Search research articles
Contact Us
Filters
Showing results (11-20 of 24) with videos related to
Page
of 3
Sort By:
Translational Behavioral Medicine
|
February 1, 2018
Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, et al.
Aging Cell
|
September 19, 2007
Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome
Hong-Yan Du, Rachel Idol, Sara Robledo, et al.
Cancer Research
|
December 12, 2019
Rare <i>BRIP1</i> Missense Alleles Confer Risk for Ovarian and Breast Cancer
Cassandra L Moyer, Jennifer Ivanovich, Jessica L Gillespie, et al.
Human Mutation
|
June 28, 2016
MonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch Repair
Christopher J Walker, Mario A Miranda, Matthew J O'Hern, et al.
Blood
|
October 22, 2008
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements
Hong-Yan Du, Elena Pumbo, Jennifer Ivanovich, et al.
Science (New York, N.Y.)
|
June 27, 2009
DICER1 mutations in familial pleuropulmonary blastoma
D Ashley Hill, Jennifer Ivanovich, John R Priest, et al.
Cancer Medicine
|
December 22, 2015
Lymphovascular space invasion and lack of downstaging after neoadjuvant chemotherapy are strong predictors of adverse outcome in young women with locally advanced breast cancer
Shariq S Khwaja, Jennifer Ivanovich, Todd A DeWees, et al.
American Journal of Human Genetics
|
July 5, 2003
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway
Xiao-Ping Zhou, Kristin A Waite, Robert Pilarski, et al.
F1000Research
|
May 17, 2018
Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / <i>DICER1</i> syndrome: a unique variant of the two-hit tumor suppression model
Mark Brenneman, Amanda Field, Jiandong Yang, et al.
JAMA
|
April 21, 2011
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML
Daniel C Link, Laura G Schuettpelz, Dong Shen, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Translational Behavioral Medicine
|
February 1, 2018
Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, et al.
Aging Cell
|
September 19, 2007
Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome
Hong-Yan Du, Rachel Idol, Sara Robledo, et al.
Cancer Research
|
December 12, 2019
Rare <i>BRIP1</i> Missense Alleles Confer Risk for Ovarian and Breast Cancer
Cassandra L Moyer, Jennifer Ivanovich, Jessica L Gillespie, et al.
Human Mutation
|
June 28, 2016
MonoSeq Variant Caller Reveals Novel Mononucleotide Run Indel Mutations in Tumors with Defective DNA Mismatch Repair
Christopher J Walker, Mario A Miranda, Matthew J O'Hern, et al.
Blood
|
October 22, 2008
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements
Hong-Yan Du, Elena Pumbo, Jennifer Ivanovich, et al.
Science (New York, N.Y.)
|
June 27, 2009
DICER1 mutations in familial pleuropulmonary blastoma
D Ashley Hill, Jennifer Ivanovich, John R Priest, et al.
Cancer Medicine
|
December 22, 2015
Lymphovascular space invasion and lack of downstaging after neoadjuvant chemotherapy are strong predictors of adverse outcome in young women with locally advanced breast cancer
Shariq S Khwaja, Jennifer Ivanovich, Todd A DeWees, et al.
American Journal of Human Genetics
|
July 5, 2003
Germline PTEN promoter mutations and deletions in Cowden/Bannayan-Riley-Ruvalcaba syndrome result in aberrant PTEN protein and dysregulation of the phosphoinositol-3-kinase/Akt pathway
Xiao-Ping Zhou, Kristin A Waite, Robert Pilarski, et al.
F1000Research
|
May 17, 2018
Temporal order of RNase IIIb and loss-of-function mutations during development determines phenotype in pleuropulmonary blastoma / <i>DICER1</i> syndrome: a unique variant of the two-hit tumor suppression model
Mark Brenneman, Amanda Field, Jiandong Yang, et al.
JAMA
|
April 21, 2011
Identification of a novel TP53 cancer susceptibility mutation through whole-genome sequencing of a patient with therapy-related AML
Daniel C Link, Laura G Schuettpelz, Dong Shen, et al.
Page
of 3