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There are 2782 results for: content related to: Hyperactive Transforming Growth Factor-β1 Signaling Potentiates Skeletal Defects in a Neurofibromatosis Type 1 Mouse Model

  1. You have free access to this content
    Nf1 Haploinsufficiency Alters Myeloid Lineage Commitment and Function, Leading to Deranged Skeletal Homeostasis

    Journal of Bone and Mineral Research

    Volume 30, Issue 10, October 2015, Pages: 1840–1851, Steven D Rhodes, Hao Yang, Ruizhi Dong, Keshav Menon, Yongzheng He, Zhaomin Li, Shi Chen, Karl W Staser, Li Jiang, Xiaohua Wu, Xianlin Yang, Xianghong Peng, Khalid S Mohammad, Theresa A Guise, Mingjiang Xu and Feng-Chun Yang

    Version of Record online : 21 MAY 2015, DOI: 10.1002/jbmr.2538

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    Combined MEK Inhibition and BMP2 Treatment Promotes Osteoblast Differentiation and Bone Healing in Nf1Osx−/− Mice

    Journal of Bone and Mineral Research

    Volume 30, Issue 1, January 2015, Pages: 55–63, Jean de la Croix Ndong, David M Stevens, Guillaume Vignaux, Sasidhar Uppuganti, Daniel S Perrien, Xiangli Yang, Jeffry S Nyman, Eva Harth and Florent Elefteriou

    Version of Record online : 26 DEC 2014, DOI: 10.1002/jbmr.2316

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    Neurofibromin Deficiency-Associated Transcriptional Dysregulation Suggests a Novel Therapy for Tibial Pseudoarthrosis in NF1

    Journal of Bone and Mineral Research

    Volume 29, Issue 12, December 2014, Pages: 2636–2642, Nandina Paria, Tae-Joon Cho, In Ho Choi, Nobuhiro Kamiya, Kay Kayembe, Rong Mao, Rebecca L Margraf, Gerlinde Obermosser, Ila Oxendine, David W Sant, Mi Hyun Song, David A Stevenson, David H Viskochil, Carol A Wise, Harry KW Kim and Jonathan J Rios

    Version of Record online : 12 DEC 2014, DOI: 10.1002/jbmr.2298

  4. 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

  5. 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

  6. 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

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    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

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    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

  9. 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

  10. 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

  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

  12. NF1 Molecular Characterization and Neurofibromatosis Type I Genotype–Phenotype Correlation: The French Experience

    Human Mutation

    Volume 34, Issue 11, November 2013, Pages: 1510–1518, Audrey Sabbagh, Eric Pasmant, Apolline Imbard, Armelle Luscan, Magali Soares, Hélène Blanché, Ingrid Laurendeau, Salah Ferkal, Michel Vidaud, Stéphane Pinson, Christine Bellanné-Chantelot, Dominique Vidaud, the members of the NF France Network, Béatrice Parfait and Pierre Wolkenstein

    Version of Record online : 26 AUG 2013, DOI: 10.1002/humu.22392

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    Nf1 mutant mice with p19ARF gene loss develop accelerated hematopoietic disease resembling acute leukemia with a variable phenotype

    American Journal of Hematology

    Volume 86, Issue 7, July 2011, Pages: 579–585, Stephen M. Wiesner, Jennifer L. Geurts, Miechaleen D. Diers, Rachel J. Bergerson, Diane E. Hasz, Kelly J. Morgan and David A. Largaespada

    Version of Record online : 16 JUN 2011, DOI: 10.1002/ajh.22035

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    Hyperactivation of mTOR critically regulates abnormal osteoclastogenesis in neurofibromatosis type 1

    Journal of Orthopaedic Research

    Volume 30, Issue 1, January 2012, Pages: 144–152, Junrong Ma, Mi Li, Janet Hock and Xijie Yu

    Version of Record online : 11 JUL 2011, DOI: 10.1002/jor.21497

  15. Neurofibromin physically interacts with the N-terminal domain of focal adhesion kinase

    Molecular Carcinogenesis

    Volume 48, Issue 11, November 2009, Pages: 1005–1017, Frederick Kweh, Min Zheng, Elena Kurenova, Margaret Wallace, Vita Golubovskaya and William G. Cance

    Version of Record online : 28 MAY 2009, DOI: 10.1002/mc.20552

  16. Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions

    Human Mutation

    Volume 31, Issue 10, October 2010, Pages: 1163–1173, Angelika C. Roehl, Julia Vogt, Tanja Mussotter, Antje N. Zickler, Helene Spöti, Josef Högel, Nadia A. Chuzhanova, Katharina Wimmer, Lan Kluwe, Victor-Felix Mautner, David N. Cooper and Hildegard Kehrer-Sawatzki

    Version of Record online : 28 SEP 2010, DOI: 10.1002/humu.21340

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    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

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    Multiple roles of NF1 in the melanocyte lineage

    Pigment Cell & Melanoma Research

    Volume 29, Issue 4, July 2016, Pages: 417–425, Lionel Larribère and Jochen Utikal

    Version of Record online : 20 JUN 2016, DOI: 10.1111/pcmr.12488

  19. Mosaic type-1 NF1 microdeletions as a cause of both generalized and segmental neurofibromatosis type-1 (NF1)

    Human Mutation

    Volume 32, Issue 2, February 2011, Pages: 213–219, Ludwine Messiaen, Julia Vogt, Kathrin Bengesser, Chuanhua Fu, Fady Mikhail, Eduard Serra, Carles Garcia-Linares, David N. Cooper, Conxi Lazaro and Hildegard Kehrer-Sawatzki

    Version of Record online : 28 JAN 2011, DOI: 10.1002/humu.21418

  20. Polymorphism in the neurofibromin gene, Nf1, is associated with antagonistic selection on wing size and development time in Drosophila melanogaster

    Molecular Ecology

    Volume 22, Issue 10, May 2013, Pages: 2716–2725, Siu F. Lee, Ying Chen Eyre-Walker, Rahul V. Rane, Caroline Reuter, Giovanna Vinti, Lea Rako, Linda Partridge and Ary A. Hoffmann

    Version of Record online : 18 MAR 2013, DOI: 10.1111/mec.12301