Guo C - Search Results

1

Deletion of 11q23 is a frequent event in the evolution of MYCN single-copy high-risk neuroblastomas.

Guo C, White PS, Hogarty MD, Brodeur GM, Gerbing R, Stram DO, Maris JM. Guo C, et al. Med Pediatr Oncol. 2000 Dec;35(6):544-6. doi: 10.1002/1096-911x(20001201)35:6<544::aid-mpo10>3.0.co;2-2. Med Pediatr Oncol. 2000. PMID: 11107113

2

No evidence for the presence of an imprinted neuroblastoma suppressor gene within chromosome sub-band 1p36.3.

Hogarty MD, Winter CL, Liu X, Guo C, White PS, Look AT, Brodeur GM, Maris JM. Hogarty MD, et al. Among authors: guo c. Cancer Res. 2002 Nov 15;62(22):6481-4. Cancer Res. 2002. PMID: 12438240

3

ID2 expression is not associated with MYCN amplification or expression in human neuroblastomas.

Wang Q, Hii G, Shusterman S, Mosse Y, Winter CL, Guo C, Zhao H, Rappaport E, Hogarty MD, Maris JM. Wang Q, et al. Among authors: guo c. Cancer Res. 2003 Apr 1;63(7):1631-5. Cancer Res. 2003. PMID: 12670915

4

Allelic deletion at 11q23 is common in MYCN single copy neuroblastomas.

Guo C, White PS, Weiss MJ, Hogarty MD, Thompson PM, Stram DO, Gerbing R, Matthay KK, Seeger RC, Brodeur GM, Maris JM. Guo C, et al. Oncogene. 1999 Sep 2;18(35):4948-57. doi: 10.1038/sj.onc.1202887. Oncogene. 1999. PMID: 10490829

5

Loss of heterozygosity at 1p36 independently predicts for disease progression but not decreased overall survival probability in neuroblastoma patients: a Children's Cancer Group study.

Maris JM, Weiss MJ, Guo C, Gerbing RB, Stram DO, White PS, Hogarty MD, Sulman EP, Thompson PM, Lukens JN, Matthay KK, Seeger RC, Brodeur GM. Maris JM, et al. Among authors: guo c. J Clin Oncol. 2000 May;18(9):1888-99. doi: 10.1200/JCO.2000.18.9.1888. J Clin Oncol. 2000. PMID: 10784629

6

Identification of a 1-megabase consensus region of deletion at 1p36.3 in primary neuroblastomas.

Hogarty MD, Liu X, Guo C, Thompson PM, Weiss MJ, White PS, Sulman EP, Brodeur GM, Maris JM. Hogarty MD, et al. Among authors: guo c. Med Pediatr Oncol. 2000 Dec;35(6):512-5. doi: 10.1002/1096-911x(20001201)35:6<512::aid-mpo2>3.0.co;2-d. Med Pediatr Oncol. 2000. PMID: 11107105

7

Localization of a hereditary neuroblastoma predisposition gene to 16p12-p13.

Weiss MJ, Guo C, Shusterman S, Hii G, Mirensky TL, White PS, Hogarty MD, Rebbeck TR, Teare D, Urbanek M, Brodeur GM, Maris JM. Weiss MJ, et al. Among authors: guo c. Med Pediatr Oncol. 2000 Dec;35(6):526-30. doi: 10.1002/1096-911x(20001201)35:6<526::aid-mpo5>3.0.co;2-s. Med Pediatr Oncol. 2000. PMID: 11107108

8

Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma.

Maris JM, Guo C, White PS, Hogarty MD, Thompson PM, Stram DO, Gerbing R, Matthay KK, Seeger RC, Brodeur GM. Maris JM, et al. Among authors: guo c. Med Pediatr Oncol. 2001 Jan;36(1):24-7. doi: 10.1002/1096-911X(20010101)36:1<24::AID-MPO1007>3.0.CO;2-7. Med Pediatr Oncol. 2001. PMID: 11464895

9

Loss of heterozygosity for chromosome 14q in neuroblastoma.

Thompson PM, Seifried BA, Kyemba SK, Jensen SJ, Guo C, Maris JM, Brodeur GM, Stram DO, Seeger RC, Gerbing R, Matthay KK, Matise TC, White PS. Thompson PM, et al. Among authors: guo c. Med Pediatr Oncol. 2001 Jan;36(1):28-31. doi: 10.1002/1096-911X(20010101)36:1<28::AID-MPO1008>3.0.CO;2-0. Med Pediatr Oncol. 2001. PMID: 11464899

10

Comprehensive analysis of chromosome 1p deletions in neuroblastoma.

Maris JM, Guo C, Blake D, White PS, Hogarty MD, Thompson PM, Rajalingam V, Gerbing R, Stram DO, Matthay KK, Seeger RC, Brodeur GM. Maris JM, et al. Among authors: guo c. Med Pediatr Oncol. 2001 Jan;36(1):32-6. doi: 10.1002/1096-911X(20010101)36:1<32::AID-MPO1009>3.0.CO;2-0. Med Pediatr Oncol. 2001. PMID: 11464900

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