Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Hemalatha Kuppusamy"'
Autor:
Jitra Kriangkum, Sarah N Motz, Tanner Mack, Sara Beiggi, Eva Baigorri, Hemalatha Kuppusamy, Andrew R Belch, James B Johnston, Linda M Pilarski
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137232 (2015)
The immunoglobulin heavy chain (IGH) gene rearrangement in chronic lymphocytic leukemia (CLL) provides a unique molecular signature; however, we demonstrate that 26/198 CLL patients (13%) had more than one IGH rearrangement, indicating the power of m
Externí odkaz:
https://doaj.org/article/7f4617d9519e44029a8c3809cf2e4678
Autor:
Hemalatha Kuppusamy, Helga M Ogmundsdottir, Eva Baigorri, Amanda Warkentin, Hlif Steingrimsdottir, Vilhelmina Haraldsdottir, Michael J Mant, John Mackey, James B Johnston, Sophia Adamia, Andrew R Belch, Linda M Pilarski
Publikováno v:
PLoS ONE, Vol 9, Iss 6, p e100691 (2014)
Genetic variations in the hyaluronan synthase 1 gene (HAS1) influence HAS1 aberrant splicing. HAS1 is aberrantly spliced in malignant cells from multiple myeloma (MM) and Waldenstrom macroglobulinemia (WM), but not in their counterparts from healthy
Externí odkaz:
https://doaj.org/article/3b3843e51fba436ebe244549f552ce0a
Publikováno v:
Journal of Biological Chemistry. 284:18840-18850
Most human genes undergo alternative splicing, but aberrant splice forms are hallmarks of many cancers, usually resulting from mutations initiating abnormal exon skipping, intron retention, or the introduction of a new splice sites. We have identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9791a57af0a6ba2a23bc9efdb021a3ad
https://doi.org/10.1074/jbc.m109.013813
https://doi.org/10.1074/jbc.m109.013813
Autor:
Sara Beiggi, James B. Johnston, Tanner Mack, Linda M. Pilarski, Jitra Kriangkum, Hemalatha Kuppusamy, Sarah N. Motz, Eva Baigorri, Andrew Belch
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137232 (2015)
PLoS ONE
PLoS ONE
The immunoglobulin heavy chain (IGH) gene rearrangement in chronic lymphocytic leukemia (CLL) provides a unique molecular signature; however, we demonstrate that 26/198 CLL patients (13%) had more than one IGH rearrangement, indicating the power of m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2efd782c166dd246b878343b81024ec
http://europepmc.org/articles/PMC4564241?pdf=render
http://europepmc.org/articles/PMC4564241?pdf=render
Autor:
Andrew Belch, Hlif Steingrimsdottir, James B. Johnston, John R. Mackey, Linda M. Pilarski, Sophia Adamia, Eva Baigorri, Michael J. Mant, Vilhelmína Haraldsdóttir, Helga M. Ögmundsdóttir, Hemalatha Kuppusamy, Amanda Warkentin
Publikováno v:
PLoS ONE
PLoS ONE, Vol 9, Iss 6, p e100691 (2014)
PLoS ONE, Vol 9, Iss 6, p e100691 (2014)
Genetic variations in the hyaluronan synthase 1 gene (HAS1) influence HAS1 aberrant splicing. HAS1 is aberrantly spliced in malignant cells from multiple myeloma (MM) and Waldenstrom macroglobulinemia (WM), but not in their counterparts from healthy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff456921fb1b07db33d4d24c58c158b6
http://europepmc.org/articles/PMC4065063
http://europepmc.org/articles/PMC4065063
Publikováno v:
The Journal of biological chemistry. 284(28)
Most human genes undergo alternative splicing, but aberrant splice forms are hallmarks of many cancers, usually resulting from mutations initiating abnormal exon skipping, intron retention, or the introduction of a new splice sites. We have identifie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a8f53300ec957e96aa2c029b0dd1db70
https://pubmed.ncbi.nlm.nih.gov/19451652
https://pubmed.ncbi.nlm.nih.gov/19451652
Autor:
Steven P. Treon, Michael J. Mant, Tony Reiman, Jitra Kriangkum, Jennifer Hodges, Hemalatha Kuppusamy, Sophia Adamia, Linda M. Pilarski, Patrick M. Pilarski, Andrew R. Belch, Anirban Ghosh, Amanda A. Reichert
Publikováno v:
Blood. 112(13)
To characterize genetic contributions toward aberrant splicing of the hyaluronan synthase 1 (HAS1) gene in multiple myeloma (MM) and Waldenstrom macroglobulinemia (WM), we sequenced 3616 bp in HAS1 exons and introns involved in aberrant splicing, fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84a8ab29b3e68330e8e72747a2b58b7
https://pubmed.ncbi.nlm.nih.gov/18815290
https://pubmed.ncbi.nlm.nih.gov/18815290
Autor:
Jitra Kriangkum, James B. Johnston, Hemalatha Kuppusamy, Andrew Belch, Spencer B. Gibson, Vilhelmina Haraldsdottir, Sunita Ghosh, Hlif Steingrimsdottir, Amanda Warkentin, Helga M. Ögmundsdóttir, Linda M. Pilarski
Publikováno v:
Blood. 118:3930-3930
Abstract 3930 Risk associations with genetic changes, especially SNPs, can be most meaningfully interpreted when the functional relevance of the involved gene(s) is known. Further, using targeted sequencing to detect SNPs provides for unequivocal all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e41f4c5a859cf89179eb3d36a429309
https://doi.org/10.1182/blood.v118.21.3930.3930
https://doi.org/10.1182/blood.v118.21.3930.3930
Publikováno v:
Blood. 114:2841-2841
Abstract 2841 Poster Board II-817 Introduction: Monoclonal gammopathy of undetermined significance (MGUS) is the most common plasma cell disorder. A small proportion of MGUS transform to multiple myeloma (MM) or other B lineage malignancies. Hyaluron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cae5d83be9fac664790a72d5c4f28b4f
https://doi.org/10.1182/blood.v114.22.2841.2841
https://doi.org/10.1182/blood.v114.22.2841.2841
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