Human Genome Epidemiology Literature Finder
Records 1 - 26 (of 26 Records) |
Query Trace: PTPRJ[original query] |
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Single nucleotide polymorphism analysis in the human phosphatase PTPrj gene using matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry. Rapid communications in mass spectrometry : RCM 2004 18 (19): 2249-54. Powell Ned, Dudley Ed, Morishita Mariko, Bogdanova Tetyana, Tronko Mykola, Thomas Ger |
The tyrosine phosphatase PTPRJ/DEP-1 genotype affects thyroid carcinogenesis. Oncogene 2004 Nov 23 (52): 8432-8. Iuliano Rodolfo, Le Pera Ilaria, Cristofaro Carmela, Baudi Francesco, Arturi Franco, Pallante Pierlorenzo, Martelli Maria Luisa, Trapasso Francesco, Chiariotti Lorenzo, Fusco Alfre |
Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer. Human molecular genetics 2005 Aug 14 (16): 2349-56. Lesueur Fabienne, Pharoah Paul D, Laing Stewart, Ahmed Shahana, Jordan Clare, Smith Paula L, Luben Robert, Wareham Nicholas J, Easton Douglas F, Dunning Alison M, Ponder Bruce A |
PTPRJ haplotypes and colorectal cancer risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008 Oct 17 (10): 2782-5. Toland Amanda E, Rozek Laura S, Presswala Shafaq, Rennert Gad, Gruber Stephen |
Missense polymorphisms of PTPRJ and PTPN13 genes affect susceptibility to a variety of human cancers. Journal of cancer research and clinical oncology 2010 Feb 136 (2): 249-59. Mita Yuichiro, Yasuda Yukiko, Sakai Akiko, Yamamoto Hiromasa, Toyooka Shinichi, Gunduz Mehmet, Tanabe Shunsuke, Naomoto Yoshio, Ouchida Mamoru, Shimizu Ken |
Role of PTPRJ genotype in papillary thyroid carcinoma risk. Endocrine-related cancer 2010 Dec 17 (4): 1001-6. Iuliano Rodolfo, Palmieri Dario, He Huiling, Iervolino Angela, Borbone Eleonora, Pallante Pierlorenzo, Cianflone Alessandra, Nagy Rebecca, Alder Hansjuerg, Calin George A, Trapasso Francesco, Giordano Carla, Croce Carlo M, de la Chapelle Albert, Fusco Alfre |
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
Leukemia 2012 May 26 (5): 902-9. Ellinghaus E, Stanulla M, Richter G, Ellinghaus D, te Kronnie G, Cario G, Cazzaniga G, Horstmann M, Panzer Grümayer R, Cavé H, Trka J, Cinek O, Teigler-Schlegel A, ElSharawy A, Häsler R, Nebel A, Meissner B, Bartram T, Lescai F, Franceschi C, Giordan M, Nürnberg P, Heinzow B, Zimmermann M, Schreiber S, Schrappe M, Franke |
Genome-wide disease association study in chewing tobacco associated oral cancers. Oral oncology 2012 Sep 48 (9): 831-5. Bhatnagar Renu, Dabholkar Jyoti, Saranath Dhananja |
Colorectal cancer susceptibility variants alter risk of breast cancer in a Chinese Han population. Genetics and molecular research : GMR 2013 12 (4): 6268-74. Wei W, Jiang M, Luo L, Li Z, Wang P, Dong W |
Proinflammatory genotype is associated with the frailty phenotype in the English Longitudinal Study of Ageing. Aging clinical and experimental research 2015 Aug . Mekli Krisztina, Nazroo James Y, Marshall Alan D, Kumari Meena, Pendleton Ne |
No impact of PTPN22, PTPRJ and ACP1 genes polymorphisms on the risk of immune thrombocytopenia in French adult patients. Thrombosis research 2016 Apr 144 76-78. Lioger Bertrand, Rollin Jerome, Vayne Caroline, Perret-Gallix Kevin, Pouplard Claire, Godeau Bertrand, Michel Marc, Gruel Yv |
De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS genetics 2016 Apr 12 (4): e1005963. Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan |
Customized Array Comparative Genomic Hybridization Analysis of 25 Phosphatase-encoding Genes in Colorectal Cancer Tissues. Cancer genomics & proteomics 2016 12 14 (1): 69-74. Laczmanska Izabela, Skiba Pawel, Karpinski Pawel, Bebenek Marek, Sasiadek Maria |
Additive effects of genetic variants associated with intraocular pressure in primary open-angle glaucoma. PloS one 2017 12 (8): e0183709. Mabuchi Fumihiko, Mabuchi Nakako, Sakurada Yoichi, Yoneyama Seigo, Kashiwagi Kenji, Iijima Hiroyuki, Yamagata Zentaro, Takamoto Mitsuko, Aihara Makoto, Iwata Takeshi, Kawase Kazuhide, Shiga Yukihiro, Nishiguchi Koji M, Nakazawa Toru, Ozaki Mineo, Araie Makoto, |
Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine malignant melanoma by integrated comparative genomic analysis. PLoS genetics 2018 9 14 (9): e1007589. Hendricks William P D, Zismann Victoria, Sivaprakasam Karthigayini, Legendre Christophe, Poorman Kelsey, Tembe Waibhav, Perdigones Nieves, Kiefer Jeffrey, Liang Winnie, DeLuca Valerie, Stark Mitchell, Ruhe Alison, Froman Roe, Duesbery Nicholas S, Washington Megan, Aldrich Jessica, Neff Mark W, Huentelman Matthew J, Hayward Nicholas, Brown Kevin, Thamm Douglas, Post Gerald, Khanna Chand, Davis Barbara, Breen Matthew, Sekulic Alexander, Trent Jeffrey |
Comments on: "Meta-analysis of association between Arg326Gln (rs1503185) and Gln276Pro (rs1566734) polymorphisms of PTPRJ gene and cancer risk". Journal of applied genetics 2019 Jul . Gholami Morteza, M Amoli Mah |
Cross-species genomic landscape comparison of human mucosal melanoma with canine oral and equine melanoma. Nature communications 2019 1 10 (1): 353. Wong Kim, van der Weyden Louise, Schott Courtney R, Foote Alastair, Constantino-Casas Fernando, Smith Sionagh, Dobson Jane M, Murchison Elizabeth P, Wu Hong, Yeh Iwei, Fullen Douglas R, Joseph Nancy, Bastian Boris C, Patel Rajiv M, Martincorena Inigo, Robles-Espinoza Carla Daniela, Iyer Vivek, Kuijjer Marieke L, Arends Mark J, Brenn Thomas, Harms Paul W, Wood Geoffrey A, Adams David |
Meta-analysis of association between Arg326Gln (rs1503185) and Gln276Pro (rs1566734) polymorphisms of PTPRJ gene and cancer risk. Journal of applied genetics 2019 1 60 (1): 57-62. Laczmanska Izabela, Sasiadek Maria |
Dominantly Inherited Hereditary Nonpolyposis Colorectal Cancer Not Caused by MMR Genes. Journal of clinical medicine 2020 6 9 (6): . Terradas Mariona, Capellá Gabriel, Valle Lau |
Candidate genes for hereditary colorectal cancer: Mutational screening and systematic review. Human mutation 2020 May . Belhadj Sami, Terradas Mariona, Munoz-Torres Pau M, Aiza Gemma, Navarro Matilde, Capellá Gabriel, Valle Lau |
Centenarian Exomes as a Tool for Evaluating the Clinical Relevance of Germline Tumor Suppressor Mutations. Technology in cancer research & treatment 0 19 1533033820911082. Balabanski Lubomir, Serbezov Dimitar, Nikolova Dragomira, Antonova Olga, Nesheva Desislava, Hammoudeh Zora, Vazharova Radoslava, Karachanak-Yankova Sena, Staneva Rada, Mihaylova Marta, Damyanova Vera, Hadjidekova Savina, Toncheva Dra |
Association Between rs12037447, rs146732504, rs151078858, rs55723436, and rs6094136 Polymorphisms and Kawasaki Disease in the Population of Polish Children.
Frontiers in pediatrics 2021 9 624798. Buda Piotr, Chyb Maciej, Smorczewska-Kiljan Anna, Wieteska-Klimczak Anna, Paczesna Agata, Kowalczyk-Domaga?a Monika, Okarska-Napiera?a Magdalena, Sobalska-Kwapis Marta, Grochowalski ?ukasz, S?omka Marcin, Sitek Aneta, Ksia ?yk Janusz, Strapagiel Domin |
Discovering Genotype Variants in an Infant with VACTERL through Clinical Exome Sequencing: A Support for Personalized Risk Assessment and Disease Prevention. Pediatric reports 2021 1 13 (1): 45-56. Pelizzo Gloria, Chiricosta Luigi, Mazzon Emanuela, Zuccotti Gian Vincenzo, Avanzini Maria Antonietta, Croce Stefania, Lima Mario, Bramanti Placido, Calcaterra Valer |
Integrated genomic analyses of acral and mucosal melanomas nominate novel driver genes. Genome medicine 2022 06 14 (1): 65. Wang Meng, Banik Ishani, Shain A Hunter, Yeh Iwei, Bastian Boris |
DNA Copy Number Alterations and Copy Neutral Loss of Heterozygosity in Adult Ph-Negative Acute B-Lymphoblastic Leukemia: Focus on the Genes Involved. International journal of molecular sciences 2023 12 24 (24): . Natalya Risinskaya, Maria Gladysheva, Abdulpatakh Abdulpatakhov, Yulia Chabaeva, Valeriya Surimova, Olga Aleshina, Anna Yushkova, Olga Dubova, Nikolay Kapranov, Irina Galtseva, Sergey Kulikov, Tatiana Obukhova, Andrey Sudarikov, Elena Parovichniko |
Identification of Novel Genetic Risk Factors for Focal Segmental Glomerulosclerosis in Children: Results From the Chronic Kidney Disease in Children (CKiD) Cohort.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2023 1 . Durand Axelle, Winkler Cheryl A, Vince Nicolas, Douillard Venceslas, Geffard Estelle, Binns-Roemer Elizabeth, Ng Derek K, Gourraud Pierre-Antoine, Reidy Kimberley, Warady Bradley, Furth Susan, Kopp Jeffrey B, Kaskel Frederick J, Limou Soph |
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- Page last updated:Apr 22, 2024
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