Dwi U Kemaladewi

Dwi U Kemaladewi

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Dwi U Kemaladewi

Dwi U Kemaladewi

Publications by authors named "Dwi U Kemaladewi"

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12Publications

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A mutation-independent approach for muscular dystrophy via upregulation of a modifier gene.

Nature 2019 08 24;572(7767):125-130. Epub 2019 Jul 24.

Program in Genetics and Genome Biology, the Hospital for Sick Children Research Institute, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/s41586-019-1430-xDOI Listing
August 2019

Expanding the Boundaries of RNA Sequencing as a Diagnostic Tool for Rare Mendelian Disease.

Am J Hum Genet 2019 03 28;104(3):466-483. Epub 2019 Feb 28.

Division of Neurology, the Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1X8, Canada; Program in Genetics and Genome Biology, Research Institute, the Hospital for Sick Children, Toronto, ON M5G 0A4, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S00029297193001
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http://dx.doi.org/10.1016/j.ajhg.2019.01.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407525PMC
March 2019

Exon Snipping in Duchenne Muscular Dystrophy.

Trends Mol Med 2016 Mar 5;22(3):187-189. Epub 2016 Feb 5.

Genetics and Genome Biology Program, the Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; Department of Pediatrics, University of Toronto, Toronto, ON, Canada; Division of Clinical and Metabolic Genetics, the Hospital for Sick Children, Toronto, ON, Canada; Centre for Genetic Medicine, the Hospital for Sick Children, Toronto, ON, Canada. Electronic address:

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http://www.cell.com/trends/molecular-medicine/pdf/S1471-4914
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http://dx.doi.org/10.1016/j.molmed.2016.01.007DOI Listing
March 2016

Spell Checking Nature: Versatility of CRISPR/Cas9 for Developing Treatments for Inherited Disorders.

Am J Hum Genet 2016 Jan 10;98(1):90-101. Epub 2015 Dec 10.

Program in Genetics and Genome Biology, Research Institute, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON M5S 1A8, Canada; Department of Paediatrics, University of Toronto, Toronto, ON M5G 1X8, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada; Centre for Genetic Medicine, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. Electronic address:

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http://www.cell.com/cms/attachment/2040911867/2054828527/mmc
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http://linkinghub.elsevier.com/retrieve/pii/S000292971500457
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http://dx.doi.org/10.1016/j.ajhg.2015.11.012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716669PMC
January 2016

Cell-type specific regulation of myostatin signaling.

FASEB J 2012 Apr 27;26(4):1462-72. Epub 2011 Dec 27.

Center for Human and Clinical Genetics, Leiden University Medical Center, Postzone S4-P, PO Box 9600, 2300RC, Leiden, The Netherlands.

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http://dx.doi.org/10.1096/fj.11-191189DOI Listing
April 2012

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy.

BMC Med Genomics 2011 Apr 20;4:36. Epub 2011 Apr 20.

Center for Human and Clinical Genetics, Leiden University Medical Center, Postzone S4-P, PO Box 9600, Leiden, 2300RC, the Netherlands.

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http://dx.doi.org/10.1186/1755-8794-4-36DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107769PMC
April 2011