Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 43 Records) |
| Query Trace: Disease and MBP[original query] |
|---|
| [Relationship between mannose-binding protein gene polymorphisms and disease progression and HBV DNA in patients with chronic HBV infection]. Zhonghua shi yan he lin chuang bing du xue za zhi = Zhonghua shiyan he linchuang bingduxue zazhi = Chinese journal of experimental and clinical virology 2012 Apr 26 (2): 90-2. Zheng Rui-Dan, Chen Jian-Neng, Gao Jian-Ping, Zhuang Qun-Ying, Zhu Qing-Chuan, Lu Yan-Hui, Lin Zhen-Qun, Hong Wu-Hua, Li Qing-Duan, Chen Z |
| Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing. Genome medicine 2013 5 (4): 30. Heitzer Ellen, Ulz Peter, Belic Jelena, Gutschi Stefan, Quehenberger Franz, Fischereder Katja, Benezeder Theresa, Auer Martina, Pischler Carina, Mannweiler Sebastian, Pichler Martin, Eisner Florian, Haeusler Martin, Riethdorf Sabine, Pantel Klaus, Samonigg Hellmut, Hoefler Gerald, Augustin Herbert, Geigl Jochen B, Speicher Michael |
| Interaction between HLA-DRB1-DQB1 haplotypes in Sardinian multiple sclerosis population. PloS one 2013 8 (4): e59790. Cocco Eleonora, Murru Raffaele, Costa Gianna, Kumar Amit, Pieroni Enrico, Melis Cristina, Barberini Luigi, Sardu Claudia, Lorefice Lorena, Fenu Giuseppe, Frau Jessica, Coghe Giancarlo, Carboni Nicola, Marrosu Maria Giovan |
| Comparable autoantibody serum levels against amyloid- and inflammation-associated proteins in Parkinson's disease patients and controls. PloS one 2014 9 (2): e88604. Maetzler Walter, Apel Anja, Langkamp Markus, Deuschle Christian, Dilger Sarah Selina, Stirnkorb Johannes Georg, Schulte Claudia, Schleicher Erwin, Gasser Thomas, Berg Danie |
| Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease. Gastroenterology 2015 Jul . Kelsen Judith R, Dawany Noor, Moran Christopher J, Petersen Britt-Sabina, Sarmady Mahdi, Sasson Ariella, Pauly-Hubbard Helen, Martinez Alejandro, Maurer Kelly, Soong Joanne, Rappaport Eric, Franke Andre, Keller Andreas, Winter Harland S, Mamula Petar, Piccoli David, Artis David, Sonnenberg Gregory F, Daly Mark, Sullivan Kathleen E, Baldassano Robert N, Devoto Marcel |
| Genomic instability in the PARK2 locus is associated with Parkinson's disease. Journal of applied genetics 2015 Apr . Ambroziak Wojciech, Koziorowski Dariusz, Duszyc Kinga, Górka-Skoczylas Paulina, Potulska-Chromik Anna, S?awek Jaros?aw, Hoffman-Zacharska Doro |
| Identification of ITPA on chromosome 20 as a susceptibility gene for young-onset tuberculosis. Human genome variation 2016 3 15067. Nakauchi Ayaka, Wong Jing Hao, Mahasirimongkol Surakameth, Yanai Hideki, Yuliwulandari Rika, Mabuchi Akihiko, Liu Xiaoxi, Mushiroda Taisei, Wattanapokayakit Sukanya, Miyagawa Taku, Keicho Naoto, Tokunaga Katsus |
| Impact of Mannose-Binding Protein Gene Polymorphisms in Omani Sickle Cell Disease Patients. Mediterranean journal of hematology and infectious diseases 2016 8 (1): e2016013. Zachariah Mathew, Al Zadjali Shoaib, Bashir Wafa, Al Ambusaidi Rahma, Misquith Rhea, Wali Yasser, Pathare An |
| Combination of Myelin Basic Protein Gene Polymorphisms with HLA-DRB1*1501 in Iranian Patients with Multiple Sclerosis. Iranian journal of immunology : IJI 2017 Sep 14 (3): 231-239. Nejati Parham, Attar Marzieh, Rahimian Maryam, Fathi Davood, Shahbazi Maj |
| A pharmacogenetic signature of high response to Copaxone in late-phase clinical-trial cohorts of multiple sclerosis. Genome medicine 2017 May 9 (1): 50. Ross Colin J, Towfic Fadi, Shankar Jyoti, Laifenfeld Daphna, Thoma Mathis, Davis Matthew, Weiner Brian, Kusko Rebecca, Zeskind Ben, Knappertz Volker, Grossman Iris, Hayden Michael |
| Variation within MBP gene predicts disease course in multiple sclerosis. Brain and behavior 2017 04 7 (4): e00670. Zhou Yuan, Simpson Steve, Charlesworth Jac C, van der Mei Ingrid, Lucas Robyn M, Ponsonby Anne-Louise, , Taylor Bruce |
| [Inflammatory factors and immunophenotypes in adjustment disorders]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2018 118 (3): 83-88. Klyushnik T P, Nikitina V B, Androsova L V, Vetlugina T P, Zozulya S A, Aksenov M M, Bokhan N |
| Identification of 55,000 Replicated DNA Methylation QTL. Scientific reports 2018 12 8 (1): 17605. McRae Allan F, Marioni Riccardo E, Shah Sonia, Yang Jian, Powell Joseph E, Harris Sarah E, Gibson Jude, Henders Anjali K, Bowdler Lisa, Painter Jodie N, Murphy Lee, Martin Nicholas G, Starr John M, Wray Naomi R, Deary Ian J, Visscher Peter M, Montgomery Grant |
| Genomic Features of Metastatic Testicular Sex Cord Stromal Tumors. European urology focus 2019 6 5 (5): 748-755. Necchi Andrea, Bratslavsky Gennady, Shapiro Oleg, Elvin Julia A, Vergilio Jo-Anne, Killian Jonathan K, Ngo Nhu, Ramkissoon Shakti, Severson Eric, Hemmerich Amanda C, Ali Siraj M, Chung Jon H, Reddy Prasanth, Miller Vincent A, Schrock Alexa B, Gay Laurie M, Ross Jeffrey S, Jacob Joseph |
| Gene expression over the course of schizophrenia: from clinical high-risk for psychosis to chronic stages. NPJ schizophrenia 2019 Mar 5 (1): 5. Ota Vanessa Kiyomi, Moretti Patricia Natalia, Santoro Marcos Leite, Talarico Fernanda, Spindola Leticia Maria, Xavier Gabriela, Carvalho Carolina Muniz, Marques Diogo Ferri, Costa Giovany Oliveira, Pellegrino Renata, de Jong Simone, Cordeiro Quirino, Hakonarson Hakon, Breen Gerome, Noto Cristiano, Bressan Rodrigo Affonseca, Gadelha Ary, Jesus Mari Jair de, Belangero Sintia |
| A dominant RAD51C pathogenic splicing variant predisposes to breast and ovarian cancer in the Newfoundland population due to founder effect. Molecular genetics & genomic medicine 2019 11 8 (2): e1070. Dawson Lesa M, Smith Kerri N, Werdyani Salem, Ndikumana Robyn, Penney Cindy, Wiede Louisa L, Smith Kendra L, Pater Justin A, MacMillan Andrée, Green Jane, Drover Sheila, Young Terry-Lynn, O'Rielly Darren |
| A Polymorphism Within the MBP Gene Is Associated With a Higher Relapse Number in Male Patients of Multiple Sclerosis. Frontiers in immunology 2020 11 771. Espino-Paisán Laura, Agudo-Jiménez Teresa, Rosales-Martínez Isabel, López-Cotarelo Pilar, García-Martínez María Ángel, Domínguez-Mozo María Inmaculada, Pérez-Pérez Silvia, Dieli-Crimi Romina, Comabella Manuel, Urcelay Elena, Álvarez-Lafuente Rober |
| Human leukocyte antigen association with familial steroid-sensitive nephrotic syndrome. European journal of pediatrics 2020 3 179 (9): 1481-1486. Korsgaard Trine, Joshi Shivani, Andersen Rene F, Moeller Kristina, Seeman Tomás, Podracká Ludmila, Eiberg Hans, Rittig Sør |
| A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders. Current Alzheimer research 2020 Nov . El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Na |
| Association of the Lactase Persistence Haplotype Block With Disease Risk in Populations of European Descent. Frontiers in genetics 2020 11 11 558762. Joslin Shannon E K, Durbin-Johnson Blythe P, Britton Monica, Settles Matthew L, Korf Ian, Lemay Danielle |
Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.
PloS one 2021 9 16 (9): e0247287. Ashvetiya Tamara, Fan Sherry X, Chen Yi-Ju, Williams Charles H, O'Connell Jeffery R, Perry James A, Hong Charles |
| [Specific features of immunological reactions in elderly and young patients with exacerbation of schizophrenia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2021 3 121 (2): 53-59. Klyushnik T P, Barkhatova A N, Sheshenin V S, Androsova L V, Zozulya S A, Otman I N, Pochueva V |
| Influence of Genetic Polymorphisms on Clinical Outcomes of Glatiramer Acetate in Multiple Sclerosis Patients. Journal of personalized medicine 2021 Oct 11 (10): . Zarzuelo-Romero María José, Pérez-Ramírez Cristina, Cura Yasmín, Carrasco-Campos María Isabel, Marangoni-Iglecias Luciana María, Ramírez-Tortosa María Carmen, Jiménez-Morales Alber |
| Phase Ib study of anlotinib combined with TQB2450 in pretreated advanced biliary tract cancer and biomarker analysis. Hepatology (Baltimore, Md.) 2022 May . Zhou Jun, Sun Yongkun, Zhang Wen, Yuan Jiajia, Peng Zhi, Wang Wei, Gong Jifang, Yang Lin, Cao Yanshuo, Zhao Hong, Chen Chao, Wang Weifeng, Shen Lin, Zhou Aipi |
| Novel synthetic lethality drug target in urothelial bladder cancer based on MTAP genomic loss. Urologic oncology 2022 11 41 (2): 109.e15-109.e22. Basin Michael F, Bratslavsky Gennady, Nahhas Nathan, Basnet Alina, Goldberg Hanan, Necchi Andrea, Sokol Ethan S, Ramkissoon Shakti H, Huang Richard S P, Ross Jeffrey S, Jacob Joseph |
| The kinetics of blast clearance are associated with copy number alterations in childhood B-cell acute lymphoblastic leukemia. Neoplasia (New York, N.Y.) 2022 10 35 100840. Urba?ska Zuzanna, Lejman Monika, Taha Joanna, Madzio Joanna, Ostrowska Kinga, Miarka-Walczyk Karolina, Wypyszczak Kamila, Styka Borys, Jakubowska Justyna, S?dek ?ukasz, Szczepa?ski Tomasz, Sta?czak Marcin, Fendler Wojciech, M?ynarski Wojciech, Pastorczak Aga |
| Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis. International journal of molecular sciences 2022 10 23 (19): . Horjus Julia, van Mourik-Banda Tineke, Heerings Marco A P, Hakobjan Marina, De Witte Ward, Heersema Dorothea J, Jansen Anne J, Strijbis Eva M M, de Jong Brigit A, Slettenaar Astrid E J, Zeinstra Esther M P E, Hoogervorst Erwin L J, Franke Barbara, Kruijer Wiebe, Jongen Peter J, Visser Leo J, Poelmans Gee |
| Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor. Biomedicines 2022 1 10 (1): . Abondio Paolo, Sarno Stefania, Giuliani Cristina, Laganà Valentina, Maletta Raffaele, Bernardi Livia, Bruno Francesco, Colao Rosanna, Puccio Gianfranco, Frangipane Francesca, Borroni Barbara, Van Broeckhoven Christine, Luiselli Donata, Bruni Amal |
| Astrocytic response mediated by the CLU risk allele inhibits OPC proliferation and myelination in a human iPSC model. Cell reports 2023 7 42 (8): 112841. Zhenqing Liu, Jianfei Chao, Cheng Wang, Guihua Sun, Daniel Roeth, Wei Liu, Xianwei Chen, Li Li, E Tian, Lizhao Feng, Hayk Davtyan, Mathew Blurton-Jones, Markus Kalkum, Yanhong S |
| Clinical and genomic profiling of a patient with a de novo ring chromosome 18: a case report highlighting autoimmune and neurological implications. Molecular cytogenetics 2024 12 17 (1): 31. Annalaura Montanari, Paola Caforio, Annalisa Paparella, Paola Casieri, Maria Cristina Nuzzi, Maria Fatima Antonucci, Claudia Rita Catacchio, Marilina Tampoia, Mattia Gentile, Roberta Bucci, Valerio Cecinati, Angelo Cellamare, Francesca Antonac |
- Page last reviewed:Feb 1, 2024
- Content source: