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  1. 1
    Intraductal tubulopapillary neoplasms of the bile ducts: clinicopathologic, immunohistochemical, and molecular analysis of 20 cases

    Intraductal tubulopapillary neoplasms of the bile ducts: clinicopathologic, immunohistochemical, and molecular analysis of 20 cases by Anna Melissa Schlitter, Kee‐Taek Jang, Günter Klöppel, Burcu Saka, Seung‐Mo Hong, Hye‐Jeong Choi, G. Johan A. Offerhaus, Ralph H. Hruban, Yoh Zen, Björn Konukiewitz, Ivonne Regel, Michael Allgäuer, Serdar Balcı, Olca Baştürk, Michelle D. Reid, Iréne Esposito, Volkan Adsay

    Published 2015
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  2. 2
    Use of multivariate analysis to suggest a new molecular classification of colorectal cancer

    Use of multivariate analysis to suggest a new molecular classification of colorectal cancer by Enric Domingo, Rajarajan Ramamoorthy, Dahmane Oukrif, Daniel Norris Rosmarin, Michal Presz, Haitao Wang, Hannah Pulker, Helen Lockstone, Tarjei S. Hveem, Treena Cranston, Håvard E. Danielsen, Marco Novelli, Brian R Davidson, Zheng‐Zhou Xu, Peter L. Molloy, Elaine Johnstone, Chris Holmes, Rachel Midgley, David Kerr, Oliver M. Sieber, Ian Tomlinson

    Published 2012
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  3. 3
    Clinical Implications of Genetic Defects in G Proteins

    Clinical Implications of Genetic Defects in G Proteins by Michael A. Levine

    Published 1999
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  4. 4
    Postnatal Establishment of Allelic Gαs Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous Gαs Disruption

    Postnatal Establishment of Allelic Gαs Silencing as a Plausible Explanation for Delayed Onset of Parathyroid Hormone Resistance Owing to Heterozygous Gαs Disruption by Serap Turan, Eduardo Fernández‐Rebollo, Cumhur Aydın, Teuta Zoto Mustafayev, Monica Reyes, George S. Bounoutas, Min Chen, Lee S. Weinstein, Reinhold G. Erben, Vladimir Marshansky, Murat Bastepe

    Published 2013
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  5. 5
    Targeted next‐generation sequencing of cancer genes dissects the molecular profiles of intraductal papillary neoplasms of the pancreas

    Targeted next‐generation sequencing of cancer genes dissects the molecular profiles of intraductal papillary neoplasms of the pancreas by Eliana Amato, Marco Dal Molin, Andrea Mafficini, Jun Yu, Giuseppe Malleo, Borislav C. Rusev, Matteo Fassan, Davide Antonello, Yoshihiko Sadakari, M. Paola Castelli, Giuseppe Zamboni, Anirban Maitra, Roberto Salvia, Ralph H. Hruban, Claudio Bassi, Paola Capelli, Rita T. Lawlor, Michael Goggins, Aldo Scarpa

    Published 2014
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  6. 6
    A mutation spectrum that includes GNAS, KRAS and TP53 may be shared by mucinous neoplasms of the appendix

    A mutation spectrum that includes GNAS, KRAS and TP53 may be shared by mucinous neoplasms of the appendix by Kieko Hara, Tsuyoshi Saito, Takuo Hayashi, Alkam Yimit, Michiko Takahashi, Keiko Mitani, Makoto Takahashi, Takashi Yao

    Published 2015
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  7. 7
    Epigenetic instability of imprinted genes in human cancers

    Epigenetic instability of imprinted genes in human cancers by Joomyeong Kim, Corey L. Bretz, Suman Lee

    Published 2015
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  8. 8
    Whole-Genome Sequencing of Growth Hormone (GH)-Secreting Pituitary Adenomas

    Whole-Genome Sequencing of Growth Hormone (GH)-Secreting Pituitary Adenomas by Niko Välimäki, Hande Demi̇r, Esa Pitkänen, Eevi Kaasinen, Atte Karppinen, Leena Kivipelto, Camilla Schalin‐Jäntti, Lauri A. Aaltonen, Auli Karhu

    Published 2015
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  9. 9
    Whole‐exome sequencing of pancreatic neoplasms with acinar differentiation

    Whole‐exome sequencing of pancreatic neoplasms with acinar differentiation by Yuchen Jiao, Raluca Yonescu, G. Johan A. Offerhaus, David S. Klimstra, Anirban Maitra, James R. Eshleman, James G. Herman, Weijie Poh, Lorraine Pelosof, Christopher L. Wolfgang, Bert Vogelstein, Kenneth W. Kinzler, Ralph H. Hruban, Nickolas Papadopoulos, Laura D. Wood

    Published 2013
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  10. 10
    Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (sporPHP1B)

    Similar frequency of paternal uniparental disomy involving chromosome 20q (patUPD20q) in Japanese and Caucasian patients affected by sporadic pseudohypoparathyroidism type Ib (spor... by Rieko Takatani, Masanori Minagawa, Angelo Molinaro, Monica Reyes, Kaori Kinoshita, Tomozumi Takatani, Itsuro Kazukawa, Misako Nagatsuma, Kenichi Kashimada, Kenichi Sato, Kazuyuki Matsushita, Fumio Nomura, Naoki Shimojo, Harald Jüppner

    Published 2015
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  11. 11
    Expression of imprinted genes in placenta is associated with infant neurobehavioral development

    Expression of imprinted genes in placenta is associated with infant neurobehavioral development by Benjamin B. Green, Maya Kappil, Luca Lambertini, David A. Armstrong, Dylan J. Guerin, Andrew J. Sharp, Barry M. Lester, Jia Chen, Carmen J. Marsit

    Published 2015
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  12. 12
    A Combination of Molecular Markers and Clinical Features Improve the Classification of Pancreatic Cysts

    A Combination of Molecular Markers and Clinical Features Improve the Classification of Pancreatic Cysts by Simeon Springer, Yuxuan Wang, Marco Dal Molin, David L. Masica, Yuchen Jiao, Isaac Kinde, Amanda L. Blackford, Siva P. Raman, Christopher L. Wolfgang, Tyler M. Tomita, Noushin Niknafs, Christopher Douville, Janine Ptak, Lisa Dobbyn, Peter J. Allen, David S. Klimstra, Mark Schattner, C. Max Schmidt, Michele Yip-Schneider, Oscar W. Cummings, Randall E. Brand, Herbert J. Zeh, Aatur D. Singhi, Aldo Scarpa, Roberto Salvia, Giuseppe Malleo, Giuseppe Zamboni, Massimo Falconi, Jin‐Young Jang, Sun‐Whe Kim, Wooil Kwon, Seung‐Mo Hong, Ki Byung Song, Song Cheol Kim, Niall Swan, Jean Murphy, Justin Geoghegan, William R. Brugge, Carlos Fernández‐del Castillo, Mari Mino‐Kenudson, Richard D. Schulick, Barish H. Edil, Volkan Adsay, Jorge Paulino, Jeanin E. van Hooft, Shinichi Yachida, Satoshi Nara, Nobuyoshi Hiraoka, Kenji Yamao, Susuma Hijioka, Van der Merwe, Michael Goggins, Marcia I. Canto, Nita Ahuja, Kenzo Hirose, Martin A. Makary, Matthew J. Weiss, John L. Cameron, Meredith E. Pittman, James R. Eshleman, Luis A. Díaz, Nickolas Papadopoulos, Kenneth W. Kinzler, Rachel Karchin, Ralph H. Hruban, Bert Vogelstein, Anne Marie Lennon

    Published 2015
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  13. 13
    The human <i>GNAS1</i> gene is imprinted and encodes distinct paternally and biallelically expressed G proteins

    The human <i>GNAS1</i> gene is imprinted and encodes distinct paternally and biallelically expressed G proteins by Bruce E. Hayward, Mamoru Kamiya, Lisa Strain, Veronica Moran, Roderick Campbell, Yoshihide Hayashizaki, David T. Bonthron

    Published 1998
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  14. 14
    Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors

    Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors by Gerald Goh, Ute I. Scholl, James M. Healy, Murim Choi, Manju L. Prasad, Carol Nelson‐Williams, John W. Kunstman, John W. Kuntsman, Reju Korah, Anna‐Carinna Suttorp, Dimo Dietrich, Matthias Haase, Holger S. Willenberg, Peter Stålberg, Per Hellman, Göran Åkerström, Peyman Björklund, Tobias Carling, Richard P. Lifton

    Published 2014
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  15. 15
    Heterozygous inactivation of <i>Gnas</i> in adipose-derived mesenchymal progenitor cells enhances osteoblast differentiation and promotes heterotopic ossification

    Heterozygous inactivation of <i>Gnas</i> in adipose-derived mesenchymal progenitor cells enhances osteoblast differentiation and promotes heterotopic ossification by Robert J. Pignolo, Meiqi Xu, Elizabeth S. Russell, Alec Richardson, Josef Kaplan, Paul C. Billings, Frederick S. Kaplan, Eileen M. Shore

    Published 2011
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  16. 16
    Quantitative Analysis of Methylation Defects and Correlation With Clinical Characteristics in Patients With Pseudohypoparathyroidism Type I and GNAS Epigenetic Alterations

    Quantitative Analysis of Methylation Defects and Correlation With Clinical Characteristics in Patients With Pseudohypoparathyroidism Type I and GNAS Epigenetic Alterations by Francesca Marta Elli, Luisa De Sanctis, Valentina Bollati, Letizia Tarantini, Marcello Filopanti, Anna Maria Barbieri, Erika Peverelli, Paolo Beck‐Peccoz, Anna Spada, Giovanna Mantovani

    Published 2014
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  17. 17
    A GNAS Mutation Found in Pancreatic Intraductal Papillary Mucinous Neoplasms Induces Drastic Alterations of Gene Expression Profiles with Upregulation of Mucin Genes

    A GNAS Mutation Found in Pancreatic Intraductal Papillary Mucinous Neoplasms Induces Drastic Alterations of Gene Expression Profiles with Upregulation of Mucin Genes by Hirotake Komatsu, Etsuko Tanji, Naoaki Sakata, Takeshi Aoki, Fuyuhiko Motoi, Takeshi Naitoh, Yu Katayose, Shinichi Egawa, Michiaki Unno, Toru Furukawa

    Published 2014
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  18. 18
    Paediatric Pituitary Adenomas: A Decade of Change

    Paediatric Pituitary Adenomas: A Decade of Change by Federica Guaraldi, Helen L. Storr, Lucia Ghizzoni, Ezio Ghigo, Martin O. Savage

    Published 2014
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  19. 19
    Whole-exome sequencing uncovers frequent GNAS mutations in intraductal papillary mucinous neoplasms of the pancreas

    Whole-exome sequencing uncovers frequent GNAS mutations in intraductal papillary mucinous neoplasms of the pancreas by Toru Furukawa, Yuko Kuboki, Etsuko Tanji, Shoko Yoshida, Takashi Hatori, Masakazu Yamamoto, Noriyuki Shibata, Kyoko Shimizu, Naoyuki Kamatani, Keiko Shiratori

    Published 2011
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  20. 20
    Recurrent <i>GNAS</i> Mutations Define an Unexpected Pathway for Pancreatic Cyst Development

    Recurrent <i>GNAS</i> Mutations Define an Unexpected Pathway for Pancreatic Cyst Development by Jian Wu, Hanno Matthaei, Anirban Maitra, Marco Dal Molin, Laura D. Wood, James R. Eshleman, Michael Goggins, Marcia I. Canto, Richard D. Schulick, Barish H. Edil, Christopher L. Wolfgang, Alison P. Klein, Luis A. Díaz, Peter J. Allen, C. Max Schmidt, Kenneth W. Kinzler, Nickolas Papadopoulos, Ralph H. Hruban, Bert Vogelstein

    Published 2011
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