Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: CBLB[original query] |
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CBLB variants in type 1 diabetes and their genetic interaction with CTLA4. Journal of leukocyte biology 2005 1 77 (4): 579-85. Bergholdt Regine, Taxvig Camilla, Eising Stefanie, Nerup Jørn, Pociot Flemmi |
The CBLB gene and Graves' disease in children. Journal of pediatric endocrinology & metabolism : JPEM 2005 Nov 18 (11): 1119-26. Chen Chia-Ching, Huang Chi-Yu, Huang Fu-Yuan, Dang Ching-Wen, Lin Chiung-Ling, Lo Fu-Sung, Lin Chao-Hsu, Tsang Ching-Cheng, Li Hsin-Jung, Liu Hsin-Fu, Chu Chen-Chung, Lin Marie, Lee Yann-Ji |
Interaction analysis of the CBLB and CTLA4 genes in type 1 diabetes. Journal of leukocyte biology 2007 Mar 81 (3): 581-3. Payne Felicity, Cooper Jason D, Walker Neil M, Lam Alex C, Smink Luc J, Nutland Sarah, Stevens Helen E, Hutchings Jayne, Todd John |
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.
Nature genetics 2010 Jun 42 (6): 495-7. Sanna Serena, Pitzalis Maristella, Zoledziewska Magdalena, Zara Ilenia, Sidore Carlo, Murru Raffaele, Whalen Michael B, Busonero Fabio, Maschio Andrea, Costa Gianna, Melis Maria Cristina, Deidda Francesca, Poddie Fausto, Morelli Laura, Farina Gabriele, Li Yun, Dei Mariano, Lai Sandra, Mulas Antonella, Cuccuru Gianmauro, Porcu Eleonora, Liang Liming, Zavattari Patrizia, Moi Loredana, Deriu Elisa, Urru M Francesca, Bajorek Michele, Satta Maria Anna, Cocco Eleonora, Ferrigno Paola, Sotgiu Stefano, Pugliatti Maura, Traccis Sebastiano, Angius Andrea, Melis Maurizio, Rosati Giulio, Abecasis Gonçalo R, Uda Manuela, Marrosu Maria Giovanna, Schlessinger David, Cucca Frances |
Association of the CBLB gene with multiple sclerosis: new evidence from a replication study in an Italian population. Journal of medical genetics 2011 Mar 48 (3): 210-1. Corrado Lucia, Bergamaschi Laura, Barizzone Nadia, Fasano Maria Edvige, Guerini Franca R, Salvetti Marco, Galimberti Daniela, Benedetti Maria Donata, Leone Maurizio, D'Alfonso Sand |
CBL, CBLB, TET2, ASXL1, and IDH1/2 mutations and additional chromosomal aberrations constitute molecular events in chronic myelogenous leukemia. Blood 2011 May 117 (21): e198-206. Makishima Hideki, Jankowska Anna M, McDevitt Michael A, O'Keefe Christine, Dujardin Simon, Cazzolli Heather, Przychodzen Bartlomiej, Prince Courtney, Nicoll John, Siddaiah Harish, Shaik Mohammed, Szpurka Hadrian, Hsi Eric, Advani Anjali, Paquette Ronald, Maciejewski Jaroslaw |
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes. Multiple sclerosis (Houndmills, Basingstoke, England) 2011 Dec . Varadé J, Comabella M, Ortiz MA, Arroyo R, Fernández O, Pinto-Medel MJ, Fedetz M, Izquierdo G, Lucas M, López Gómez C, Catalá Rabasa A, Alcina A, Matesanz F, Alloza I, Antigüedad A, García-Barcina M, Otaegui D, Olascoaga J, Saiz A, Blanco Y, Montalbán X, Vandenbroeck K, Urcelay E |
Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
Fatty acid desaturase 1 polymorphisms are associated with coronary heart disease in a Chinese population. Chinese medical journal 2012 Mar 125 (5): 801-6. Liu Si-jun, Zhi Hong, Chen Pei-zhan, Chen Wei, Lu Feng, Ma Gen-shan, Dai Jun-cheng, Shen Chong, Liu Nai-feng, Hu Zhi-bin, Wang Hui, Shen Hong-bi |
CBL mutations in myeloproliferative neoplasms are also found in the gene's proline-rich domain and in patients with the V617FJAK2. Haematologica 2012 Feb . Aranaz P, Hurtado C, Erquiaga I, Migueliz I, Ormazabal C, Cristobal I, Garcia-Delgado M, Novo FJ, Vizmanos JL |
A multiple sclerosis-associated variant of CBLB links genetic risk with type I IFN function. Journal of immunology (Baltimore, Md. : 1950) 2014 Nov 193 (9): 4439-47. Stürner Klarissa Hanja, Borgmeyer Uwe, Schulze Christian, Pless Ole, Martin Rola |
Single Nucleotide Polymorphisms in CBLB, a Regulator of T-Cell Response, Predict Radiation Pneumonitis and Outcomes After Definitive Radiotherapy for Non-Small-Cell Lung Cancer. Clinical lung cancer 2015 Nov . Li Peng, Wang Xiaohong, Liu Zhensheng, Liu Hongliang, Xu Ting, Wang HuiJuan, Gomez Daniel R, Nguyen Quynh-Nhu, Wang Li-E, Teng Yuee, Song Yipeng, Komaki Ritsuko, Welsh James W, Wei Qingyi, Liao Zhongxi |
The effect of MVK-MMAB variants, their haplotypes and G×E interactions on serum lipid levels and the risk of coronary heart disease and ischemic stroke. Oncotarget 2017 Sep 8 (42): 72801-72817. Miao Liu, Yin Rui-Xing, Huang Feng, Chen Wu-Xian, Cao Xiao-Li, Wu Jin-Zh |
Association between the MVK and MMAB polymorphisms and serum lipid levels. Oncotarget 2017 Sep 8 (41): 70378-70393. Miao Liu, Yin Rui-Xing, Pan Shang-Ling, Yang Shuo, Yang De-Zhai, Lin Wei-Xio |
Autozygosity mapping of methylmalonic acidemia associated genes by short tandem repeat markers facilitates the identification of five novel mutations in an Iranian patient cohort. Metabolic brain disease 2018 7 33 (5): 1689-1697. Shafaat Mehdi, Alaee Mohammad Reza, Rahmanifar Ali, Setoodeh Aria, Razzaghy-Azar Maryam, Bagherian Hamideh, Bagheri Samira Dabbagh, Zafarghandi Motlagh Fatemeh, Hashemi Mehrdad, Abiri Maryam, Zeinali Siro |
Single nucleotide polymorphisms of casitas B-lineage lymphoma proto-oncogene-b predict outcomes of patients with advanced non-small cell lung cancer after first-line platinum based doublet chemotherapy. Journal of thoracic disease 2018 Mar 10 (3): 1635-1647. Li Peng, Liu Hong-Liang, Zhang Zhi-Qiang, Lv Xiao-Dong, Chang Yu-Xi, Wang Hui-Juan, Ma Jie, Ma Zhi-Yong, Qu Xiu-Juan, Teng Yue |
Mutation analysis of genes related to methylmalonic acidemia: identification of eight novel mutations. Molecular biology reports 2019 2 46 (1): 271-285. Keyfi Fatemeh, Abbaszadegan Mohammad R, Sankian Mojtaba, Rolfs Arndt, Orolicki Slobodanka, Pournasrollah Mohammad, Alijanpour Morteza, Varasteh Abdolre |
Application of Artificial Neural Network for Prediction of Risk of Multiple Sclerosis Based on Single Nucleotide Polymorphism Genotypes. Journal of molecular neuroscience : MN 2020 3 70 (7): 1081-1087. Ghafouri-Fard Soudeh, Taheri Mohammad, Omrani Mir Davood, Daaee Amir, Mohammad-Rahimi Hosse |
Exploring the Potential Genetic Heterogeneity in the Incidence of Hoof Disorders in Austrian Fleckvieh and Braunvieh Cattle. Frontiers in genetics 2020 12 11 577116. Kosi?ska-Selbi Barbara, Suchocki Tomasz, Egger-Danner Christa, Schwarzenbacher Hermann, Fr?szczak Magdalena, Szyda Joan |
Pharmacogenetic Predictors of Response to Interferon Beta Therapy in Multiple Sclerosis. Molecular neurobiology 2021 Jun . Carrasco-Campos María Isabel, Pérez-Ramírez Cristina, Macías-Cortés Elena, Puerta-García Elena, Sánchez-Pozo Antonio, Arnal-García Carmen, Barrero-Hernández Francisco Javier, Calleja-Hernández Miguel Ángel, Jiménez-Morales Alberto, Cañadas-Garre Mari |
Engrafted Donor-Derived Clonal Hematopoiesis after Allogenic Hematopoietic Cell Transplantation is Associated with Chronic Graft-versus-Host Disease Requiring Immunosuppressive Therapy, but no Adverse Impact on Overall Survival or Relapse. Transplantation and cellular therapy 2021 4 27 (8): 662.e1-662.e9. Newell Laura F, Williams Todd, Liu James, Yu Yun, Chen Yiyi, Booth Georgeann C, Knight Rebekah J, Goslee Kelli R, Cook Rachel J, Leonard Jessica, Meyers Gabrielle, Traer Elie, Press Richard D, Fan Guang, Wang Ying, Raess Philipp W, Maziarz Richard T, Dunlap Jennif |
Genome-wide meta-analysis implicates variation affecting mast cell biology in urticaria. The Journal of allergy and clinical immunology 2023 9 . Sheila Mary McSweeney, Jake Saklatvala, Rossella Rispoli, Clarisse Ganier, Grzegorz Woszczek, Laurent Thomas, Kristian Hveem, Mari Løset, Nick Dand, Christos Tziotzios, Michael Simpson, John Alexander McGra |
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry. Genome medicine 2023 1 15 (1): 7. Mueller Stefanie H, Lai Alvina G, Valkovskaya Maria, Michailidou Kyriaki, Bolla Manjeet K, Wang Qin, Dennis Joe, Lush Michael, Abu-Ful Zomoruda, Ahearn Thomas U, Andrulis Irene L, Anton-Culver Hoda, Antonenkova Natalia N, Arndt Volker, Aronson Kristan J, Augustinsson Annelie, Baert Thais, Freeman Laura E Beane, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Blomqvist Carl, Bogdanova Natalia V, Bojesen Stig E, Bonanni Bernardo, Brenner Hermann, Brucker Sara Y, Buys Saundra S, Castelao Jose E, Chan Tsun L, Chang-Claude Jenny, Chanock Stephen J, Choi Ji-Yeob, Chung Wendy K, , Colonna Sarah V, , Cornelissen Sten, Couch Fergus J, Czene Kamila, Daly Mary B, Devilee Peter, Dörk Thilo, Dossus Laure, Dwek Miriam, Eccles Diana M, Ekici Arif B, Eliassen A Heather, Engel Christoph, Evans D Gareth, Fasching Peter A, Fletcher Olivia, Flyger Henrik, Gago-Dominguez Manuela, Gao Yu-Tang, García-Closas Montserrat, García-Sáenz José A, Genkinger Jeanine, Gentry-Maharaj Aleksandra, Grassmann Felix, Guénel Pascal, Gündert Melanie, Haeberle Lothar, Hahnen Eric, Haiman Christopher A, Håkansson Niclas, Hall Per, Harkness Elaine F, Harrington Patricia A, Hartikainen Jaana M, Hartman Mikael, Hein Alexander, Ho Weang-Kee, Hooning Maartje J, Hoppe Reiner, Hopper John L, Houlston Richard S, Howell Anthony, Hunter David J, Huo Dezheng, , Ito Hidemi, Iwasaki Motoki, Jakubowska Anna, Janni Wolfgang, John Esther M, Jones Michael E, Jung Audrey, Kaaks Rudolf, Kang Daehee, Khusnutdinova Elza K, Kim Sung-Won, Kitahara Cari M, Koutros Stella, Kraft Peter, Kristensen Vessela N, Kubelka-Sabit Katerina, Kurian Allison W, Kwong Ava, Lacey James V, Lambrechts Diether, Le Marchand Loic, Li Jingmei, Linet Martha, Lo Wing-Yee, Long Jirong, Lophatananon Artitaya, Mannermaa Arto, Manoochehri Mehdi, Margolin Sara, Matsuo Keitaro, Mavroudis Dimitrios, Menon Usha, Muir Kenneth, Murphy Rachel A, Nevanlinna Heli, Newman William G, Niederacher Dieter, O'Brien Katie M, Obi Nadia, Offit Kenneth, Olopade Olufunmilayo I, Olshan Andrew F, Olsson Håkan, Park Sue K, Patel Alpa V, Patel Achal, Perou Charles M, Peto Julian, Pharoah Paul D P, Plaseska-Karanfilska Dijana, Presneau Nadege, Rack Brigitte, Radice Paolo, Ramachandran Dhanya, Rashid Muhammad U, Rennert Gad, Romero Atocha, Ruddy Kathryn J, Ruebner Matthias, Saloustros Emmanouil, Sandler Dale P, Sawyer Elinor J, Schmidt Marjanka K, Schmutzler Rita K, Schneider Michael O, Scott Christopher, Shah Mitul, Sharma Priyanka, Shen Chen-Yang, Shu Xiao-Ou, Simard Jacques, Surowy Harald, Tamimi Rulla M, Tapper William J, Taylor Jack A, Teo Soo Hwang, Teras Lauren R, Toland Amanda E, Tollenaar Rob A E M, Torres Diana, Torres-Mejía Gabriela, Troester Melissa A, Truong Thérèse, Vachon Celine M, Vijai Joseph, Weinberg Clarice R, Wendt Camilla, Winqvist Robert, Wolk Alicja, Wu Anna H, Yamaji Taiki, Yang Xiaohong R, Yu Jyh-Cherng, Zheng Wei, Ziogas Argyrios, Ziv Elad, Dunning Alison M, Easton Douglas F, Hemingway Harry, Hamann Ute, Kuchenbaecker Karoline |
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- Page last updated:Apr 16, 2024
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