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Characterization of the GNAQ promoter and association of increased Gq expression with cardiac hypertrophy in humans. [electronic resource] by
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- Erdmann, Jeanette
- Savidou, Danai
- Heusch, Gerd
- Leineweber, Kirsten
- Jakob, Heinz
- Hense, Hans-Werner
- Löwel, Hannelore
- Brockmeyer, Norbert H
- Schunkert, Heribert
- Siffert, Winfried
Producer: 20081113
In:
European heart journal vol. 29
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4662.
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Osteoblast expression of an engineered Gs-coupled receptor dramatically increases bone mass. [electronic resource] by
- Hsiao, Edward C
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- Chang, Wei C
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- Peng, Jeffrey
- Nguyen, Trieu D
- Manalac, Carlota
- Halloran, Bernard P
- Conklin, Bruce R
- Nissenson, Robert A
Producer: 20080225
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 105
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A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. [electronic resource] by
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- Stamper, Brendan D
- Gordon, Christopher T
- Johnson, Jason M
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- Smith, Joshua D
- Emery, Sarah B
- Lyonnet, Stanislas
- Amiel, Jeanne
- Holder, Muriel
- Heggie, Andrew A
- Bamshad, Michael J
- Nickerson, Deborah A
- Cox, Timothy C
- Hing, Anne V
- Horst, Jeremy A
- Cunningham, Michael L
Producer: 20120625
In:
American journal of human genetics vol. 90
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G-protein-independent coupling of MC4R to Kir7.1 in hypothalamic neurons. [electronic resource] by
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- Digby, Gregory J
- Sebag, Julien A
- Millhauser, Glenn L
- Palomino, Rafael
- Matthews, Robert
- Gillyard, Taneisha
- Panaro, Brandon L
- Tough, Iain R
- Cox, Helen M
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Producer: 20150430
In:
Nature vol. 520
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4670.
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SNX14 is a bifunctional negative regulator for neuronal 5-HT6 receptor signaling. [electronic resource] by
- Ha, Chang Man
- Park, Daehun
- Kim, Yoonju
- Na, Myeongsu
- Panda, Surabhi
- Won, Sehoon
- Kim, Hyun
- Ryu, Hoon
- Park, Zee Yong
- Rasenick, Mark M
- Chang, Sunghoe
Producer: 20160208
In:
Journal of cell science vol. 128
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Lack of association between autonomously functioning thyroid nodules and germline polymorphisms of the thyrotropin receptor and Gαs genes in a mild to moderate iodine-deficient Caucasian population. [electronic resource] by
- Vicchio, Teresa Manuela
- Giovinazzo, Salvatore
- Certo, Rosaria
- Cucinotta, Mariapaola
- Micali, Carmelo
- Baldari, Sergio
- Benvenga, Salvatore
- Trimarchi, Francesco
- Campennì, Alfredo
- Ruggeri, Rosaria Maddalena
Producer: 20150624
In:
Journal of endocrinological investigation vol. 37
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4675.
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- Rogers, Angela
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- Stewart, Michelle
- Paudyal, Anju
- Hough, Tertius A
- Nesbit, M Andrew
- Wells, Sara
- Vincent, Tonia L
- Brown, Stephen Dm
- Cox, Roger D
- Thakker, Rajesh V
Producer: 20190621
In:
JCI insight vol. 2
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Atrx inactivation drives disease-defining phenotypes in glioma cells of origin through global epigenomic remodeling. [electronic resource] by
- Danussi, Carla
- Bose, Promita
- Parthasarathy, Prasanna T
- Silberman, Pedro C
- Van Arnam, John S
- Vitucci, Mark
- Tang, Oliver Y
- Heguy, Adriana
- Wang, Yuxiang
- Chan, Timothy A
- Riggins, Gregory J
- Sulman, Erik P
- Lang, Frederick F
- Creighton, Chad J
- Deneen, Benjamin
- Miller, C Ryan
- Picketts, David J
- Kannan, Kasthuri
- Huse, Jason T
Producer: 20181212
In:
Nature communications vol. 9
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