Zobrazeno 1 - 10 of 13 pro vyhledávání: '"K C, Halling"'
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CLIN-PATHOLOGY
Autor: D. Alexandru, R. Satyadev, W. So, S. H. Lee, Y. S. Lee, Y.-K. Hong, C. S. Kang, S. D. Rodgers, B. J. Marascalchi, R. G. Strom, H. Riina, U. Samadani, A. Frempong-Boadu, R. Babu, C. Sen, D. Zagzag, M. D. Anderson, T. W. Abel, P. L. Moots, Y. Odia, B. A. Orr, C. G. Eberhart, F. Rodriguez, R. T. Sweis, J. Lavingia, J. Connelly, E. Cochran, M. van den Bent, C. Hartmann, M. Preusser, T. Strobel, H. J. Dubbink, J. M. Kros, A. von Deimling, B. Boisselier, M. Sanson, K. C. Halling, K. L. Diefes, K. Aldape, C. Giannini, F. J. Rodriguez, A. H. Ligon, I. Horkayne-Szakaly, E. J. Rushing, K. L. Ligon, N. Vena, D. I. Garcia, J. Douglas Cameron, A. Raghunathan, K. Wani, T. S. Armstrong, E. Vera-Bolanos, M. Fouladi, A. Gajjar, S. Goldman, N. L. Lehman, P. Metellus, T. Mikkelsen, M. J. T. Necesito-Reyes, A. Omuro, R. J. Packer, S. Partap, I. F. Pollack, M. D. Prados, H. Ian Robbins, R. Soffietti, J. Wu, M. R. Gilbert, K. D. Aldape, M. Prosniak, L. A. Harshyne, D. W. Andrews, D. Craig Hooper, N. Kagawa, N. Hosen, N. Kijima, R. Hirayama, Y. Chiba, F. Yamamoto, M. Kinoshita, N. Hashimoto, Y. Fujimoto, T. Yoshimine, J. Hu, M. Nuno, C. Patil, J. Rudnick, S. Phuphanich, S. Bannykh, R. Chu, J. Yu, K. Black, J. Choi, D. Kim, K. W. Shim, S. H. Kim, H. Kanno, H. Nishihara, S. Tanaka, T. Yanagi, P. Buczkowicz, D.-A. Khuong-Quang, P. Rakopoulos, E. Bouffet, A. Morrison, U. Bartels, S. M. Pfister, N. Jabado, C. Hawkins, B. D. Weinberg, K. L. Newell, P. Kumar, F. Wang, S. Venneti, M. Madden, T. Coyne, J. Phillips, D. Gorovets, J. Huse, J. Kofler, C. Lu, T. Tihan, L. Sullivan, M. Santi, A. Judkins, C. Thompson, A. Perry, J. B. Iorgulescu, I. Laufer, M. Hameed, E. Lis, P. Boland, R. Komotar, M. Bilsky, A. C. Amato-Watkins, J. Neal, A. D. Rees, J. S. Davies, C. Hayhurst, C. Lu-Emerson, M. Snuderl, C. Davidson, N. D. Kirkpatrick, Y. Huang, D. G. Duda, M. Ancukiewicz, A. Stemmer-Rachamimov, T. T. Batchelor, R. K. Jain, B. Ellezam, B. J. Theeler, Z. S. Sadighi, V. Mehta, M.-D. T. Tran, A. M. Adesina, V. K. Puduvalli, J. M. Bruner
Publikováno v: Neuro-Oncology. 14:vi106-vi111
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69b537326c459c7679e9153e0e97fc1a
https://doi.org/10.1093/neuonc/nos233
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2
Microsatellite instability testing
Autor: Y R, Parc, K C, Halling
Publikováno v: Methods in molecular medicine. 50
Microsatellites are tandem repeats of simple sequences that occur abundantly and are randomly interspersed throughout the human genome. They typically consist of 10-50 copies of 1-6 bp motifs, and are characterized by a high degree of polymorphism. D
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e85530bb5f9b170292dc11af45de938b
https://pubmed.ncbi.nlm.nih.gov/21318817
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3
Immunohistochemical Analysis for hMLH1 and hMSH2 Expression in Colorectal Cancer
Autor: K C, Halling, P C, Roche
Publikováno v: Methods in molecular medicine. 50
Defective DNA mismatch repair (MMR) occurs in the majority of tumors from patients with hereditary non-polyposis colorectal cancer (HNPCC) and approx 15% of sporadic colorectal cancer (CRC) (1,2). In HNPCC-associated tumors, defective MMR is most oft
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::058610903f1544f7f341173da289ddd2
https://pubmed.ncbi.nlm.nih.gov/21318818
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4
DNA mismatch repair genes hMLH1, hMSH2, and hMSH6 are not inactivated in bronchioloalveolar carcinomas of the lung
Autor: M C, Aubry, K C, Halling, J L, Myers, H D, Tazelaar, P, Yang, S N, Thibodeau
Publikováno v: Cancer. 92(11)
Defective DNA mismatch repair (MMR) appears to be rare in nonsmall cell carcinomas of the lung. Defective DNA MMR results from genetic or epigenetic alterations that inactivate the DNA MMR genes hMLH1 or hMSH2, and rarely hMSH6. The loss of normal DN
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f9d4d32414e3f6242a3b1b7ac30e9d1d
https://pubmed.ncbi.nlm.nih.gov/11753964
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5
A comparison of cytology and fluorescence in situ hybridization for the detection of urothelial carcinoma
Autor: K C, Halling, W, King, I A, Sokolova, R G, Meyer, H M, Burkhardt, A C, Halling, J C, Cheville, T J, Sebo, S, Ramakumar, C S, Stewart, S, Pankratz, D J, O'Kane, S A, Seelig, M M, Lieber, R B, Jenkins
Publikováno v: The Journal of urology. 164(5)
We determine the relative sensitivities of cytology and fluorescence in situ hybridization (FISH) for the detection of urothelial carcinoma.A mixture of fluorescent labeled probes to the centromeres of chromosomes 3, 7 and 17, and band 9p21 (P16/CDKN
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6a8a1f37ebd12e46e892323c5a0707c3
https://pubmed.ncbi.nlm.nih.gov/11025767
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6
HMSH6 alterations in patients with microsatellite instability-low colorectal cancer
Autor: Y R, Parc, K C, Halling, L, Wang, E R, Christensen, J M, Cunningham, A J, French, L J, Burgart, T L, Price-Troska, P C, Roche, S N, Thibodeau
Publikováno v: Cancer research. 60(8)
Two microsatellite instability (MSI) phenotypes have been described in colorectal cancer (CRC): MSI-H (instability at30% of the loci examined) and MSI-L (MSI at 1-30% of the loci examined). The MSI-H phenotype, observed in both hereditary nonpolyposi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f0a1137c4d244fa0592ab54ab3a97250
https://pubmed.ncbi.nlm.nih.gov/10786688
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7
Microsatellite instability and hMLH1/hMSH2 expression in young endometrial carcinoma patients: associations with family history and histopathology
Autor: Y R, Parc, K C, Halling, L J, Burgart, S K, McDonnell, D J, Schaid, S N, Thibodeau, A C, Halling
Publikováno v: International journal of cancer. 86(1)
Endometrial cancer is the second most common malignancy in patients with hereditary nonpolyposis colorectal cancer (HNPCC). The age at diagnosis of HNPCC-associated endometrial cancer is approximately 15 years younger than for sporadic endometrial ca
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fca0f5a883858e5a9c7b2f8665b1eeb5
https://pubmed.ncbi.nlm.nih.gov/10728595
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8
Hereditary desmoid disease in a family with a germline Alu I repeat mutation of the APC gene
Autor: K C, Halling, C R, Lazzaro, R, Honchel, J A, Bufill, S M, Powell, C A, Arndt, N M, Lindor
Publikováno v: Human heredity. 49(2)
Two families with autosomal dominantly inherited desmoid tumors have recently been shown to have germline mutations at the 3' end of the APC gene. We subsequently identified an Amish family with autosomal dominantly inherited desmoid tumors. Genetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8d6b0bc2113e0af3684e57fd6605ccd8
https://pubmed.ncbi.nlm.nih.gov/10077730
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10
Altered expression of hMSH2 and hMLH1 in tumors with microsatellite instability and genetic alterations in mismatch repair genes
Autor: S N, Thibodeau, A J, French, P C, Roche, J M, Cunningham, D J, Tester, N M, Lindor, G, Moslein, S M, Baker, R M, Liskay, L J, Burgart, R, Honchel, K C, Halling
Publikováno v: Cancer research. 56(21)
To date, at least four genes involved in DNA mismatch repair (MMR) have been demonstrated to be altered in the germline of patients with hereditary nonpolyposis colon cancer: hMSH2, hMLH1, hPMS1, and hPMS2. Additionally, loss of MMR function has been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ec7243cafef5a0efcc04e6138319f7aa
https://pubmed.ncbi.nlm.nih.gov/8895729
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