMB-GIRDLE MUSCULAR-DYSTROPHY TYPE 2A, The American journal of pathology, 153(4), 1998, pp. 1169-1179
DYSTROBREVIN DEFICIENCY AT THE SARCOLEMMA OF PATIENTS WITH MUSCULAR-DYSTROPHY
Authors: METZINGER L BLAKE DJ SQUIER MV ANDERSON LVB DECONINCK AE NAWROTZKI R HILTONJONES D DAVIES KE
Citation: L. Metzinger et al., DYSTROBREVIN DEFICIENCY AT THE SARCOLEMMA OF PATIENTS WITH MUSCULAR-DYSTROPHY, Human molecular genetics, 6(7), 1997, pp. 1185-1191
ABSENCE OF CALPAIN-3 IN A FORM OF LIMB-GIRDLE MUSCULAR-DYSTROPHY (LGMD2A)
Authors: SPENCER MJ TIDBALL JG ANDERSON LVB BUSHBY KMD HARRIS JB PASSOSBUENO MR SOMER H VAINZOF M ZATZ M
Citation: Mj. Spencer et al., ABSENCE OF CALPAIN-3 IN A FORM OF LIMB-GIRDLE MUSCULAR-DYSTROPHY (LGMD2A), Journal of the neurological sciences, 146(2), 1997, pp. 173-178
DYSTROPHINOPATHY OR SARCOGLYCANOPATHY - THE IMPORTANCE OF A FULL DIAGNOSTIC-ASSESSMENT IN SUSPECTED MANIFESTING CARRIERS OF DUCHENNE AND BECKER MUSCULAR-DYSTROPHY
Authors: BUSHBY K ANDERSON LVB SEWRY C POGUE R TAYLOR J POLLITT C MUNTONI F
Citation: K. Bushby et al., DYSTROPHINOPATHY OR SARCOGLYCANOPATHY - THE IMPORTANCE OF A FULL DIAGNOSTIC-ASSESSMENT IN SUSPECTED MANIFESTING CARRIERS OF DUCHENNE AND BECKER MUSCULAR-DYSTROPHY, Journal of Medical Genetics, 34, 1997, pp. 522-522
A ROLE OF DYSTROGLYCAN IN SCHWANNOMA CELL-ADHESION TO LAMININ
Authors: MATSUMURA K CHIBA A YAMADA H FUKUTAOHI H FUJITA S ENDO T KOBATA A ANDERSON LVB KANAZAWA I CAMPBELL KP SHIMIZU T
Citation: K. Matsumura et al., A ROLE OF DYSTROGLYCAN IN SCHWANNOMA CELL-ADHESION TO LAMININ, The Journal of biological chemistry, 272(21), 1997, pp. 13904-13910
UTROPHIN ABUNDANCE IS REDUCED AT NEUROMUSCULAR-JUNCTIONS OF PATIENTS WITH BOTH INHERITED AND ACQUIRED ACETYLCHOLINE-RECEPTOR DEFICIENCIES
Authors: SLATER CR YOUNG C WOOD SJ BEWICK GS ANDERSON LVB BAXTER P FAWCETT PRW ROBERTS M JACOBSON L KUKS J VINCENT A NEWSOMDAVIS J
Citation: Cr. Slater et al., UTROPHIN ABUNDANCE IS REDUCED AT NEUROMUSCULAR-JUNCTIONS OF PATIENTS WITH BOTH INHERITED AND ACQUIRED ACETYLCHOLINE-RECEPTOR DEFICIENCIES, Brain, 120, 1997, pp. 1513-1531
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
OPTIMIZED PROTEIN DIAGNOSIS IN THE AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES
Authors: ANDERSON LVB
Citation: Lvb. Anderson, OPTIMIZED PROTEIN DIAGNOSIS IN THE AUTOSOMAL RECESSIVE LIMB-GIRDLE MUSCULAR-DYSTROPHIES, Neuromuscular disorders, 6(6), 1996, pp. 443-446
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
RESEARCH DATABASE FOR DYSTROPHIN GENE AND PROTEIN EXPRESSION - 35TH ENMC WORKSHOP, 6-8 OCTOBER 1995, NAARDEN, THE NETHERLANDS
Authors: ANDERSON LVB
Citation: Lvb. Anderson, RESEARCH DATABASE FOR DYSTROPHIN GENE AND PROTEIN EXPRESSION - 35TH ENMC WORKSHOP, 6-8 OCTOBER 1995, NAARDEN, THE NETHERLANDS, Neuromuscular disorders, 6(3), 1996, pp. 219-219
DYSTROPHIN AND THE DYSTROPHIN-ASSOCIATED GLYCOPROTEIN, BETA-DYSTROGLYCAN, CO-LOCALIZE IN PHOTORECEPTOR SYNAPTIC COMPLEXES OF THE HUMAN RETINA
Authors: DRENCKHAHN D HOLBACH M NESS W SCHMITZ F ANDERSON LVB
Citation: D. Drenckhahn et al., DYSTROPHIN AND THE DYSTROPHIN-ASSOCIATED GLYCOPROTEIN, BETA-DYSTROGLYCAN, CO-LOCALIZE IN PHOTORECEPTOR SYNAPTIC COMPLEXES OF THE HUMAN RETINA, Neuroscience, 73(2), 1996, pp. 605-612
COSTAMERIC DISTRIBUTION OF BETA-DYSTROGLYCAN (43KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN) IN NORMAL AND DYSTROPHIN-DEFICIENT HUMAN SKELETAL-MUSCLE
Authors: HERRMANN R ANDERSON LVB VOIT T
Citation: R. Herrmann et al., COSTAMERIC DISTRIBUTION OF BETA-DYSTROGLYCAN (43KDA DYSTROPHIN-ASSOCIATED GLYCOPROTEIN) IN NORMAL AND DYSTROPHIN-DEFICIENT HUMAN SKELETAL-MUSCLE, Biochemical Society transactions, 24(2), 1996, pp. 501-506
DISTRIBUTION OF UTROPHIN MESSENGER-RNA IN RAT SKELETAL-MUSCLE
Authors: VATER R YOUNG C LINDSAY SJ ANDERSON LVB SLATER CR
Citation: R. Vater et al., DISTRIBUTION OF UTROPHIN MESSENGER-RNA IN RAT SKELETAL-MUSCLE, The Journal of general physiology, 108(2), 1996, pp. 80-80
DYSTROGLYCAN IS A DUAL RECEPTOR FOR AGRIN AND LAMININ-2 IN SCHWANN-CELL MEMBRANE
Authors: YAMADA H DENZER AJ HORI H TANAKA T ANDERSON LVB FUJITA S FUKUTAOHI H SHIMIZU T RUEGG MA MATSUMURA K
Citation: H. Yamada et al., DYSTROGLYCAN IS A DUAL RECEPTOR FOR AGRIN AND LAMININ-2 IN SCHWANN-CELL MEMBRANE, The Journal of biological chemistry, 271(38), 1996, pp. 23418-23423
THE EXPRESSION OF DYSTROPHIN-ASSOCIATED GLYCOPROTEINS DURING SKELETAL-MUSCLE DEGENERATION AND REGENERATION - AN IMMUNOFLUORESCENCE STUDY
Authors: VATER R HARRIS JB ANDERSON LVB ROBERDS SL CAMPBELL KP CULLEN MJ
Citation: R. Vater et al., THE EXPRESSION OF DYSTROPHIN-ASSOCIATED GLYCOPROTEINS DURING SKELETAL-MUSCLE DEGENERATION AND REGENERATION - AN IMMUNOFLUORESCENCE STUDY, Journal of neuropathology and experimental neurology, 54(4), 1995, pp. 557-569
DELETION STATUS AND INTELLECTUAL IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY
Authors: BUSHBY KMD APPLETON R ANDERSON LVB WELCH JL KELLY P GARDNERMEDWIN D
Citation: Kmd. Bushby et al., DELETION STATUS AND INTELLECTUAL IMPAIRMENT IN DUCHENNE MUSCULAR-DYSTROPHY, Developmental Medicine and Child Neurology, 37(3), 1995, pp. 260-269
BECKER MUSCULAR-DYSTROPHY WITH ONSET AFTER 60 YEARS
Authors: HEALD A ANDERSON LVB BUSHBY KMD SHAW PJ
Citation: A. Heald et al., BECKER MUSCULAR-DYSTROPHY WITH ONSET AFTER 60 YEARS, Neurology, 44(12), 1994, pp. 2388-2390
Risultati: 1-20 |