Pearson PL - Search Results

1

The recurrent translocation t(14;20)(q32;q12) in multiple myeloma results in aberrant expression of MAFB: a molecular and genetic analysis of the chromosomal breakpoint.

Boersma-Vreugdenhil GR, Kuipers J, Van Stralen E, Peeters T, Michaux L, Hagemeijer A, Pearson PL, Clevers HC, Bast BJ. Boersma-Vreugdenhil GR, et al. Among authors: pearson pl. Br J Haematol. 2004 Aug;126(3):355-63. doi: 10.1111/j.1365-2141.2004.05050.x. Br J Haematol. 2004. PMID: 15257707 Free article.

2

Fluorescence in situ hybridization analysis shows the frequent occurrence of 14q32.3 rearrangements with involvement of immunoglobulin switch regions in myeloma cell lines.

Kuipers J, Vaandrager JW, Weghuis DO, Pearson PL, Scheres J, Lokhorst HM, Clevers H, Bast BJ. Kuipers J, et al. Among authors: pearson pl. Cancer Genet Cytogenet. 1999 Mar;109(2):99-107. doi: 10.1016/s0165-4608(98)00157-5. Cancer Genet Cytogenet. 1999. PMID: 10087940

3

Genetic mapping of the copper toxicosis locus in Bedlington terriers to dog chromosome 10, in a region syntenic to human chromosome region 2p13-p16.

van de Sluis BJ, Breen M, Nanji M, van Wolferen M, de Jong P, Binns MM, Pearson PL, Kuipers J, Rothuizen J, Cox DW, Wijmenga C, van Oost BA. van de Sluis BJ, et al. Among authors: pearson pl. Hum Mol Genet. 1999 Mar;8(3):501-7. doi: 10.1093/hmg/8.3.501. Hum Mol Genet. 1999. PMID: 9949209

4

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p.

Dauwerse JG, Kievits T, Beverstock GC, van der Keur D, Smit E, Wessels HW, Hagemeijer A, Pearson PL, van Ommen GJ, Breuning MH. Dauwerse JG, et al. Among authors: pearson pl. Cytogenet Cell Genet. 1990;53(2-3):126-8. doi: 10.1159/000132911. Cytogenet Cell Genet. 1990. PMID: 2369839

5

Genotype-phenotype correlations in families with deletions in the von Hippel-Lindau (VHL) gene.

Hes F, Zewald R, Peeters T, Sijmons R, Links T, Verheij J, Matthijs G, Leguis E, Mortier G, van der Torren K, Rosman M, Lips C, Pearson P, van der Luijt R. Hes F, et al. Hum Genet. 2000 Apr;106(4):425-31. doi: 10.1007/s004390000265. Hum Genet. 2000. PMID: 10830910

6

Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISH.

Giltay JC, Kastrop PM, Tiemessen CH, van Inzen WG, Scheres JM, Pearson PL. Giltay JC, et al. Among authors: pearson pl. Cytogenet Cell Genet. 1999;84(1-2):67-72. doi: 10.1159/000015217. Cytogenet Cell Genet. 1999. PMID: 10343106

7

Proceedings: Localization of gene markers to regions of the human X chromosome by segregation of X-autosome translocations in somatic cell hybrids.

Pearson PL, van der Linden AG, Hagemeijer A. Pearson PL, et al. Cytogenet Cell Genet. 1974;13(1):136-42. doi: 10.1159/000130257. Cytogenet Cell Genet. 1974. PMID: 4827480 No abstract available.

8

The genetic analysis of cancer.

Pearson PL, Van der Luijt RB. Pearson PL, et al. J Intern Med. 1998 Jun;243(6):413-7. doi: 10.1046/j.1365-2796.1998.00343.x. J Intern Med. 1998. PMID: 9681837 Free article. Review.

9

A genomewide screen in a four-generation Dutch family with celiac disease: evidence for linkage to chromosomes 6 and 9.

van Belzen MJ, Vrolijk MM, Meijer JW, Crusius JB, Pearson PL, Sandkuijl LA, Houwen RH, Wijmenga C. van Belzen MJ, et al. Among authors: pearson pl. Am J Gastroenterol. 2004 Mar;99(3):466-71. doi: 10.1111/j.1572-0241.2004.04072.x. Am J Gastroenterol. 2004. PMID: 15056087

10

Characterization and chromosomal localization of five canine ATOX1 pseudogenes.

van de Sluis B, Nanji MS, Breen M, Pearson PL, Oost BA, Cox DW, Wijmenga C. van de Sluis B, et al. Among authors: pearson pl. Cytogenet Cell Genet. 2001;93(1-2):105-8. doi: 10.1159/000056959. Cytogenet Cell Genet. 2001. PMID: 11474190

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