White I - Search Results

1

A murine replication protein accumulates temporarily in the heterochromatic regions of nuclei prior to initiation of DNA replication.

Starborg M, Brundell E, Gell K, Larsson C, White I, Daneholt B, Höög C. Starborg M, et al. Among authors: white i. J Cell Sci. 1995 Mar;108 ( Pt 3):927-34. doi: 10.1242/jcs.108.3.927. J Cell Sci. 1995. PMID: 7622621

2

The human NOTCH1, 2, and 3 genes are located at chromosome positions 9q34, 1p13-p11, and 19p13.2-p13.1 in regions of neoplasia-associated translocation.

Larsson C, Lardelli M, White I, Lendahl U. Larsson C, et al. Among authors: white i. Genomics. 1994 Nov 15;24(2):253-8. doi: 10.1006/geno.1994.1613. Genomics. 1994. PMID: 7698746

3

Localization of the human soluble epoxide hydrolase gene (EPHX2) to chromosomal region 8p21-p12.

Larsson C, White I, Johansson C, Stark A, Meijer J. Larsson C, et al. Among authors: white i. Hum Genet. 1995 Mar;95(3):356-8. doi: 10.1007/BF00225209. Hum Genet. 1995. PMID: 7868134

4

Predisposition for breast cancer in carriers of constitutional translocation 11q;22q.

Lindblom A, Sandelin K, Iselius L, Dumanski J, White I, Nordenskjöld M, Larsson C. Lindblom A, et al. Among authors: white i. Am J Hum Genet. 1994 May;54(5):871-6. Am J Hum Genet. 1994. PMID: 8178827 Free PMC article.

5

Chromosomal localization of six human forkhead genes, freac-1 (FKHL5), -3 (FKHL7), -4 (FKHL8), -5 (FKHL9), -6 (FKHL10), and -8 (FKHL12).

Larsson C, Hellqvist M, Pierrou S, White I, Enerbäck S, Carlsson P. Larsson C, et al. Among authors: white i. Genomics. 1995 Dec 10;30(3):464-9. doi: 10.1006/geno.1995.1266. Genomics. 1995. PMID: 8825632

6

Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidism.

Farnebo F, Teh BT, Dotzenrath C, Wassif WS, Svensson A, White I, Betz R, Goretzki P, Sandelin K, Farnebo LO, Larsson C. Farnebo F, et al. Among authors: white i. Hum Genet. 1997 Mar;99(3):342-9. doi: 10.1007/s004390050369. Hum Genet. 1997. PMID: 9050920

7

Loss of ZDHHC15 expression in a woman with a balanced translocation t(X;15)(q13.3;cen) and severe mental retardation.

Mansouri MR, Marklund L, Gustavsson P, Davey E, Carlsson B, Larsson C, White I, Gustavson KH, Dahl N. Mansouri MR, et al. Among authors: white i. Eur J Hum Genet. 2005 Aug;13(8):970-7. doi: 10.1038/sj.ejhg.5201445. Eur J Hum Genet. 2005. PMID: 15915161

8

PGD for dystrophin gene deletions using fluorescence in situ hybridization.

Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E. Malmgren H, et al. Among authors: white i. Mol Hum Reprod. 2006 May;12(5):353-6. doi: 10.1093/molehr/gal039. Epub 2006 Apr 11. Mol Hum Reprod. 2006. PMID: 16608904

9

22q11.2 microduplication in two patients with bladder exstrophy and hearing impairment.

Lundin J, Söderhäll C, Lundén L, Hammarsjö A, White I, Schoumans J, Läckgren G, Kockum CC, Nordenskjöld A. Lundin J, et al. Among authors: white i. Eur J Med Genet. 2010 Mar-Apr;53(2):61-5. doi: 10.1016/j.ejmg.2009.11.004. Epub 2010 Jan 4. Eur J Med Genet. 2010. PMID: 20045748

10

Meiotic segregation analyses of reciprocal translocations in spermatozoa and embryos: no support for predictive value regarding PGD outcome.

Haapaniemi Kouru K, Malmgren H, White I, Rodriguez Sanchez A, Syk Lundberg E. Haapaniemi Kouru K, et al. Among authors: white i. Reprod Biomed Online. 2017 Jun;34(6):645-652. doi: 10.1016/j.rbmo.2017.02.013. Epub 2017 Mar 14. Reprod Biomed Online. 2017. PMID: 28336162

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