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Refinado por: Nome da Publicação: Blood Advances remover
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1
Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations
Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations
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Telomere biology disorder prevalence and phenotypes in adults with familial hematologic and/or pulmonary presentations

Feurstein, Simone ; Adegunsoye, Ayodeji ; Mojsilovic, Danijela ; Vij, Rekha ; West DePersia, Allison H. ; Rajagopal, Padma Sheila ; Osman, Afaf ; Collins, Robert H. ; Kim, Raymond H. ; Gore, Steven D. ; Greenberg, Peter ; Godley, Lucy A. ; Li, Zejuan ; del Gaudio, Daniela ; Subramanian, Hari Prasanna ; Das, Soma ; Walsh, Tom ; Gulsuner, Suleyman ; Segal, Jeremy P. ; Husain, Aliya N. ; Gurbuxani, Sandeep ; King, Mary-Claire ; Strek, Mary E. ; Churpek, Jane E.

Blood advances, 2020-10, Vol.4 (19), p.4873-4886 [Periódico revisado por pares]

United States: Elsevier Inc

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2
TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML
TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML
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TP53 mutation defines a unique subgroup within complex karyotype de novo and therapy-related MDS/AML

Weinberg, Olga K. ; Siddon, Alexa ; Madanat, Yazan F. ; Gagan, Jeffrey ; Arber, Daniel A. ; Dal Cin, Paola ; Narayanan, Damodaran ; Ouseph, Madhu M. ; Kurzer, Jason H. ; Hasserjian, Robert P.

Blood advances, 2022-05, Vol.6 (9), p.2847-2853 [Periódico revisado por pares]

United States: Elsevier Inc

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3
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants
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ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants

Luo, Xi ; Feurstein, Simone ; Mohan, Shruthi ; Porter, Christopher C. ; Jackson, Sarah A. ; Keel, Sioban ; Chicka, Michael ; Brown, Anna L. ; Kesserwan, Chimene ; Agarwal, Anupriya ; Luo, Minjie ; Li, Zejuan ; Ross, Justyne E. ; Baliakas, Panagiotis ; Pineda-Alvarez, Daniel ; DiNardo, Courtney D. ; Bertuch, Alison A. ; Mehta, Nikita ; Vulliamy, Tom ; Wang, Ying ; Nichols, Kim E. ; Malcovati, Luca ; Walsh, Michael F. ; Rawlings, Lesley H. ; McWeeney, Shannon K. ; Soulier, Jean ; Raimbault, Anna ; Routbort, Mark J. ; Zhang, Liying ; Ryan, Gabriella ; Speck, Nancy A. ; Plon, Sharon E. ; Wu, David ; Godley, Lucy A.

Blood advances, 2019-10, Vol.3 (20), p.2962-2979 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Prospective evaluation of prognostic impact of KIT mutations on acute myeloid leukemia with RUNX1-RUNX1T1 and CBFB-MYH11
Prospective evaluation of prognostic impact of KIT mutations on acute myeloid leukemia with RUNX1-RUNX1T1 and CBFB-MYH11
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Prospective evaluation of prognostic impact of KIT mutations on acute myeloid leukemia with RUNX1-RUNX1T1 and CBFB-MYH11

Ishikawa, Yuichi ; Kawashima, Naomi ; Atsuta, Yoshiko ; Sugiura, Isamu ; Sawa, Masashi ; Dobashi, Nobuaki ; Yokoyama, Hisayuki ; Doki, Noriko ; Tomita, Akihiro ; Kiguchi, Toru ; Koh, Shiro ; Kanamori, Heiwa ; Iriyama, Noriyoshi ; Kohno, Akio ; Moriuchi, Yukiyoshi ; Asada, Noboru ; Hirano, Daiki ; Togitani, Kazuto ; Sakura, Toru ; Hagihara, Maki ; Tomikawa, Tatsuki ; Yokoyama, Yasuhisa ; Asou, Norio ; Ohtake, Shigeki ; Matsumura, Itaru ; Miyazaki, Yasushi ; Naoe, Tomoki ; Kiyoi, Hitoshi

Blood advances, 2020-01, Vol.4 (1), p.66-75 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Molecular mechanisms mediating relapse following ivosidenib monotherapy in IDH1-mutant relapsed or refractory AML
Molecular mechanisms mediating relapse following ivosidenib monotherapy in IDH1-mutant relapsed or refractory AML
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Molecular mechanisms mediating relapse following ivosidenib monotherapy in IDH1-mutant relapsed or refractory AML

Choe, Sung ; Wang, Hongfang ; DiNardo, Courtney D. ; Stein, Eytan M. ; de Botton, Stéphane ; Roboz, Gail J. ; Altman, Jessica K. ; Mims, Alice S. ; Watts, Justin M. ; Pollyea, Daniel A. ; Fathi, Amir T. ; Tallman, Martin S. ; Kantarjian, Hagop M. ; Stone, Richard M. ; Quek, Lynn ; Konteatis, Zenon ; Dang, Lenny ; Nicolay, Brandon ; Nejad, Parham ; Liu, Guowen ; Zhang, Vickie ; Liu, Hua ; Goldwasser, Meredith ; Liu, Wei ; Marks, Kevin ; Bowden, Chris ; Biller, Scott A. ; Attar, Eyal C. ; Wu, Bin

Blood advances, 2020-05, Vol.4 (9), p.1894-1905 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Prognostic impact of CEBPA bZIP domain mutation in acute myeloid leukemia
Prognostic impact of CEBPA bZIP domain mutation in acute myeloid leukemia
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Prognostic impact of CEBPA bZIP domain mutation in acute myeloid leukemia

Wakita, Satoshi ; Sakaguchi, Masahiro ; Oh, Iekuni ; Kako, Shinichi ; Toya, Takashi ; Najima, Yuho ; Doki, Noriko ; Kanda, Junya ; Kuroda, Junya ; Mori, Shinichiro ; Satake, Atsushi ; Usuki, Kensuke ; Ueki, Toshimitsu ; Uoshima, Nobuhiko ; Kobayashi, Yutaka ; Kawata, Eri ; Tajika, Kenji ; Nagao, Yuhei ; Shono, Katsuhiro ; Shibusawa, Motoharu ; Tadokoro, Jiro ; Kayamori, Kensuke ; Hagihara, Masao ; Uchiyama, Hitoji ; Uchida, Naoyuki ; Kubota, Yasushi ; Kimura, Shinya ; Nagoshi, Hisao ; Ichinohe, Tatsuo ; Kurosawa, Saiko ; Motomura, Sayuri ; Hashimoto, Akiko ; Muto, Hideharu ; Sato, Eriko ; Ogata, Masao ; Mitsuhashi, Kenjiro ; Ando, Jun ; Marumo, Atsushi ; Omori, Ikuko ; Fujiwara, Yusuke ; Terada, Kazuki ; Yui, Shunsuke ; Arai, Kunihito ; Kitano, Tomoaki ; Miyata, Miho ; Kurosawa, Akiyo ; Mizoguchi, Ayumi ; Komatsu, Norio ; Fukuda, Takahiro ; Ohashi, Kazuteru ; Kanda, Yoshinobu ; Inokuchi, Koiti ; Yamaguchi, Hiroki

Blood advances, 2022-01, Vol.6 (1), p.238-247 [Periódico revisado por pares]

United States: Elsevier Inc

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7
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML
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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML

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

Blood advances, 2020-03, Vol.4 (6), p.1131-1144 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Prognostic and therapeutic impacts of mutant TP53 variant allelic frequency in newly diagnosed acute myeloid leukemia
Prognostic and therapeutic impacts of mutant TP53 variant allelic frequency in newly diagnosed acute myeloid leukemia
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Prognostic and therapeutic impacts of mutant TP53 variant allelic frequency in newly diagnosed acute myeloid leukemia

Short, Nicholas J. ; Montalban-Bravo, Guillermo ; Hwang, Hyunsoo ; Ning, Jing ; Franquiz, Miguel J. ; Kanagal-Shamanna, Rashmi ; Patel, Keyur P. ; DiNardo, Courtney D. ; Ravandi, Farhad ; Garcia-Manero, Guillermo ; Takahashi, Koichi ; Konopleva, Marina ; Daver, Naval ; Issa, Ghayas C. ; Andreeff, Michael ; Kantarjian, Hagop ; Kadia, Tapan M.

Blood advances, 2020-11, Vol.4 (22), p.5681-5689 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Outcomes of older patients with NPM1-mutated AML: current treatments and the promise of venetoclax-based regimens
Outcomes of older patients with NPM1-mutated AML: current treatments and the promise of venetoclax-based regimens
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Outcomes of older patients with NPM1-mutated AML: current treatments and the promise of venetoclax-based regimens

Lachowiez, Curtis A. ; Loghavi, Sanam ; Kadia, Tapan M. ; Daver, Naval ; Borthakur, Gautam ; Pemmaraju, Naveen ; Naqvi, Kiran ; Alvarado, Yesid ; Yilmaz, Musa ; Short, Nicholas ; Ohanian, Maro ; Pierce, Sherry R. ; Patel, Keyur P. ; Qiao, Wei ; Ning, Jing ; Sasaki, Koji ; Takahashi, Koichi ; Jabbour, Elias ; Andreeff, Michael ; Ravandi, Farhad ; Kantarjian, Hagop M. ; Konopleva, Marina ; DiNardo, Courtney D.

Blood advances, 2020-04, Vol.4 (7), p.1311-1320 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma
Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma
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Frequent germline mutations of HAVCR2 in sporadic subcutaneous panniculitis-like T-cell lymphoma

Polprasert, Chantana ; Takeuchi, Yasuhide ; Kakiuchi, Nobuyuki ; Yoshida, Kenichi ; Assanasen, Thamathorn ; Sitthi, Wimonmas ; Bunworasate, Udomsak ; Pirunsarn, Arunrat ; Wudhikarn, Kitsada ; Lawasut, Panisinee ; Uaprasert, Noppacharn ; Kongkiatkamon, Sunisa ; Moonla, Chatphatai ; Sanada, Masashi ; Akita, Nobuhiro ; Takeda, June ; Fujii, Yoichi ; Suzuki, Hiromichi ; Nannya, Yasuhito ; Shiraishi, Yuichi ; Chiba, Kenichi ; Tanaka, Hiroko ; Miyano, Satoru ; Rojnuckarin, Ponlapat ; Ogawa, Seishi ; Makishima, Hideki

Blood advances, 2019-02, Vol.3 (4), p.588-595 [Periódico revisado por pares]

United States: Elsevier Inc

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