Nancarrow J - Search Results

1

Fragile X genotype characterized by an unstable region of DNA.

Yu S, Pritchard M, Kremer E, Lynch M, Nancarrow J, Baker E, Holman K, Mulley JC, Warren ST, Schlessinger D, et al. Yu S, et al. Among authors: nancarrow j. Science. 1991 May 24;252(5009):1179-81. doi: 10.1126/science.252.5009.1179. Science. 1991. PMID: 2031189

2

Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.

Nancarrow JK, Kremer E, Holman K, Eyre H, Doggett NA, Le Paslier D, Callen DF, Sutherland GR, Richards RI. Nancarrow JK, et al. Science. 1994 Jun 24;264(5167):1938-41. doi: 10.1126/science.8009225. Science. 1994. PMID: 8009225

3

Genetic mapping of new RFLPs at Xq27-q28.

Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL, et al. Suthers GK, et al. Among authors: nancarrow j. Genomics. 1991 Jan;9(1):37-43. doi: 10.1016/0888-7543(91)90218-4. Genomics. 1991. PMID: 1672291

4

Chromosomal fragile site FRA16D and DNA instability in cancer.

Mangelsdorf M, Ried K, Woollatt E, Dayan S, Eyre H, Finnis M, Hobson L, Nancarrow J, Venter D, Baker E, Richards RI. Mangelsdorf M, et al. Among authors: nancarrow j. Cancer Res. 2000 Mar 15;60(6):1683-9. Cancer Res. 2000. PMID: 10749140

5

Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.

Callen DF, Baker E, Lane S, Nancarrow J, Thompson A, Whitmore SA, MacLennan DH, Berger R, Cherif D, Järvelä I, et al. Callen DF, et al. Among authors: nancarrow j. Am J Hum Genet. 1991 Dec;49(6):1372-7. Am J Hum Genet. 1991. PMID: 1746562 Free PMC article.

6

A refined physical map of the long arm of human chromosome 16.

Chen LZ, Harris PC, Apostolou S, Baker E, Holman K, Lane SA, Nancarrow JK, Whitmore SA, Stallings RL, Hildebrand CE, et al. Chen LZ, et al. Among authors: nancarrow jk. Genomics. 1991 Jun;10(2):308-12. doi: 10.1016/0888-7543(91)90313-4. Genomics. 1991. PMID: 2071140

7

Molecular basis of p(CCG)n repeat instability at the FRA16A fragile site locus.

Nancarrow JK, Holman K, Mangelsdorf M, Hori T, Denton M, Sutherland GR, Richards RI. Nancarrow JK, et al. Hum Mol Genet. 1995 Mar;4(3):367-72. doi: 10.1093/hmg/4.3.367. Hum Mol Genet. 1995. PMID: 7795589

8

A PCR-based genetic linkage map of human chromosome 16.

Shen Y, Kozman HM, Thompson A, Phillips HA, Holman K, Nancarrow J, Lane S, Chen LZ, Apostolou S, Doggett NA, et al. Shen Y, et al. Among authors: nancarrow j. Genomics. 1994 Jul 1;22(1):68-76. doi: 10.1006/geno.1994.1346. Genomics. 1994. PMID: 7959793

9

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells.

Ried K, Finnis M, Hobson L, Mangelsdorf M, Dayan S, Nancarrow JK, Woollatt E, Kremmidiotis G, Gardner A, Venter D, Baker E, Richards RI. Ried K, et al. Among authors: nancarrow jk. Hum Mol Genet. 2000 Jul 1;9(11):1651-63. doi: 10.1093/hmg/9.11.1651. Hum Mol Genet. 2000. PMID: 10861292

10

High-resolution cytogenetic-based physical map of human chromosome 16.

Callen DF, Doggett NA, Stallings RL, Chen LZ, Whitmore SA, Lane SA, Nancarrow JK, Apostolou S, Thompson AD, Lapsys NM, et al. Callen DF, et al. Among authors: nancarrow jk. Genomics. 1992 Aug;13(4):1178-85. doi: 10.1016/0888-7543(92)90035-q. Genomics. 1992. PMID: 1505951

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