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Haematologica
|
November 6, 2025
TNF-α signaling drives myeloid skewing and clonal expansion of stem and progenitors in <i>RUNX1</i>-familial platelet disorder
Mona Mohammadhosseini, Aishwarya Sahasrabudhe, Luiza H Ostrowski, et al.
Aesthetic Surgery Journal
|
October 29, 2024
Evaluation of Permanent Nipple-Areolar Complex Sensitivity Loss Following Reduction Mammaplasty
Stephanie Francalancia, Mary Lou, Damon McIntire, et al.
American Journal of Hematology
|
September 12, 2017
Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities
Tao Cai, Xiang Chen, Jinchen Li, et al.
Immunity
|
May 24, 2011
Gain-of-function Pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in mice
Jae Jin Chae, Young-Hun Cho, Geun-Shik Lee, et al.
Blood
|
October 22, 2009
Differential requirement for Gata1 DNA binding and transactivation between primitive and definitive stages of hematopoiesis in zebrafish
Christiane L Belele, Milton A English, Jagman Chahal, et al.
Blood
|
October 12, 2017
<i>Chd7</i> deficiency delays leukemogenesis in mice induced by <i>Cbfb-MYH11</i>
Tao Zhen, Erika M Kwon, Ling Zhao, et al.
British Journal of Haematology
|
May 29, 2025
Pregnancy and delivery outcomes in individuals with RUNX1-Familial Platelet Disorder
Natalie T Deuitch, Lylach Haizler-Cohen, Amra Kajdic, et al.
Plos One
|
April 6, 2012
Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects
Shobi Veleri, Kevin Bishop, Damian E Dalle Nogare, et al.
Plos Pathogens
|
March 22, 2014
Activation of HIV-1 from latent infection via synergy of RUNX1 inhibitor Ro5-3335 and SAHA
Zachary Klase, Venkat S R K Yedavalli, Laurent Houzet, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
November 10, 2009
LC/MS characterization of impurities and degradation products of a potent antitumor peptidic dimer, CU201
Jennie Wang, Vidhya Krishnamoorthi, Euphemia Wang, et al.
Page
of 15
Search research articles
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Showing results (81-90 of 144) with videos related to
Sort By:
Page
of 15
Haematologica
|
November 6, 2025
TNF-α signaling drives myeloid skewing and clonal expansion of stem and progenitors in <i>RUNX1</i>-familial platelet disorder
Mona Mohammadhosseini, Aishwarya Sahasrabudhe, Luiza H Ostrowski, et al.
Aesthetic Surgery Journal
|
October 29, 2024
Evaluation of Permanent Nipple-Areolar Complex Sensitivity Loss Following Reduction Mammaplasty
Stephanie Francalancia, Mary Lou, Damon McIntire, et al.
American Journal of Hematology
|
September 12, 2017
Identification of novel mutations in the HbF repressor gene BCL11A in patients with autism and intelligence disabilities
Tao Cai, Xiang Chen, Jinchen Li, et al.
Immunity
|
May 24, 2011
Gain-of-function Pyrin mutations induce NLRP3 protein-independent interleukin-1β activation and severe autoinflammation in mice
Jae Jin Chae, Young-Hun Cho, Geun-Shik Lee, et al.
Blood
|
October 22, 2009
Differential requirement for Gata1 DNA binding and transactivation between primitive and definitive stages of hematopoiesis in zebrafish
Christiane L Belele, Milton A English, Jagman Chahal, et al.
Blood
|
October 12, 2017
<i>Chd7</i> deficiency delays leukemogenesis in mice induced by <i>Cbfb-MYH11</i>
Tao Zhen, Erika M Kwon, Ling Zhao, et al.
British Journal of Haematology
|
May 29, 2025
Pregnancy and delivery outcomes in individuals with RUNX1-Familial Platelet Disorder
Natalie T Deuitch, Lylach Haizler-Cohen, Amra Kajdic, et al.
Plos One
|
April 6, 2012
Knockdown of Bardet-Biedl syndrome gene BBS9/PTHB1 leads to cilia defects
Shobi Veleri, Kevin Bishop, Damian E Dalle Nogare, et al.
Plos Pathogens
|
March 22, 2014
Activation of HIV-1 from latent infection via synergy of RUNX1 inhibitor Ro5-3335 and SAHA
Zachary Klase, Venkat S R K Yedavalli, Laurent Houzet, et al.
Journal of Pharmaceutical and Biomedical Analysis
|
November 10, 2009
LC/MS characterization of impurities and degradation products of a potent antitumor peptidic dimer, CU201
Jennie Wang, Vidhya Krishnamoorthi, Euphemia Wang, et al.
Page
of 15