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Items: 20

1.
CTNNB1 Gene Mutations, Pituitary Transcription Factors, and MicroRNA Expression Involvement in the Pathogenesis of Adamantinomatous Craniopharyngiomas
Marina Lanciotti Campanini, Leandro Machado Colli, Beatriz Maria Carvalho Paixao, Tatiana Pereira Freitas Cabral, Fernando Colbari Amaral, Helio Rubens Machado, Luciano Serafin Neder, Fabiano Saggioro, Ayrton Custodio Moreira, Sonir Roberto Rauber Antonini, Margaret de Castro
Horm Cancer. 2010 Aug; 1(4): 187–196. Published online 2010 Nov 2. doi: 10.1007/s12672-010-0041-7
PMCID:
PMC10358030
AbstractArticlePDF–185K
2.
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
AbstractArticlePDF–2.2M
3.
Impact of cytosine methylation on DNA binding specificities of human transcription factors
Yimeng Yin, Ekaterina Morgunova, Arttu Jolma, Eevi Kaasinen, Biswajyoti Sahu, Syed Khund-Sayeed, Pratyush K. Das, Teemu Kivioja, Kashyap Dave, Fan Zhong, Kazuhiro R. Nitta, Minna Taipale, Alexander Popov, Paul A. Ginno, Silvia Domcke, Jian Yan, Dirk Schübeler, Charles Vinson, Jussi Taipale
Science. Author manuscript; available in PMC 2021 Mar 30.
Published in final edited form as: Science. 2017 May 5; 356(6337): eaaj2239. doi: 10.1126/science.aaj2239
PMCID:
PMC8009048
AbstractArticlePDF–2.6M
4.
Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis
Viola Alesi, Maria Lisa Dentici, Silvia Genovese, Sara Loddo, Emanuele Bellacchio, Valeria Orlando, Silvia Di Tommaso, Giorgia Catino, Chiara Calacci, Giusy Calvieri, Daniele Pompili, Graziamaria Ubertini, Bruno Dallapiccola, Rossella Capolino, Antonio Novelli
Int J Mol Sci. 2021 Jan; 22(2): 750. Published online 2021 Jan 13. doi: 10.3390/ijms22020750
PMCID:
PMC7828579
AbstractArticlePDF–1.6M
5.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M
6.
Architecture of the human interactome defines protein communities and disease networks
Edward L. Huttlin, Raphael J. Bruckner, Joao A. Paulo, Joe R. Cannon, Lily Ting, Kurt Baltier, Greg Colby, Fana Gebreab, Melanie P. Gygi, Hannah Parzen, John Szpyt, Stanley Tam, Gabriela Zarraga, Laura Pontano-Vaites, Sharan Swarup, Anne E. White, Devin K. Schweppe, Ramin Rad, Brian K. Erickson, Robert A. Obar, K.G. Guruharsha, Kejie Li, Spyros Artavanis-Tsakonas, Steven P. Gygi, J. Wade Harper
Nature. Author manuscript; available in PMC 2017 Nov 17.
Published in final edited form as: Nature. 2017 May 25; 545(7655): 505–509. Published online 2017 May 17. doi: 10.1038/nature22366
PMCID:
PMC5531611
AbstractArticlePDF–2.7M
7.
HESX1 Mutations in Patients with Congenital Hypopituitarism: Variable Phenotypes with the Same Genotype
Qing Fang, Anna Flavia Figueredo Benedetti, Qianyi Ma, Louise Gregory, Jun Z. Li, Mehul Dattani, Abdollah Sadeghi-Nejad, Ivo J.P. Arnhold, Berenice Bilharinho de Mendonça, Sally A. Camper, Luciani R. Carvalho
Clin Endocrinol (Oxf) Author manuscript; available in PMC 2017 Sep 1.
Published in final edited form as: Clin Endocrinol (Oxf). 2016 Sep; 85(3): 408–414. Published online 2016 Apr 28. doi: 10.1111/cen.13067
PMCID:
PMC4988903
AbstractArticlePDF–486K
8.
Phospho-tyrosine dependent protein–protein interaction network
Arndt Grossmann, Nouhad Benlasfer, Petra Birth, Anna Hegele, Franziska Wachsmuth, Luise Apelt, Ulrich Stelzl
Mol Syst Biol. 2015 Mar; 11(3): 0794. Published online 2015 Mar 26. doi: 10.15252/msb.20145968
PMCID:
PMC4380928
AbstractArticlePDF–1.9M
9.
The identification of HESX1 mutations in Kallmann syndrome
Kayce Newbern, Nithya Natrajan, Hyung-Goo Kim, Lynn .P. Chorich, Lisa Halvorson, Richard S. Cameron, Lawrence C. Layman
Fertil Steril. Author manuscript; available in PMC 2014 Jun 1.
Published in final edited form as: Fertil Steril. 2013 Jun; 99(7): 1831–1837. Published online 2013 Mar 1. doi: 10.1016/j.fertnstert.2013.01.149
PMCID:
PMC3888813
AbstractArticlePDF–1.3M
10.
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
AbstractArticlePDF–1.0M
11.
Candidate Gene Sequencing of LHX2, HESX1, and SOX2 in a Large Schizencephaly Cohort
Cecilia Mellado, Annapurna Poduri, Danielle Gleason, Princess C Elhosary, Brenda J Barry, Jennifer N Partlow, Bernard S Chang, Gary M Shaw, A James Barkovich, Christopher A Walsh
Am J Med Genet A. 2010 Nov; 152A(11): 2736–2742. Published online 2010 Oct 11. doi: 10.1002/ajmg.a.33684
PMCID:
PMC2965295
AbstractArticlePDF–113K
12.
Corepressors TLE1 and TLE3 Interact with HESX1 and PROP1
Luciani R. Carvalho, Michelle L. Brinkmeier, Frederic Castinetti, Buffy S. Ellsworth, Sally A. Camper
Mol Endocrinol. 2010 Apr; 24(4): 754–765. Published online 2010 Feb 24. doi: 10.1210/me.2008-0359
PMCID:
PMC2852357
AbstractArticle
13.
An atlas of combinatorial transcriptional regulation in mouse and man
The FANTOM consortium and RIKEN Omics Science Center
Cell. Author manuscript; available in PMC 2011 Mar 5.
Published in final edited form as: Cell. 2010 Mar 5; 140(5): 744–752. doi: 10.1016/j.cell.2010.01.044
Correction in:
volume 141 on page 369
PMCID:
PMC2836267
AbstractArticlePDF–2.2M
14.
Role of Conserved Salt Bridges in Homeodomain Stability and DNA Binding
Mario Torrado, Julia Revuelta, Carlos Gonzalez, Francisco Corzana, Agatha Bastida, Juan Luis Asensio
J Biol Chem. 2009 Aug 28; 284(35): 23765–23779. Published online 2009 Jun 26. doi: 10.1074/jbc.M109.012054
PMCID:
PMC2749150
AbstractArticlePDF–4.7M
15.
A Novel Dominant Negative Mutation of OTX2 Associated with Combined Pituitary Hormone Deficiency
Daniel Diaczok, Christopher Romero, Janice Zunich, Ian Marshall, Sally Radovick
J Clin Endocrinol Metab. 2008 Nov; 93(11): 4351–4359. Published online 2008 Aug 26. doi: 10.1210/jc.2008-1189
PMCID:
PMC2582563
AbstractArticle
16.
DNMT1 interacts with the developmental transcriptional repressor HESX1
Ezat Sajedi, Carles Gaston-Massuet, Cynthia L. Andoniadou, Massimo Signore, Paul J. Hurd, Mehul Dattani, Juan Pedro Martinez-Barbera
Biochim Biophys Acta. 2008 Jan; 1783(1): 131–143. doi: 10.1016/j.bbamcr.2007.08.010
PMCID:
PMC2233781
AbstractArticle
17.
The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)
Genome Res. 2004 Oct; 14(10b): 2121–2127. doi: 10.1101/gr.2596504
Correction in:
Genome Res. 2006 Jun; 16(6): 804.
PMCID:
PMC528928
AbstractArticlePDF–140K
18.
Temporal regulation of a paired-like homeodomain repressor/TLE corepressor complex and a related activator is required for pituitary organogenesis
Jeremy S. Dasen, Juan-Pedro Martinez Barbera, Thomas S. Herman, Shawn O' Connell, Lorin Olson, BongGun Ju, Jessica Tollkuhn, Sung Hee Baek, David W. Rose, Michael G. Rosenfeld
Genes Dev. 2001 Dec 1; 15(23): 3193–3207. doi: 10.1101/gad.932601
PMCID:
PMC312840
AbstractArticlePDF–1.1M
19.
A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction
Luciani R. Carvalho, Kathryn S. Woods, Berenice B. Mendonca, Nathalie Marcal, Andrea L. Zamparini, Stefano Stifani, Joshua M. Brickman, Ivo J.P. Arnhold, Mehul T. Dattani
J Clin Invest. 2003 Oct 15; 112(8): 1192–1201. doi: 10.1172/JCI18589
PMCID:
PMC213489
AbstractArticlePDF–1.8M
20.
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences
Mammalian Gene Collection (MGC) Program Team
Proc Natl Acad Sci U S A. 2002 Dec 24; 99(26): 16899–16903. Published online 2002 Dec 11. doi: 10.1073/pnas.242603899
PMCID:
PMC139241
AbstractArticlePDF–118K

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