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There are 8200 results for: content related to: Rescue of genomic information in adult acute lymphoblastic leukaemia (ALL) with normal/failed cytogenetics: a GIMEMA centralized biological study

  1. Tumorigenic properties of neurofibromin-deficient Schwann cells in culture and as syngrafts in Nf1 knockout mice

    Journal of Neuroscience Research

    Volume 82, Issue 3, 1 November 2005, Pages: 357–367, Min Wu, Margaret R. Wallace and David Muir

    Version of Record online : 22 SEP 2005, DOI: 10.1002/jnr.20646

  2. Identification of Large NF1 Duplications Reciprocal to NAHR-Mediated Type-1 NF1 Deletions

    Human Mutation

    Volume 35, Issue 12, December 2014, Pages: 1469–1475, Hildegard Kehrer-Sawatzki, Kathrin Bengesser, Tom Callens, Fady Mikhail, Chuanhua Fu, Morten Hillmer, Martha E. Walker, Howard M. Saal, Yves Lacassie, David N. Cooper and Ludwine Messiaen

    Version of Record online : 24 NOV 2014, DOI: 10.1002/humu.22692

  3. Neurofibromatosis 1 (NF1) heterozygosity results in a cell-autonomous growth advantage for astrocytes

    Glia

    Volume 33, Issue 4, 15 March 2001, Pages: 314–323, Michaela Livia Bajenaru, Jessica Donahoe, Teresa Corral, Karlyne M. Reilly, Sean Brophy, Angel Pellicer and David H. Gutmann

    Version of Record online : 21 FEB 2001, DOI: 10.1002/1098-1136(20010315)33:4<314::AID-GLIA1030>3.0.CO;2-Q

  4. You have free access to this content
    A murine model of neurofibromatosis type 1 tibial pseudarthrosis featuring proliferative fibrous tissue and osteoclast-like cells

    Journal of Bone and Mineral Research

    Volume 27, Issue 1, January 2012, Pages: 68–78, Jad El-Hoss, Kate Sullivan, Tegan Cheng, Nicole YC Yu, Justin D Bobyn, Lauren Peacock, Kathy Mikulec, Paul Baldock, Ian E Alexander, Aaron Schindeler and David G Little

    Version of Record online : 22 DEC 2011, DOI: 10.1002/jbmr.528

  5. You have free access to this content
    Local low-dose lovastatin delivery improves the bone-healing defect caused by Nf1 loss of function in osteoblasts

    Journal of Bone and Mineral Research

    Volume 25, Issue 7, July 2010, Pages: 1658–1667, Weixi Wang, Jeffry S Nyman, Heather E Moss, Gloria Gutierrez, Gregory R Mundy, Xiangli Yang and Florent Elefteriou

    Version of Record online : 29 JAN 2010, DOI: 10.1002/jbmr.42

  6. You have free access to this content
    Neurofibromatosis-1 gene deletions and mutations in de novo adult acute myeloid leukemia

    American Journal of Hematology

    Volume 88, Issue 4, April 2013, Pages: 306–311, Elise Boudry-Labis, Catherine Roche-Lestienne, Olivier Nibourel, Nicolas Boissel, Christine Terre, Christine Perot, Virginie Eclache, Nathalie Gachard, Isabelle Tigaud, Ghislaine Plessis, Wendy Cuccuini, Sandrine Geffroy, Céline Villenet, Martin Figeac, Frederic Leprêtre, Aline Renneville, Meyling Cheok, Jean Soulier, Hervé Dombret, Claude Preudhomme and On behalf of the French ALFA group

    Version of Record online : 5 MAR 2013, DOI: 10.1002/ajh.23403

  7. Tissue-specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells

    Human Mutation

    Volume 33, Issue 3, March 2012, Pages: 541–550, Angelika C. Roehl, Tanja Mussotter, David N. Cooper, Lan Kluwe, Katharina Wimmer, Josef Högel, Marion Zetzmann, Julia Vogt, Victor-Felix Mautner and Hildegard Kehrer-Sawatzki

    Version of Record online : 23 JAN 2012, DOI: 10.1002/humu.22013

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    Hyperactive Transforming Growth Factor-β1 Signaling Potentiates Skeletal Defects in a Neurofibromatosis Type 1 Mouse Model

    Journal of Bone and Mineral Research

    Volume 28, Issue 12, December 2013, Pages: 2476–2489, Steven D Rhodes, Xiaohua Wu, Yongzheng He, Shi Chen, Hao Yang, Karl W Staser, Jiapeng Wang, Ping Zhang, Chang Jiang, Hiroki Yokota, Ruizhi Dong, Xianghong Peng, Xianlin Yang, Sreemala Murthy, Mohamad Azhar, Khalid S Mohammad, Mingjiang Xu, Theresa A Guise and Feng-Chun Yang

    Version of Record online : 19 NOV 2013, DOI: 10.1002/jbmr.1992

  9. Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patients

    Genes, Chromosomes and Cancer

    Volume 45, Issue 10, October 2006, Pages: 893–904, Thomas De Raedt, Ophélia Maertens, Magdalena Chmara, Hilde Brems, Ine Heyns, Raf Sciot, Elisa Majounie, Meena Upadhyaya, Sofie De Schepper, Frank Speleman, Ludwine Messiaen, Joris Robert Vermeesch and Eric Legius

    Version of Record online : 7 JUL 2006, DOI: 10.1002/gcc.20353

  10. Assessment of the potential pathogenicity of missense mutations identified in the GTPase-activating protein (GAP)-related domain of the neurofibromatosis type-1 (NF1) gene

    Human Mutation

    Volume 33, Issue 12, December 2012, Pages: 1687–1696, Laura Thomas, Mark Richards, Matthew Mort, Elaine Dunlop, David N. Cooper and Meena Upadhyaya

    Version of Record online : 6 AUG 2012, DOI: 10.1002/humu.22162

  11. Neurofibromin-deficient Schwann cells have increased lysophosphatidic acid dependent survival and migration—implications for increased neurofibroma formation during pregnancy

    Glia

    Volume 55, Issue 5, 1 April 2007, Pages: 527–536, Todd D. Nebesio, Wenyu Ming, Shi Chen, Travis Clegg, Jin Yuan, Yanzhu Yang, Selina A. Estwick, Yan Li, Xiaohong Li, Cynthia M. Hingtgen and Feng-Chun Yang

    Version of Record online : 18 JAN 2007, DOI: 10.1002/glia.20482

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    NF1 mRNA biogenesis: Effect of the genomic milieu in splicing regulation of the NF1 exon 37 region

    FEBS Letters

    Volume 580, Issue 18, August 07, 2006, Pages: 4449–4456, Marco Baralle, Natasa Skoko, Anna Knezevich, Laura De Conti, Dario Motti, Madhuri Bhuvanagiri, Diana Baralle, Emanuele Buratti and Francisco E. Baralle

    Version of Record online : 14 JUL 2006, DOI: 10.1016/j.febslet.2006.07.018

  13. Influence of duration of phosphoric acid pre-etching on bond durability of universal adhesives and surface free-energy characteristics of enamel

    European Journal of Oral Sciences

    Volume 124, Issue 4, August 2016, Pages: 377–386, Akimasa Tsujimoto, Wayne W. Barkmeier, Toshiki Takamizawa, Hidehiko Watanabe, William W. Johnson, Mark A. Latta and Masashi Miyazaki

    Version of Record online : 18 JUN 2016, DOI: 10.1111/eos.12284

  14. Fungi Use Efficient Algorithms for the Exploration of Microfluidic Networks

    Small

    Volume 2, Issue 10, October 2006, Pages: 1212–1220, Kristi L. Hanson, Dan V. Nicolau Jr., Luisa Filipponi, Lisen Wang, Abraham P. Lee and Dan V. Nicolau

    Version of Record online : 17 AUG 2006, DOI: 10.1002/smll.200600105

  15. New recurrent balanced translocations in acute myeloid leukemia and myelodysplastic syndromes: Cancer and leukemia group B 8461

    Genes, Chromosomes and Cancer

    Volume 52, Issue 4, April 2013, Pages: 385–401, Alison Walker, Krzysztof Mrózek, Jessica Kohlschmidt, Kathleen W. Rao, Mark J. Pettenati, Lisa J. Sterling, Guido Marcucci, Andrew J. Carroll, Clara D. Bloomfield and for the Alliance for Clinical Trials in Oncology

    Version of Record online : 10 DEC 2012, DOI: 10.1002/gcc.22036

  16. Neurofibromatosis Type I (NF1)

    Standard Article

    eLS

    David Viskochil

    Published Online : 15 SEP 2009, DOI: 10.1002/9780470015902.a0005534.pub2

  17. Chromosome 17 loss-of-heterozygosity studies in benign and malignant tumors in neurofibromatosis type 1

    Genes, Chromosomes and Cancer

    Volume 28, Issue 4, August 2000, Pages: 425–431, Sonja A. Rasmussen, Jennifer Overman, Susanne A.M. Thomson, Steven D. Colman, Corinne R. Abernathy, Rachael E. Trimpert, Rebecca Moose, Gurinder Virdi, Kyle Roux, Mislen Bauer, Amyn M. Rojiani, Bernard L. Maria, David Muir and Margaret R. Wallace

    Version of Record online : 14 JUN 2000, DOI: 10.1002/1098-2264(200008)28:4<425::AID-GCC8>3.0.CO;2-E

  18. Neurofibromatosis Type 1

    Standard Article

    Management of Genetic Syndromes

    David Viskochil

    Published Online : 14 JAN 2005, DOI: 10.1002/0471695998.mgs031

  19. A severe form of Noonan syndrome and autosomal dominant café-au-lait spots – evidence for different genetic origins

    Acta Paediatrica

    Volume 98, Issue 4, April 2009, Pages: 693–698, Anna-Maja Nyström, Sara Ekvall, Bo Strömberg, Gerd Holmström, Ann-Charlotte Thuresson, Göran Annerén and Marie-Louise Bondeson

    Version of Record online : 19 DEC 2008, DOI: 10.1111/j.1651-2227.2008.01170.x

  20. Detection of copy number changes at the NF1 locus with improved high-resolution array CGH

    Clinical Genetics

    Volume 72, Issue 3, September 2007, Pages: 238–244, MH Shen, K Mantripragada, JP Dumanski, I Frayling and M Upadhyaya

    Version of Record online : 13 AUG 2007, DOI: 10.1111/j.1399-0004.2007.00858.x