Artículos de revistas sobre el tema "ANKRD26"
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Husnain, Muhammad, Trent Wang, Maikel Valdes, James Hoffman y Lazaros Lekakis. "Multiple Myeloma in a Patient with ANKRD26-Related Thrombocytopenia Successfully Treated with Combination Therapy and Autologous Stem Cell Transplant". Case Reports in Hematology 2019 (2 de junio de 2019): 1–3. http://dx.doi.org/10.1155/2019/9357572.
Texto completoNecchi, Vittorio, Alessandra Balduini, Patrizia Noris, Serena Barozzi, Patrizia Sommi, Christian di Buduo, Carlo Balduini, Enrico Solcia y Alessandro Pecci. "Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia". Thrombosis and Haemostasis 109, n.º 02 (2013): 263–71. http://dx.doi.org/10.1160/th12-07-0497.
Texto completoErdomaeva, Ya A., D. V. Fedorova, P. A. Zharkov, M. A. Kurnikova, S. G. Mann y E. V. Raykina. "ANKRD26-related thrombocytopenia: case report and literature review of inherited thrombocytopenias with predisposition to malignancies". Pediatric Hematology/Oncology and Immunopathology 18, n.º 3 (13 de septiembre de 2019): 54–61. http://dx.doi.org/10.24287/1726-1708-2019-18-3-54-61.
Texto completoNoris, Patrizia, Silverio Perrotta, Marco Seri, Alessandro Pecci, Chiara Gnan, Giuseppe Loffredo, Nuria Pujol-Moix et al. "Mutations in ANKRD26 are responsible for a frequent form of inherited thrombocytopenia: analysis of 78 patients from 21 families". Blood 117, n.º 24 (16 de junio de 2011): 6673–80. http://dx.doi.org/10.1182/blood-2011-02-336537.
Texto completoGuison, Jérôme, Gilles Blaison, Oana Stoica, Remy Hurstel, Marie Favier y Remi Favier. "Idiopathic pulmonary embolism in a case of severe family ANKRD26 thrombocytopenia". Mediterranean Journal of Hematology and Infectious Diseases 9, n.º 1 (16 de junio de 2017): e2017038. http://dx.doi.org/10.4084/mjhid.2017.038.
Texto completoKojić, Snežana. "MARP Protein Family: A Possible Role in Molecular Mechanisms of Tumorigenesis". Journal of Medical Biochemistry 29, n.º 3 (1 de julio de 2010): 157–64. http://dx.doi.org/10.2478/v10011-010-0024-9.
Texto completoVincenot, Anne, Marie-Françoise Hurtaud-Roux, Olivier René, Sylvie Binard, Odile Fenneteau y Nicole Schlegel. "ANKRD26 normocytic thrombocytopenia: a family report". Annales de biologie clinique 74, n.º 3 (mayo de 2016): 317–22. http://dx.doi.org/10.1684/abc.2016.1142.
Texto completoNoris, Patrizia, Remi Favier, Marie-Christine Alessi, Amy E. Geddis, Shinji Kunishima, Paula G. Heller, Paola Giordano et al. "ANKRD26-related thrombocytopenia and myeloid malignancies". Blood 122, n.º 11 (12 de septiembre de 2013): 1987–89. http://dx.doi.org/10.1182/blood-2013-04-499319.
Texto completoMorozova, D. S., A. A. Martyanov, M. A. Panteleev, P. A. Zharkov, D. V. Fedorova y A. N. Sveshnikova. "Observation of granulocyte function during ex vivo thrombus formation for patients with ANKRD26-associated thrombocytopenia". Pediatric Hematology/Oncology and Immunopathology 19, n.º 1 (28 de marzo de 2020): 27–34. http://dx.doi.org/10.24287/1726-1708-2020-19-1-27-34.
Texto completoGnan, Chiara, Patrizia Noris, Felisa C. Molinas, Shinji Kunishima, Paula Graciela Heller, Akihiro Iguchi, Alessandro Pecci et al. "Mutations Identified in Thrombocytopenia THC2 Are Likely to Dysregulate ANKRD26 Expression". Blood 118, n.º 21 (18 de noviembre de 2011): 708. http://dx.doi.org/10.1182/blood.v118.21.708.708.
Texto completoEisfeld, Ann-Kathrin, Jessica Kohlschmidt, Krzysztof Mrózek, Alice S. Mims, Christopher J. Walker, Deedra Nicolet, James S. Blachly et al. "Mutations in Genes Associated with Familial Predisposition to Myeloid Neoplasms: Their Frequency and Associations with Pretreatment Characteristics in Adult Patients (Pts) with Presumably Sporadic De Novo Acute Myeloid Leukemia (AML)". Blood 132, Supplement 1 (29 de noviembre de 2018): 1478. http://dx.doi.org/10.1182/blood-2018-99-120085.
Texto completoPolokhov, D. M., D. V. Fedorova, A. V. Pshonkin, A. A. Ignatova, E. A. Ponomarenko, M. Yu Aleksenko, I. V. Mersiyanova et al. "Platelet phenotype in children with ANKRD26-related thrombocytopenia". Pediatric Hematology/Oncology and Immunopathology 20, n.º 2 (22 de mayo de 2021): 65–73. http://dx.doi.org/10.24287/1726-1708-2021-20-2-65-73.
Texto completoCoelho, D. Pereira, J. Azevedo, P. Martinho, T. Nascimento, S. Marini, A. Barbosa Ribeiro, E. Cortesão et al. "PS1496 ANKRD26-RELATED THROMBOCYTOPENIA: STUDY OF 3 FAMILIES". HemaSphere 3, S1 (junio de 2019): 689. http://dx.doi.org/10.1097/01.hs9.0000564244.71382.2b.
Texto completoAl Daama, Saad A., Yousef H. Housawi, Walid Dridi, Mohammed Sager, F. George Otieno, Cuiping Hou, Lyam Vasquez et al. "A missense mutation in ANKRD26 segregates with thrombocytopenia". Blood 122, n.º 3 (18 de julio de 2013): 461–62. http://dx.doi.org/10.1182/blood-2013-03-489344.
Texto completoKuzmanovic, Teodora, Metis Hasipek, Samuel Li, Thomas Laframboise, Valeria Visconte, Sunisa Kongkiatkamon, Seth J. Corey et al. "ANKRD26 Coding Variants in Myeloid Neoplasia". Blood 140, Supplement 1 (15 de noviembre de 2022): 4013–15. http://dx.doi.org/10.1182/blood-2022-170645.
Texto completoHo, Thanh, Juliana Perez Botero, William J. Hogan, Saad S. Kenderian, Naseema Gangat, Ayalew Tefferi, Roshini S. Abraham et al. "Clinical Spectrum of Germline Mutations with Predisposition to Myeloid Neoplasms- 2016 World Health Organization Classification Update". Blood 128, n.º 22 (2 de diciembre de 2016): 300. http://dx.doi.org/10.1182/blood.v128.22.300.300.
Texto completoCantor, Alan, Md Almamun, Nah-Young Shin y Daniel Yuan. "2004 – GERMLINE ANKRD26 MUTATIONS IN FAMILIAL THROMBOCYTOPENIA AND LEUKEMIA PREDISPOSITION". Experimental Hematology 111 (2022): S33. http://dx.doi.org/10.1016/j.exphem.2022.07.036.
Texto completoBluteau, Dominique, Alessandra Balduini, Nathalie Balayn, Manuela Currao, Paquita Nurden, Caroline Deswarte, Guy Leverger et al. "Thrombocytopenia-associated mutations in the ANKRD26 regulatory region induce MAPK hyperactivation". Journal of Clinical Investigation 124, n.º 2 (16 de enero de 2014): 580–91. http://dx.doi.org/10.1172/jci71861.
Texto completoDong, X. J., H. P. Guan, Q. D. Zhang, M. Yerle y B. Liu. "Mapping of porcine ANKRD1, ANKRD2, ANKRD23, VGLL2 and VGLL4 using somatic cell and radiation hybrid panels". Animal Genetics 38, n.º 4 (agosto de 2007): 424–25. http://dx.doi.org/10.1111/j.1365-2052.2007.01613.x.
Texto completoKraemer, Bjoern y Andrew Weyrich. "Polyubiquinated protein depots in platelets and megakaryocytes from patients with ANKRD26-RT". Thrombosis and Haemostasis 109, n.º 02 (2013): 180. http://dx.doi.org/10.1160/th13-01-0025.
Texto completoStaubitz, Julia Isabelle, Thomas Johannes Musholt, Arno Schad, Erik Springer, Hauke Lang, Krishnaraj Rajalingam, Wilfried Roth y Nils Hartmann. "ANKRD26-RET - A novel gene fusion involving RET in papillary thyroid carcinoma". Cancer Genetics 238 (octubre de 2019): 10–17. http://dx.doi.org/10.1016/j.cancergen.2019.07.002.
Texto completoChen, Ming-Huei, Lisa R. Yanek, Joshua D. Backman, John D. Eicher, Jennifer E. Huffman, Yoav Ben-Shlomo, Andrew D. Beswick et al. "Exome-chip meta-analysis identifies association between variation in ANKRD26 and platelet aggregation". Platelets 30, n.º 2 (29 de noviembre de 2017): 164–73. http://dx.doi.org/10.1080/09537104.2017.1384538.
Texto completoAcs, Peter, Peter O. Bauer, Balazs Mayer, Tapan Bera, Rhonda Macallister, Eva Mezey y Ira Pastan. "A novel form of ciliopathy underlies hyperphagia and obesity in Ankrd26 knockout mice". Brain Structure and Function 220, n.º 3 (16 de marzo de 2014): 1511–28. http://dx.doi.org/10.1007/s00429-014-0741-9.
Texto completoBera, T. K., X. F. Liu, M. Yamada, O. Gavrilova, E. Mezey, L. Tessarollo, M. Anver, Y. Hahn, B. Lee y I. Pastan. "A model for obesity and gigantism due to disruption of the Ankrd26 gene". Proceedings of the National Academy of Sciences 105, n.º 1 (27 de diciembre de 2007): 270–75. http://dx.doi.org/10.1073/pnas.0710978105.
Texto completoKuzmanovic, Teodora, Bhumika J. Patel, Jibran Durrani, Hassan Awada, Cassandra M. Kerr, Bartlomiej P. Przychodzen, Samuel Li et al. "ANKRD26 Coding Variants Presenting with Giant Platelets and a Predisposition to Myeloid Neoplasia". Blood 134, Supplement_1 (13 de noviembre de 2019): 4233. http://dx.doi.org/10.1182/blood-2019-130520.
Texto completoNestorovic, Aleksandra, Jovana Jasnic-Savovic, Georgine Faulkner, Dragica Radojkovic y Snezana Kojic. "Ankrd1-mediated signaling is supported by its interaction with zonula occludens-1". Archives of Biological Sciences 66, n.º 3 (2014): 1233–42. http://dx.doi.org/10.2298/abs1403233n.
Texto completoGlembotsky, Ana C., Rosana F. Marta, Yesica R. Espasandin, Nora P. Goette, Fernando Negro, Noris Patrizia, Anna Savoia et al. "Application of a Diagnostic Algorithm for Inherited Thrombocytopenia Patients in the Setting of a Developing Country". Blood 118, n.º 21 (18 de noviembre de 2011): 1163. http://dx.doi.org/10.1182/blood.v118.21.1163.1163.
Texto completoМ.Ю., Донников,, Илларионов, Р.А., Изотова, Т.А., Колбасин, Л.Н. y Коваленко, Л.В. "Evaluation of the effectiveness of next generation sequencing in the clinical practice of the medical genetic consultation in Khanty-Mansi region". Nauchno-prakticheskii zhurnal «Medicinskaia genetika, n.º 9 (30 de septiembre de 2022): 38–40. http://dx.doi.org/10.25557/2073-7998.2022.09.38-40.
Texto completoTsumura, Aaron M., Brian J. Druker, Diana Brewer, Richard Press y Theodore P. Braun. "BCR-ABL+ Chronic Myeloid Leukemia Arising in a Family With Inherited ANKRD26-Related Thrombocytopenia". JCO Precision Oncology, n.º 5 (febrero de 2021): 415–17. http://dx.doi.org/10.1200/po.20.00318.
Texto completoFiore, Mathieu, Noémie Saut, Marie-Christine Alessi y Jean-François Viallard. "Successful use of eltrombopag for surgical preparation in a patient with ANKRD26-related thrombocytopenia". Platelets 27, n.º 8 (8 de junio de 2016): 828–29. http://dx.doi.org/10.1080/09537104.2016.1190446.
Texto completoRaciti, G. A., T. K. Bera, O. Gavrilova y I. Pastan. "Partial inactivation of Ankrd26 causes diabetes with enhanced insulin responsiveness of adipose tissue in mice". Diabetologia 54, n.º 11 (13 de agosto de 2011): 2911–22. http://dx.doi.org/10.1007/s00125-011-2263-9.
Texto completoVrzalova, Zuzana, Katerina Stano Kozubik, Lenka Radova, Jakub Trizuljak, Sarka Pospisilova y Michael Doubek. "Characterization of Pathogenic Variants Associated with Hereditary Thrombocytopenias in Families from the Czech Republic". Blood 134, Supplement_1 (13 de noviembre de 2019): 2343. http://dx.doi.org/10.1182/blood-2019-122696.
Texto completoZhang, Bing, Yoonha Choi, Dana Ng, Ziming Weng, Clara Lo, Yohannes Ghebremariam, Engin Özkan et al. "Identification Of The Disease-Causing Mutation In Autosomal Dominant Familial Immune Thrombocytopenia By Genome-Wide Linkage Analysis and Whole Genome Sequencing". Blood 122, n.º 21 (15 de noviembre de 2013): 565. http://dx.doi.org/10.1182/blood.v122.21.565.565.
Texto completoLazaro, Estibaliz, Clémence Houssin, Loic Sentilhes, Laura Blouin y Mathieu Fiore. "Successful management of a pregnant woman with severe ANKRD26-related thrombocytopenia and anti-HPA-5b alloimmunization". Platelets 31, n.º 6 (12 de octubre de 2019): 827–29. http://dx.doi.org/10.1080/09537104.2019.1678116.
Texto completoLiu, Xiu-Fen, Tapan K. Bera, Charissa Kahue, Thelma Escobar, Zhaoliang Fei, Gregory A. Raciti y Ira Pastan. "ANKRD26 and Its Interacting Partners TRIO, GPS2, HMMR and DIPA Regulate Adipogenesis in 3T3-L1 Cells". PLoS ONE 7, n.º 5 (30 de mayo de 2012): e38130. http://dx.doi.org/10.1371/journal.pone.0038130.
Texto completoKirály, Péter Attila, Krisztián Kállay, Dóra Marosvári, Gábor Benyó, Anita Szőke, Judit Csomor y Csaba Bödör. "Familiáris myelodysplasiás szindróma és akut myeloid leukaemia klinikai és genetikai háttere". Orvosi Hetilap 157, n.º 8 (febrero de 2016): 283–89. http://dx.doi.org/10.1556/650.2016.30375.
Texto completoKewan, Tariq, Ryan Noss, Lucy A. Godley, Heesun J. Rogers y Hetty E. Carraway. "Inherited Thrombocytopenia Caused by Germline ANKRD26 Mutation Should Be Considered in Young Patients With Suspected Myelodysplastic Syndrome". Journal of Investigative Medicine High Impact Case Reports 8 (enero de 2020): 232470962093894. http://dx.doi.org/10.1177/2324709620938941.
Texto completoBalduini, Alessandra, Hana Raslova, Christian A. Di Buduo, Alessandro Donada, Matthias Ballmaier, Manuela Germeshausen y Carlo L. Balduini. "Clinic, pathogenic mechanisms and drug testing of two inherited thrombocytopenias, ANKRD26-related Thrombocytopenia and MYH9-related diseases". European Journal of Medical Genetics 61, n.º 11 (noviembre de 2018): 715–22. http://dx.doi.org/10.1016/j.ejmg.2018.01.014.
Texto completoPerez Botero, J., J. L. Oliveira, D. Chen, K. K. Reichard, D. S. Viswanatha, P. L. Nguyen, R. K. Pruthi et al. "ASXL1 mutated chronic myelomonocytic leukemia in a patient with familial thrombocytopenia secondary to germline mutation in ANKRD26". Blood Cancer Journal 5, n.º 5 (mayo de 2015): e315-e315. http://dx.doi.org/10.1038/bcj.2015.41.
Texto completoPorter, Christopher C. "Germ line mutations associated with leukemias". Hematology 2016, n.º 1 (2 de diciembre de 2016): 302–8. http://dx.doi.org/10.1182/asheducation-2016.1.302.
Texto completoDifilippo, Emma Catherine, Alejandro Ferrer, Laura Schultz-Rogers, Naseema Gangat, Shakila P. Khan, Aref Al-Kali, Abhishek A. Mangaonkar et al. "Spectrum of Hematological Malignancies in 130 Patients with Germline Predisposition Syndromes - Mayo Clinic Germline Predisposition Study". Blood 136, Supplement 1 (5 de noviembre de 2020): 34–35. http://dx.doi.org/10.1182/blood-2020-139050.
Texto completoIqbal, Zafar, Muhammad Absar, Tanveer Akhtar, Aamer Aleem, Abid Jameel, Sulman Basit, Anhar Ullah et al. "Integrated Genomic Analysis Identifies ANKRD36 Gene as a Novel and Common Biomarker of Disease Progression in Chronic Myeloid Leukemia". Biology 10, n.º 11 (15 de noviembre de 2021): 1182. http://dx.doi.org/10.3390/biology10111182.
Texto completoPecci, A., P. Noris y C. L. Balduini. "Inherited thrombocytopenias". Hämostaseologie 32, n.º 04 (2012): 259–70. http://dx.doi.org/10.5482/ha12050001.
Texto completoChurpek, Jane E. "Inherited Predisposition to Myelodysplastic Syndrome and Acute Leukemia". Blood 124, n.º 21 (6 de diciembre de 2014): SCI—31—SCI—31. http://dx.doi.org/10.1182/blood.v124.21.sci-31.sci-31.
Texto completoStano Kozubik, K., J. Trizuljak, Z. Vrzalova, L. Radova, I. Blahakova, J. Stika, P. Smejkal et al. "P1648: ANALYSIS OF ANKRD26 GENE 5’UTR VARIANTS IN A COHORT OF CZECH PATIENTS WITH SUSPECTED HEREDITARY HEMATOLOGICAL DISORDER". HemaSphere 6 (junio de 2022): 1529–30. http://dx.doi.org/10.1097/01.hs9.0000849448.51581.9a.
Texto completoAverina, M., H. Jensvoll, H. Strand y M. Sovershaev. "A novel ANKRD26 gene variant causing inherited thrombocytopenia in a family of Finnish origin: Another brick in the wall?" Thrombosis Research 151 (marzo de 2017): 41–43. http://dx.doi.org/10.1016/j.thromres.2017.01.001.
Texto completoXu, Xiaofei, Lan Zhang, Shengjie Wang, Keyi Jin, Chen DAN y Jian Huang. "Relapse with BCR-ABL1 Elevation in Chronic Myeloid Leukemia after Progression to Multiple Myeloma from Monoclonal Gammopathy of Undetermined Significance with a Persistent KMT2D Mutation". Blood 138, Supplement 1 (5 de noviembre de 2021): 4608. http://dx.doi.org/10.1182/blood-2021-145904.
Texto completoLouzil, Jan, Jana Stikarova, Dana Provaznikova, Ingrid Hrachovinova, Tereza Fenclova, Jan Musil, Martin Radek et al. "Diagnosing Czech Patients with Inherited Platelet Disorders". International Journal of Molecular Sciences 23, n.º 22 (19 de noviembre de 2022): 14386. http://dx.doi.org/10.3390/ijms232214386.
Texto completoBogomolovas, Julius, Kathrin Brohm, Jelena Čelutkienė, Giedrė Balčiūnaitė, Daiva Bironaitė, Virginija Bukelskienė, Dainius Daunoravičus et al. "Induction of Ankrd1 in Dilated Cardiomyopathy Correlates with the Heart Failure Progression". BioMed Research International 2015 (2015): 1–9. http://dx.doi.org/10.1155/2015/273936.
Texto completoBastida, José María, José Ramón Gonzalez-Porras, José Rivera y María Luisa Lozano. "Role of Thrombopoietin Receptor Agonists in Inherited Thrombocytopenia". International Journal of Molecular Sciences 22, n.º 9 (21 de abril de 2021): 4330. http://dx.doi.org/10.3390/ijms22094330.
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