Falk MJ - Search Results

1

Limitations of preimplantation genetic diagnosis for mitochondrial DNA diseases.

Mitalipov S, Amato P, Parry S, Falk MJ. Mitalipov S, et al. Among authors: falk mj. Cell Rep. 2014 May 22;7(4):935-7. doi: 10.1016/j.celrep.2014.05.004. Cell Rep. 2014. PMID: 24856294 Free PMC article. No abstract available.

2

Mitochondrial genetic diseases.

Falk MJ, Sondheimer N. Falk MJ, et al. Curr Opin Pediatr. 2010 Dec;22(6):711-6. doi: 10.1097/MOP.0b013e3283402e21. Curr Opin Pediatr. 2010. PMID: 21045694 Free PMC article. Review.

3

Human Placental Transcriptome Reveals Critical Alterations in Inflammation and Energy Metabolism with Fetal Sex Differences in Spontaneous Preterm Birth.

Lien YC, Zhang Z, Cheng Y, Polyak E, Sillers L, Falk MJ, Ischiropoulos H, Parry S, Simmons RA. Lien YC, et al. Among authors: falk mj. Int J Mol Sci. 2021 Jul 23;22(15):7899. doi: 10.3390/ijms22157899. Int J Mol Sci. 2021. PMID: 34360662 Free PMC article.

4

Neurodevelopmental manifestations of mitochondrial disease.

Falk MJ. Falk MJ. J Dev Behav Pediatr. 2010 Sep;31(7):610-21. doi: 10.1097/DBP.0b013e3181ef42c1. J Dev Behav Pediatr. 2010. PMID: 20814259 Free PMC article. Review.

5

Mitochondrial disorders and the eye.

Schrier SA, Falk MJ. Schrier SA, et al. Among authors: falk mj. Curr Opin Ophthalmol. 2011 Sep;22(5):325-31. doi: 10.1097/ICU.0b013e328349419d. Curr Opin Ophthalmol. 2011. PMID: 21730846 Free PMC article. Review.

6

Molecular profiling of mitochondrial dysfunction in Caenorhabditis elegans.

Polyak E, Zhang Z, Falk MJ. Polyak E, et al. Among authors: falk mj. Methods Mol Biol. 2012;837:241-55. doi: 10.1007/978-1-61779-504-6_17. Methods Mol Biol. 2012. PMID: 22215553 Free PMC article.

7

Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataracts.

Schrier SA, Wong LJ, Place E, Ji JQ, Pierce EA, Golden J, Santi M, Anninger W, Falk MJ. Schrier SA, et al. Among authors: falk mj. Discov Med. 2012 Feb;13(69):143-50. Discov Med. 2012. PMID: 22369973 Free PMC article.

8

Molecular genetic testing for mitochondrial disease: from one generation to the next.

McCormick E, Place E, Falk MJ. McCormick E, et al. Among authors: falk mj. Neurotherapeutics. 2013 Apr;10(2):251-61. doi: 10.1007/s13311-012-0174-1. Neurotherapeutics. 2013. PMID: 23269497 Free PMC article. Review.

9

Mitochondrial disease genetic diagnostics: optimized whole-exome analysis for all MitoCarta nuclear genes and the mitochondrial genome.

Falk MJ, Pierce EA, Consugar M, Xie MH, Guadalupe M, Hardy O, Rappaport EF, Wallace DC, LeProust E, Gai X. Falk MJ, et al. Discov Med. 2012 Dec;14(79):389-99. Discov Med. 2012. PMID: 23272691 Free PMC article.

10

Integrated transcriptome analysis across mitochondrial disease etiologies and tissues improves understanding of common cellular adaptations to respiratory chain dysfunction.

Zhang Z, Falk MJ. Zhang Z, et al. Among authors: falk mj. Int J Biochem Cell Biol. 2014 May;50:106-11. doi: 10.1016/j.biocel.2014.02.012. Epub 2014 Feb 22. Int J Biochem Cell Biol. 2014. PMID: 24569120 Free PMC article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

197 results

Search Page

Filters