PMC Links for GEO Profiles (Select 98864165) - PMC

Federica Campolo, Chiara Capponi, Maria Grazia Tarsitano, Marta Tenuta, Carlotta Pozza, Daniele Gianfrilli, Fabio Magliocca, Mary A. Venneri, Elena Vicini, Andrea Lenzi, Andrea M. Isidori, Federica Barbagallo

Front Endocrinol (Lausanne) 2022; 13: 1010924. Published online 2022 Oct 7. doi: 10.3389/fendo.2022.1010924

PMCID:: PMC9585345

Abstract Article PDF–6.6M

Select item 83145474.

SNX27-driven membrane localisation of OTULIN antagonises linear ubiquitination and NF-κB signalling activation

Ruona Shi, Xue Shi, Dajiang Qin, Shibing Tang, Michiel Vermeulen, Xiaofei Zhang

Cell Biosci. 2021; 11: 146. Published online 2021 Jul 27. doi: 10.1186/s13578-021-00659-5

PMCID:: PMC8314547

Abstract Article PDF–3.7M

Select item 81650305.

Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome

Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi

Cell. Author manuscript; available in PMC 2022 May 27.

Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011

PMCID:: PMC8165030

Abstract Article PDF–2.2M

Select item 71404506.

Hypermethylation of UCHL1 Promotes Metastasis of Nasopharyngeal Carcinoma by Suppressing Degradation of Cortactin (CTTN)

Yin Zhao, Yuan Lei, Shi-Wei He, Ying-Qin Li, Ya-Qin Wang, Xiao-Hong Hong, Ye-Lin Liang, Jun-Yan Li, Yang Chen, Wei-Jie Luo, Pan-Pan Zhang, Xiao-Jing Yang, Qing-Mei He, Jun Ma, Na Liu, Ling-Long Tang

Cells. 2020 Mar; 9(3): 559. Published online 2020 Feb 27. doi: 10.3390/cells9030559

Correction in:: Cells. 2024 May; 13(10): 816.

PMCID:: PMC7140450

Abstract Article PDF–4.3M

Select item 47645737.

A deep proteomics perspective on CRM1-mediated nuclear export and nucleocytoplasmic partitioning

Koray Kırlı, Samir Karaca, Heinz Jürgen Dehne, Matthias Samwer, Kuan Ting Pan, Christof Lenz, Henning Urlaub, Dirk Görlich

eLife. 2015; 4: e11466. Published online 2015 Dec 17. doi: 10.7554/eLife.11466

PMCID:: PMC4764573

Abstract Article PDF–5.7M

Select item 42498718.

Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network

Jennifer R. Malinowski, Joshua C. Denny, Suzette J. Bielinski, Melissa A. Basford, Yuki Bradford, Peggy L. Peissig, David Carrell, David R. Crosslin, Jyotishman Pathak, Luke Rasmussen, Jennifer Pacheco, Abel Kho, Katherine M. Newton, Rongling Li, Iftikhar J. Kullo, Christopher G. Chute, Rex L. Chisholm, Gail P. Jarvik, Eric B. Larson, Catherine A. McCarty, Daniel R. Masys, Dan M. Roden, Mariza de Andrade, Marylyn D. Ritchie, Dana C. Crawford

PLoS One. 2014; 9(12): e111301. Published online 2014 Dec 1. doi: 10.1371/journal.pone.0111301

PMCID:: PMC4249871

Abstract Article PDF–941K

Select item 35671759.

A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function

Eleonora Porcu, Marco Medici, Giorgio Pistis, Claudia B. Volpato, Scott G. Wilson, Anne R. Cappola, Steffan D. Bos, Joris Deelen, Martin den Heijer, Rachel M. Freathy, Jari Lahti, Chunyu Liu, Lorna M. Lopez, Ilja M. Nolte, Jeffrey R. O'Connell, Toshiko Tanaka, Stella Trompet, Alice Arnold, Stefania Bandinelli, Marian Beekman, Stefan Böhringer, Suzanne J. Brown, Brendan M. Buckley, Clara Camaschella, Anton J. M. de Craen, Gail Davies, Marieke C. H. de Visser, Ian Ford, Tom Forsen, Timothy M. Frayling, Laura Fugazzola, Martin Gögele, Andrew T. Hattersley, Ad R. Hermus, Albert Hofman, Jeanine J. Houwing-Duistermaat, Richard A. Jensen, Eero Kajantie, Margreet Kloppenburg, Ee M. Lim, Corrado Masciullo, Stefano Mariotti, Cosetta Minelli, Braxton D. Mitchell, Ramaiah Nagaraja, Romana T. Netea-Maier, Aarno Palotie, Luca Persani, Maria G. Piras, Bruce M. Psaty, Katri Räikkönen, J. Brent Richards, Fernando Rivadeneira, Cinzia Sala, Mona M. Sabra, Naveed Sattar, Beverley M. Shields, Nicole Soranzo, John M. Starr, David J. Stott, Fred C. G. J. Sweep, Gianluca Usala, Melanie M. van der Klauw, Diana van Heemst, Alies van Mullem, Sita H.Vermeulen, W. Edward Visser, John P. Walsh, Rudi G. J. Westendorp, Elisabeth Widen, Guangju Zhai, Francesco Cucca, Ian J. Deary, Johan G. Eriksson, Luigi Ferrucci, Caroline S. Fox, J. Wouter Jukema, Lambertus A. Kiemeney, Peter P. Pramstaller, David Schlessinger, Alan R. Shuldiner, Eline P. Slagboom, André G. Uitterlinden, Bijay Vaidya, Theo J. Visser, Bruce H. R. Wolffenbuttel, Ingrid Meulenbelt, Jerome I. Rotter, Tim D. Spector, Andrew A. Hicks, Daniela Toniolo, Serena Sanna, Robin P. Peeters, Silvia Naitza

PLoS Genet. 2013 Feb; 9(2): e1003266. Published online 2013 Feb 7. doi: 10.1371/journal.pgen.1003266

PMCID:: PMC3567175

Abstract Article PDF–1.6M

Select item 355630910.

Phosphodiesterase 8B gene polymorphism in women with recurrent miscarriage: A retrospective case control study

Michaela Granfors, Helena Karypidis, Frida Hosseini, Lottie Skjöldebrand-Sparre, Anneli Stavreus-Evers, Katarina Bremme, Britth-Marie Landgren, Inger Sundström-Poromaa, Anna-Karin Wikström, Helena Åkerud

BMC Med Genet. 2012; 13: 121. Published online 2012 Dec 13. doi: 10.1186/1471-2350-13-121

PMCID:: PMC3556309

Abstract Article PDF–155K

Select item 336098511.

Identification of novel genetic variants in phosphodiesterase 8B (PDE8B), a cAMP specific phosphodiesterase highly expressed in the adrenal cortex, in a cohort of patients with adrenal tumors

Anya Rothenbuhler, Anelia Horvath, Rossella Libé, Fabio Rueda Faucz, Amato Fratticci, Marie Laure Raffin Sanson, Delphine Vezzosi, Monalisa Azevedo, Isaak Levi, Madson Q Almeida, Maya Lodish, Maria Nesterova, Jérôme Bertherat, Constantine A Stratakis

Clin Endocrinol (Oxf) Author manuscript; available in PMC 2013 Aug 1.

Published in final edited form as: Clin Endocrinol (Oxf). 2012 Aug; 77(2): 195–199. doi: 10.1111/j.1365-2265.2012.04366.x

Correction in:: volume 77 on page 943

PMCID:: PMC3360985

Abstract Article PDF–471K

Select item 332102312.

Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci

Nicholas Eriksson, Joyce Y. Tung, Amy K. Kiefer, David A. Hinds, Uta Francke, Joanna L. Mountain, Chuong B. Do

PLoS One. 2012; 7(4): e34442. Published online 2012 Apr 6. doi: 10.1371/journal.pone.0034442

PMCID:: PMC3321023

Abstract Article PDF–750K

Select item 317805913.

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas

Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042

PMCID:: PMC3178059

Abstract Article PDF–1.0M

Select item 314056014.

Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search

Jason L. Stein, Derrek P. Hibar, Sarah K. Madsen, Mathew Khamis, Katie L. McMahon, Greig I. de Zubicaray, Narelle K. Hansell, Grant W. Montgomery, Nicholas G. Martin, Margaret J. Wright, Andrew J. Saykin, Clifford R. Jack, Jr, Michael W. Weiner, Arthur W. Toga, Paul M. Thompson, Alzheimer’s Disease Neuroimaging Initiative

Mol Psychiatry. Author manuscript; available in PMC 2012 Mar 1.

Published in final edited form as: Mol Psychiatry. 2011 Sep; 16(9): 927–881. Published online 2011 Apr 19. doi: 10.1038/mp.2011.32

PMCID:: PMC3140560

Abstract Article PDF–641K

Select item 313680915.

Abnormalities of cAMP signaling are present in adrenocortical lesions associated with ACTH-independent Cushing syndrome despite the absence of mutations in known genes

Eirini I. Bimpaki, Maria Nesterova, Constantine A. Stratakis

Eur J Endocrinol. Author manuscript; available in PMC 2011 Jul 15.

Published in final edited form as: Eur J Endocrinol. 2009 Jul; 161(1): 153–161. Published online 2009 May 8. doi: 10.1530/EJE-09-0027

PMCID:: PMC3136809

Abstract Article PDF–976K

Select item 308074516.

A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement

Peter N Taylor, Vijay Panicker, Adrian Sayers, Beverley Shields, Ahmed Iqbal, Alexandra P Bremner, John P Beilby, Peter J Leedman, Andrew T Hattersley, Bijay Vaidya, Timothy Frayling, Jonathan Evans, Jonathan H Tobias, Nicholas J Timpson, John P Walsh, Colin M Dayan

Eur J Endocrinol. 2011 May; 164(5): 773–780. doi: 10.1530/EJE-10-0938

PMCID:: PMC3080745

Abstract Article PDF–151K

Select item 289646417.

Personalized Smoking Cessation: Interactions between Nicotine Dose, Dependence and Quit-Success Genotype Score

Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl

Mol Med. 2010 Jul-Aug; 16(7-8): 247–253. Published online 2010 Mar 17. doi: 10.2119/molmed.2009.00159

Correction in:: Mol Med. 2012; 18(1): 729.

PMCID:: PMC2896464

Abstract Article PDF–2.4M

Select item 286755418.

Haplotype Analysis of the Promoter Region of Phosphodiesterase Type 8B (PDE8B) in Correlation with Inactivating PDE8B Mutation and the Serum Thyroid-Stimulating Hormone Levels

Anelia Horvath, Fabio Faucz, Gabriela P. Finkielstain, Maria Eleni Nikita, Anya Rothenbuhler, Madson Almeida, Veronica Mericq, Constantine A. Stratakis

Thyroid. 2010 Apr; 20(4): 363–367. doi: 10.1089/thy.2009.0260

PMCID:: PMC2867554

Abstract Article PDF–148K

Select item 280175519.

Autosomal-Dominant Striatal Degeneration Is Caused by a Mutation in the Phosphodiesterase 8B Gene

Silke Appenzeller, Anja Schirmacher, Hartmut Halfter, Sebastian Bäumer, Manuela Pendziwiat, Vincent Timmerman, Peter De Jonghe, Klára Fekete, Florian Stögbauer, Peter Lüdemann, Margret Hund, Elgar Susanne Quabius, E. Bernd Ringelstein, Gregor Kuhlenbäumer

Am J Hum Genet. 2010 Jan 8; 86(1): 83–87. doi: 10.1016/j.ajhg.2009.12.003

PMCID:: PMC2801755

Abstract Article PDF–448K

Select item 267114820.

A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex

Anelia Horvath, Christoforos Giatzakis, Kitman Tsang, Elizabeth Greene, Paulo Osorio, Sosipatros Boikos, Rossella Libè, Yianna Patronas, Audrey Robinson-White, Elaine Remmers, Jerôme Bertherat, Maria Nesterova, Constantine A. Stratakis

Eur J Hum Genet. Author manuscript; available in PMC 2009 Apr 21.

Published in final edited form as: Eur J Hum Genet. 2008 Oct; 16(10): 1245–1253. Published online 2008 Apr 23. doi: 10.1038/ejhg.2008.85

PMCID:: PMC2671148

Abstract Article PDF–1.3M

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