Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mary E. Neilly"'
Publikováno v:
Leukemialymphoma. 5(5-6)
We have identified a family in which three members developed B-cell lymphoproliferative disorders within a nine month period. The 33 year old proband and his mother have hairy cell leukemia, and his 37 year old brother developed a large cell lymphoma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c738c299855d499cbc1afd6a23beb6f
https://pubmed.ncbi.nlm.nih.gov/27463340
https://pubmed.ncbi.nlm.nih.gov/27463340
Autor:
Yanming Zhang, Elizabeth M. Davis, Janet D. Rowley, Brigitte Schlegelberger, Heidrun D. Gerr, Michele L. Nassin, Mary E. Neilly, Nimanthi Jayathilaka
Publikováno v:
Cancer Genetics and Cytogenetics. 176:131-136
The PRDX4 gene located at Xp22 codes for a member of the peroxiredoxin gene family. Genes within this family exhibit thioredoxin-dependent peroxidase activity and have been implicated in cellular functioning, including proliferation and differentiati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56835fc7924438a083963a3afadb8e3a
https://doi.org/10.1016/j.cancergencyto.2007.03.010
https://doi.org/10.1016/j.cancergencyto.2007.03.010
Autor:
Rui Su, Pumin Zhang, Xi Jiang, Zhixiang Zuo, Sandeep Gurbuxani, Lichuan Tang, Huilin Huang, Xi Qin, Hengyou Weng, Shenglai Li, Chenying Li, Ping Chen, Chuan He, Mary E. Neilly, Hao Huang, Xiao Wang, Zejuan Li, Richard A. Larson, Jie Jin, Jennifer Strong, Gia-Ming Hong, Xiaocheng Weng, Yungui Wang, Jianjun Chen, Yuanyuan Li, Chao Hu, Stephen Arnovitz
Publikováno v:
Blood. 128:2706-2706
Introduction N 6-methyladenosine (m6A) is the most abundant internal modification in messenger RNA (mRNA) mainly occurring at consensus motif of G[G>A]m6AC[U>A>C]. Despite the functional importance of m6A modification in various fundamental bioproces
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b859defde53500dff5ad5a1fe96e911
https://doi.org/10.1182/blood.v128.22.2706.2706
https://doi.org/10.1182/blood.v128.22.2706.2706
Autor:
Xi Jiang, Hao Huang, Hengyou Weng, Yuanyuan Li, Jinhua Wang, Zejuan Li, Mary E. Neilly, Shenglai Li, Stephen Arnovitz, Ping Chen, Yungui Wang, Jianjun Chen
Publikováno v:
Blood. 124:1011-1011
Approximately 10% of human acute leukemias are involved in chromosomal translocations between the mixed lineage leukemia (MLL) gene and over 50 partner genes. MLL-rearranged leukemias occur preferentially in infant and young children and are often as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dae6945cb2bf92e55523cfd0512f559
https://doi.org/10.1182/blood.v124.21.1011.1011
https://doi.org/10.1182/blood.v124.21.1011.1011
Autor:
Zejuan Li, Jiwang Zhang, Tobias Herold, Zhixiang Zuo, Hengyou Weng, Michelle M. Le Beau, Mary E. Neilly, Ping Chen, Justin Salat, Bryan Ulrich, Yuanyuan Li, Yang Yang, Sandeep Gurbuxani, Hao Huang, Stefan K. Bohlander, Richard A. Larson, Chao Hu, Xi Jiang, Stephen Arnovitz, Shenglai Li, Jason Bugno, Jie Jin, Yungui Wang, Seungpyo Hong, Jianjun Chen
Publikováno v:
Blood. 124:886-886
Acute myeloid leukemia (AML) is one of the most common and fatal forms of hematopoietic malignancies with diverse chromosomal and molecular abnormalities. The majority of AML patients do not survive more than 5 years. Advanced genomic studies reveal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df5c11fa1a81b04b0fb41e4ce55b5306
https://doi.org/10.1182/blood.v124.21.886.886
https://doi.org/10.1182/blood.v124.21.886.886
Autor:
Shantel, Corbin, Mary E, Neilly, Rafael, Espinosa, Elizabeth M, Davis, Timothy W, McKeithan, Michelle M, Le Beau
Publikováno v:
Cancer research. 62(12)
The FRA3B, at 3p14.2, lies within the fragile histidine triad (FHIT) gene and is the most highly expressed of the common fragile sites observed when DNA replication is perturbed by aphidicolin. Common fragile sites are highly unstable regions of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f32a2c6a974c2de8c6e9e1d16a170a88
https://pubmed.ncbi.nlm.nih.gov/12067991
https://pubmed.ncbi.nlm.nih.gov/12067991
Autor:
Rafael Espinosa, Michelle M. Le Beau, Thomas W. Glover, Feyruz V. Rassool, David I. Smith, Mary E. Neilly, Timothy W. McKeithan
Publikováno v:
Human molecular genetics. 7(4)
The FRA3B at 3p14.2 is the most highly expressed of the common fragile sites observed when DNA replication is perturbed by aphidicolin or folate stress. The molecular basis for chromosome fragility at FRA3B is unknown. In contrast to the rare fragile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0a48cf1f5f83b6807936e4d626678cf
https://pubmed.ncbi.nlm.nih.gov/9499431
https://pubmed.ncbi.nlm.nih.gov/9499431
Autor:
Timothy W. McKeithan, Feyruz V. Rassool, Mei-Ling Shen, Mary E. Neilly, Ferenc Boldog, Robert M. McCarroll, Rafael Espinosa, S. Tiong Ong, Harry A. Drabkin, Michelle M. Le Beau
Publikováno v:
Genomics. 35(1)
Despite several lines of evidence suggesting that common chromosomal fragile sites are biologically important as hot spots for recombination, their structure remains unknown. We showed previously that the plasmid pSV2neo preferentially integrates int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c875eee6fdf2f7c5449eda926c2e7551
https://pubmed.ncbi.nlm.nih.gov/8661111
https://pubmed.ncbi.nlm.nih.gov/8661111
Autor:
Timothy W. McKeithan, Feyruz V. Rassool, R. Espinosa, Mary E. Neilly, M M Le Beau, E van Melle
Fragile sites are specific regions of chromosomes that are prone to breakage. In cells cultured under conditions that induce fragile site expression, high levels of inter- and intrachromosomal recombination have been observed involving chromosomal ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::818ece8beff3608646fb18768e959d82
https://europepmc.org/articles/PMC52147/
https://europepmc.org/articles/PMC52147/
Publikováno v:
Europe PubMed Central
Comparative gene mapping analysis in mammals suggests that the major histocompatibility complex (MHC) genes map syntenic with genes, such as glyoxylase 1 (GLO1). In man, the MHC locus and other genes of this syntenic group map to chromosome band 6p21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb06a28d98a1326fd14b25ffb5d6ff97
https://doi.org/10.1159/000134064
https://doi.org/10.1159/000134064