Zobrazeno 1 - 10
of 25
pro vyhledávání: '"V. V. Murty"'
Autor:
V. V. Murty, Vijay K. Garg
Publikováno v:
ICDCS
We study the problem of determining which message ordering specifications can be implemented in a distributed system. Further, if a specafication can be implemented, we give a technique to determine whether it can be implemented by tagging informatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49a53746186a3439466afc852d5bf617
https://doi.org/10.1109/icdcs.1997.603392
https://doi.org/10.1109/icdcs.1997.603392
Autor:
A, Chatterjee, H A, Pulido, S, Koul, N, Beleño, A, Perilla, H, Posso, M, Manusukhani, V V, Murty
Publikováno v:
Cancer research. 61(5)
Allelic deletions on the short arm of chromosome 6 (6p) are one of the common, possibly early, genetic changes that occur in the pathogenesis of cervical carcinoma (CC). Previous loss of heterozygosity (LOH) studies in CC identified a number of criti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf86859ab3706bc007899219c6bba1e8
https://pubmed.ncbi.nlm.nih.gov/11280775
https://pubmed.ncbi.nlm.nih.gov/11280775
Publikováno v:
Cancer genetics and cytogenetics. 123(2)
Combined cytogenetic, chromosome painting, and spectral karyotyping (SKY) analyses in a case of hepatoblastoma revealed a karyotype of 49,XY,+Y,+der(2)t(2;3)(q35;q25),der(3)t(1;3)(q12; q25),+20. Trisomy 1q, 2, and 20 identified in the present case ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::08990cb731372011c2bc7e23497d8a62
https://pubmed.ncbi.nlm.nih.gov/11150606
https://pubmed.ncbi.nlm.nih.gov/11150606
Autor:
H A, Pulido, M J, Fakruddin, A, Chatterjee, E D, Esplin, N, Beleño, G, Martinez, H, Posso, G A, Evans, V V, Murty
Publikováno v:
Cancer research. 60(23)
Previous functional and deletion mapping studies on cervical cancer (CC) have implicated one or more tumor suppressor genes (TSGs) on chromosome 11 at q13 and q22-24 regions. Of these, the 11q22-24 region exhibits frequent allelic deletions in a vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::810e762951a150fa817d69c63fd35e52
https://pubmed.ncbi.nlm.nih.gov/11118052
https://pubmed.ncbi.nlm.nih.gov/11118052
Autor:
S, Bala, H, Oliver, B, Renault, K, Montgomery, S, Dutta, P, Rao, J, Houldsworth, R, Kucherlapati, X, Wang, R S, Chaganti, V V, Murty
Publikováno v:
Genes, chromosomescancer. 28(3)
Cytogenetic and molecular analyses have shown that the chromosome band 12q22 is recurrently deleted in male germ cell tumors (GCTs), indicating the presence of a candidate tumor suppressor gene (TSG) in this region. To identify the TSG, we mapped the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c9c75b953535806a1d4aee008c9c6c3
https://pubmed.ncbi.nlm.nih.gov/10862031
https://pubmed.ncbi.nlm.nih.gov/10862031
Autor:
S P, Schantz, Q, Huang, K, Shah, V V, Murty, T C, Hsu, G, Yu, P E, Andersen, A G, Huvos, R S, Chaganti
Publikováno v:
Carcinogenesis. 21(6)
The interaction between environmental exposures and host susceptibility may lead to specific mutational events within head and neck squamous cell carcinoma (HNSCC). Furthermore, this interplay may determine not only the probability of cancer developm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f2ec7c6e83bf70065db5fb41baa033f7
https://pubmed.ncbi.nlm.nih.gov/10837016
https://pubmed.ncbi.nlm.nih.gov/10837016
Publikováno v:
Cancer genetics and cytogenetics. 111(1)
A patient with BCR/ABL negative myeloproliferative syndrome with a 46,XY,del(3)(q21), t(4;15)(p16;q24) karyotype is described. Fluorescence in situ hybridization performed with chromosomes 4 and 15 painting probes confirmed a novel reciprocal (4;15)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e5a60938c19fc59669a405ce97e01fd1
https://pubmed.ncbi.nlm.nih.gov/10326585
https://pubmed.ncbi.nlm.nih.gov/10326585
Autor:
V V, Murty, R S, Chaganti
Publikováno v:
Seminars in oncology. 25(2)
Adult human male germ cell tumors (GCTs) arise by transformation of germ cells (GCs). The transformed GCs exhibit pluripotentiality to differentiate into embryonic, extra-embryonic, and somatic tissue types, and are highly sensitive to cisplatin-base
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::31a06e2f4d65ff1cc7bcc58fa2d7df68
https://pubmed.ncbi.nlm.nih.gov/9562446
https://pubmed.ncbi.nlm.nih.gov/9562446
Publikováno v:
Oncogene. 12(12)
Cytogenetic and loss of heterozygosity (LOH) studies of chromosome 5 in male germ cell tumors (GCTs) previously reported suggested the presence of one or more tumor suppressor genes (TSGs) on this chromosome which may play a role in the development o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c481e336b3aed7a8bdbb210700810297
https://pubmed.ncbi.nlm.nih.gov/8700532
https://pubmed.ncbi.nlm.nih.gov/8700532
Publikováno v:
Blood. 86(8)
The t(11;14)(q13;q32) translocation, which juxtaposes the BCL1 oncogene with the Ig heavy chain locus, has been associated with an uncommon subtype of non-Hodgkin's lymphoma (NHL) termed mantle cell lymphoma (MCL). To date, no molecular marker that s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::774086415f905ff1525ab3428d5d2184
https://pubmed.ncbi.nlm.nih.gov/7579380
https://pubmed.ncbi.nlm.nih.gov/7579380