Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Patricia T Greipp

Showing results (71-80 of 124) with videos related to

Pageof 13
Sort By:
Cancer Genetics|January 7, 2020
Secondary acquisition of BCR-ABL1 fusion in de novo GATA2-MECOM positive acute myeloid leukemia with subsequent emergence of a rare KMT2A-ASXL2 fusionPatrick R Blackburn, Li Huang, Andrew Dalovisio, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 22, 2017
Gastroblastoma harbors a recurrent somatic MALAT1-GLI1 fusion geneRondell P Graham, Asha A Nair, Jaime I Davila, et al.
Journal of Neuroendocrinology|February 13, 2025
Alternative lengthening of telomeres and Ki-67 proliferation index provide complementary information on recurrence risk after resection of pancreatic neuroendocrine tumorsHallbera Gudmundsdottir, Rondell P Graham, Patricia T Greipp, et al.
Leukemia & Lymphoma|October 3, 2018
Elderly acute lymphoblastic leukemia: a Mayo Clinic study of 124 patientsKevin C Miller, Aref Al-Kali, Mithun V Shah, et al.
Transplantation and Cellular Therapy|April 8, 2021
Impact of Novel Targeted Therapies and Cytogenetic Risk Groups on Outcome After Allogeneic Transplantation for Adult ALLZaid H Abdel Rahman, Michael G Heckman, Kevin Miller, et al.
American Journal of Clinical Pathology|June 6, 2018
Defining Lymphoplasmacytic Lymphoma: Does MYD88L265P Define a Pathologically Distinct Entity Among Patients With an IgM Paraprotein and Bone Marrow-Based Low-Grade B-Cell Lymphomas With Plasmacytic Differentiation?Hong Fang, Prashant Kapoor, Wilson I Gonsalves, et al.
Genes, Chromosomes & Cancer|May 31, 2022
Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studiesMarie-France Gagnon, Holly E Berg, Reid G Meyer, et al.
Cold Spring Harbor Molecular Case Studies|April 3, 2019
Detection of a cryptic <i>NUP214/ABL1</i> gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
Cancer Genetics|November 1, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasmsRashmi Kanagal-Shamanna, Jennelle C Hodge, Tracy Tucker, et al.
Genes, Chromosomes & Cancer|March 21, 2020
Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemiaPatrick R Blackburn, James B Smadbeck, Iya Znoyko, et al.
Pageof 13

Showing results (71-80 of 124) with videos related to

Sort By:
Pageof 13
Cancer Genetics|January 7, 2020
Secondary acquisition of BCR-ABL1 fusion in de novo GATA2-MECOM positive acute myeloid leukemia with subsequent emergence of a rare KMT2A-ASXL2 fusionPatrick R Blackburn, Li Huang, Andrew Dalovisio, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|July 22, 2017
Gastroblastoma harbors a recurrent somatic MALAT1-GLI1 fusion geneRondell P Graham, Asha A Nair, Jaime I Davila, et al.
Journal of Neuroendocrinology|February 13, 2025
Alternative lengthening of telomeres and Ki-67 proliferation index provide complementary information on recurrence risk after resection of pancreatic neuroendocrine tumorsHallbera Gudmundsdottir, Rondell P Graham, Patricia T Greipp, et al.
Leukemia & Lymphoma|October 3, 2018
Elderly acute lymphoblastic leukemia: a Mayo Clinic study of 124 patientsKevin C Miller, Aref Al-Kali, Mithun V Shah, et al.
Transplantation and Cellular Therapy|April 8, 2021
Impact of Novel Targeted Therapies and Cytogenetic Risk Groups on Outcome After Allogeneic Transplantation for Adult ALLZaid H Abdel Rahman, Michael G Heckman, Kevin Miller, et al.
American Journal of Clinical Pathology|June 6, 2018
Defining Lymphoplasmacytic Lymphoma: Does MYD88L265P Define a Pathologically Distinct Entity Among Patients With an IgM Paraprotein and Bone Marrow-Based Low-Grade B-Cell Lymphomas With Plasmacytic Differentiation?Hong Fang, Prashant Kapoor, Wilson I Gonsalves, et al.
Genes, Chromosomes & Cancer|May 31, 2022
Typical, atypical and cryptic t(15;17)(q24;q21) (PML::RARA) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual-color dual-fusion FISH studiesMarie-France Gagnon, Holly E Berg, Reid G Meyer, et al.
Cold Spring Harbor Molecular Case Studies|April 3, 2019
Detection of a cryptic <i>NUP214/ABL1</i> gene fusion by mate-pair sequencing (MPseq) in a newly diagnosed case of pediatric T-lymphoblastic leukemiaJess F Peterson, Beth A Pitel, Stephanie A Smoley, et al.
Cancer Genetics|November 1, 2018
Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasmsRashmi Kanagal-Shamanna, Jennelle C Hodge, Tracy Tucker, et al.
Genes, Chromosomes & Cancer|March 21, 2020
Cryptic and atypical KMT2A-USP2 and KMT2A-USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemiaPatrick R Blackburn, James B Smadbeck, Iya Znoyko, et al.
Pageof 13