White PS - Search Results

1

Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification.

Fong CT, Dracopoli NC, White PS, Merrill PT, Griffith RC, Housman DE, Brodeur GM. Fong CT, et al. Among authors: white ps. Proc Natl Acad Sci U S A. 1989 May;86(10):3753-7. doi: 10.1073/pnas.86.10.3753. Proc Natl Acad Sci U S A. 1989. PMID: 2566996 Free PMC article.

2

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.

Moley JF, Brother MB, Fong CT, White PS, Baylin SB, Nelkin B, Wells SA, Brodeur GM. Moley JF, et al. Among authors: white ps. Cancer Res. 1992 Feb 15;52(4):770-4. Cancer Res. 1992. PMID: 1346584

3

Loss of heterozygosity for chromosomes 1 or 14 defines subsets of advanced neuroblastomas.

Fong CT, White PS, Peterson K, Sapienza C, Cavenee WK, Kern SE, Vogelstein B, Cantor AB, Look AT, Brodeur GM. Fong CT, et al. Among authors: white ps. Cancer Res. 1992 Apr 1;52(7):1780-5. Cancer Res. 1992. PMID: 1551108

4

Use of the single-strand conformation polymorphism technique to detect loss of heterozygosity in neuroblastoma.

White PS, Kaufman BA, Marshall HN, Brodeur GM. White PS, et al. Genes Chromosomes Cancer. 1993 Jun;7(2):102-8. doi: 10.1002/gcc.2870070207. Genes Chromosomes Cancer. 1993. PMID: 7687451

5

A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3.

White PS, Maris JM, Beltinger C, Sulman E, Marshall HN, Fujimori M, Kaufman BA, Biegel JA, Allen C, Hilliard C, Valentine MB, Look AT, Enomoto H, Sakiyama S, Brodeur GM. White PS, et al. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5520-4. doi: 10.1073/pnas.92.12.5520. Proc Natl Acad Sci U S A. 1995. PMID: 7777541 Free PMC article.

6

Linkage mapping of the tumor necrosis factor receptor 2 (TNFR2) gene to 1p36.2 using the single-strand conformation polymorphism technique.

Kaufman BA, White PS, Steinbrueck T, Donis-Keller H, Brodeur GM. Kaufman BA, et al. Among authors: white ps. Hum Genet. 1994 Oct;94(4):418-22. doi: 10.1007/BF00201604. Hum Genet. 1994. PMID: 7927340

7

Characterization of the region of consistent deletion within 1p36 in neuroblastomas.

White PS, Fujimori M, Marshall HN, Kaufman BA, Brodeur GM. White PS, et al. Prog Clin Biol Res. 1994;385:3-9. Prog Clin Biol Res. 1994. PMID: 7972224 No abstract available.

8

A complex single strand conformational polymorphism (SSCP) in the tumor necrosis factor receptor 2 (TNFR2) gene on chromosome 1p36.2.

Kaufman BA, White PS, Brodeur G. Kaufman BA, et al. Among authors: white ps. Hum Mol Genet. 1993 Jun;2(6):824. doi: 10.1093/hmg/2.6.824-a. Hum Mol Genet. 1993. PMID: 8394764 No abstract available.

9

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: white ps. J Clin Oncol. 2000 May;18(9):1888-99. doi: 10.1200/JCO.2000.18.9.1888. J Clin Oncol. 2000. PMID: 10784629

10

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. Among authors: white ps. 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

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