Frengen E - Search Results

1

Biallelic NDUFA4 Deletion Causes Mitochondrial Complex IV Deficiency in a Patient with Leigh Syndrome.

Misceo D, Strømme P, Bitarafan F, Chawla MS, Sheng Y, Bach de Courtade SM, Eide L, Frengen E. Misceo D, et al. Among authors: frengen e. Genes (Basel). 2024 Apr 17;15(4):500. doi: 10.3390/genes15040500. Genes (Basel). 2024. PMID: 38674434 Free PMC article.

2

Isolation of region-specific probes from pig chromosome 6 by coincidence cloning.

Frengen E, Thomsen PD, Schmitz A, Frelat G, Davies W. Frengen E, et al. Mamm Genome. 1994 Aug;5(8):497-502. doi: 10.1007/BF00369319. Mamm Genome. 1994. PMID: 7949734

3

Construction of bacterial artificial chromosome (BAC/PAC) libraries.

Osoegawa K, de Jong PJ, Frengen E, Ioannou PA. Osoegawa K, et al. Among authors: frengen e. Curr Protoc Hum Genet. 2001 May;Chapter 5:Unit 5.15. doi: 10.1002/0471142905.hg0515s21. Curr Protoc Hum Genet. 2001. PMID: 18428289

4

Imaging tumor-stroma interactions during chemotherapy reveals contributions of the microenvironment to resistance.

Nakasone ES, Askautrud HA, Kees T, Park JH, Plaks V, Ewald AJ, Fein M, Rasch MG, Tan YX, Qiu J, Park J, Sinha P, Bissell MJ, Frengen E, Werb Z, Egeblad M. Nakasone ES, et al. Among authors: frengen e. Cancer Cell. 2012 Apr 17;21(4):488-503. doi: 10.1016/j.ccr.2012.02.017. Cancer Cell. 2012. PMID: 22516258 Free PMC article.

5

Alternative transcripts of the candidate tumor suppressor gene, WWOX, are expressed at high levels in human breast tumors.

Driouch K, Prydz H, Monese R, Johansen H, Lidereau R, Frengen E. Driouch K, et al. Among authors: frengen e. Oncogene. 2002 Mar 14;21(12):1832-40. doi: 10.1038/sj.onc.1205273. Oncogene. 2002. PMID: 11896615

6

A core MYC gene expression signature is prominent in basal-like breast cancer but only partially overlaps the core serum response.

Chandriani S, Frengen E, Cowling VH, Pendergrass SA, Perou CM, Whitfield ML, Cole MD. Chandriani S, et al. Among authors: frengen e. PLoS One. 2009 Aug 19;4(8):e6693. doi: 10.1371/journal.pone.0006693. PLoS One. 2009. PMID: 19690609 Free PMC article.

7

Cloning and characterization of MDDX28, a putative dead-box helicase with mitochondrial and nuclear localization.

Valgardsdottir R, Brede G, Eide LG, Frengen E, Prydz H. Valgardsdottir R, et al. Among authors: frengen e. J Biol Chem. 2001 Aug 24;276(34):32056-63. doi: 10.1074/jbc.M011629200. Epub 2001 May 11. J Biol Chem. 2001. PMID: 11350955 Free article.

8

[Structural variation in the human genome contributes to variation of traits].

Barøy T, Misceo D, Frengen E. Barøy T, et al. Among authors: frengen e. Tidsskr Nor Laegeforen. 2008 Sep 11;128(17):1951-5. Tidsskr Nor Laegeforen. 2008. PMID: 18787571 Free article. Review. Norwegian.

9

A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient.

Misceo D, Bjørgo K, Ormerod E, Ringen Ø, Rocchi M, van der Hagen CB, Frengen E. Misceo D, et al. Among authors: frengen e. Am J Med Genet A. 2008 Dec 15;146A(24):3230-3. doi: 10.1002/ajmg.a.32582. Am J Med Genet A. 2008. PMID: 19012337 No abstract available.

10

A partial trisomy 1q patient with a deletion 1q22 and an insertion 1(q42q44) into 1q22.

Misceo D, Rocchi M, van der Hagen CB, Frengen E. Misceo D, et al. Among authors: frengen e. Am J Med Genet A. 2009 Feb;149A(2):290-3. doi: 10.1002/ajmg.a.32623. Am J Med Genet A. 2009. PMID: 19161140 Review. No abstract available.

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