Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Natalia Gonzalez Paz"'
Autor:
Arif H. Kamal, Sumithra J. Mandrekar, Natalia Gonzalez-Paz, Patricia T. Greipp, Eric W. Schaefer, Philip R. Greipp, Prashant Kapoor, Shaji Kumar
Publikováno v:
Mayo Clinic Proceedings. 85:905-912
OBJECTIVE To determine clinical features, natural history, and outcome of a well-defined cohort of 25 consecutive patients with idiopathic systemic capillary leak syndrome (SCLS) evaluated at a tertiary care center. PATIENTS AND METHODS Records of pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4cd9549ee3736cf172c39c0cae62944
https://doi.org/10.4065/mcp.2010.0159
https://doi.org/10.4065/mcp.2010.0159
Autor:
Ruifang Xu, C. Aguilera, Syed M. Jalal, J.M. Hernández-Rivas, Enrique M. Ocio, Angela Dispenzieri, Morie A. Gertz, Roelandt F.J. Schop, P R Greipp, Norma C. Gutiérrez, Moro Mj, Martha Q. Lacy, R. García-Sanz, B. Gonzalez, S Van Wier, J M Hernández, R Fonseca, Natalia Gonzalez-Paz, J F San Miguel
Publikováno v:
British Journal of Haematology. 136:80-86
Fluorescence in situ hybridisation (FISH) is an effective technique for the cytogenetic analysis of Waldenstrom macroglobulinemia (WM), but the potential impact of molecular cytogenetics on disease evolution and as a prognostic marker is still unknow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b44e67c329c08aaac81df8af092035a
https://doi.org/10.1111/j.1365-2141.2006.06389.x
https://doi.org/10.1111/j.1365-2141.2006.06389.x
Autor:
Morie A. Gertz, Natalia Gonzalez Paz, Roshini S. Abraham, Angela Dispenzieri, Tammy Price-Troska, Diane E. Grill, Rafael Fonseca, Karla V. Ballman, Michelle K. Manske
Publikováno v:
Blood. 105:794-803
Immunoglobulin light chain amyloidosis (AL) is characterized by a clonal expansion of plasma cells within the bone marrow. Gene expression analysis was used to identify a unique molecular profile for AL using enriched plasma cells (CD138+) from the b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d3a0ef111c27882a51e79c0ef79507
https://doi.org/10.1182/blood-2004-04-1424
https://doi.org/10.1182/blood-2004-04-1424
Autor:
Doris N. Savoy, Natalia Gonzalez-Paz, Rafael Fonseca, Ellen A. Weiss, Martin E. Fernandez-Zapico, Daniel D. Billadeau, Raul Urrutia, Suresh T. Chari, Julian R. Molina, Thomas C. Smyrk
Publikováno v:
Cancer Cell. 7(1):39-49
Herein, we show that the hematopoietic-specific GEF VAV1 is ectopically expressed in primary pancreatic adenocarcinomas due to demethylation of the gene promoter. Interestingly, VAV1-positive tumors had a worse survival rate compared to VAV1-negative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::007db466b6ed103b02d48ff4ae5f6a40
The recurrent IgH translocations are highly associated with nonhyperdiploid variant multiple myeloma
Autor:
Morie A. Gertz, Martin M. Oken, Jerry M. Winkler, Gordon W. Dewald, Rafael Fonseca, Robert A. Kyle, Emily A. Blood, Natalia Gonzalez-Paz, Carina S. Debes-Marun, Philip R. Greipp, Martha Q. Lacy, Sandra C. Bryant, Angela Dispenzieri, Rafael Santana-Davila, Elisa B. Picken
Publikováno v:
Blood. 102:2562-2567
Aneuploid is ubiquitous in multiple myeloma (MM), and 4 cytogenetic subcategories are recognized: hypodiploid (associated with a shorter survival), pseudodiploid, hyperdiploid, and near-tetraploid MM. The hypodiploid, pseudodiploid, and near-tetraplo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::908a16f129a332ea6a8edba5773f0e02
https://doi.org/10.1182/blood-2003-02-0493
https://doi.org/10.1182/blood-2003-02-0493
Autor:
B Van Ness, Kim Henderson, Tammy Price-Troska, Wee Joo Chng, R Fonseca, Natalia Gonzalez-Paz, S Van Wier, Susanna Jacobus, S V Rajkumar, Patricia T. Greipp, Emily A. Blood, Martin M. Oken
Publikováno v:
Leukemia. 21:582-584
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f28c7f6bcdb016f15d33fa55ccb10020
https://doi.org/10.1038/sj.leu.2404524
https://doi.org/10.1038/sj.leu.2404524
Autor:
Natalia Gonzalez-Paz, Marta Chesi, Tae-Hoon Chung, George Mulligan, Siok Bian Ng, T Troska-Price, Wee Joo Chng, P L Bergsagel, Gaofeng Huang, R Fonseca
Publikováno v:
Leukemia
Events mediating transformation from the pre-malignant monoclonal gammopathy of undetermined significance (MGUS) to multiple myeloma (MM) are unknown. We analyzed a gene expression datasets generated on the Affymetrix U133 platform from 22 MGUS and 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9330a612caa566e2e9fd1bac4b0e3944
https://pubmed.ncbi.nlm.nih.gov/21468039
https://pubmed.ncbi.nlm.nih.gov/21468039
Autor:
Patricia T. Greipp, Kim Henderson, Susanna Jacobus, Wee Joo Chng, B Van Ness, R Fonseca, Natalia Gonzalez-Paz, Robert A. Kyle, Tammy Price-Troska, S Van Wier, S V Rajkumar, Martin M. Oken
Primary genetic abnormalities in myeloma (MM) such as trisomies of chromosomes 3, 5, 7, 9, 11, 15, 19 and 21 associated with hyperdiploid MM and translocations involving the immunoglobulin heavy chain (IgH) locus on chromosome 14q32 and three main re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d90e8f362488794436d9e21ebd40e519
https://europepmc.org/articles/PMC3864109/
https://europepmc.org/articles/PMC3864109/
Autor:
Rebecca F. McClure, Martha Q. Lacy, Morie A. Gertz, Wee Joo Chng, Paul J. Kurtin, Emily A. Blood, Kimberly J. Henderson, Angela Dispenzieri, Rafael Fonseca, C. David James, Martin M. Oken, Gregory J. Ahmann, Natalia Gonzalez-Paz, Philip R. Greipp, Brian G Van Ness
Publikováno v:
Blood. 109(3)
The biological and clinical implications of p16 gene methylation in multiple myeloma (MM) are still unclear despite previous studies. In this comprehensive study, using methylation-specific PCR (MS-PCR), we show that p16 methylation is relatively com
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64667f60c9ea41a6f9c23cc2b827fccd
https://pubmed.ncbi.nlm.nih.gov/17244692
https://pubmed.ncbi.nlm.nih.gov/17244692
Autor:
Angela Dispenzieri, Robert A. Kyle, Rafael Santana-Davila, Elisa B. Picken, Sandra C. Bryant, S V Rajkumar, C S Debes-Marun, Natalia Gonzalez-Paz, Martha Q. Lacy, T. E. Witzig, Jerry M. Winkler, John A. Lust, Rafael Fonseca, Morie A. Gertz, P R Greipp, Gordon W. Dewald
Publikováno v:
Leukemia. 17(2)
The nonrandom recurrent nature of chromosome abnormalities in myeloma suggests a role for them in disease pathogenesis. We performed a careful cytogenetic analysis of patients with abnormal karyotypes (n = 254), to discern patterns of association, se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eac79d75a07d48fd0798bd7ee7963389
https://pubmed.ncbi.nlm.nih.gov/14712294
https://pubmed.ncbi.nlm.nih.gov/14712294