نتائج البحث - "Andrea, A. J."

1

Rare variants in Fanconi anemia genes are enriched in acute myeloid leukemia

المساهمون: Maung, Kyaw Ze Ya, Leo, Paul J, Bassal, Mahmoud, Casolari, Debora A, Bray, Sarah C, Singhal, Deepak, Samaraweera, Saumya E, Nguyen, Tran, Cildir, Gökhan, Tergaonkar, Vinay, Lewis, Ian, Brown, Anna L, D'Andrea, Richard J, Gonda, Thomas J

المصدر: Blood Cancer Journal, Vol 8, Iss 6, Pp 1-5 (2018)
Blood Cancer Journal

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2185a7cffd743552938423e09196d9b9
http://link.springer.com/article/10.1038/s41408-018-0090-7

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2

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

المؤلفون: Andrew Dubowsky, Jinghua Feng, Amanda Wells, Stefan Fröhling, Meryl Altree, Andreas W. Schreiber, Sue Morgan, Lesley Rawlings, Richard J D'Andrea, Anna L. Brown, Chan-Eng Chong, Joëlle Michaud, Andrew H. Wei, Georges Natsoulis, Jeffrey Suttle, Rachel Susman, Cassandra Vakulin, Tilmann Bochtler, Uday R. Popat, Mark S. Currie, Paul Wang, Milena Babic, Ella J Wilkins, Christopher N. Hahn, Miriam Fine, Xiaochun Li, Jessica Burdett, Belinda Mercorella, Catherine Carmichael, Nigel Patton, Denae Henry, Marshall S. Horwitz, Peer Arts, Kerry Phillips, Julian Cooney, Sarah Moore, Sally Mapp, Nicola K. Poplawski, Thuong Ha, Sarah L King-Smith, Louise Jaensch, Shai Izraeli, Devendra K Hiwase, Julia Dobbins, Lucy A. Godley, Cecily Forsyth, Kenneth F. Bradstock, Carolyn M. Butcher, Helen Mar Fan, Grace McKavanagh, Hugh Y. Rienhoff, Hamish S. Scott, Mario Nicola, Elli Papaemmanuil, Ping Cannon, Ian D. Lewis, Claire C. Homan, Peter J. Brautigan, Alwin Krämer

المساهمون: Brown, Anna L, Arts, Peer, Babic, Milena, Dobbins, Julia, Feng, Jinghua, Ha, Thuong, Homan, Claire C, King-Smith, Sarah L, Li, Xiao-Chun, Brautigan, Peter, Butcher, Carolyn, D'Andrea, Richard J, Hahn, Christopher N, Scott, Hamish S

المصدر: Blood advances. 4(6)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30cc21538186700c18e024f443315b4b
https://pubmed.ncbi.nlm.nih.gov/32208489

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3

Targeting sphingosine kinase 1 induces MCL1-dependent cell death in acute myeloid leukemia

المؤلفون: Saumya E. Samaraweera, Diana Iarossi, Alexander C. Lewis, Ian D. Lewis, Angel F. Lopez, Melissa R. Pitman, Richard J D'Andrea, Andrew H. Wei, Hayley S. Ramshaw, Craig T. Wallington-Beddoe, John Toubia, Stuart M. Pitson, Jason A. Powell, Wenying Zhu, Nik Cummings, Daniel Thomas, Paul A.B. Moretti

المساهمون: Powell, Jason A, Lewis, Alexander C, Zhu, Wenying, Toubia, John, Pitman, Melissa R, Wallington-Beddoe, Craig T, Moretti, Paul AB, Iarossi, Diana, Samaraweera, Saumya E, Cummings, Nik, Ramshaw, Hayley S, Thomas, Daniel, Wei, Andrew H, Lopez, Angel F, D'Andrea, Richard J, Lewis, Ian D, Pitson, Stuart M

المصدر: Blood

مصطلحات موضوعية: 0301 basic medicine, Myeloid, CD34, Biochemistry, myeloid leukemia, Amino Acid Chloromethyl Ketones, Mice, chemistry.chemical_compound, Mice, Inbred NOD, Sphingosine, hemic and lymphatic diseases, Molecular Targeted Therapy, human AML cells, Myeloid Neoplasia, Cell Death, biology, Gene Expression Regulation, Leukemic, Myeloid leukemia, Hematology, Amino Alcohols, Caspase Inhibitors, Leukemia, Myeloid, Acute, Phosphotransferases (Alcohol Group Acceptor), Receptors, Lysosphingolipid, Leukemia, xenografts, medicine.anatomical_structure, Sphingosine kinase 1, Caspases, Neoplastic Stem Cells, Quinolines, Female, Signal Transduction, Immunology, Bone Marrow Cells, SPHK1, 03 medical and health sciences, Cell Line, Tumor, medicine, aspase-dependent cell death, Animals, Humans, Progenitor cell, Protein Kinase Inhibitors, MCL1 degradation, Cell Biology, medicine.disease, Survival Analysis, Xenograft Model Antitumor Assays, Myeloid Cell Leukemia Sequence 1 Protein, 030104 developmental biology, chemistry, Cancer research, biology.protein, Lysophospholipids

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6dac0b862c63e5c5eea38557824efcf
https://doi.org/10.1182/blood-2016-06-720433

4

Genomic subtyping and therapeutic targeting of acute erythroleukemia

المؤلفون: Marcus B. Valentine, L. Bik To, Ian D. Lewis, Stephen P. Hunger, Guangchun Song, Eric J. Enemark, Elliot Stieglitz, Laura J. Janke, Edgar Sioson, Andrew H. Wei, Yongjin Li, Ji Wen, Lei Shi, Catherine Carmichael, Hamish S. Scott, Katherine Masih, Richard J D'Andrea, Rhonda E. Ries, Shirley Kow Yin Kham, Virginia Valentine, Anna L. Brown, R. Coleman Lindsley, Sarah M. Morris, Benjamin L. Ebert, Chunxu Qu, Manja Meggendorfer, Franco Locatelli, Giuseppe Basso, Ilaria Iacobucci, Daisuke Tomizawa, Benjamin T. Kile, John K. Choi, Michael Rusch, Paula Marlton, Thomas B. Alexander, Stanley Pounds, Torsten Haferlach, Allen Eng Juh Yeoh, Nobutaka Kiyokawa, Deqing Pei, Xiaotu Ma, Debbie Payne-Turner, Mignon L. Loh, Charles G. Mullighan, Soheil Meshinchi, Christopher N. Hahn, Cheng Cheng, Xin Zhou

المساهمون: Iacobucci, Ilaria, Wen, Ji, Meggendorfer, Manja, Choi, John K, Lewis, Ian D, D'Andrea, Richard J, Brown, Anna L, Scott, Hamish S, Hahn, Christopher N, Mullighan, Charles G

المصدر: Nature genetics, vol 51, iss 4

مصطلحات موضوعية: Male, Myeloid, Erythroblastic, Medical and Health Sciences, 0302 clinical medicine, hemic and lymphatic diseases, 2.1 Biological and endogenous factors, Aetiology, Child, Cancer, Pediatric, 0303 health sciences, Leukemia, biology, Acute erythroid leukemia, Myeloid leukemia, Nuclear Proteins, Hematology, Genomics, Biological Sciences, Prognosis, KMT2A, medicine.anatomical_structure, Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA, Child, Preschool, Myeloid-Lymphoid Leukemia Protein, Female, acute myeloid-leukemia, Nucleophosmin, Biotechnology, Adult, Pediatric Research Initiative, NPM1, Adolescent, Pediatric Cancer, Childhood Leukemia, erythroleukemia, Acute, Article, 03 medical and health sciences, Young Adult, Rare Diseases, acute erythroid leukemia, acute lymphoblastic-leukemia, world-health-organization, myelodysplastic syndrome, clonal hematopoiesis, crystal-structures, cell-line, gene, mutations, Genetics, medicine, Humans, Preschool, 030304 developmental biology, Homeodomain Proteins, Infant, Newborn, Infant, Newborn, medicine.disease, fms-Like Tyrosine Kinase 3, Fms-Like Tyrosine Kinase 3, Mutation, Cancer research, biology.protein, Leukemia, Erythroblastic, Acute, Tumor Suppressor Protein p53, 030217 neurology & neurosurgery, Developmental Biology

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f0d821e777167627bd37dcd271acd9
https://hdl.handle.net/10807/230059

5

Apparent ‘JAK2 -negative’ polycythaemia vera due to compound mutations in exon 14

المؤلفون: Sarah Moore, Tran Nguyen, Richard J D'Andrea, David M. Ross, Merel J. M. Van Velzen, Christopher N. Hahn, Debora A. Casolari, Ing Soo Tiong, Hamish S. Scott, Daniela Zantomio

المساهمون: Tiong, Ing Soo, Casolari, Debora A, Moore, Sarah, Nguyen, Tran, Van Velzen, Merel JM, Zantomio, Daniela, Scott, Hamish S, D'Andrea, Richard J, Hahn, Christopher N, Ross, David M

المصدر: British Journal of Haematology. 178:333-336

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bcd5374e4d799413489fdcf610bf132
https://doi.org/10.1111/bjh.14126

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6

miR-155 as a potential target of IL-3 signaling in primary AML cells

المؤلفون: Richard J D'Andrea, Michelle Perugini, Hayley S. Ramshaw, Chung H. Kok, Teresa Sadras

المساهمون: Sadras, Teresa, Kok, Chung H, Perugini, Michelle, Ramshaw, Hayley S, D'Andrea, Richard J

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::251df53aef27a2c696067a7f6cf90739
https://hdl.handle.net/11541.2/129746

7

Gaq signaling is required for the maintenance of MLL-AF9-induced acute myeloid leukemia

المؤلفون: Estrella Gonzales-Aloy, Hangyu Yi, Debora A. Casolari, Michelle Haber, Murray D. Norris, Jingyi Wang, Richard J D'Andrea, Florida Voli, Tao Liu, Ivor Lewis, Tsz Kan Fung, Jacqueline Lynch, Chintae So, Amie Brown, Bo Liu

المساهمون: Lynch, Jennifer R, Yi, Hangyu, Casolari, Debora A, Voli, Florida, Gonzales-Aloy, Estrella, Fung, Tsz Kan, Liu, Bing, Brown, Anna L, Liu, Tao, Haber, Michelle, Norris, Murray D, Lewis, Ian D, So, Chi Wai Eric, D'Andrea, Richard J D, Wang, Jenny Yingzi

المصدر: Leukemia. 30(8)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33fa98f211e42043f0b1d61375486c25
https://pubmed.ncbi.nlm.nih.gov/26859074

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8

Novel germ line DDX41 mutations define families with a lower age of MDS/AML onset and lymphoid malignancies

المساهمون: Lewinsohn, Maya, Brown, Anna L, Weinel, Luke M, Phung, Connie, Chong, Chan-Eng, D'Andrea, Richard J, Scott, Hamish S

المصدر: Blood. 127(8)

مصطلحات موضوعية: 0301 basic medicine, Male, Genotype, Immunology, DNA Mutational Analysis, Follicular lymphoma, Fluorescent Antibody Technique, Bioinformatics, medicine.disease_cause, Biochemistry, Germline, DEAD-box RNA Helicases, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, hemic and lymphatic diseases, Medicine, Missense mutation, Humans, Genetic Predisposition to Disease, Age of Onset, Germ-Line Mutation, Aged, Aged, 80 and over, Mutation, business.industry, Myelodysplastic syndromes, Myeloid leukemia, Cell Biology, Hematology, families, Middle Aged, mutations, medicine.disease, germline DDX41 mutations, Pedigree, lymphoid malignancies, Leukemia, Myeloid, Acute, 030104 developmental biology, Phenotype, 030220 oncology & carcinogenesis, Myelodysplastic Syndromes, Cancer research, Female, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df8b3bba2cbe44729865dbfaf9be5183
https://pubmed.ncbi.nlm.nih.gov/26917736

9

Investigation of a Novel Cyclin-Dependent-Kinase (CDK) Inhibitor Cdki-73 As an Effective Treatment Option for MLL-AML

المؤلفون: Muhammed H. Rahaman, Julian Adams, Diana Iarossi, Richard B. Lock, Ben Noll, Jennifer Richmond, Ka Leung Li, Luen Bik To, Ian D. Lewis, Shudong Wang, Sarah C Bray, Longjin Zhong, Richard J D'Andrea

المساهمون: Li, Ka Leung, Bray, Sarah C, Iarossi, Diana, Adams, Julian, Zhong, Longjin, Noll, Ben, Rahaman, Muhammed H, Richmond, Jennifer, To, Luen Bik, Lewis, Ian D, Lock, Richard B, Wang, Shudong, D'Andrea, Richard J

المصدر: Blood. 126:1365-1365

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc9ad016906f35796837dae16eaa2ea3
https://doi.org/10.1182/blood.v126.23.1365.1365

10

Self-reverting mutations partially correct the blood phenotype in a Diamond Blackfan Anemia patient

المؤلفون: Sarah Moore, Ross D. Hannan, Amanda Tirimacco, Christopher Barnett, Amee J George, Ben Saxon, Miriam Fine, Luen Bik To, Chun Chun Young, Christopher N. Hahn, Hamish S. Scott, Jinghua Feng, Richard J D'Andrea, Andreas W. Schreiber, David M. Lawrence, Alexandra L. Yeoman, Sarah C Bray, Parvathy Venugopal

المساهمون: Venugopal, Parvathy, Moore, Sarah, Lawrence, David M, George, Amee J, Hannan, Ross D, Bray, Sarah CE, To, Luen Bik, D'Andrea, Richard J, Feng, Jinghua, Tirimacco, Amanda, Yeoman, Alexandra L, Young, Chun Chun, Fine, Miriam, Schreiber, Andreas W, Hahn, Christopher N, Barnett, Christopher, Saxon, Ben, Scott, Hamish S

المصدر: BASE-Bielefeld Academic Search Engine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1c896a2c9dee486829e48b1c6e8508a
http://hdl.handle.net/2440/110952

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