Jakobs PM - Search Results

1

Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.

Hejna JA, Timmers CD, Reifsteck C, Bruun DA, Lucas LW, Jakobs PM, Toth-Fejel S, Unsworth N, Clemens SL, Garcia DK, Naylor SL, Thayer MJ, Olson SB, Grompe M, Moses RE. Hejna JA, et al. Among authors: jakobs pm. Am J Hum Genet. 2000 May;66(5):1540-51. doi: 10.1086/302896. Epub 2000 Apr 12. Am J Hum Genet. 2000. PMID: 10762542 Free PMC article.

2

The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population.

Whitney MA, Jakobs P, Kaback M, Moses RE, Grompe M. Whitney MA, et al. Hum Mutat. 1994;3(4):339-41. doi: 10.1002/humu.1380030402. Hum Mutat. 1994. PMID: 8081385

3

Microcell mediated chromosome transfer maps the Fanconi anaemia group D gene to chromosome 3p.

Whitney M, Thayer M, Reifsteck C, Olson S, Smith L, Jakobs PM, Leach R, Naylor S, Joenje H, Grompe M. Whitney M, et al. Among authors: jakobs pm. Nat Genet. 1995 Nov;11(3):341-3. doi: 10.1038/ng1195-341. Nat Genet. 1995. PMID: 7581463

4

Fanconi anemia cells have a normal gene structure for topoisomerase I.

Saito H, Grompe M, Neeley TL, Jakobs PM, Moses RE. Saito H, et al. Among authors: jakobs pm. Hum Genet. 1994 May;93(5):583-6. doi: 10.1007/BF00202828. Hum Genet. 1994. PMID: 8168839

5

A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews.

Whitney MA, Saito H, Jakobs PM, Gibson RA, Moses RE, Grompe M. Whitney MA, et al. Among authors: jakobs pm. Nat Genet. 1993 Jun;4(2):202-5. doi: 10.1038/ng0693-202. Nat Genet. 1993. PMID: 8348157

6

Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure.

Jakobs PM, Sahaayaruban P, Saito H, Reifsteck C, Olson S, Joenje H, Moses RE, Grompe M. Jakobs PM, et al. Somat Cell Mol Genet. 1996 Mar;22(2):151-7. doi: 10.1007/BF02369905. Somat Cell Mol Genet. 1996. PMID: 8782494

7

Complementation group assignments in Fanconi anemia fibroblast cell lines from North America.

Jakobs PM, Fiddler-Odell E, Reifsteck C, Olson S, Moses RE, Grompe M. Jakobs PM, et al. Somat Cell Mol Genet. 1997 Jan;23(1):1-7. doi: 10.1007/BF02679950. Somat Cell Mol Genet. 1997. PMID: 9217996

8

Embryonic stem cells can be used to construct hybrid cell lines containing a single, selectable murine chromosome.

Jakobs PM, Smith L, Thayer M, Grompe M. Jakobs PM, et al. Mamm Genome. 1999 Apr;10(4):381-4. doi: 10.1007/s003359901006. Mamm Genome. 1999. PMID: 10087297

9

ERCC1 is required for FANCD2 focus formation.

McCabe KM, Hemphill A, Akkari Y, Jakobs PM, Pauw D, Olson SB, Moses RE, Grompe M. McCabe KM, et al. Among authors: jakobs pm. Mol Genet Metab. 2008 Sep-Oct;95(1-2):66-73. doi: 10.1016/j.ymgme.2008.06.009. Epub 2008 Jul 30. Mol Genet Metab. 2008. PMID: 18672388 Free PMC article.

10

Spontaneous deletion in the FMR1 gene in a patient with fragile X syndrome and cherubism.

Quan F, Grompe M, Jakobs P, Popovich BW. Quan F, et al. Hum Mol Genet. 1995 Sep;4(9):1681-4. doi: 10.1093/hmg/4.9.1681. Hum Mol Genet. 1995. PMID: 8541863 No abstract available.

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