31
Views
72
CrossRef citations to date
0
Altmetric
Article

Functional Effects of PTPN11 (SHP2) Mutations Causing LEOPARD Syndrome on Epidermal Growth Factor-Induced Phosphoinositide 3-Kinase/AKT/Glycogen Synthase Kinase 3β Signaling

, , , , , , , , , , , & show all
Pages 2498-2507 | Received 19 May 2009, Accepted 17 Feb 2010, Published online: 20 Mar 2023

Keep up to date with the latest research on this topic with citation updates for this article.

Read on this site (3)

Giulio Calcagni, Marta Unolt, Maria Cristina Digilio, Anwar Baban, Paolo Versacci, Marco Tartaglia, Antonio Baldini & Bruno Marino. (2017) Congenital heart disease and genetic syndromes: new insights into molecular mechanisms. Expert Review of Molecular Diagnostics 17:9, pages 861-870.
Read now
Shinya Kusakari, Fumihito Saitow, Yukio Ago, Koji Shibasaki, Miho Sato-Hashimoto, Yasunori Matsuzaki, Takenori Kotani, Yoji Murata, Hirokazu Hirai, Toshio Matsuda, Hidenori Suzuki, Takashi Matozaki & Hiroshi Ohnishi. (2015) Shp2 in Forebrain Neurons Regulates Synaptic Plasticity, Locomotion, and Memory Formation in Mice. Molecular and Cellular Biology 35:9, pages 1557-1572.
Read now
Panna Tandon, Frank L. Conlon & Joan M. Taylor. (2012) ROCKs cause SHP-wrecks and broken hearts. Small GTPases 3:4, pages 209-212.
Read now

Articles from other publishers (69)

Chunxiao He, Zhiyong Peng, Dengyang Zhang, Yao Guo, Tianqi Liang, Yuming Zhao, Liuting Yu, Qi Zhang, Zhiguang Chang, Yan Xiao, Na Li, Hongman Xue, Shunjie Wu, Zhizhuang Joe Zhao, Changhua Zhang & Yun Chen. (2023) Sunitinib selectively targets leukemogenic signaling of mutant SHP2 in juvenile myelomonocytic leukemia. Biochemical Pharmacology 213, pages 115588.
Crossref
Hongmei Luo, Zhongzhou Yang, Jie Li, Hengwei Jin, Mingyang Jiang & Congjia Shan. (2023) Deletion of PDK1 Caused Cardiac Malmorphogenesis and Heart Defects Due to Profound Protein Phosphorylation Changes Mediated by SHP2. Journal of Cardiovascular Translational Research.
Crossref
Atsushi Fujita, Mitsuhiro Kato, Hidenori Sugano, Yasushi Iimura, Hiroharu Suzuki, Jun Tohyama, Masafumi Fukuda, Yosuke Ito, Shimpei Baba, Tohru Okanishi, Hideo Enoki, Ayataka Fujimoto, Akiyo Yamamoto, Kentaro Kawamura, Shinsuke Kato, Ryoko Honda, Tomonori Ono, Hideaki Shiraishi, Kiyoshi Egawa, Kentaro Shirai, Shinji Yamamoto, Itaru Hayakawa, Hisashi Kawawaki, Ken Saida, Naomi Tsuchida, Yuri Uchiyama, Kohei Hamanaka, Satoko Miyatake, Takeshi Mizuguchi, Mitsuko Nakashima, Hirotomo Saitsu, Noriko Miyake, Akiyoshi Kakita & Naomichi Matsumoto. (2023) An integrated genetic analysis of epileptogenic brain malformed lesions. Acta Neuropathologica Communications 11:1.
Crossref
M. A. Siano, R. Pivonello, M. Salerno, M. Falco, C. Mauro, D. De Brasi, A. Klain, S. Sestito, A. De Luca, V. Pinna, C. Simeoli, D. Concolino, Ciro Gabriele Mainolfi, T. Mannarino, P. Strisciuglio, M. Tartaglia & D. Melis. (2022) Endocrine system involvement in patients with RASopathies: A case series. Frontiers in Endocrinology 13.
Crossref
Sadaf Naz. 2022. Auditory System - Function and Disorders. Auditory System - Function and Disorders.
Jae-Sung Yi, Sravan Perla, Yan Huang, Kana Mizuno, Frank J. Giordano, Alexander A. Vinks & Anton M. Bennett. (2021) Low-dose Dasatinib Ameliorates Hypertrophic Cardiomyopathy in Noonan Syndrome with Multiple Lentigines. Cardiovascular Drugs and Therapy 36:4, pages 589-604.
Crossref
Maria I. Kontaridis, Amy E. Roberts, Lisa Schill, Lisa Schoyer, Beth Stronach, Gregor Andelfinger, Yoko Aoki, Marni E. Axelrad, Annette Bakker, Anton M. Bennett, Alberto Broniscer, Pau Castel, Caitlin A. Chang, Lukas Cyganek, Tirtha K. Das, Jeroen Hertog, Emilia Galperin, Shruti Garg, Bruce D. Gelb, Kristiana Gordon, Tamar Green, Karen W. Gripp, Maxim Itkin, Maija Kiuru, Bruce R. Korf, Jeff R. Livingstone, Alejandro López‐Juárez, Pilar L. Magoulas, Sahar Mansour, Theresa Milner, Elisabeth Parker, Elizabeth I. Pierpont, Kevin Plouffe, Katherine A. Rauen, Suma P. Shankar, Shane B. Smith, David A. Stevenson, Marco Tartaglia, Richard Van, Morgan E. Wagner, Stephanie M. Ware & Martin Zenker. (2022) The seventh international RASopathies symposium: Pathways to a cure—expanding knowledge, enhancing research, and therapeutic discovery . American Journal of Medical Genetics Part A 188:6, pages 1915-1927.
Crossref
Maike Krenz. (2022) Friend or foe? Unraveling the complex roles of protein tyrosine phosphatases in cardiac disease and development. Cellular Signalling 93, pages 110297.
Crossref
Yuan Zhang, Wei Lu, Qing Zhao, Jindong Chen, Tiancong Wang & Jun Ji. (2022) The role of the protein tyrosine phosphatase SHP2 in ossification . Developmental Dynamics 251:5, pages 748-758.
Crossref
Jiao Kong & Ya-Qiu Long. (2022) Recent advances in the discovery of protein tyrosine phosphatase SHP2 inhibitors. RSC Medicinal Chemistry 13:3, pages 246-257.
Crossref
Yihui Song, Shu Wang, Min Zhao, Xinyu Yang & Bin Yu. (2022) Strategies Targeting Protein Tyrosine Phosphatase SHP2 for Cancer Therapy. Journal of Medicinal Chemistry 65:4, pages 3066-3079.
Crossref
Yihui Song, Min Zhao, Huiqing Zhang & Bin Yu. (2022) Double-edged roles of protein tyrosine phosphatase SHP2 in cancer and its inhibitors in clinical trials. Pharmacology & Therapeutics 230, pages 107966.
Crossref
A. Gulhan Ercan-Sencicek, Saravanakkumar Chennappan, Kelly Aromalaran & Maria Irene Kontaridis. 2022. Current Progress in iPSC Disease Modeling. Current Progress in iPSC Disease Modeling 65 110 .
Javier-Fernando Montero-Bullón, Óscar González-Velasco, María Isidoro-García & Jesus Lacal. (2021) Integrated in silico MS-based phosphoproteomics and network enrichment analysis of RASopathy proteins. Orphanet Journal of Rare Diseases 16:1.
Crossref
Massimiliano Anselmi & Jochen S. Hub. (2021) The loops of the N-SH2 binding cleft do not serve as allosteric switch in SHP2 activation. Proceedings of the National Academy of Sciences 118:17.
Crossref
Rebeca Lorca, Luca Pannone, Elías Cuesta‐Llavona, Gianfranco Bocchinfuso, Julian Rodríguez‐Reguero, Giovanna Carpentieri, Inés Hernando, Elisabetta Flex, Marco Tartaglia, Eliecer Coto, Juan Gómez & Simone Martinelli. (2021) Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2 ‐related disorders . Clinical Genetics 99:3, pages 457-461.
Crossref
Alexsandra C. Malaquias & Alexander A.L. Jorge. (2021) Activation of the MAPK pathway (RASopathies) and partial growth hormone insensitivity. Molecular and Cellular Endocrinology 519, pages 111040.
Crossref
Lisa M. Vincent, Karen W. Gripp & Heather Mason-Suares. 2021. Clinical DNA Variant Interpretation. Clinical DNA Variant Interpretation 389 398 .
Marialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, Andreas Hahn, Amir Peleg, Alina German, Christina Lissewski, Simona Coppola, Francesca Pantaleoni, Luisa Kocherscheid, Franziska Altmüller, Denny Schanze, Thushiha Logeswaran, Soheyla Chahrokh-Zadeh, Anna Munzig, Saeideh Nakhaei-Rad, Hélène Cavé, Mohammad R Ahmadian, Marco Tartaglia & Martin Zenker. (2020) Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy. Human Molecular Genetics 29:11, pages 1772-1783.
Crossref
Emmanuelle Ranza, Anne Guimier, Alain Verloes, Yline Capri, Charles Marques, Martine Auclair, Michèle Mathieu‐Dramard, Gilles Morin, Julien Thevenon, Laurence Faivre, Christel Thauvin‐Robinet, A. Micheil Innes, David A. Dyment, Corinne Vigouroux & Jeanne Amiel. (2020) Overlapping phenotypes between SHORT and Noonan syndromes in patients with PTPN11 pathogenic variants . Clinical Genetics 98:1, pages 10-18.
Crossref
Catherine Hall, Hongtao Yu & Eunhee Choi. (2020) Insulin receptor endocytosis in the pathophysiology of insulin resistance. Experimental & Molecular Medicine 52:6, pages 911-920.
Crossref
Ruo-Yu Zhang, Zhi-Hong Yu, Lan Chen, Chad D. Walls, Sheng Zhang, Li Wu & Zhong-Yin Zhang. (2020) Mechanistic insights explain the transforming potential of the T507K substitution in the protein-tyrosine phosphatase SHP2. Journal of Biological Chemistry 295:18, pages 6187-6201.
Crossref
Dadong Shen, Wenxia Chen, Jinlin Zhu, Guofeng Wu, Runpu Shen, Meiyang Xi & Haopeng Sun. (2020) Therapeutic potential of targeting SHP2 in human developmental disorders and cancers. European Journal of Medicinal Chemistry 190, pages 112117.
Crossref
Mohamed El Kholy, Heba Elsedfy, Laurence Perin, Walid Abi Habid, Nathalie Thibaud, Mauro Bozzola, Sylvie Rossignol, Patricia Leneuve, François Godeau, Sandra Chantot-Bastaraud, Irène Netchine & Yves Le Bouc. (2019) Normal Growth despite Combined Pituitary Hormone Deficiency. Hormone Research in Paediatrics 92:2, pages 133-142.
Crossref
Colin J. Dinsmore & Philippe Soriano. (2018) MAPK and PI3K signaling: At the crossroads of neural crest development. Developmental Biology 444, pages S79-S97.
Crossref
Mylène Tajan, Romain Paccoud, Sophie Branka, Thomas Edouard & Armelle Yart. (2018) The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway. Endocrine Reviews 39:5, pages 676-700.
Crossref
Xu Ding, Wei Yang, Xiao-Dan Liu, Xi Yang, Huan-Min Wang & Jun Tai. (2018) Spinal SHP2 Contributes to Exaggerated Incisional Pain in Adult Rats Subjected to Neonatal and Adult Incisions via PI3K. Neuroscience 385, pages 102-120.
Crossref
Mylène TajanJulie Pernin-Grandjean, Nicolas Beton, Isabelle Gennero, Florence Capilla, Benjamin G Neel, Toshiyuki Araki, Philippe ValetMaithé Tauber, Jean-Pierre Salles, Armelle YartThomas Edouard. (2018) Noonan syndrome-causing SHP2 mutants impair ERK-dependent chondrocyte differentiation during endochondral bone growth. Human Molecular Genetics 27:13, pages 2276-2289.
Crossref
Giulio Calcagni, Rachele Adorisio, Simone Martinelli, Giorgia Grutter, Anwar Baban, Paolo Versacci, Maria Cristina Digilio, Fabrizio Drago, Bruce D. Gelb, Marco Tartaglia & Bruno Marino. (2018) Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies. Heart Failure Clinics 14:2, pages 225-235.
Crossref
Hong Zheng, Wen-Mei YuRonald R. Waclaw, Maria I. Kontaridis, Benjamin G. Neel & Cheng-Kui Qu. (2018) Gain-of-function mutations in the gene encoding the tyrosine phosphatase SHP2 induce hydrocephalus in a catalytically dependent manner. Science Signaling 11:522.
Crossref
Lijun Wang, Caterina Iorio, Kevin Yan, Howard Yang, Sunao Takeshita, Sumin Kang, Benjamin G. Neel & Wentian Yang. (2018) A ERK/RSK‐mediated negative feedback loop regulates M‐CSF–evoked PI3K/AKT activation in macrophages. The FASEB Journal 32:2, pages 875-887.
Crossref
Rajika Roy & Maike Krenz. (2017) Heterozygous deletion of AKT1 rescues cardiac contractility, but not hypertrophy, in a mouse model of Noonan Syndrome with Multiple Lentigines. Journal of Molecular and Cellular Cardiology 112, pages 83-90.
Crossref
Luca Pannone, Gianfranco Bocchinfuso, Elisabetta Flex, Cesare Rossi, Giuseppina Baldassarre, Christina Lissewski, Francesca Pantaleoni, Federica Consoli, Francesca Lepri, Monia Magliozzi, Massimiliano Anselmi, Silvia Delle Vigne, Giovanni Sorge, Kadri Karaer, Goran Cuturilo, Alessandro Sartorio, Sigrid Tinschert, Maria Accadia, Maria C. Digilio, Giuseppe Zampino, Alessandro De Luca, Hélène Cavé, Martin Zenker, Bruce D. Gelb, Bruno Dallapiccola, Lorenzo Stella, Giovanni B. Ferrero, Simone Martinelli & Marco Tartaglia. (2017) Structural, Functional, and Clinical Characterization of a Novel PTPN11 Mutation Cluster Underlying Noonan Syndrome . Human Mutation 38:4, pages 451-459.
Crossref
Chuan Chen, Fan Liang, Bo Chen, Zhongyi Sun, Tongdan Xue, Runlei Yang & Duqiang Luo. (2017) Identification of demethylincisterol A 3 as a selective inhibitor of protein tyrosine phosphatase Shp2. European Journal of Pharmacology 795, pages 124-133.
Crossref
Salvatore Corallino, Leo K. Iwai, Leo S. Payne, Paul H. Huang, Francesca Sacco, Gianni Cesareni & Luisa Castagnoli. (2016) Alterations in the phosphoproteomic profile of cells expressing a non-functional form of the SHP2 phosphatase. New Biotechnology 33:5, pages 524-536.
Crossref
Jessica Lauriol, Janel R. Cabrera, Ashbeel Roy, Kimberly Keith, Sara M. Hough, Federico Damilano, Bonnie Wang, Gabriel C. Segarra, Meaghan E. Flessa, Lauren E. Miller, Saumya Das, Roderick Bronson, Kyu-Ho Lee & Maria I. Kontaridis. (2016) Developmental SHP2 dysfunction underlies cardiac hypertrophy in Noonan syndrome with multiple lentigines. Journal of Clinical Investigation 126:8, pages 2989-3005.
Crossref
Catie Cessans, Virginie Ehlinger, Catherine Arnaud, Armelle Yart, Yline Capri, Pascal Barat, Benoit Cammas, Didier Lacombe, Régis Coutant, Albert David, Sabine Baron, Jacques Weill, Bruno Leheup, Marc Nicolino, Jean-Pierre Salles, Alain Verloes, Maithé Tauber, Hélène Cavé & Thomas Edouard. (2016) Growth patterns of patients with Noonan syndrome: correlation with age and genotype. European Journal of Endocrinology 174:5, pages 641-650.
Crossref
Rosario Alarcón-Cabrera, Felipe Partarrieu-Mejías & Nicolás Peña-Toro. (2016) Síndrome LEOPARD diagnosticado en un adulto. Piel 31:5, pages 376-378.
Crossref
Jan M Wit, Wilma Oostdijk, Monique Losekoot, Hermine A van Duyvenvoorde, Claudia A L Ruivenkamp & Sarina G Kant. (2016) MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature. European Journal of Endocrinology 174:4, pages R145-R173.
Crossref
Saori Noda, Atsushi Takahashi, Takeru Hayashi, Sei-ichi Tanuma & Masanori Hatakeyama. (2016) Determination of the catalytic activity of LEOPARD syndrome-associated SHP2 mutants toward parafibromin, a bona fide SHP2 substrate involved in Wnt signaling. Biochemical and Biophysical Research Communications 469:4, pages 1133-1139.
Crossref
Alessandro Dema, Ekaterina Perets, Maike Svenja Schulz, Veronika Anita Deák & Enno Klussmann. (2015) Pharmacological targeting of AKAP-directed compartmentalized cAMP signalling. Cellular Signalling 27:12, pages 2474-2487.
Crossref
Mylène Tajan, Audrey de Rocca Serra, Philippe Valet, Thomas Edouard & Armelle Yart. (2015) SHP2 sails from physiology to pathology. European Journal of Medical Genetics 58:10, pages 509-525.
Crossref
Bruce D. Gelb, Amy E. Roberts & Marco Tartaglia. (2015) Cardiomyopathies in Noonan syndrome and the other RASopathies. Progress in Pediatric Cardiology 39:1, pages 13-19.
Crossref
Sarah A. Clay, Timothy L. Domeier, Laurin M. Hanft, Kerry S. McDonald & Maike Krenz. (2015) Elevated Ca 2+ transients and increased myofibrillar power generation cause cardiac hypercontractility in a model of Noonan syndrome with multiple lentigines . American Journal of Physiology-Heart and Circulatory Physiology 308:9, pages H1086-H1095.
Crossref
Michelle A. Edwards, Kathryn Crombie, Christine Schramm & Maike Krenz. (2015) The Q510E mutation in Shp2 perturbs heart valve development by increasing cell migration. Journal of Applied Physiology 118:1, pages 124-131.
Crossref
Wei Qiu, Xiaonan Wang, Vladimir Romanov, Ashley Hutchinson, Andrés Lin, Maxim Ruzanov, Kevin P Battaile, Emil F Pai, Benjamin G Neel & Nickolay Y Chirgadze. (2014) Structural insights into Noonan/LEOPARD syndrome-related mutants of protein-tyrosine phosphatase SHP2 (PTPN11). BMC Structural Biology 14:1.
Crossref
Nobuhiro Kamiya, Harry K.W. Kim & Philip D. King. (2014) Regulation of bone and skeletal development by the SHP-2 protein tyrosine phosphatase. Bone 69, pages 55-60.
Crossref
Mylène TajanAurélie BatutThomas CadoudalSimon DeleruyelleSophie Le GonidecCéline Saint LaurentMaëlle VomscheidEstelle WanecqKarine TréguerAudrey De Rocca Serra-NédélecClaire VinelMarie-Adeline MarquesJoffrey PozzoOksana KunduzovaJean-Pierre SallesMaithé TauberPatrick Raynal, Hélène Cavé, Thomas EdouardPhilippe ValetArmelle Yart. (2014) LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity. Proceedings of the National Academy of Sciences 111:42.
Crossref
ZHONGQIAN HU, HAOSHU FANG, XINYI WANG, DANLEI CHEN, ZHUO CHEN & SIYING WANG. (2014) Overexpression of SHP2 tyrosine phosphatase promotes the tumorigenesis of breast carcinoma. Oncology Reports 32:1, pages 205-212.
Crossref
Zhi-Hong Yu, Ruo-Yu Zhang, Chad D. Walls, Lan Chen, Sheng Zhang, Li Wu, Sijiu Liu & Zhong-Yin Zhang. (2014) Molecular Basis of Gain-of-Function LEOPARD Syndrome-Associated SHP2 Mutations. Biochemistry 53:25, pages 4136-4151.
Crossref
Monica Bonetti, Jeroen Paardekooper Overman, Federico Tessadori, Emily Noël, Jeroen Bakkers & Jeroen den Hertog. (2014) Noonan and LEOPARD syndrome Shp2 variants induce heart displacement defects in zebrafish. Development 141:9, pages 1961-1970.
Crossref
Monica Bonetti, Virginia Rodriguez-Martinez, Jeroen Paardekooper Overman, John Overvoorde, Mark van Eekelen, Chris Jopling & Jeroen den Hertog. (2014) Distinct and Overlapping Functions of ptpn11 Genes in Zebrafish Development. PLoS ONE 9:4, pages e94884.
Crossref
. 2014. The Melanocytic Proliferations. The Melanocytic Proliferations 44 64 .
Christine Schramm, Michelle A. Edwards & Maike Krenz. (2013) New Approaches to Prevent LEOPARD Syndrome-associated Cardiac Hypertrophy by Specifically Targeting Shp2-dependent Signaling. Journal of Biological Chemistry 288:25, pages 18335-18344.
Crossref
Philip E. LapinskiMelissa F. MeyerGen-Sheng FengNobuhiro Kamiya & Philip D. King. (2013) Deletion of SHP-2 in mesenchymal stem cells causes growth retardation, limb and chest deformity, and calvarial defects in mice. Disease Models & Mechanisms.
Crossref
Maria I. Kontaridis, Eleni V. Geladari & Charalampia V. Geladari. 2013. Protein Tyrosine Phosphatase Control of Metabolism. Protein Tyrosine Phosphatase Control of Metabolism 147 167 .
Anna Keyte & Mary Redmond Hutson. (2012) The neural crest in cardiac congenital anomalies. Differentiation 84:1, pages 25-40.
Crossref
René Eulenfeld, Anna Dittrich, Christina Khouri, Pia J. Müller, Barbara Mütze, Alexandra Wolf & Fred Schaper. (2012) Interleukin-6 signalling: More than Jaks and STATs. European Journal of Cell Biology 91:6-7, pages 486-495.
Crossref
Audrey De Rocca Serra-NédélecThomas EdouardKarine TréguerMylène TajanToshiyuki ArakiMarie DanceMarianne Mus, Alexandra Montagner, Maïté TauberJean-Pierre Salles, Philippe ValetBenjamin G. NeelPatrick RaynalArmelle Yart. (2012) Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature. Proceedings of the National Academy of Sciences 109:11, pages 4257-4262.
Crossref
Christine Schramm, Deborah M. Fine, Michelle A. Edwards, Ashley N. Reeb & Maike Krenz. (2012) The PTPN11 loss-of-function mutation Q510E-Shp2 causes hypertrophic cardiomyopathy by dysregulating mTOR signaling . American Journal of Physiology-Heart and Circulatory Physiology 302:1, pages H231-H243.
Crossref
Eduardo Calonje, Thomas Brenn & Alexander Lazar. 2012. McKee's Pathology of the Skin. McKee's Pathology of the Skin 912 934 .
T. Edouard & J. P. Salles. 2012. Aspects biologiques, moléculaires et cliniques de l’axe GH/IGF-I. Aspects biologiques, moléculaires et cliniques de l’axe GH/IGF-I 15 25 .
Hidekazu Ishida, Shigetoyo Kogaki, Jun Narita, Hiroaki Ichimori, Nobutoshi Nawa, Yoko Okada, Kunihiko Takahashi & Keiichi Ozono. (2011) LEOPARD-type SHP2 mutant Gln510Glu attenuates cardiomyocyte differentiation and promotes cardiac hypertrophy via dysregulation of Akt/GSK-3β/β-catenin signaling. American Journal of Physiology-Heart and Circulatory Physiology 301:4, pages H1531-H1539.
Crossref
Martin Zenker. (2011) Clinical manifestations of mutations in RAS and related intracellular signal transduction factors. Current Opinion in Pediatrics 23:4, pages 443-451.
Crossref
Jessica Lauriol & Maria I. Kontaridis. (2011) PTPN11-Associated Mutations in the Heart: Has LEOPARD Changed Its RASpots?. Trends in Cardiovascular Medicine 21:4, pages 97-104.
Crossref
Talita M. Marin, Kimberly Keith, Benjamin Davies, David A. Conner, Prajna Guha, Demetrios Kalaitzidis, Xue Wu, Jessica Lauriol, Bo Wang, Michael Bauer, Roderick Bronson, Kleber G. Franchini, Benjamin G. Neel & Maria I. Kontaridis. (2011) Rapamycin reverses hypertrophic cardiomyopathy in a mouse model of LEOPARD syndrome–associated PTPN11 mutation. Journal of Clinical Investigation 121:3, pages 1026-1043.
Crossref
Emanuela Ferrari, Michele Tinti, Stefano Costa, Salvatore Corallino, Aurelio Pio Nardozza, Andrew Chatraryamontri, Arnaud Ceol, Gianni Cesareni & Luisa Castagnoli. (2011) Identification of New Substrates of the Protein-tyrosine Phosphatase PTP1B by Bayesian Integration of Proteome Evidence. Journal of Biological Chemistry 286:6, pages 4173-4185.
Crossref
Marco Tartaglia, Bruce D. Gelb & Martin Zenker. (2011) Noonan syndrome and clinically related disorders. Best Practice & Research Clinical Endocrinology & Metabolism 25:1, pages 161-179.
Crossref
Marco Tartaglia & Bruce D. Gelb. (2010) Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms. Annals of the New York Academy of Sciences 1214:1, pages 99-121.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.