Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Diane L, Pickering"'
Autor:
Bhavana J. Dave, Pamela A. Althof, Rachel A. Harris, Diane L. Pickering, Jadd M. Stevens, Jennifer N. Sanmann, Lynette M. Smith
Publikováno v:
Leukemia research. 110
The clinical implications of deletions within chromosome 14q32 in CLL pathogenesis remain unclear. We examined the frequency of 14q32 deletions among CLL cases by karyotype and FISH, categorized the variation using genomic microarray, and assessed th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bda52b5e23bb5dc2c15222cff4ab6fc
https://pubmed.ncbi.nlm.nih.gov/34293710
https://pubmed.ncbi.nlm.nih.gov/34293710
Autor:
John A. Crolla, Justin Paschall, David H. Ledbetter, Morag N. Collinson, Ramaswamy K. Iyer, Vineith Kaul, Erin B. Kaminsky, Arthur R. Brothman, John G. Compton, Amy E. Fuller, Diane L. Pickering, Emily Aston, Todd Ackley, Stephen T. Warren, Erik C. Thorland, Sarah J. Beal, Shashirekha Shetty, Deanna M. Church, M. Katharine Rudd, Brian Bunke, Troy J. Gliem, Andres Moreno-De-Luca, Gabriele Richard, Daniel Moreno-De-Luca, Christa Lese Martin, Warren G. Sanger, Sarah T. South, Dawn Kunig, Heidi Whitby, Jennifer G. Mulle, Shuwen Huang, Swaroop Aradhya, Michael R. Rossi, Denae M. Golden
Publikováno v:
Genetics in Medicine. 13:777-784
Purpose: Copy number variants have emerged as a major cause of human disease such as autism and intellectual disabilities. Because copy number variants are common in normal individuals, determining the functional and clinical significance of rare cop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9599117d4d4b5c9274afa79f0f6715ab
https://doi.org/10.1097/gim.0b013e31822c79f9
https://doi.org/10.1097/gim.0b013e31822c79f9
Autor:
Jadd M. Stevens, Warren G. Sanger, Diane L. Pickering, Ann Haskins Olney, Denae M. Golden, James D. Eudy, Bhavana J. Dave
Publikováno v:
Genetics in Medicine. 10:262-266
Purpose: Cytogenetic investigations are useful for etiologic determinations of mental retardation, developmental delay, multiple congenital anomalies, and pregnancy complications; however, the causes remain elusive in a majority of cases despite high
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca08d30af5f76bf1c37fe9109ca7af2
https://doi.org/10.1097/gim.0b013e31816b64ad
https://doi.org/10.1097/gim.0b013e31816b64ad
Autor:
George E. Wright, Javeed Iqbal, Lisa M. Rimsza, Lynette M. Smith, Diane L. Pickering, Smrati Jain, Julie M. Vose, Jan Delabie, Timothy C. Greiner, Douglas E. Horsman, Dennis D. Weisenburger, C. P. Hans, Elias Campo, Hans Konrad Müller-Hermelink, Bhavana J. Dave, Yulei Shen, Elaine S. Jaffe, Andreas Rosenwald, Timothy W. McKeithan, Kai Fu, German Ott, Joseph M. Connors, Warren G. Sanger, Louis M. Staudt, K. Patel, J. Ji, Randy D. Gascoyne, W. C. Chan
Publikováno v:
Leukemia. 21:2332-2343
Gene expression profiling of diffuse large B-cell lymphoma (DLBCL) has revealed biologically and prognostically distinct subgroups: germinal center B-cell-like (GCB), activated B-cell-like (ABC) and primary mediastinal (PM) DLBCL. The BCL6 gene is of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bda8b555bd3f95ede16cfe6900c7a0
https://doi.org/10.1038/sj.leu.2404856
https://doi.org/10.1038/sj.leu.2404856
Autor:
Kellie Neth, Guimei Zhou, Henry T. Lynch, Brigid Quinn-Laquer, Jane F. Lynch, Diane L. Pickering, Wing C. Chan, Warren G. Sanger, Patricia Aoun, Cynthia Page, Dennis D. Weisenburger, Patrice Watson
Publikováno v:
American Journal of Clinical Pathology. 127:31-38
B-cell chronic lymphocytic leukemia (B-CLL) is a heterogeneous disease that may exhibit familial clustering. We examined the cytogenetic, immunophenotypic, and VH gene usage characteristics of a family with B-CLL affecting 7 members in 3 generations.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abad6e088035e778cfea45dee516895b
https://doi.org/10.1309/pftpll4hck2d1erk
https://doi.org/10.1309/pftpll4hck2d1erk
Autor:
Robert Tanner, Hagelstrom, James, Ford, Gwendolyn M, Reiser, Marilu, Nelson, Diane L, Pickering, Pamela A, Althof, Warren G, Sanger, Peter F, Coccia
Publikováno v:
Pediatric bloodcancer. 63(3)
Male breast cancer (MBC) is unusual, especially in young adults. Most cases of MBC as a secondary malignancy relate to the previous treatment with ionizing radiation. MBC can be associated with mutations in hereditary cancer predisposition syndrome g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2d924c8d35ddd26ca9fdcc4862f0ac3
https://pubmed.ncbi.nlm.nih.gov/26468640
https://pubmed.ncbi.nlm.nih.gov/26468640
Autor:
Mitchell S. Cairo, Eric J. Lowe, David L. Zwick, Diane L. Pickering, Warren G. Sanger, Sherrie L. Perkins, Ginny Davenport, Minnie Abromowitch
Publikováno v:
British Journal of Haematology. 131:624-627
Anaplastic large cell lymphoma (ALCL) comprises 10-15% of childhood non-Hodgkin lymphomas (NHL). Systemic ALCL is highly associated with anaplastic lymphoma kinase (ALK) gene translocations with over-expression of ALK protein. We studied ALK rearrang
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c737c406f70bbd4327f20522c8b2dbb3
https://doi.org/10.1111/j.1365-2141.2005.05808.x
https://doi.org/10.1111/j.1365-2141.2005.05808.x
Autor:
Michelle M. Hess, Christine M. Higgins, Warren G. Sanger, Diane L. Pickering, Wing C. Chan, Dennis D. Weisenburger, Bhavana J. Dave
Publikováno v:
Cancer Genetics and Cytogenetics. 153:115-121
Diffuse large B-cell lymphoma (DLBCL), the most common subtype of adult non-Hodgkin lymphoma (NHL), is infrequently seen in adolescents and is rare in children. Due to the infrequency of the disease, single institution-based cytogenetic and fluoresce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42b416bd8f8a2a52de5d65f2ea51867e
https://doi.org/10.1016/j.cancergencyto.2004.01.008
https://doi.org/10.1016/j.cancergencyto.2004.01.008
Autor:
Diane L. Pickering, Sherrie L. Perkins, Warren G. Sanger, Cheryl M. Coffin, Holly Zhou, Melissa H. Cessna, Sheryl R. Tripp, Clark Daines
Publikováno v:
Modern Pathology. 15:931-938
Abnormalities of chromosome 2p23 with expression of ALK1 and p80 occur in both inflammatory myofibroblastic tumor (IMT) and anaplastic large cell lymphoma. This immunohistochemical study investigates whether the ALK family of neoplasms includes fibro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e715887d4c40782930f9bfdd8744cdfb
https://doi.org/10.1097/01.mp.0000026615.04130.1f
https://doi.org/10.1097/01.mp.0000026615.04130.1f
Autor:
Ronald Levy, Diane L. Pickering, James O. Armitage, Izidore S. Lossos, Timothy C. Greiner, Louis M. Staudt, Dennis D. Weisenburger, Roger A. Warnke, Wing C. Chan, James C. Lynch, James Z. Huang, Ash A. Alizadeh, Warren G. Sanger
Publikováno v:
Blood. 99:2285-2290
Recently we have identified subgroups of de novo primary diffuse large B-cell lymphoma (DLBCL) based on complementary DNA microarray-generated gene expression profiles. To correlate the gene expression profiles with cytogenetic abnormalities in these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15586e4ded536f5f682ee14b251b0930
https://doi.org/10.1182/blood.v99.7.2285
https://doi.org/10.1182/blood.v99.7.2285