Search Results - "LUTCHMAN, M"

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2 by Rouleau, Guy A, Merel, Philippe, Lutchman, Mohini, Sanson, Marc, Zucman, Jessica, Marineau, Claude, Hoang-Xuan, Khé, Demczuk, Suzanne, Desmaze, Chantal, Plougastel, Béatrice, Pulst, Stefan M, Lenoir, Gilbert, Bijlsma, Emilia, Fashold, Raimund, Dumanski, Jan, Jong, Pieter de, Parry, Dilys, Eldrige, Roswell, Aurias, Alain, Delattre, Olivier, Thomas, Gilles

“…Neurofibromatosis type 2 (NF2) is a monogenic dominantly inherited disease predisposing carriers to develop nervous system tumours. To identify the genetic…”
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Reassignment of the EPB4.1 gene to 1p36 and assessment of its involvement in neuroblastomas by Huang, S, Lichtenauer, U D, Pack, S, Wang, C, Kim, A C, Lutchman, M, Koch, C A, Torres-Cruz, J, Huang, S C, Benz, Jr, E J, Christiansen, H, Dockhorn-Dworniczak, B, Poremba, C, Vortmeyer, A O, Chishti, A H, Zhuang, Z

“…EPB4.1 has been previously mapped to human chromosome 1p33-p34.2. In contradiction to this chromosomal location, we have mapped EPB4.1-1p36 by using…”
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Neurofibromatosis type 2: a new mechanism of tumor suppression by Lutchman, Mohini, Rouleau, Guy A.

“…Neurofibromatosis type 2 (NF2) is an autosomal dominant disease which predisposes primarily to CNS tumors such as schwannomas (vestibular and spinal),…”
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Radiation hybrid mapping of EPB41L1, a novel protein 4.1 homologue, to human chromosome 20q11.2-q12 by Kim, A C, Van Huffel, C, Lutchman, M, Chishti, A H

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Reassignment of the EPB4·1 gene to 1p36 and assessment of its involvement in neuroblastomas by Huang, S., Lichtenauer, U. D., Pack, S., Wang, C., Kim, A. C., Lutchman, M., Koch, C. A., Torres-Cruz, J., Huang, S.-C., Benz Jr, E. J., Christiansen, H., Dockhorn-Dworniczak, B., Poremba, C., Vortmeyer, A. O., Chishti, A. H., Zhuang, Z.

“…Objectives EPB4·1 has been previously mapped to human chromosome 1p33‐p34.2. In contradiction to this chromosomal location, we have mapped EPB4·1–1p36 by using…”
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Schwannomin: new insights into this member of the band 4.1 superfamily by Belliveau, M J, Lutchman, M, Claudio, J O, Marineau, C, Rouleau, G A

“…Neurofibromatosis type 2 (NF2) is an autosomal dominant disease characterized by the development of central nervous system tumours. The NF2 gene was recently…”
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HMG-CoA reductase inhibitors promote cholesterol-dependent Akt/PKB translocation to membrane domains in endothelial cells by SKALETZ-ROROWSKI, Adriane, LUTCHMAN, Mohini, KUREISHI, Yasuko, LEFER, David J, FAUST, Jerry R, WALSH, Kenneth

“…Recent results have shown that 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors referred to as statins rapidly activate the protein kinase…”
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A Pvull RFLP at the HOX 1.4 homeobox locus (HOX1D) by Goto, J., Figlewicz, D.A., Lutchman, M., Ruddle, F., Rouleau, G.A.

“…Images…”
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Neurofibromatosis 2 tumor suppressor protein colocalizes with ezrin and CD44 and associates with actin-containing cytoskeleton by Sainio, M, Zhao, F, Heiska, L, Turunen, O, den Bakker, M, Zwarthoff, E, Lutchman, M, Rouleau, G A, Jääskeläinen, J, Vaheri, A, Carpén, O

“…Neurofibromatosis 2 (NF2) protein (merlin; schwannomin) is a tumor suppressor involved in tumorigenesis of NF2-associated and sporadic schwannomas and…”
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Complete deficiency of glycophorin A in red blood cells from mice with targeted inactivation of the band 3 (AE1) gene by HASSOUN, Y. H, HANADA, T, LUTCHMAN, M, SAHR, K. E, PALEK, J, HANSPAL, M, CHISHTI, A. H

“…Glycophorin A is the major transmembrane sialoglycoprotein of red blood cells. It has been shown to contribute to the expression of the MN and Wright blood…”
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The neurofibromatosis type 2 gene product, Schwannomin, suppresses growth of NIH 3T3 cells by LUTCHMAN, N, ROULEAU, G. A

“…Cancer is a multistep process that involves the activation of oncogenes and the inactivation of antioncogenes. Recently, a new putative tumor suppressor, the…”
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Complete Deficiency of Glycophorin A in Red Blood Cells From Mice With Targeted Inactivation of the Band 3 (AE1) Gene by Hassoun, Hani, Hanada, Toshihiko, Lutchman, Mohini, Sahr, Kenneth E., Palek, Jiri, Hanspal, Manjit, Chishti, Athar H.

“…Glycophorin A is the major transmembrane sialoglycoprotein of red blood cells. It has been shown to contribute to the expression of the MN and Wright blood…”
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Neurofibromatosis type 2: A new mechanism of tumor suppression by Lutchman, M, Rouleau, G A

“…Neurofibromatosis type 2 (NF2) is an autosomal dominant disease which predisposes primarily to CNS tumors such as schwannomas (vestibular and spinal),…”
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Targeted Inactivation of Murine Band 3 (AE1) Gene Produces a Hypercoagulable State Causing Widespread Thrombosis In Vivo by Hassoun, Hani, Wang, Ying, Vassiliadis, John, Lutchman, Mohini, Palek, Jiri, Aish, Leo, Aish, Irene S., Liu, Shih-Chun, Chishti, Athar H.

“…Only 5% to 10% of band 3 null mice survive the neonatal period. To determine the cause of death, 3 adult and 11 newborn band 3 null mice were submitted for…”
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Fontan Liver Lesions: Not Always HCC by Haeffele, Christiane, Aggarwal, Avin, Lutchman, Glen, Veldtman, Gruschen R., Wu, Fred M., Lui, George K.

“…A 24-year-old Fontan procedure patient underwent surveillance liver cardiac magnetic resonance imaging. Findings were suggestive of hepatocellular… A…”
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Widespread but cell type-specific expression of the mouse neurofibromatosis type 2 gene by Claudio, J O, Lutchman, M, Rouleau, G A

“…Neurofibromatosis type 2 (NF2) is an autosomal dominant disease in which loss of function mutations of the NF2 gene lead to the development of schwannomas,…”
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Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus by Sanson, M, Marineau, C, Desmaze, C, Lutchman, M, Ruttledge, M, Baron, C, Narod, S, Delattre, O, Lenoir, G, Thomas, G

“…Neurofibromatosis type 2 (NF2) is an autosomal dominant disease which predisposes to the development of schwannomas, meningiomas, ependymomas, and juvenile…”
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Reassignment of the EPB4.I gene to Ip36 and assessment of its involvement in neuroblastomas by HUANG, S, LICHTENAUER, U. D, CHRISTIANSEN, H, DOCKHORN-DWORNICZAK, B, POREMBA, C, VORTMEYER, A. O, CHISHTI, A. H, ZHUANG, Z, PACK, S, WANG, C, KIM, A. C, LUTCHMAN, M, KOCH, C. A, TORRES-CRUZ, J, HUANG, S.-C, BENZ, E. J

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cDNA sequence, genomic structure, and expression of the mouse dematin gene (Epb4.9) by Azim, A C, Kim, A C, Lutchman, M, Andrabi, S, Peters, L L, Chishti, A H

“…Dematin (protein 4.9 region) is an actin-bundling phosphoprotein of the erythroid membrane cytoskeleton (Rana et al. 1993; Azim et al. 1995). Although much is…”
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Targeted inactivation of murine band 3 (AE1) gene produces a hypercoagulable state causing widespread thrombosis in vivo by HASSOUN, H, YING WANG, VASSILIADIS, J, LUTCHMAN, M, PALEK, J, AISH, L, AISH, I. S, LIU, S.-C, CHISHTI, A. H

“…Only 5% to 10% of band 3 null mice survive the neonatal period. To determine the cause of death, 3 adult and 11 newborn band 3 null mice were submitted for…”
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