Yandell DW - Search Results

1

Brief report: lymphoma of donor origin occurring in the porta hepatis of a transplanted liver.

Spiro IJ, Yandell DW, Li C, Saini S, Ferry J, Powelson J, Katkov WN, Cosimi AB. Spiro IJ, et al. Among authors: yandell dw. N Engl J Med. 1993 Jul 1;329(1):27-9. doi: 10.1056/NEJM199307013290105. N Engl J Med. 1993. PMID: 8505941 Free article. No abstract available.

2

Elevated frequency of microsatellite mutations in TK6 human lymphoblast clones selected for mutations at the thymidine kinase locus.

Li CY, Yandell DW, Little JB. Li CY, et al. Among authors: yandell dw. Mol Cell Biol. 1994 Jul;14(7):4373-9. doi: 10.1128/mcb.14.7.4373-4379.1994. Mol Cell Biol. 1994. PMID: 8007946 Free PMC article.

3

Molecular mechanisms of spontaneous and induced loss of heterozygosity in human cells in vitro.

Li CY, Yandell DW, Little JB. Li CY, et al. Among authors: yandell dw. Somat Cell Mol Genet. 1992 Jan;18(1):77-87. doi: 10.1007/BF01233450. Somat Cell Mol Genet. 1992. PMID: 1546370

4

[Hypervariable regions (HVR) as genetic markers in tumor diagnosis. Methodological principles and their use in pathologic diagnosis].

Poremba C, Yandell DW, Spiro IJ, Heidl G, Böcker W, Dockhorn-Dworniczak B. Poremba C, et al. Among authors: yandell dw. Pathologe. 1994 Apr;15(2):113-8. doi: 10.1007/s002920050033. Pathologe. 1994. PMID: 8197067 German.

5

Evidence for coincident mutations in human lymphoblast clones selected for functional loss of a thymidine kinase gene.

Li CY, Yandell DW, Little JB. Li CY, et al. Among authors: yandell dw. Mol Carcinog. 1992;5(4):270-7. doi: 10.1002/mc.2940050407. Mol Carcinog. 1992. PMID: 1497803

6

Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene.

Wiggs J, Nordenskjöld M, Yandell D, Rapaport J, Grondin V, Janson M, Werelius B, Petersen R, Craft A, Riedel K, et al. Wiggs J, et al. N Engl J Med. 1988 Jan 21;318(3):151-7. doi: 10.1056/NEJM198801213180305. N Engl J Med. 1988. PMID: 2892131

7

Immature teratomas of different origin carried by a pregnant mother and her fetus.

Poremba C, Dockhorn-Dworniczak B, Merritt V, Li CY, Heidl G, Tauber PF, Böcker W, Yandell DW. Poremba C, et al. Among authors: yandell dw. Diagn Mol Pathol. 1993 Jun;2(2):131-6. Diagn Mol Pathol. 1993. PMID: 8269278

8

Oncogenic point mutations in the human retinoblastoma gene: their application to genetic counseling.

Yandell DW, Campbell TA, Dayton SH, Petersen R, Walton D, Little JB, McConkie-Rosell A, Buckley EG, Dryja TP. Yandell DW, et al. N Engl J Med. 1989 Dec 21;321(25):1689-95. doi: 10.1056/NEJM198912213212501. N Engl J Med. 1989. PMID: 2594029

9

Two prostate carcinoma cell lines demonstrate abnormalities in tumor suppressor genes.

Rubin SJ, Hallahan DE, Ashman CR, Brachman DG, Beckett MA, Virudachalam S, Yandell DW, Weichselbaum RR. Rubin SJ, et al. Among authors: yandell dw. J Surg Oncol. 1991 Jan;46(1):31-6. doi: 10.1002/jso.2930460108. J Surg Oncol. 1991. PMID: 1986144

10

Chromosome 17p deletions and p53 gene mutations associated with the formation of malignant neurofibrosarcomas in von Recklinghausen neurofibromatosis.

Menon AG, Anderson KM, Riccardi VM, Chung RY, Whaley JM, Yandell DW, Farmer GE, Freiman RN, Lee JK, Li FP, et al. Menon AG, et al. Among authors: yandell dw. Proc Natl Acad Sci U S A. 1990 Jul;87(14):5435-9. doi: 10.1073/pnas.87.14.5435. Proc Natl Acad Sci U S A. 1990. PMID: 2142531 Free PMC article.

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