نتائج البحث - "Forte, Gabriella M. A."

1

Academic Journal

Import of extracellular ATP in yeast and man modulates AMPK and TORC1 signalling

المؤلفون: Forte, Gabriella M., Davie, Elizabeth, Lie, Shervi, Franz-Wachtel, Mirita, Ovens, Ashley J., Wang, Tingting, Oakhill, Jonathan S., Macek, Boris, Hagan, Iain M., Petersen, Janni

مصطلحات موضوعية: RESEARCH ARTICLE

وصف الملف: text/html

Relation: http://jcs.biologists.org/cgi/content/short/132/7/jcs223925; http://dx.doi.org/10.1242/jcs.223925

الاتاحة: http://jcs.biologists.org/cgi/content/short/132/7/jcs223925
https://doi.org/10.1242/jcs.223925

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2

Academic Journal

Phosphorylation of the amino-terminus of the AGC kinase Gad8 prevents its interaction with TORC2

المؤلفون: Du, Wei, Forte, Gabriella M, Smith, Duncan, Petersen, Janni

مصطلحات موضوعية: Gad8, PKC, SGK1, Schizosaccharomyces pombe, TORC2

Relation: Du W, Forte GM, Smith D, Petersen J. Phosphorylation of the amino-terminus of the AGC kinase Gad8 prevents its interaction with TORC2. Open Biol. 2016 Mar;6(3). pii: 150189. doi:10.1098/rsob.150189.; http://hdl.handle.net/2328/36167; https://doi.org/10.1098/rsob.150189

الاتاحة: http://hdl.handle.net/2328/36167
https://doi.org/10.1098/rsob.150189

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3

Academic Journal

N-terminal acetylation inhibits protein targeting to the endoplasmic reticulum

المؤلفون: Forte, Gabriella M A, Pool, Martin R., Stirling, Colin J.

المصدر: Forte , G M A , Pool , M R & Stirling , C J 2011 , ' N-terminal acetylation inhibits protein targeting to the endoplasmic reticulum ' , PLoS Biology , vol. 9 , no. 5 , e1001073 , pp. 1-13 . https://doi.org/10.1371/journal.pbio.1001073

Relation: https://research.manchester.ac.uk/en/publications/402aafcf-1757-4eb1-ae3f-2dca8f027187

الاتاحة: https://research.manchester.ac.uk/en/publications/402aafcf-1757-4eb1-ae3f-2dca8f027187
https://doi.org/10.1371/journal.pbio.1001073
http://www.plosbiology.org/article/fetchObjectAttachment.action?uri=info%3Adoi%2F10.1371%2Fjournal.pbio.1001073&representation=PDF

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4

Academic Journal

mTORC1 directly inhibits AMPK to promote cell proliferation under nutrient stress

المؤلفون: Ling, Naomi X.Y., Kaczmarek, Adrian, Hoque, Ashfaqul, Davie, Elizabeth, Ngoei, Kevin R. W., Morrison, Kaitlin R., Smiles, William J., Forte, Gabriella M., Wang, Tingting, Lie, Shervi, Dite, Toby A., Langendorf, Christopher G., Scott, John W., Oakhill, Jonathan S., Petersen, Janni

المصدر: Ling , N X Y , Kaczmarek , A , Hoque , A , Davie , E , Ngoei , K R W , Morrison , K R , Smiles , W J , Forte , G M , Wang , T , Lie , S , Dite , T A , Langendorf , C G , Scott , J W , Oakhill , J S & Petersen , J 2020 , ' mTORC1 directly inhibits AMPK to promote cell proliferation under nutrient stress ' , Nature Metabolism , vol. 2 , no. 1 , pp. 41-49 . https://doi.org/10.1038/s42255-019-0157-1

مصطلحات موضوعية: /dk/atira/pure/subjectarea/asjc/2700/2712, name=Endocrinology, Diabetes and Metabolism, /dk/atira/pure/subjectarea/asjc/2700/2737, name=Physiology (medical), /dk/atira/pure/subjectarea/asjc/2700/2724, name=Internal Medicine, /dk/atira/pure/subjectarea/asjc/1300/1307, name=Cell Biology

الاتاحة: https://discovery.dundee.ac.uk/en/publications/cf13767e-b364-48ab-911f-97bfd6e564f9
https://doi.org/10.1038/s42255-019-0157-1
http://www.scopus.com/inward/record.url?scp=85078318076&partnerID=8YFLogxK

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5

Academic Journal

Characterization of Human Disease Phenotypes Associated with Mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

المؤلفون: Crow, Yanick J., Chase, Diana S., Schmidt, Johanna Lowenstein, Szynkiewicz, Marcin, Forte, Gabriella M. A., Gornall, Hannah L., Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel Hamid, Mohamed S., Abdel Salam, Ghada M., Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon Shalev, Stavit, Arellano, Montse, Aswani, Vijay, Babul Hirji, Riyana, Baildam, Eileen M., Bahi Buisson, Nadia, Bailey, Kathryn M., Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W., Bernard, Genevieve, Bianchi, Marika, de Villemeur, Thierry Billette, Blair, Edward M., Bloom, Miriam, Burlina, Alberto B., Carpanelli, Maria Luisa, Carvalho, Daniel R., Castro Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E., Chitayat, David A., Collins, Abigail E., Sierra Corcoles, Concepcion, Cordeiro, Nuno J. V., Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C., De Goede, Christian G. E. L., De Laet, Corinne, De Waele, Liesbeth M. H., Denzler, Ines, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C., Ferrie, Colin D., Figueiredo, Antonio, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R., Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Lent, Khan, Nasaim, King, Mary D., Kirk, Edwin P., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, La Piana, Roberta, Lim, Ming J., Lin, Jean Pierre S. M., Linnankivi, Tarja, Mackay, Mark T., Marom, Daphna R., Lourenco, Charles Marques, Mckee, Shane A., Moroni, Isabella, Morton, Jenny E. V., Moutard, Marie Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez Enamorado, Noemi, Oades, Patrick J., Ostergaard, John R., Perez Duenas, Belen, Prendiville, Julie S., Ramesh, Venkateswaran, Rasmussen, Magnhild, Regal, Luc, Ricci, Federica, Rio, Marlene, Rodriguez, Diana, Roubertie, Agathe, Salvatici, Elisabetta, Segers, Karin A., Sinha, Gyanranjan P., Soler, Doriette, Spiegel, Ronen, Stoedberg, Tommy I., Straussberg, Rachel, Swoboda, Kathryn J., Suri, Mohnish, Tacke, Uta, Tan, Tiong Y., Naude, Johann te Water, Teik, Keng Wee, Thomas, Maya Mary, Till, Marianne, Tonduti, Davide, Van Coster, Rudy Noel, van der Knaap, Marjo S., Vassallo, Grace, Vijzelaar, Raymon, Vogt, Julie, Wallace, Geoffrey B., Wassmer, Evangeline, Webb, Hannah J., Whitehouse, William P., Whitney, Robyn N., Zaki, Maha S., Zuberi, Sameer M., Livingston, John H., Rozenberg, Flore, Lebon, Pierre, Vanderver, Adeline, Rice, Gillian I., ARIAUDO, GIADA, D'ARRIGO, STEFANO, FAZZI, ELISA MARIA, OLIVIERI, IVANA, VALENTE, ENZA MARIA, ORCESI, SIMONA

المساهمون: Crow, Yanick J., Chase, Diana S., Schmidt, Johanna Lowenstein, Szynkiewicz, Marcin, Forte, Gabriella M. A., Gornall, Hannah L., Oojageer, Anthony, Anderson, Beverley, Pizzino, Amy, Helman, Guy, Abdel Hamid, Mohamed S., Abdel Salam, Ghada M., Ackroyd, Sam, Aeby, Alec, Agosta, Guillermo, Albin, Catherine, Allon Shalev, Stavit, Arellano, Montse, Ariaudo, Giada, Aswani, Vijay, Babul Hirji, Riyana, Baildam, Eileen M., Bahi Buisson, Nadia, Bailey, Kathryn M., Barnerias, Christine, Barth, Magalie, Battini, Roberta, Beresford, Michael W., Bernard, Genevieve, Bianchi, Marika, de Villemeur, Thierry Billette, Blair, Edward M., Bloom, Miriam, Burlina, Alberto B., Carpanelli, Maria Luisa, Carvalho, Daniel R., Castro Gago, Manuel, Cavallini, Anna, Cereda, Cristina, Chandler, Kate E., Chitayat, David A., Collins, Abigail E., Sierra Corcoles, Concepcion, Cordeiro, Nuno J. V., Crichiutti, Giovanni, Dabydeen, Lyvia, Dale, Russell C., D'Arrigo, Stefano, De Goede, Christian G. E. L., De Laet, Corinne, De Waele, Liesbeth M. H., Denzler, Ine, Desguerre, Isabelle, Devriendt, Koenraad, Di Rocco, Maja, Fahey, Michael C., Fazzi, ELISA MARIA, Ferrie, Colin D., Figueiredo, Antonio, Gener, Blanca, Goizet, Cyril, Gowrinathan, Nirmala R., Gowrishankar, Kalpana, Hanrahan, Donncha, Isidor, Bertrand, Kara, Lent, Khan, Nasaim, King, Mary D., Kirk, Edwin P., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre, Lauffer, Heinz, Laugel, Vincent, La Piana, Roberta, Lim, Ming J., Lin, Jean Pierre S. M., Linnankivi, Tarja, Mackay, Mark T., Marom, Daphna R., Lourenco, Charles Marque, Mckee, Shane A., Moroni, Isabella, Morton, Jenny E. V., Moutard, Marie Laure, Murray, Kevin, Nabbout, Rima, Nampoothiri, Sheela, Nunez Enamorado, Noemi, Oades, Patrick J., Olivieri, Ivana, Ostergaard, John R., Perez Duenas, Belen, Prendiville, Julie S., Ramesh, Venkateswaran, Rasmussen, Magnhild, Regal, Luc, Ricci, Federica, Rio, Marlene, Rodriguez, Diana

Relation: info:eu-repo/semantics/altIdentifier/pmid/25604658; info:eu-repo/semantics/altIdentifier/wos/WOS:000348843600007; volume:167; issue:2; firstpage:296; lastpage:312; numberofpages:17; journal:AMERICAN JOURNAL OF MEDICAL GENETICS. PART A; http://hdl.handle.net/11571/1180853; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84921417123

الاتاحة: http://hdl.handle.net/11571/1180853
https://doi.org/10.1002/ajmg.a.36887

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6

Assessment of interferon-related biomarkers in Aicardi-Gouti?¨res syndrome associated with mutations in TREX1 RNASEH2A RNASEH2B RNASEH2C SAMHD1 and ADAR: a case-control study

المؤلفون: Rice, Gillian I, Forte, Gabriella M A, Szynkiewicz, Marcin, Chase, Diana S, Aeby, Alec, Abdel-Hamid, Mohamed S, Ackroyd, Sam, Allcock, Rebecca, Bailey, Kathryn M, Balottin, Umberto, Barnerias, Christine, Bernard, Genevieve, Bodemer, Christine, Botella, Maria P, Cereda, Cristina, Chandler, Kate E, Dabydeen, Lyvia, Dale, Russell C, De Laet, Corinne, De Goede, Christian G E L, del Toro, Mireia, Effat, Laila, Enamorado, Noemi Nunez, Fazzi, Elisa, Gener, Blanca, Haldre, Madli, Lin, Jean-Pierre S-M, Livingston, John H, Lourenco, Charles Marques, Marques, Wilson, Oades, Patrick, Peterson, Pärt, Rasmussen, Magnhild, Roubertie, Agathe, Schmidt, Johanna Loewenstein, Shalev, Stavit A, Simon, Rogelio, Spiegel, Ronen, Swoboda, Kathryn J, Temtamy, Samia A, Vassallo, Grace, Vilain, Catheline N, Vogt, Julie, Wermenbol, Vanessa, Whitehouse, William P, Soler, Doriette, Olivieri, Ivana, Orcesi, Simona, Aglan, Mona S, Zaki, Maha S, Abdel-Salam, Ghada M H, Vanderver, Adeline, Kisand, Kai, Rozenberg, Flore, Lebon, Pierre, Crow, Yanick J

المصدر: The Lancet Neurology; Vol 12

URL الوصول: https://explore.openaire.eu/search/publication?articleId=ec_fp7health::45aef8e13a83a94ddb1028a57e61563f

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7

Academic Journal

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type i interferon signaling

المؤلفون: Rice, Gillian I., Del Toro Duany, Yoandris, Jenkinson, Emma M., Forte, Gabriella M. A., Anderson, Beverley H., Ariaudo, Giada, Bader Meunier, Brigitte, Baildam, Eileen M., Battini, Roberta, Beresford, Michael W., Casarano, Manuela, Chouchane, Mondher, Cimaz, Rolando, Collins, Abigail E., Cordeiro, Nuno J. V., Dale, Russell C., Davidson, Joyce E., De Waele, Liesbeth, Desguerre, Isabelle, Faivre, Laurence, Isidor, Bertrand, Lagae, Lieven, Latchman, Andrew R., Lebon, Pierre, Li, Chumei, Livingston, John H., Lourenço, Charles M., Mancardi, Maria Margherita, Masurel Paulet, Alice, Mcinnes, Iain B., Menezes, Manoj P., Mignot, Cyril, O'Sullivan, James, Orcesi, Simona, Picco, Paolo P., Riva, Enrica, Robinson, Robert A., Rodriguez, Diana, Salvatici, Elisabetta, Scott, Christiaan, Szybowska, Marta, Tolmie, John L., Vanderver, Adeline, Vanhulle, Catherine, Vieira, Jose Pedro, Webb, Kate, Whitney, Robyn N., Williams, Simon G., Wolfe, Lynne A., Zuberi, Sameer M., Hur, Sun, Crow, Yanick J., FAZZI, Elisa Maria

المساهمون: Rice Gillian I., Del Toro Duany Yoandri, Jenkinson Emma M., Forte Gabriella M. A., Anderson Beverley H., Ariaudo Giada, Bader Meunier Brigitte, Baildam Eileen M., Battini Roberta, Beresford Michael W., Casarano Manuela, Chouchane Mondher, Cimaz Rolando, Collins Abigail E., Cordeiro Nuno J. V., Dale Russell C., Davidson Joyce E., De Waele Liesbeth, Desguerre Isabelle, Faivre Laurence, Fazzi Elisa Maria, Isidor Bertrand, Lagae Lieven, Latchman Andrew R., Lebon Pierre, Li Chumei, Livingston John H., Lourenço Charles M., Mancardi Maria Margherita, Masurel Paulet Alice, Mcinnes Iain B., Menezes Manoj P., Mignot Cyril, O'Sullivan Jame, Orcesi Simona, Picco Paolo P., Riva Enrica, Robinson Robert A., Rodriguez Diana, Salvatici Elisabetta, Scott Christiaan, Szybowska Marta, Tolmie John L., Vanderver Adeline, Vanhulle Catherine, Vieira Jose Pedro, Webb Kate, Whitney Robyn N., Williams Simon G., Wolfe Lynne A., Zuberi Sameer M., Hur Sun, Crow Yanick J.

وصف الملف: STAMPA

Relation: info:eu-repo/semantics/altIdentifier/pmid/24686847; info:eu-repo/semantics/altIdentifier/wos/WOS:000335422900020; volume:46; issue:5; firstpage:503; lastpage:509; numberofpages:7; journal:NATURE GENETICS; http://hdl.handle.net/11379/468029; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84899495767; http://www.nature.com/ng/index.html

الاتاحة: http://hdl.handle.net/11379/468029
https://doi.org/10.1038/ng.2933
http://www.nature.com/ng/index.html

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8

Academic Journal

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

المؤلفون: Rice, Gillian I, del Toro Duany, Yoandris, Jenkinson, Emma M, Forte, Gabriella M A, Anderson, Beverley H, Ariaudo, Giada, Bader-Meunier, Brigitte, Baildam, Eileen M, Battini, Roberta, Beresford, Michael W, Casarano, Manuela, Chouchane, Mondher, Cimaz, Rolando, Collins, Abigail E, Cordeiro, Nuno J V, Dale, Russell C, Davidson, Joyce E, De Waele, Liesbeth, Desguerre, Isabelle, Faivre, Laurence, Fazzi, Elisa, Isidor, Bertrand, Lagae, Lieven, Latchman, Andrew R, Lebon, Pierre, Li, Chumei, Livingston, John H, Lourenço, Charles M, Mancardi, Maria Margherita, Masurel-Paulet, Alice, McInnes, Iain B, Menezes, Manoj P, Mignot, Cyril, O'Sullivan, James, Orcesi, Simona, Picco, Paolo P, Riva, Enrica, Robinson, Robert A, Rodriguez, Diana, Salvatici, Elisabetta, Scott, Christiaan, Szybowska, Marta, Tolmie, John L, Vanderver, Adeline, Vanhulle, Catherine, Vieira, Jose Pedro, Webb, Kate, Whitney, Robyn N, Williams, Simon G, Wolfe, Lynne A, Zuberi, Sameer M, Hur, Sun, Crow, Yanick J

Relation: Nature Genetics vol:46 issue:5 pages:503-9; https://lirias.kuleuven.be/handle/123456789/461658

الاتاحة: https://lirias.kuleuven.be/handle/123456789/461658

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9

Academic Journal

Synonymous mutations in RNASEH2A create cryptic splice sites impairing RNase H2 enzyme function in aicardi-Goutières syndrome

المصدر: Crow , Y , Rice , G I , Reijns , M A M , Coffin , S R , Forte , G M A , Anderson , B , Szynkiewicz , M , Gornall , H , Gent , D , Leitch , A , Botella , M P , Fazzi , E , Gener , B , Lagae , L , Olivieri , I , Orcesi , S , Swoboda , K J , Perrino , F W , Jackson , A P & Crow , Y J 2013 , ' Synonymous mutations in RNASEH2A create cryptic ....

مصطلحات موضوعية: AGS, Aicardi-Goutières syndrome, RNASEH2A, Splicing, Synonymous mutations

الاتاحة: https://research.manchester.ac.uk/en/publications/5729d202-62c1-46be-b9d0-7759e4f9a10c
https://doi.org/10.1002/humu.22336

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