Human Genome Epidemiology Literature Finder
Rare Diseases
Records 1 - 29 (of 29 Records) |
Query Trace: Chronic Myeloproliferative Disorders[original query] |
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Factor V Leiden mutation carriership and venous thromboembolism in polycythemia vera and essential thrombocythemia. American journal of hematology 2002 Sep 71 (1): 1-6. Ruggeri Marco, Gisslinger Heinz, Tosetto Alberto, Rintelen Claudia, Mannhalter Christine, Pabinger Ingrid, Heis Navide, Castaman Giancarlo, Missiaglia Edoardo, Lechner Klaus, Rodeghiero Frances |
Frequent occurrence of anticardiolipin antibodies, Factor V Leiden mutation, and perturbed endothelial function in chronic myeloproliferative disorders. American journal of hematology 2002 Mar 69 (3): 185-91. Jensen Morten Krogh, de Nully Brown Peter, Thorsen Sixtus, Hasselbalch Hans Ca |
Mpl Baltimore: a thrombopoietin receptor polymorphism associated with thrombocytosis. Proceedings of the National Academy of Sciences of the United States of America 2004 Aug 101 (31): 11444-7. Moliterno Alison R, Williams Donna M, Gutierrez-Alamillo Laura I, Salvatori Roberto, Ingersoll Roxann G, Spivak Jerry |
The JAK2 V617F mutation in de novo acute myelogenous leukemias. Oncogene 2006 Mar 25 (9): 1434-6. Lee J W, Kim Y G, Soung Y H, Han K J, Kim S Y, Rhim H S, Min W S, Nam S W, Park W S, Lee J Y, Yoo N J, Lee S |
Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis. American journal of clinical pathology 2006 Apr 125 (4): 625-33. Murugesan Gurunathan, Aboudola Samer, Szpurka Hadrian, Verbic Mary Ann, Maciejewski Jaroslaw P, Tubbs Raymond R, Hsi Eric |
Incidence and significance of the JAK2 V617F mutation in patients with chronic myeloproliferative disorders. Irish journal of medical science 0 176 (2): 105-9. Langabeer S E, Ni Ainle F, Conneally E, Lawler |
Incidence of the JAK2 V617F mutation among patients with splanchnic or cerebral venous thrombosis and without overt chronic myeloproliferative disorders. Journal of thrombosis and haemostasis : JTH 2007 Apr 5 (4): 708-14. De Stefano V, Fiorini A, Rossi E, Za T, Farina G, Chiusolo P, Sica S, Leone |
[Clinical study on relationship between JAK2 V617F mutation and chronic myeloproliferative disorders]. Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi 2008 Feb 29 (2): 105-9. Zhang Yue, Li Lin, Nie Ling, Yu Yang, Yang Yi-Hong, Zhang Zhan-Qiang, Yang Lin, Xu Shi-Cai, Xiao Zhi-Ji |
A sensitive detection method for MPLW515L or MPLW515K mutation in chronic myeloproliferative disorders with locked nucleic acid-modified probes and real-time polymerase chain reaction. The Journal of molecular diagnostics : JMD 2008 Sep 10 (5): 435-41. Pancrazzi Alessandro, Guglielmelli Paola, Ponziani Vanessa, Bergamaschi Gaetano, Bosi Alberto, Barosi Giovanni, Vannucchi Alessandro |
Prevalence of the JAK2-V617F mutation in Taiwanese patients with chronic myeloproliferative disorders. Internal medicine journal 2008 Jun 38 (6): 422-6. Lieu C-H, Wu H-S, Hon Y-C, Tsai W-H, Yang C-F, Wang C-C, Lin Y-C, Shih C-H, Hsu H |
Detection of the JAK2 V617F missense mutation by high resolution melting analysis and its validation. Clinica chimica acta; international journal of clinical chemistry 2009 Jul . Er TK, Chang JG, Hsieh LL, Lin SK, Wang LH, Lin CW, Chang CS, Liu TC |
[The quantitative assay and clinical significance of JAK2V617F mutation in 131 patients with chronic myeloproliferative disorders]. Zhonghua nei ke za zhi 2009 Feb 48 (2): 140-3. Shen Yi-Min, Chao Hong-Ying, Zhang Ri, Feng Yu-Feng, Cen Jian-Nong, Yao Li, Shen Hong-Jie, Zhu Zi-Ling, Xue Yong-Qu |
HFE C282Y mutation as a genetic modifier influencing disease susceptibility for chronic myeloproliferative disease. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Mar 18 (3): 929-34. Andrikovics Hajnalka, Meggyesi Nora, Szilvasi Aniko, Tamaska Julia, Halm Gabriella, Lueff Sandor, Nahajevszky Sarolta, Egyed Miklos, Varkonyi Judit, Mikala Gabor, Sipos Andrea, Kalasz Laszlo, Masszi Tamas, Tordai Atti |
MPLW515L mutation in acute megakaryoblastic leukaemia. Leukemia 2009 May 23 (5): 852-5. Hussein K, Bock O, Theophile K, Schulz-Bischof K, Porwit A, Schlue J, Jonigk D, Kreipe |
Quantitative assay for Janus kinase 2 (JAK2) mutation in Chinese patients with chronic myeloproliferative disorders. The Journal of international medical research 0 37 (1): 37-46. Shen Y-M, Chao H-Y, Zhang R, Feng Y-F, Cen J-N, Yao L, Shen H-J, Zhu Z-L, Xue Y |
[Detection and clinical significance of JAK2 mutation in 412 patients with chronic myeloproliferative neoplasms]. Zhonghua zhong liu za zhi [Chinese journal of oncology] 2009 Jul 31 (7): 510-4. Chao Hong-Ying, Fan Zheng, Zhang Ri, Shen Yi-Min, Chen Wan, Fei Hai-Rong, Zhu Zi-Ling, Feng Yu-Feng, Chen Zi-Xing, Xue Yong-Qu |
Clinical significance of V617F mutation of the JAK2 gene in patients with chronic myeloproliferative disorders. Hematology (Amsterdam, Netherlands) 2009 Dec 14 (6): 323-30. Basquiera Ana L, Soria Néstor W, Ryser Ricardo, Salguero Miriam, Moiraghi Beatriz, Sackmann Federico, Sturich Ana G, Borello Adriana, Berretta Adriana, Bonafé Miriam, Barral José Moreno, Palazzo Emilio D, García Juan |
JAK2 mutations in Asian patients with essential thrombocythaemia. Internal medicine journal 2011 Feb 41 (2): 191-6. Wong G-C, Kam G L S, Koay E S |
Sex differences in the JAK2 V617F allele burden in chronic myeloproliferative disorders. Haematologica 2010 Jul 95 (7): 1090-7. Stein Brady L, Williams Donna M, Wang Nae-Yuh, Rogers Ophelia, Isaacs Mary Ann, Pemmaraju Naveen, Spivak Jerry L, Moliterno Alison |
Prevalence of JAK2 V617F mutation in Indian patients with chronic myeloproliferative disorders. The Indian journal of medical research 2010 Oct 132 423-7. Sazawal Sudha, Bajaj Jyoti, Chikkara Sunita, Jain Sonal, Bhargava Rahul, Mahapatra Manoranjan, Saxena Re |
MPL mutation profile in JAK2 mutation-negative patients with myeloproliferative disorders. Diagnostic molecular pathology : the American journal of surgical pathology, part B 2011 Mar 20 (1): 34-9. Ma Wanlong, Zhang Xi, Wang Xiuqiang, Zhang Zhong, Yeh Chen-Hsiung, Uyeji Jennifer, Albitar Mah |
Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera. Molecular biology reports 2012 Sep 39 (9): 8663-7. Karkucak Mutlu, Yakut Tahsin, Ozkocaman Vildan, Ozkalemkas Fahir, Ali Ridvan, Bayram Murat, Gorukmez Orhan, Ocakoglu Gokh |
A study of JAK2 (V617F) gene mutation in patients with chronic myeloproliferative disorders. La Clinica terapeutica 2012 163 (2): 109-13. Hamidah N H, Farisah N R, Azlinda A B, Wong F L, Das S, Fadillah S A W, Ainoon |
Janus kinase (JAK) 2 V617F mutation in Asian Indians with cerebral venous thrombosis and without overt myeloproliferative disorders. Journal of the neurological sciences 2012 Sep . De T, Prabhakar P, Nagaraja D, Christopher R |
Low frequency of c-MPL gene mutations in Iranian patients with Philadelphia-negative myeloproliferative disorders. Iranian journal of pediatric hematology and oncology 2015 5 (1): 43-9. Ghotaslou A, Nadali F, Chahardouli B, Alizad Ghandforosh N, Rostami S H, Alimoghaddam K, Ghavamzadeh |
Matrix Metalloproteinases 2 and 9 Polymorphism in Patients With Myeloproliferative Diseases: A STROBE-Compliant Observational Study. Medicine 2015 Apr 94 (16): e732. Maral Senem, Acar Muradiye, Balcik Ozlem Sahin, Uctepe Eyyup, Hatipoglu Omer Faruk, Akdeniz Derya, Altun Hatice Uludag, Kosar Ali, Gunduz Mehmet, Gunduz Es |
Diagnostic value of the JAK2 V617F mutation for latent chronic myeloproliferative disorders in patients with Budd-Chiari syndrome and/or portal vein thrombosis. The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2015 Jan 26 (1): 42-8. Karaköse Süleyman, Oruç Nevin, Zengin Melia, Akarca Ulus Salih, Ersöz Gal |
Low frequency of V617F mutation in JAK2 gene in Indian patients with hepatic venous outflow obstruction and extrahepatic portal venous obstruction. Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology 2016 Sep . Rai Praveer, Kumar Pankaj, Mishra Swapnil, Aggarwal Rake |
FAS/FASL gene polymorphisms in Turkish patients with chronic myeloproliferative disorders. Archives of medical science : AMS 2017 Mar 13 (2): 426-432. Ozdemirkiran Fusun Gediz, Nalbantoglu Sinem, Gokgoz Zafer, Payzin Bahriye Kadriye, Vural Filiz, Cagirgan Seckin, Berdeli Af |
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- Page last updated:May 13, 2024
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