Добірка наукової літератури з теми "ANKRD11"
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Статті в журналах з теми "ANKRD11"
Zhao, Youshan, Feng Xu, Juan Guo, Sida Zhao, Chunkang Chang, and Xiao Li. "Dysregulation of ANKRD11 Influenced Hematopoisis By Histone Acetylation-Mediated Gene Expression in Myelodysplastic Syndrome." Blood 128, no. 22 (December 2, 2016): 4292. http://dx.doi.org/10.1182/blood.v128.22.4292.4292.
Повний текст джерелаGao, Fenqi, Xiu Zhao, Bingyan Cao, Xin Fan, Xiaoqiao Li, Lele Li, Shengbin Sui, Zhe Su, and Chunxiu Gong. "Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature." Journal of Personalized Medicine 12, no. 3 (March 5, 2022): 407. http://dx.doi.org/10.3390/jpm12030407.
Повний текст джерелаBestetti, Ilaria, Milena Crippa, Alessandra Sironi, Francesca Tumiatti, Maura Masciadri, Marie Falkenberg Smeland, Swati Naik, et al. "Expanding the Molecular Spectrum of ANKRD11 Gene Defects in 33 Patients with a Clinical Presentation of KBG Syndrome." International Journal of Molecular Sciences 23, no. 11 (May 25, 2022): 5912. http://dx.doi.org/10.3390/ijms23115912.
Повний текст джерелаParenti, Ilaria, Mark B. Mallozzi, Irina Hüning, Cristina Gervasini, Alma Kuechler, Emanuele Agolini, Beate Albrecht, et al. "ANKRD11 variants: KBG syndrome and beyond." Clinical Genetics 100, no. 2 (May 14, 2021): 187–200. http://dx.doi.org/10.1111/cge.13977.
Повний текст джерелаKojić, Snežana. "MARP Protein Family: A Possible Role in Molecular Mechanisms of Tumorigenesis." Journal of Medical Biochemistry 29, no. 3 (July 1, 2010): 157–64. http://dx.doi.org/10.2478/v10011-010-0024-9.
Повний текст джерелаNeilsen, P. M., K. M. Cheney, C. W. Li, J. D. Chen, J. E. Cawrse, R. B. Schulz, J. A. Powell, R. Kumar, and D. F. Callen. "Identification of ANKRD11 as a p53 coactivator." Journal of Cell Science 121, no. 21 (October 7, 2008): 3541–52. http://dx.doi.org/10.1242/jcs.026351.
Повний текст джерелаKim, Hyo Jeong, Eunhae Cho, Jong Bum Park, Woo Young Im, and Hyon J. Kim. "A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion." European Journal of Medical Genetics 58, no. 2 (February 2015): 86–94. http://dx.doi.org/10.1016/j.ejmg.2014.11.003.
Повний текст джерелаYoungs, Erin L., Jessica A. Hellings, and Merlin G. Butler. "ANKRD11 gene deletion in a 17-year-old male." Clinical Dysmorphology 20, no. 3 (July 2011): 170–71. http://dx.doi.org/10.1097/mcd.0b013e328346f6ae.
Повний текст джерелаLim, Sue Ping, Nick C. Wong, Rachel J. Suetani, Kristen Ho, Jane Lee Ng, Paul M. Neilsen, Peter G. Gill, Raman Kumar, and David F. Callen. "Specific-site methylation of tumour suppressor ANKRD11 in breast cancer." European Journal of Cancer 48, no. 17 (November 2012): 3300–3309. http://dx.doi.org/10.1016/j.ejca.2012.03.023.
Повний текст джерелаSacharow, Stephanie, Deling Li, Yao Shan Fan, and Mustafa Tekin. "Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome." American Journal of Medical Genetics Part A 158A, no. 3 (February 3, 2012): 547–52. http://dx.doi.org/10.1002/ajmg.a.34436.
Повний текст джерелаДисертації з теми "ANKRD11"
Ackermann, Sarah [Verfasser], and Thomas [Akademischer Betreuer] Meyer. "Mutationsanalyse des ANKRD1-Gens bei Patienten mit dilatativer Kardiomyopathie / Sarah Ackermann. Betreuer: Thomas Meyer." Marburg : Philipps-Universität Marburg, 2012. http://d-nb.info/1021498874/34.
Повний текст джерелаJimenez, Carrera Adriana Patricia [Verfasser]. "Functional characterisation of ANKRD1 and its regulation by RASSF1A and YAP1 signalling / Adriana Patricia Jimenez Carrera." Gießen : Universitätsbibliothek, 2017. http://d-nb.info/1131551214/34.
Повний текст джерелаFütterer, Jane Wong. "Characterisation of a novel protein, ANKRD18A, implicated in a severe form of thrombocytopenia." Thesis, University of Birmingham, 2017. http://etheses.bham.ac.uk//id/eprint/7511/.
Повний текст джерелаDonada, Alessandro. "Physiopathological mechanisms of two congenical platelet disorders : filaminopathy-A and ANKRD26-related - Thrombocytopenia 5THC2." Thesis, Sorbonne Paris Cité, 2018. https://theses.md.univ-paris-diderot.fr/DONADA_Alessandro_2_complete_2018.zip.
Повний текст джерелаInherited thrombocytopenias are a class of congenital haematological disorders affecting primarily the megakaryocytic lineage and accomunated by a decrease in platelet numbers. Almost 50 different genes have been associated to inherited platelet disorders, and huge differences exist between each disorder, in regard to clinical manifestation and pathobiology. My research interest have been focused on two different congenital thrombocytopenias: Filaminopathy A and Thrombocytopenia 2. The first disease is a X-linked syndrome associated to mutations in the gene FLNA (Filamin A), and patients display a mild to severe macrothrombocytopenia, associated with a lifelong bleeding tendency. The second disorder is an automal dominant condition caused by mutations in the 5’ UTR of the ANKRD26 gene. It is associated with dysmegakaryopoiesis, mild to severe thrombocytopenia and an increased risk to develop myeloid malignancies. To study the physiopathology of those two rare diseases, we have exploited the induced pluripotent stem cell technology to develop several patient specific cell lines. Those experimental tools revealed invaluable for the understanding of the disease physiopathology, and allowed us to describe in great details the molecular mechanisms underlying the reduction in proplatelet formation for Filaminopathy A and the predisposition to leukemia for Thrombocytopenia 2. To perform such studies, we devised a robust differentiation protocol, recapitulating efficiently the haematopoietic differentiation and easily adapted to the in vitro differentiation of multiple cell lineages. Furthermore, we exploited a genome editing technique to introduce efficiently different protein mutants, in order to dissect the molecular role of Filamin A in megakaryopoiesis. In regard of Filaminopathy A, we have been able to describe an original and novel relationship between a membrane integrin (IIb3), Filamin A and a crucial signalling pathway (RhoA) for megakaryopoiesis. Our data support a model where the absence of FLNa induces an abnormal activity of the RhoA pathway, in response to the integrin IIb3 binding to fibrinogen. Concerning the thrombocytopenia 2, we described a novel mechanism that associated the increased expression of ANKRD26 to a deregulated activity of the G-CSF-dependent signalling pathway. This anomaly impacts the normal granulopoiesis and lead to an abnormal amplification of this cell lineage, possibly increasing the risk of acquiring other mutational hits and progress towards a myeloid malignancy.In conclusion, with this work we offer a proof of concept of the potentiality of disease modeling via induced pluripotent stem cells. Our results pave the way for further studies that could advance our understanding of the physiopathology of inherited platelet disorders
Roy, Sébastien. "Étude des mécanismes gouvernant le transport intracellulaire et le contrôle de qualité des RCPG." Thèse, Université de Sherbrooke, 2014. http://savoirs.usherbrooke.ca/handle/11143/154.
Повний текст джерелаRostamirad, Shabnam. "Identification and characterization of a novel retinal protein, ANKRD33, and its interacting partner HPCAL-1." Thesis, University of British Columbia, 2010. http://hdl.handle.net/2429/27274.
Повний текст джерелаPapanikos, Frantzeskos [Verfasser], Attila [Gutachter] Tóth, and Konstantinos [Gutachter] Anastasiadis. "The role of two sex chromosome associated proteins, SCML1 and ANKRD31, in gametogenesis in mice / Frantzeskos Papanikos ; Gutachter: Attila Tóth, Konstantinos Anastasiadis." Dresden : Technische Universität Dresden, 2020. http://d-nb.info/1227196539/34.
Повний текст джерелаDuffus, Kate. "Investigation of genetic susceptibility to Rheumatoid Arthritis." Thesis, University of Manchester, 2014. https://www.research.manchester.ac.uk/portal/en/theses/investigation-of-genetic-susceptibility-to-rheumatoid-arthritis(edf01c7b-3c46-4c75-8751-6f117291c027).html.
Повний текст джерелаTachibana, Mitsuhiro. "Ankyrin repeat domain 28 (ANKRD28), a novel binding partner of DOCK180, promotes cell migration by regulating focal adhesion formation." Kyoto University, 2009. http://hdl.handle.net/2433/124284.
Повний текст джерелаLim, Sue Ping. "Epigenetics in cancer : basic and translational aspects." Thesis, 2012. http://hdl.handle.net/2440/86747.
Повний текст джерелаThesis (Ph.D.) -- University of Adelaide, School of Medicine, 2012
Тези доповідей конференцій з теми "ANKRD11"
Boriek, Aladin M., and Junaith S. Mohamed. "Knockdown Of Desmin Protein By SiRNA Up-regulates Ankrd1 Through Akt/NF-kB Signaling Pathway And Turns Ankrd1 Into Mechanosensitive In Human Airway Smooth Muscle Cells." In American Thoracic Society 2010 International Conference, May 14-19, 2010 • New Orleans. American Thoracic Society, 2010. http://dx.doi.org/10.1164/ajrccm-conference.2010.181.1_meetingabstracts.a5316.
Повний текст джерелаLee, Ting-Fang, Yen-Fan Lin, Ying-Pu Liu, and Cheng-Wen Wu. "Abstract 5508: ANKRD52 inhibited tumor metastasis in lung adenocarcinoma." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-5508.
Повний текст джерелаLopez, MA, JS Mohamed, PS Pardo та AM Boriek. "Does the Mechanosensitive NF-κB Regulate ANKRD1 in the Muscular Dystrophy with Myositis (mdm)Diaphragm?." У American Thoracic Society 2009 International Conference, May 15-20, 2009 • San Diego, California. American Thoracic Society, 2009. http://dx.doi.org/10.1164/ajrccm-conference.2009.179.1_meetingabstracts.a6131.
Повний текст джерелаLei, Ying, Beric Ross Henderson, Catherine Emmanuel, Paul Harnett, and Anna de Fazio. "Abstract 4616: Chemo-sensitisation in epithelial ovarian cancer cell lines by targeting Ankyrin Repeat Domain 1 (ANKRD1)." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4616.
Повний текст джерелаLin, Yen-Fan, Ying-Pu Liu, Ting-Fang Lee, and Cheng-Wen Wu. "Abstract 4843: ANKRD52 inhibited tumor metastasis through dephosphorylation of PAK1 in lung adenocarcinoma." In Proceedings: AACR Annual Meeting 2017; April 1-5, 2017; Washington, DC. American Association for Cancer Research, 2017. http://dx.doi.org/10.1158/1538-7445.am2017-4843.
Повний текст джерелаLee, Ting-Fang, Yin-Pu Liu, Yen-Fan Lin, Chong-Fang Hsu, and Cheng-Wen Wu. "Abstract 1782: ANKRD52 inhibited tumor metastasis through dephosphorylation of PAK1 in lung adenocarcinomas." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-1782.
Повний текст джерелаLee, Ting-Fang, Yin-Pu Liu, Yen-Fan Lin, Chong-Fang Hsu, and Cheng-Wen Wu. "Abstract 1782: ANKRD52 inhibited tumor metastasis through dephosphorylation of PAK1 in lung adenocarcinomas." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-1782.
Повний текст джерела"Differentially methylation of ANKRD53 and GATA3 genes in human miscarriages with trisomy 16." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-079.
Повний текст джерелаQian, J., and S. Nan. "307 The pathogenic mechanisms of systemic lupus erythematosus associated genes pnp, plekhf2 and ankrd44." In LUPUS 2017 & ACA 2017, (12th International Congress on SLE &, 7th Asian Congress on Autoimmunity). Lupus Foundation of America, 2017. http://dx.doi.org/10.1136/lupus-2017-000215.307.
Повний текст джерелаSong, Tianyu Y., Haixin Zhao, Hongjie Fan, Min Long, Chenlu Geng, Xiaoxiao Xie, Yang Liu, et al. "Abstract 2154: Immune pressure selects ANKRD52 mutations for cancer cells to escape T cell-mediated killing." In Proceedings: AACR Annual Meeting 2020; April 27-28, 2020 and June 22-24, 2020; Philadelphia, PA. American Association for Cancer Research, 2020. http://dx.doi.org/10.1158/1538-7445.am2020-2154.
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