Grompe M - Search Results

1

Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.

Hemphill AW, Akkari Y, Newell AH, Schultz RA, Grompe M, North PS, Hickson ID, Jakobs PM, Rennie S, Pauw D, Hejna J, Olson SB, Moses RE. Hemphill AW, et al. Among authors: grompe m. Cytogenet Genome Res. 2009;125(3):165-75. doi: 10.1159/000230001. Epub 2009 Sep 4. Cytogenet Genome Res. 2009. PMID: 19738377 Free PMC article.

2

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: grompe m. Nat Genet. 1995 Nov;11(3):341-3. doi: 10.1038/ng1195-341. Nat Genet. 1995. PMID: 7581463

3

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. Among authors: grompe m. Hum Mutat. 1994;3(4):339-41. doi: 10.1002/humu.1380030402. Hum Mutat. 1994. PMID: 8081385

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: grompe m. 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: grompe m. Nat Genet. 1993 Jun;4(2):202-5. doi: 10.1038/ng0693-202. Nat Genet. 1993. PMID: 8348157

6

Cloning and characterization of a human cDNA (INPPL1) sharing homology with inositol polyphosphate phosphatases.

Hejna JA, Saito H, Merkens LS, Tittle TV, Jakobs PM, Whitney MA, Grompe M, Friedberg AS, Moses RE. Hejna JA, et al. Among authors: grompe m. Genomics. 1995 Sep 1;29(1):285-7. doi: 10.1006/geno.1995.1247. Genomics. 1995. PMID: 8530088

7

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. Among authors: grompe m. 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.

8

Germ cell defects and hematopoietic hypersensitivity to gamma-interferon in mice with a targeted disruption of the Fanconi anemia C gene.

Whitney MA, Royle G, Low MJ, Kelly MA, Axthelm MK, Reifsteck C, Olson S, Braun RE, Heinrich MC, Rathbun RK, Bagby GC, Grompe M. Whitney MA, et al. Among authors: grompe m. Blood. 1996 Jul 1;88(1):49-58. Blood. 1996. PMID: 8704201 Free article.

9

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. Among authors: grompe m. Somat Cell Mol Genet. 1996 Mar;22(2):151-7. doi: 10.1007/BF02369905. Somat Cell Mol Genet. 1996. PMID: 8782494

10

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. Among authors: grompe m. Somat Cell Mol Genet. 1997 Jan;23(1):1-7. doi: 10.1007/BF02679950. Somat Cell Mol Genet. 1997. PMID: 9217996

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