PMC Links for GEO Profiles (Select 102745608) - PMC

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 71699834.

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

Abstract Article PDF–5.4M

Select item 67303135.

Anosmin-1 Modulates Fibroblast Growth Factor Receptor 1 Signaling in Human Gonadotropin-Releasing Hormone Olfactory Neuroblasts through a Heparan Sulfate-Dependent Mechanism

David González-Martínez, Soo-Hyun Kim, Youli Hu, Scott Guimond, Jonathan Schofield, Paul Winyard, Gabriella Barbara Vannelli, Jeremy Turnbull, Pierre-Marc Bouloux

J Neurosci. 2004 Nov 17; 24(46): 10384–10392. doi: 10.1523/JNEUROSCI.3400-04.2004

PMCID:: PMC6730313

Abstract Article PDF–540K

Select item 66235576.

FGF-2 and Anosmin-1 Are Selectively Expressed in Different Types of Multiple Sclerosis Lesions

Diego Clemente, María Cristina Ortega, Francisco Javier Arenzana, Fernando de Castro

J Neurosci. 2011 Oct 19; 31(42): 14899–14909. doi: 10.1523/JNEUROSCI.1158-11.2011

PMCID:: PMC6623557

Abstract Article PDF–4.3M

Select item 58601517.

ANOS1: a unified nomenclature for Kallmann syndrome 1 gene (KAL1) and anosmin-1

Fernando de Castro, Ruth Seal, Roberto Maggi, on behalf of Group of HGNC consultants for KAL1 nomenclature

Brief Funct Genomics. 2017 Jul; 16(4): 205–210. Published online 2016 Nov 13. doi: 10.1093/bfgp/elw037

PMCID:: PMC5860151

Abstract Article PDF–173K

Select item 58269268.

VIRMA mediates preferential m⁶A mRNA methylation in 3′UTR and near stop codon and associates with alternative polyadenylation

Yanan Yue, Jun Liu, Xiaolong Cui, Jie Cao, Guanzheng Luo, Zezhou Zhang, Tao Cheng, Minsong Gao, Xiao Shu, Honghui Ma, Fengqin Wang, Xinxia Wang, Bin Shen, Yizhen Wang, Xinhua Feng, Chuan He, Jianzhao Liu

Cell Discov. 2018; 4: 10. Published online 2018 Feb 27. doi: 10.1038/s41421-018-0019-0

PMCID:: PMC5826926

Abstract Article PDF–2.3M

Select item 55766939.

Study on molecular mechanism of ANOS1 promoting development of colorectal cancer

Lu Qi, Wenjuan Zhang, Zhiqiang Cheng, Na Tang, Yanqing Ding

PLoS One. 2017; 12(8): e0182964. Published online 2017 Aug 30. doi: 10.1371/journal.pone.0182964

PMCID:: PMC5576693

Abstract Article PDF–4.1M

Select item 464683910.

Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD)

Mark J. McCabe, Youli Hu, Louise C. Gregory, Carles Gaston-Massuet, Kyriaki S. Alatzoglou, José W. Saldanha, Angelica Gualtieri, Ajay Thankamony, Ieuan Hughes, Sharron Townshend, Juan-Pedro Martinez-Barbera, Pierre-Marc Bouloux, Mehul T. Dattani

Mol Cell Endocrinol. 2015 Dec 5; 417: 63–72. doi: 10.1016/j.mce.2015.09.010

PMCID:: PMC4646839

Abstract Article PDF–2.0M

Select item 464252211.

Point mutations in KAL1 and the mitochondrial gene MT-tRNA^cys synergize to produce Kallmann syndrome phenotype

Fei Wang, Guo-dong Huang, Hui Tian, Ying-bin Zhong, Hui-juan Shi, Zheng Li, Xian-sheng Zhang, Han Wang, Fei Sun

Sci Rep. 2015; 5: 13050. Published online 2015 Aug 17. doi: 10.1038/srep13050

PMCID:: PMC4642522

Abstract Article PDF–1.3M

Select item 446910612.

Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life

Julie Sarfati, Claire Bouvattier, Hélène Bry-Gauillard, Alejandra Cartes, Jérôme Bouligand, Jacques Young

Orphanet J Rare Dis. 2015; 10: 71. Published online 2015 Jun 9. doi: 10.1186/s13023-015-0287-9

PMCID:: PMC4469106

Abstract Article PDF–2.1M

Select item 419679113.

A novel nonsense mutation of the KAL1 gene (p.Trp204*) in Kallmann syndrome

Antonette Souto El Husny, Milene Raiol-Moraes, Milena Coelho Fernandes-Caldato, Ândrea Ribeiro-dos-Santos

Appl Clin Genet. 2014; 7: 177–182. Published online 2014 Sep 30. doi: 10.2147/TACG.S64280

PMCID:: PMC4196791

Abstract Article PDF–608K

Select item 386995014.

Anosmin-1 contributes to brain tumor malignancy through integrin signal pathways

Catherine T Choy, Haseong Kim, Ji-Young Lee, David M Williams, David Palethorpe, Greg Fellows, Alan J Wright, Ken Laing, Leslie R Bridges, Franklyn A Howe, Soo-Hyun Kim

Endocr Relat Cancer. 2014 Feb; 21(1): 85–99. Prepublished online 2013 Nov 4. doi: 10.1530/ERC-13-0181

PMCID:: PMC3869950

Abstract Article PDF–503K

Select item 373532315.

Molecular analysis of KAL-1 in a series of Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism patients from Northwestern China

Kai-Fa Tang, Qi-Fei Wu, Tie-Jun Zou, Wei Xue, Xin-Yang Wang, Jun-Ping Xing

Asian J Androl. 2009 Nov; 11(6): 711–715. Published online 2009 Sep 7. doi: 10.1038/aja.2009.52

PMCID:: PMC3735323

Abstract Article PDF–405K

Select item 364460716.

Prioritizing Genetic Testing in Patients With Kallmann Syndrome Using Clinical Phenotypes

Flavia Amanda Costa-Barbosa, Ravikumar Balasubramanian, Kimberly W. Keefe, Natalie D. Shaw, Nada Al-Tassan, Lacey Plummer, Andrew A. Dwyer, Cassandra L. Buck, Jin-Ho Choi, Stephanie B. Seminara, Richard Quinton, Dorota Monies, Brian Meyer, Janet E. Hall, Nelly Pitteloud, William F. Crowley, Jr

J Clin Endocrinol Metab. 2013 May; 98(5): E943–E953. Published online 2013 Mar 26. doi: 10.1210/jc.2012-4116

PMCID:: PMC3644607

Abstract Article

Select item 359538317.

Transforming growth factor-β regulates the expression of anosmin (KAL-1) in human retinal pigment epithelial cells

Raghavan Raju, Bixi Jian, John J. Hooks, Chandrasekharam N. Nagineni

Cytokine. Author manuscript; available in PMC 2014 Mar 1.

Published in final edited form as: Cytokine. 2013 Mar; 61(3): 724–727. Published online 2013 Jan 26. doi: 10.1016/j.cyto.2012.12.019

PMCID:: PMC3595383

Abstract Article PDF–987K

Select item 347780418.

A Census of Human Soluble Protein Complexes

Pierre C. Havugimana, G. Traver Hart, Tamás Nepusz, Haixuan Yang, Andrei L. Turinsky, Zhihua Li, Peggy I. Wang, Daniel R. Boutz, Vincent Fong, Sadhna Phanse, Mohan Babu, Stephanie A. Craig, Pingzhao Hu, Cuihong Wan, James Vlasblom, Vaqaarun-Nisa Dar, Alexander Bezginov, Gregory W. Clark, Gabriel C. Wu, Shoshana J. Wodak, Elisabeth R.M. Tillier, Alberto Paccanaro, Edward M. Marcotte, Andrew Emili

Cell. Author manuscript; available in PMC 2013 Aug 31.

Published in final edited form as: Cell. 2012 Aug 31; 150(5): 1068–1081. doi: 10.1016/j.cell.2012.08.011

PMCID:: PMC3477804

Abstract Article PDF–7.7M

Select item 317805919.

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 314308920.

Incidence, Phenotypic Features and Molecular Genetics of Kallmann Syndrome in Finland

Eeva-Maria Laitinen, Kirsi Vaaralahti, Johanna Tommiska, Elina Eklund, Mari Tervaniemi, Leena Valanne, Taneli Raivio

Orphanet J Rare Dis. 2011; 6: 41. Published online 2011 Jun 17. doi: 10.1186/1750-1172-6-41

PMCID:: PMC3143089

Abstract Article PDF–755K

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