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JAK2V617F variant allele frequency, non-driver mutations, single-nucleotide variants and polycythemia vera outcome. Journal of cancer research and clinical oncology 2022 Oct . Kandu?a Zuzanna, Janowski Micha?, Wi?ckowska Barbara, Paczkowska Edyta, Lewandowski Krzyszt |
Characteristics of patients with cerebral sinus venous thrombosis and JAK2 V617F mutation. Acta neurologica Belgica 2022 Sep . Simaan Naaem, Molad Jeremy, Honig Asaf, Filioglo Andrei, Shbat Fadi, Auriel Eitan, Barnea Rani, Hallevi Hen, Seyman Estelle, Mendel Rom, Leker Ronen R, Peretz Shlo |
JAK2 rs10974944 is associated with both V617F-positive and negative myeloproliferative neoplasms in a Vietnamese population: A potential genetic marker. Molecular genetics & genomic medicine 2022 Aug e2044. Ngoc Nguyen Thy, Hau Bui Bich, Vuong Nguyen Ba, Xuan Nguyen T |
Triple-Negativity Identifies a Subgroup of Patients with Better Overall Survival in Essential Thrombocythemia. Hematology reports 2022 Aug 14 (3): 265-269. Santoro Marco, Accurso Vincenzo, Mancuso Salvatrice, Napolitano Mariasanta, Mattana Marta, Vajana Giorgia, Russello Federica, Siragusa Serg |
Hematological relevance of JAK2 V617F and calreticulin mutations in Tunisian patients with essential thrombocythemia. Journal of clinical laboratory analysis 2022 Jun e24522. Abdelghani Maroua, Hammami Haifa, Zidi Wiem, Amouri Hassiba, Othmen Hind Ben Hadj, Farrah Ahlem, Menif Sam |
JAK2 allele burden is correlated with a risk of venous but not arterial thrombosis. Thrombosis research 2022 Mar 211 1-5. Soudet Simon, Le Roy Gaelle, Cadet Estelle, Michaud Audrey, Morel Pierre, Marolleau Jean Pierre, Sevestre Marie Antoinet |
Myelodysplastic/myeloproliferative neoplasms with ring sideroblasts and thrombocytosis (MDS/MPN-RS-T): Mayo-Moffitt collaborative study of 158 patients. Blood cancer journal 2022 2 12 (2): 26. Mangaonkar Abhishek A, Lasho Terra L, Ketterling Rhett P, Reichard Kaaren K, Gangat Naseema, Al-Kali Aref, Begna Kebede H, Pardanani Animesh, Al Ali Najla H, Talati Chetasi, Sallman David, Padron Eric, Patnaik Mrinal M, Tefferi Ayalew, Komrokji Ra |
The Pan African medical journal 2021 39 194. Sassi Hela, Menif Samia, Ammar Safa Ben, Farrah Ahlem, Othmen Hend Ben Hadj, Amouri Hassi |
Portal Thrombosis in Cirrhosis: Role of Thrombophilic Disorders. Journal of clinical medicine 2020 Aug 9 (9): . Fortea José Ignacio, Carrera Inés García, Puente Ángela, Cuadrado Antonio, Huelin Patricia, Tato Carmen Álvarez, Fernández Paloma Álvarez, Montes María Del Rocío Pérez, Céspedes Javier Nuñez, López Ana Batlle, Sanchez Francisco José González, Hoyos Marcos López, Crespo Javier, Fábrega Emil |
Next-generation sequencing in the diagnosis of non-cirrhotic splanchnic vein thrombosis. Journal of hepatology 2020 Jul . Magaz Marta, Alvarez-Larrán Alberto, Colomer Dolors, López-Guerra Mónica, García-Criado M Ángeles, Mezzano Gabriel, Belmonte Ernest, Olivas Pol, Soy Guillem, Cervantes Francisco, Darnell Anna, Ferrusquía-Acosta José, Baiges Anna, Turon Fanny, Hernández-Gea Virginia, García-Pagán Juan Carl |
ASXL1 mutations, previous vascular complications and age at diagnosis predict survival in 85 WHO-defined polycythaemia vera patients. British journal of haematology 2020 Feb . Andréasson Björn, Pettersson Helna, Wasslavik Carina, Johansson Peter, Palmqvist Lars, Asp Jul |
Thrombophilic Risk of Factor V Leiden, Prothrombin G20210A, MTHFR, and Calreticulin Mutations in Essential Thrombocythemia Egyptian Patients. Advances in hematology 2020 2020 7695129. El-Ghonemy Mohamed S, El Sharawy Solafa, Fahmi Maryan Waheeb, El-Ashwah Shaimaa, Denewer May, El-Baiomy M |
V617F-independent upregulation of JAK2 gene expression in patients with inflammatory bowel disease. Journal of cellular biochemistry 2019 May . Asadzadeh-Aghdaei Hamid, Mashayekhi Kazem, Koushki Khadijeh, Azimzadeh Pedram, Rostami-Nejad Mohammad, Amani Davar, Chaleshi Vahid, Haftcheshmeh Saeed Mohammadian, Sahebkar Amirhossein, Zali Mohammad Re |
Classical Philadelphia-negative myeloproliferative neoplasms: focus on mutations and JAK2 inhibitors. Medical oncology (Northwood, London, England) 2018 Aug 35 (9): 119. Helbig Grzego |
Selective testing for calreticulin gene mutations in patients with splanchnic vein thrombosis: A prospective cohort study. Journal of hepatology 2017 May . Poisson Johanne, Plessier Aurélie, Kiladjian Jean-Jacques, Turon Fanny, Cassinat Bruno, Andreoli Annalisa, De Raucourt Emmanuelle, Goria Odile, Zekrini Kamal, Bureau Christophe, Lorre Florence, Cervantes Francisco, Colomer Dolors, Durand François, Garcia-Pagan Juan-Carlos, Casadevall Nicole, Valla Dominique-Charles, Rautou Pierre-Emmanuel, Marzac Christophe, |
[Mutation of CALR Gene in Patients with Chronic Myeloproliferative Neoplasm and Its Clinical Significance]. Zhongguo shi yan xue ye xue za zhi 2017 Feb 25 (1): 151-156. Tang Qin, Zhang Xiu-Wen, Xia Lei, Jiang Nai- |
[The development and comparative approbation of methods of increasing sensitivity of detection of mutation V617F in gene JAK2 by pyro-sequencing]. Klinicheskaia laboratornaia diagnostika 2017 Feb 62 (2): 125-8. Dunaeva E A, Mironov K O, Subbotina T N, Olkhovsky I A, Shipulin G |
Estimation of diagnosis and prognosis in ET by assessment of CALR and JAK2 mutations and laboratory findings: a meta-analysis. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico 2017 Feb . Saki N, Shirzad R, Rahim F, Saki Malehi |
[Clinical features of essential thrombocythemia and primary myelofibrosis, depending on the molecular characteristics of disease]. Terapevticheskii arkhiv 2017 89 (7): 4-9. Melikyan A L, Subortseva I N, Sudarikov A B, Kovrigina A M, Gilyazitdinova E A, Kolosheinova T I, Abdullaev A O, Treglazova S |
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 |
Coexistence of JAK2 and CALR mutations and their clinical implications in patients with essential thrombocythemia. Oncotarget 2016 Jul . Min-Gu Kang, Hyun-Woo Choi, Jun Hyung Lee, Yong Jun Choi, Hyun-Jung Choi, Jong-Hee Shin, Soon-Pal Suh, Szardenings Michael, Hye-Ran Kim, Myung-Geun Sh |
Prognostic value of CALR vs. JAK2V617F mutations on splenomegaly, leukemic transformation, thrombosis, and overall survival in patients with primary fibrosis: a meta-analysis. Annals of hematology 2016 Jul . Pei Yu-Qing, Wu Yue, Wang Fei, Cui W |
Thrombotic risk correlates with mutational status in true essential thrombocythemia. European journal of clinical investigation 2016 Jun . Bertozzi I, Peroni E, Coltro G, Bogoni G, Cosi E, Santarossa C, Fabris F, Randi M |
Molecular biomarkers of thrombosis in myeloproliferative neoplasms. Thrombosis research 2016 Apr 140 Suppl 1 S71-5. Barbui Tiziano, Falanga An |
PO-19 - Platelet (PLT) adhesion under flow condition in essential thrombocythemia (ET) and polycythemia vera (PV) is variably influenced according to patient mutational status. Thrombosis research 2016 Apr 140 Suppl 1 S183. Vignoli A, Tessarolo S, Marchetti M, Gamba S, Piras F, Finazzi G, van der Meijden P E J, Swieringa F, Ten Cate H, Heemskerk J W M, Rambaldi A, Falanga |
Unbiased pro-thrombotic features at diagnosis in 977 thrombocythemic patients with Philadelphia-negative chronic myeloproliferative neoplasms. Leukemia research 2016 Apr 46 18-25. Gugliotta Luigi, Iurlo Alessandra, Gugliotta Gabriele, Tieghi Alessia, Specchia Giorgina, Gaidano Gianluca, Scalzulli Potito R, Rumi Elisa, Dragani Alfredo, Martinelli Vincenzo, Santoro Cristina, Randi Maria Luigia, Tagariello Giuseppe, Candoni Anna, Cattaneo Daniele, Ricco Alessandra, Palmieri Raffaele, Liberati Marina A, Langella Maria, Rago Angela, Bergamaschi Micaela, Monari Paola, Miglio Rossella, Santoro Umberto, Cacciola Rossella, Rupoli Serena, Mastrullo Lucia, Musto Pellegrino, Mazzucconi Maria Gabriella, Vignetti Marco, Cortelezzi Agostino, Vianelli Nicola, Martino Bruno, Stefano Valerio De, Passamonti Francesco, Vannucchi Alessandro M, |
Thrombophilia Profile in Budd-Chiari Syndrome and Splanchnic Vein Thrombosis: A Study from Western India. The Journal of the Association of Physicians of India 2015 Sep 63 (9): 32-5. Sawant Prabha, Vashishtha Chitranshu, Nasa Mukesh, Parikh Pathik, Patel Jignesh, Agasti Anan |
Clinical Manifestation of Calreticulin Gene Mutations in Essential Thrombocythemia without Janus Kinase 2 and MPL Mutations: A Chinese Cohort Clinical Study. Chinese medical journal 0 129 (15): 1778-1783. Sun Chao, Zhou Xin, Zou Zhi-Jian, Guo Hong-Feng, Li Jian-Yong, Qiao Ch |
Correlation Between PAI-1 Gene 4G/5G Polymorphism and the Risk of Thrombosis in Ph Chromosome-Negative Myeloproliferative Neoplasms. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 0 26 1076029620935207. Zhang Xueya, Cai Xuerong, Pan Jingx |
Predictive factors of thrombosis for patients with essential thrombocythaemia: A single center study. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 0 26 (1): 115-121. Prajs Iwona, Kuliczkowski Kazimie |
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- Page last updated:Feb 03, 2023
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