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Showing results (1001-1010 of 1,115) with videos related to
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British Journal of Haematology
|
November 23, 2017
The absolute percent deviation of IGHV mutation rather than a 98% cut-off predicts survival of chronic lymphocytic leukaemia patients treated with fludarabine, cyclophosphamide and rituximab
Preetesh Jain, Graciela M Nogueras González, Rashmi Kanagal-Shamanna, et al.
Human Genetics
|
December 15, 2010
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans
Ken Sin Lo, James G Wilson, Leslie A Lange, et al.
Journal of Lipid Research
|
July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration
Matthew B Lanktree, Clara C Elbers, Yun Li, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
August 3, 2020
Risk of pre-eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case-control study
K J Gray, V P Kovacheva, H Mirzakhani, et al.
Oncogene
|
August 11, 2010
Transcriptional upregulation of histone deacetylase 2 promotes Myc-induced oncogenic effects
G M Marshall, S Gherardi, N Xu, et al.
Blood
|
August 10, 2007
A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemia
Gabrielle S Sellick, Lynn R Goldin, Ruth W Wild, et al.
Haematologica
|
November 10, 2018
The involvement of microRNA in the pathogenesis of Richter syndrome
Katrien Van Roosbroeck, Recep Bayraktar, Steliana Calin, et al.
JCI Insight
|
February 1, 2017
Leukemia cell proliferation and death in chronic lymphocytic leukemia patients on therapy with the BTK inhibitor ibrutinib
Jan A Burger, Kelvin W Li, Michael J Keating, et al.
Human Molecular Genetics
|
January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia
Minal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Blood
|
December 12, 2018
Randomized trial of ibrutinib vs ibrutinib plus rituximab in patients with chronic lymphocytic leukemia
Jan A Burger, Mariela Sivina, Nitin Jain, et al.
Page
of 112
Search research articles
Search
Showing results (1001-1010 of 1,115) with videos related to
Sort By:
Page
of 112
British Journal of Haematology
|
November 23, 2017
The absolute percent deviation of IGHV mutation rather than a 98% cut-off predicts survival of chronic lymphocytic leukaemia patients treated with fludarabine, cyclophosphamide and rituximab
Preetesh Jain, Graciela M Nogueras González, Rashmi Kanagal-Shamanna, et al.
Human Genetics
|
December 15, 2010
Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans
Ken Sin Lo, James G Wilson, Leslie A Lange, et al.
Journal of Lipid Research
|
July 23, 2015
Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration
Matthew B Lanktree, Clara C Elbers, Yun Li, et al.
BJOG : an International Journal of Obstetrics and Gynaecology
|
August 3, 2020
Risk of pre-eclampsia in patients with a maternal genetic predisposition to common medical conditions: a case-control study
K J Gray, V P Kovacheva, H Mirzakhani, et al.
Oncogene
|
August 11, 2010
Transcriptional upregulation of histone deacetylase 2 promotes Myc-induced oncogenic effects
G M Marshall, S Gherardi, N Xu, et al.
Blood
|
August 10, 2007
A high-density SNP genome-wide linkage search of 206 families identifies susceptibility loci for chronic lymphocytic leukemia
Gabrielle S Sellick, Lynn R Goldin, Ruth W Wild, et al.
Haematologica
|
November 10, 2018
The involvement of microRNA in the pathogenesis of Richter syndrome
Katrien Van Roosbroeck, Recep Bayraktar, Steliana Calin, et al.
JCI Insight
|
February 1, 2017
Leukemia cell proliferation and death in chronic lymphocytic leukemia patients on therapy with the BTK inhibitor ibrutinib
Jan A Burger, Kelvin W Li, Michael J Keating, et al.
Human Molecular Genetics
|
January 4, 2015
Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia
Minal J Menezes, Yiran Guo, Jianguo Zhang, et al.
Blood
|
December 12, 2018
Randomized trial of ibrutinib vs ibrutinib plus rituximab in patients with chronic lymphocytic leukemia
Jan A Burger, Mariela Sivina, Nitin Jain, et al.
Page
of 112