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Results: 1-25 | 26-38
Results: 1-25/38
The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy
Authors: Morris, GE
Citation: Ge. Morris, The role of the nuclear envelope in Emery-Dreifuss muscular dystrophy, TRENDS MO M, 7(12), 2001, pp. 572-577
Problems with LAP nomenclature
Authors: Wilson, KL Benavente, R Burke, B Craigie, R Foisner, R Furukawa, K Gerace, L Goldman, RD Gruenbaum, Y Harris, C Hutchison, CJ Krohne, G Morris, GE Otto, H Simon, AJ Worman, HJ
Citation: Kl. Wilson et al., Problems with LAP nomenclature, NAT CELL BI, 3(4), 2001, pp. E90-E90
The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin
Authors: Holt, I Clements, L Manilal, S Brown, SC Morris, GE
Citation: I. Holt et al., The R482Q lamin A/C mutation that causes lipodystrophy does not prevent nuclear targeting of lamin A in adipocytes or its interaction with emerin, EUR J HUM G, 9(3), 2001, pp. 204-208
The exon 2b region of the spinal muscular atophy protein, SMN, is involvedin self-association and SIP1 binding (vol 9, pg 2869, 2000)
Authors: Young, PJ Man, NT Lorson, CL Le, TT Androphy, EJ Burghes, AHM Morris, GE
Citation: Pj. Young et al., The exon 2b region of the spinal muscular atophy protein, SMN, is involvedin self-association and SIP1 binding (vol 9, pg 2869, 2000), HUM MOL GEN, 10(1), 2001, pp. 88-88
Polyphosphate interaction with aluminium-doped titania pigment particles
Authors: Taylor, ML Morris, GE Smart, RSC
Citation: Ml. Taylor et al., Polyphosphate interaction with aluminium-doped titania pigment particles, COLL SURF A, 190(3), 2001, pp. 285-294
Structure of an intermediate in the unfolding of creatine kinase
Authors: Webb, TI Morris, GE
Citation: Ti. Webb et Ge. Morris, Structure of an intermediate in the unfolding of creatine kinase, PROTEINS, 42(2), 2001, pp. 269-278
Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations
Authors: Sewry, CA Brown, SC Mercuri, E Bonne, G Feng, L Camici, G Morris, GE Muntoni, F
Citation: Ca. Sewry et al., Skeletal muscle pathology in autosomal dominant Emery-Dreifuss muscular dystrophy with lamin A/C mutations, NEUROP AP N, 27(4), 2001, pp. 281-290
Epitopes in the interacting regions of beta-dystroglycan (PPxY motif) and dystrophin (WW domain)
Authors: Pereboev, AV Ahmed, N Man, NT Morris, GE
Citation: Av. Pereboev et al., Epitopes in the interacting regions of beta-dystroglycan (PPxY motif) and dystrophin (WW domain), BBA-GEN SUB, 1527(1-2), 2001, pp. 54-60
Both emerin and lamin C depend on lamin A for localization at the nuclear envelope
Authors: Vaughan, OA Alvarez-Reyes, M Bridger, JM Broers, JLV Ramaekers, FCS Wehnert, M Morris, GE Whitfield, WGF Hutchison, CJ
Citation: Oa. Vaughan et al., Both emerin and lamin C depend on lamin A for localization at the nuclear envelope, J CELL SCI, 114(14), 2001, pp. 2577-2590
Absence of utrophin in intercalated discs of human cardiac muscle
Authors: Sewry, CA Man, NT Lynch, T Morris, GE
Citation: Ca. Sewry et al., Absence of utrophin in intercalated discs of human cardiac muscle, HISTOCHEM J, 33(1), 2001, pp. 9-12
Nuclear gems and cajal (coiled) bodies in fetal tissues: Nucleolar distribution of the spinal muscular atrophy protein, SMN
Authors: Young, PJ Le, TT Dunckley, M Man, NT Burghes, AHM Morris, GE
Citation: Pj. Young et al., Nuclear gems and cajal (coiled) bodies in fetal tissues: Nucleolar distribution of the spinal muscular atrophy protein, SMN, EXP CELL RE, 265(2), 2001, pp. 252-261
How does a g993t mutation in the emerin gene cause Emery-Dreifuss musculardystrophy?
Authors: Holt, I Clements, L Manilal, S Morris, GE
Citation: I. Holt et al., How does a g993t mutation in the emerin gene cause Emery-Dreifuss musculardystrophy?, BIOC BIOP R, 287(5), 2001, pp. 1129-1133
Dystrophin in adult zebrafish muscle
Authors: Chambers, SP Dodd, A Overall, R Sirey, T Lam, LT Morris, GE Love, DR
Citation: Sp. Chambers et al., Dystrophin in adult zebrafish muscle, BIOC BIOP R, 286(3), 2001, pp. 478-483
Methane formation during the iridium/iodide catalysed carbonylation of methanol
Authors: Ghaffar, T Charmant, JPH Sunley, GJ Morris, GE Haynes, A Maitlis, PM
Citation: T. Ghaffar et al., Methane formation during the iridium/iodide catalysed carbonylation of methanol, INORG CH C, 3(1), 2000, pp. 11-12
In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide
Authors: Bartlett, RJ Stockinger, S Denis, MM Bartlett, WT Inverardi, L Le, TT Man, NT Morris, GE Bogan, DJ Metcalf-Bogan, J Kornegay, JN
Citation: Rj. Bartlett et al., In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide, NAT BIOTECH, 18(6), 2000, pp. 615-622
In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide (vol 18, pg 615, 2000)
Authors: Bartlett, RJ Stockinger, S Denis, MM Bartlett, WT Inverardi, L Le, TT Man, TM Morris, GE Bogan, DJ Metcalf-Bogan, J Kornegay, JN
Citation: Rj. Bartlett et al., In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide (vol 18, pg 615, 2000), NAT BIOTECH, 18(11), 2000, pp. 1209-1209
Smoking, lung function and the prognosis of abdominal aortic aneurysm
Authors: Greenhalgh, RM Powell, JT Fowkes, FGR Forbes, JF Ruckley, CV Poole-Wilson, PA Browse, N Bulpitt, CJ Burnand, K Coles, EC Fletcher, A Blair, S Clark, R Devine, C Ferguson, K Hearn, S Kerracher, E Logan, S McCabe, A Meer-Baloch, R Mossa, M Rattray, A Wilson, K Brown, L Franks, P Keen, N Rose, C Hassaine, RM Horrocks, M Budd, J Horrocks, M Baird, RN Lamont, P Wilkins, DC Ashley, S Flowerdew, K Baker, A Earnshaw, J Heather, B Gibbons, C Blackett, RL Parvin, SD Harvey, DR Hedges, R Finch, D Hocken, DB Morris, GE Shearman, CP Lear, P Lewis, P Clarke, RJ Ruckley, CV Jenkins, AM Ruckley, CV Cooper, GG Engeset, J Naylor, R Stewart, G Cumming, J McCormick, J Howd, A Turner, A Harper, DR Smith, RC Chamberlain, J Jones, AG Wyatt, MG McKay, AJ Forrester, JC McCollum, P Stonebridge, PA Davidson, AIG Baker, R Forsythe, JLR Lambert, D Duncan, JL Bell, PRF Ratliff, D Callum, KG Nash, JR McPherson, DS Jenner, RE Stewart, R Armitstead, PR Barrie, WW Hamer, DB Powis, S Coen, LD Michaels, J Welsh, CL Hopkinson, BR Wenham, PW Beard, J Auckland, A Black, J Downing, R Hickey, NC Greenhalgh, RM Davies, AH Greenhalgh, RM Nott, D May, ARL McFarland, R Taylor, P Bradley, JWP Paes, T Cameron, AEP McIrvine, A Negus, D Taylor, PR Butler, CM Hoile, RW Pardy, B Ackroyd, J Hamilton, G Lane, R Giddings, AEB Dormandy, J Taylor, R Thomas, M Burnand, KJ Adiseshiah, M Pattison, P Clarke, J Colin, J Rutter, P Brearley, S Pietroni, M McCollum, CN Greaney, MG Reilly, D Paley, WG Lambert, M Hughes, R Blair, S Shand, JEG Donaldson, LA Galloway, JMD Wilkinson, AR Gough, M Mosley, J Matheson, DM Walker, M Hulton, N Aldoori, MI Yeung, CK Hearn, AR Kelly, J Durrans, D Gwynn, B Hopkinson, GB Duffield, RGM Schraibman, IG Hall, R Leveson, SH Clark, J Klimach, O
Citation: Rm. Greenhalgh et al., Smoking, lung function and the prognosis of abdominal aortic aneurysm, EUR J VAS E, 19(6), 2000, pp. 636-642
Endoluminal femoropopliteal bypass for intermittent claudication
Authors: Tisi, PV Cowan, AR Morris, GE
Citation: Pv. Tisi et al., Endoluminal femoropopliteal bypass for intermittent claudication, EUR J VAS E, 19(5), 2000, pp. 481-488
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy
Authors: Monani, UR Sendtner, M Coovert, DD Parsons, DW Andreassi, C Le, TT Jablonka, S Schrank, B Rossol, W Prior, TW Morris, GE Burghes, AHM
Citation: Ur. Monani et al., The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy, HUM MOL GEN, 9(3), 2000, pp. 333-339
The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding
Authors: Young, PJ Man, NT Lorson, CL Le, TT Androphy, EJ Burghes, AHM Morris, GE
Citation: Pj. Young et al., The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding, HUM MOL GEN, 9(19), 2000, pp. 2869-2877
Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle andheart
Authors: Lam, LT Pham, YCN Man, NT Morris, GE
Citation: Lt. Lam et al., Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle andheart, HUM MOL GEN, 9(14), 2000, pp. 2167-2173
Nuclear proteins and cell death in inherited neuromuscular disease
Authors: Morris, GE
Citation: Ge. Morris, Nuclear proteins and cell death in inherited neuromuscular disease, NEUROMUSC D, 10(4-5), 2000, pp. 217-227
Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain
Authors: Austin, RC Morris, GE Howard, PL Klamut, HJ Ray, PN
Citation: Rc. Austin et al., Expression and synthesis of alternatively spliced variants of Dp71 in adult human brain, NEUROMUSC D, 10(3), 2000, pp. 187-193
Endovascular femoropopliteal bypass
Authors: Morris, GE
Citation: Ge. Morris, Endovascular femoropopliteal bypass, ANN VASC S, 14(3), 2000, pp. 291-295
Hepatitis C epitopes from phage-displayed cDNA libraries and improved diagnosis with a chimeric antigen
Authors: Pereboeva, LA Pereboev, AV Wang, LF Morris, GE
Citation: La. Pereboeva et al., Hepatitis C epitopes from phage-displayed cDNA libraries and improved diagnosis with a chimeric antigen, J MED VIROL, 60(2), 2000, pp. 144-151
Risultati: 1-25 | 26-38