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Items: 18


Automated four-dimensional long term imaging enables single cell tracking within organotypic brain slices to study neurodevelopment and degeneration.

Linsley JW, Tripathi A, Epstein I, Schmunk G, Mount E, Campioni M, Oza V, Barch M, Javaherian A, Nowakowski TJ, Samsi S, Finkbeiner S.

Commun Biol. 2019 May 1;2:155. doi: 10.1038/s42003-019-0411-9. eCollection 2019.


The effects of chronic betaine supplementation on body composition and performance in collegiate females: a double-blind, randomized, placebo controlled trial.

Cholewa JM, Hudson A, Cicholski T, Cervenka A, Barreno K, Broom K, Barch M, Craig SAS.

J Int Soc Sports Nutr. 2018 Jul 31;15(1):37. doi: 10.1186/s12970-018-0243-x.


Assessing microscope image focus quality with deep learning.

Yang SJ, Berndl M, Michael Ando D, Barch M, Narayanaswamy A, Christiansen E, Hoyer S, Roat C, Hung J, Rueden CT, Shankar A, Finkbeiner S, Nelson P.

BMC Bioinformatics. 2018 Mar 15;19(1):77. doi: 10.1186/s12859-018-2087-4.


Exceedingly small iron oxide nanoparticles as positive MRI contrast agents.

Wei H, Bruns OT, Kaul MG, Hansen EC, Barch M, Wiśniowska A, Chen O, Chen Y, Li N, Okada S, Cordero JM, Heine M, Farrar CT, Montana DM, Adam G, Ittrich H, Jasanoff A, Nielsen P, Bawendi MG.

Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):2325-2330. doi: 10.1073/pnas.1620145114. Epub 2017 Feb 13.


Molecular imaging with engineered physiology.

Desai M, Slusarczyk AL, Chapin A, Barch M, Jasanoff A.

Nat Commun. 2016 Dec 2;7:13607. doi: 10.1038/ncomms13607.


Cell Type-Specific Circuit Mapping Reveals the Presynaptic Connectivity of Developing Cortical Circuits.

Cocas LA, Fernandez G, Barch M, Doll J, Zamora Diaz I, Pleasure SJ.

J Neurosci. 2016 Mar 16;36(11):3378-90. doi: 10.1523/JNEUROSCI.0375-15.2016.


Magneto-fluorescent core-shell supernanoparticles.

Chen O, Riedemann L, Etoc F, Herrmann H, Coppey M, Barch M, Farrar CT, Zhao J, Bruns OT, Wei H, Guo P, Cui J, Jensen R, Chen Y, Harris DK, Cordero JM, Wang Z, Jasanoff A, Fukumura D, Reimer R, Dahan M, Jain RK, Bawendi MG.

Nat Commun. 2014 Oct 9;5:5093. doi: 10.1038/ncomms6093.


Screen-based analysis of magnetic nanoparticle libraries formed using peptidic iron oxide ligands.

Barch M, Okada S, Bartelle BB, Jasanoff A.

J Am Chem Soc. 2014 Sep 10;136(36):12516-9. doi: 10.1021/ja410884e. Epub 2014 Sep 2.


Molecular characterization of distal 4q duplication in two patients using oligonucleotide array-based comparative genomic hybridization (oaCGH) analysis.

Thapa M, Asamoah A, Gowans GC, Platky KC, Barch MJ, Mouchrani P, Rajakaruna C, Hersh JH.

Am J Med Genet A. 2014 Apr;164A(4):1069-74. doi: 10.1002/ajmg.a.36396. Epub 2014 Jan 23.


Estradiol stimulates transcription of nuclear respiratory factor-1 and increases mitochondrial biogenesis.

Mattingly KA, Ivanova MM, Riggs KA, Wickramasinghe NS, Barch MJ, Klinge CM.

Mol Endocrinol. 2008 Mar;22(3):609-22. Epub 2007 Nov 29.


Structure and dynamics in DNA looped domains: CAG triplet repeat sequence dynamics probed by 2-aminopurine fluorescence.

Lee BJ, Barch M, Castner EW Jr, Völker J, Breslauer KJ.

Biochemistry. 2007 Sep 25;46(38):10756-66. Epub 2007 Aug 25.


Detecting force-induced molecular transitions with fluorescence resonant energy transfer.

Tarsa PB, Brau RR, Barch M, Ferrer JM, Freyzon Y, Matsudaira P, Lang MJ.

Angew Chem Int Ed Engl. 2007;46(12):1999-2001. doi: 10.1002/anie.200604546. No abstract available.


Chromosome 20q deletion and progression to monosomy 7 in a patient with Shwachman-Diamond syndrome without MDS/AML.

Raj AB, Bertolone SJ, Barch MJ, Hersh JH.

J Pediatr Hematol Oncol. 2003 Jun;25(6):508-9. No abstract available.


Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.

Angle B, Yen F, Hersh JH, Gowans G, Barch M.

Am J Med Genet. 2002 Aug 15;111(3):307-12.


Identification of trisomy 16 murine embryos by fluorescence in situ hybridization.

Nugent P, Barch MJ, Weston WM, Greene RM, Pisano MM.

Biotechniques. 2001 Aug;31(2):284-6, 288. No abstract available.


Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality.

Williams PG, Hersh JH, Yen FF, Barch MJ, Kleinert HE, Kunz J, Kalff-Suske M.

Clin Genet. 1997 Dec;52(6):436-41.


De novo 1;10 balanced translocation in an infant with thanatophoric dysplasia: a clue to the locus of the candidate gene.

Hersh JH, Yen FF, Peiper SC, Barch MJ, Yacoub OA, Voss DH, Roberts JL.

J Med Genet. 1995 Apr;32(4):293-5.

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