Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: JUND[original query] |
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Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study. Human molecular genetics 2013 Jan . Thevenon J, Bourredjem A, Faivre L, Cardot-Bauters C, Calender A, Murat A, Giraud S, Niccoli P, Odou MF, Borson-Chazot F, Barlier A, Lombard-Bohas C, Clauser E, Tabarin A, Parfait B, Chabre O, Castermans E, Ruszniewski P, Le Bras M, Delemer B, Bouchard P, Beckers A, Guilhem I, Rohmer V, Goichot B, Caron P, Baudin E, Chanson P, Groussin L, Du Boullay H, Weryha G, Lecomte P, Penfornis A, Bihan H, Archambeaud F, Kerlan V, Duron F, Kuhn JM, Vergès B, Rodier M, Renard M, Sadoul JL, Binquet C, Goudet P |
Higher risk of aggressive pancreatic neuroendocrine tumors in MEN1 patients with MEN1 mutations affecting the CHES1 interacting MENIN domain. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2387-91. Bartsch Detlef K, Slater Emily P, Albers Max, Knoop Richard, Chaloupka Brunhilde, Lopez Caroline L, Fendrich Volker, Kann Peter H, Waldmann Je |
Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study. European journal of endocrinology / European Federation of Endocrine Societies 2015 Sep . Thevenon Julien, Bourredjem Abderrahmane, Faivre Laurence, Bauters Catherine, Calender Alain, Lebras Maelle, Giraud Sophie, Niccoli Patricia, Odou Marie-Françoise, Borson-Chazot Francoise, Barlier Anne, Lombard-Bohas Catherine, Clauser Eric, Tabarin Antoine, Pasmant Eric, Chabre Olivier, Castermans Emilie, Ruszniewski Philippe, Bertherat Jerôme, Delemer Brigitte, Christin-Maitre Sophie, Beckers Albert, Guilhem Isabelle, Rohmer Vincent, Goichot Bernard, Caron Philippe, Baudin Eric, Chanson Philippe, Groussin Lionel, Du Boullay Helene, Weryha Georges, Lecomte Pierre, Schillo Franck, Bihan Helene, Archambeaud Francoise, Kerlan Veronique, Bourcigaux Nathalie, Kuhn Jean-Marc, Vergès Bruno, Rodier Michel, Renard Michel, Sadoul Jean Louis, Binquet Christine, Goudet Pier |
The study on polymorphisms of Sep15 and TrxR2 and the expression of AP-1 signaling pathway in Kashin-Beck disease. Bone 2018 Apr . Wu RuiPeng, Zhang RongQiang, Xiong YongMin, Sun WenYan, Li YuanYuan, Yang XiaoLi, Liu JiFeng, Jiang Yong, Guo Hao, Mo XiaoYan, Cao JunLi |
Genetic variation near CXCL12 is associated with susceptibility to HIV-related non-Hodgkin lymphoma.
Haematologica 2020 Jul . Thorball Christian W, Oudot-Mellakh Tiphaine, Ehsan Nava, Hammer Christian, Santoni Federico A, Niay Jonathan, Costagliola Dominique, Goujard Cécile, Meyer Laurence, Wang Sophia S, Hussain Shehnaz K, Theodorou Ioannis, Cavassini Matthias, Rauch Andri, Battegay Manuel, Hoffmann Matthias, Schmid Patrick, Bernasconi Enos, Günthard Huldrych F, Mohammadi Pejman, McLaren Paul J, Rabkin Charles S, Besson Caroline, Fellay Jacqu |
Transcriptomic responses to hypoxia in endometrial and decidual stromal cells. Reproduction (Cambridge, England) 2020 4 160 (1): 39-51. Rytkönen Kalle T, Heinosalo Taija, Mahmoudian Mehrad, Ma Xinghong, Perheentupa Antti, Elo Laura L, Poutanen Matti, Wagner Günter |
Regulatory SNP rs5743417 impairs constitutive expression of human ?-defensin 1 and has high frequency in Africans and Afro-Americans. International journal of immunogenetics 2020 1 47 (4): 332-341. Cruz Díaz Luis Antonio, Gutiérrez Ortega Abel, Chávez Álvarez Rocío Del Carmen, Velarde Félix Jesús Salvador, Prado Montes de Oca Ernes |
Mutator-Derived lncRNA Landscape: A Novel Insight Into the Genomic Instability of Prostate Cancer. Frontiers in oncology 2022 7 12 876531. Tang Liansha, Li Wanjiang, Xu Hang, Zheng Xiaonan, Qiu Shi, He Wenbo, Wei Qiang, Ai Jianzhong, Yang Lu, Liu Jiy |
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- Page last updated:Apr 29, 2024
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