Neilly ME - Search Results

1

Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors.

Corbin S, Neilly ME, Espinosa R 3rd, Davis EM, McKeithan TW, Le Beau MM. Corbin S, et al. Among authors: neilly me. Cancer Res. 2002 Jun 15;62(12):3477-84. Cancer Res. 2002. PMID: 12067991

2

Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA.

Rassool FV, Le Beau MM, Neilly ME, van Melle E, Espinosa R 3rd, McKeithan TW. Rassool FV, et al. Among authors: neilly me. Am J Hum Genet. 1992 Jun;50(6):1243-51. Am J Hum Genet. 1992. PMID: 1317992 Free PMC article.

3

Preferential integration of marker DNA into the chromosomal fragile site at 3p14: an approach to cloning fragile sites.

Rassool FV, McKeithan TW, Neilly ME, van Melle E, Espinosa R 3rd, Le Beau MM. Rassool FV, et al. Among authors: neilly me. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6657-61. doi: 10.1073/pnas.88.15.6657. Proc Natl Acad Sci U S A. 1991. PMID: 1862089 Free PMC article.

4

Direct cloning of DNA sequences from the common fragile site region at chromosome band 3p14.2.

Rassool FV, Le Beau MM, Shen ML, Neilly ME, Espinosa R 3rd, Ong ST, Boldog F, Drabkin H, McCarroll R, McKeithan TW. Rassool FV, et al. Among authors: neilly me. Genomics. 1996 Jul 1;35(1):109-17. doi: 10.1006/geno.1996.0329. Genomics. 1996. PMID: 8661111

5

Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction.

Le Beau MM, Rassool FV, Neilly ME, Espinosa R 3rd, Glover TW, Smith DI, McKeithan TW. Le Beau MM, et al. Among authors: neilly me. Hum Mol Genet. 1998 Apr;7(4):755-61. doi: 10.1093/hmg/7.4.755. Hum Mol Genet. 1998. PMID: 9499431

6

Localization of the Chinese hamster MHC locus to chromosome 1q17-->q18 by fluorescence in situ hybridization.

Rassool FV, Neilly ME, McGuire KL, McKeithan TW, Le Beau MM. Rassool FV, et al. Among authors: neilly me. Cytogenet Cell Genet. 1995;71(1):62-3. doi: 10.1159/000134064. Cytogenet Cell Genet. 1995. PMID: 7606930

7

Familial Lymphoproliferative Disorders with Chromosomal Fragile Site Analysis.

Moormeier JA, Neilly ME, Vardiman JW, Le Beau MM, Golomb HM. Moormeier JA, et al. Among authors: neilly me. Leuk Lymphoma. 1991;5(5-6):311-6. doi: 10.3109/10428199109067623. Leuk Lymphoma. 1991. PMID: 27463340

8

Cytogenetic and molecular study of the PRDX4 gene in a t(X;18)(p22;q23): a cautionary tale.

Gerr HD, Nassin ML, Davis EM, Jayathilaka N, Neilly ME, Schlegelberger B, Zhang Y, Rowley JD. Gerr HD, et al. Among authors: neilly me. Cancer Genet Cytogenet. 2007 Jul 15;176(2):131-6. doi: 10.1016/j.cancergencyto.2007.03.010. Cancer Genet Cytogenet. 2007. PMID: 17656256 Free PMC article.

9

Rearrangements of chromosome 3 involving bands 3q21 and 3q26 are associated with normal or elevated platelet counts in acute nonlymphocytic leukemia.

Bitter MA, Neilly ME, Le Beau MM, Pearson MG, Rowley JD. Bitter MA, et al. Among authors: neilly me. Blood. 1985 Dec;66(6):1362-70. Blood. 1985. PMID: 4063525 Free article.

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