D.U. Kemaladewi: search on Z-Library

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1

CRISPR/Cas9-mediated exon inclusion in Lama2 gene alleviates dystrophic pathology in MDC1A mouse model

Kemaladewi, D., Hyatt, E., Ivakine, Z., Cohn, R.

Journal:

Neuromuscular Disorders

Year:

2016

Language:

english

File:

PDF, 192 KB

english, 2016

2

Dual exon skipping in myostatin and dystrophin for Duchenne muscular dystrophy

Dwi U Kemaladewi, Willem MH Hoogaars, Sandra H van Heiningen, Samuel Terlouw, David JJ de Gorter, Johan T den Dunnen, Gert Jan B van Ommen, Annemieke Aartsma-Rus, Peter ten Dijke, Peter AC’t Hoen

Journal:

BMC Medical Genomics

Year:

2011

Language:

english

File:

PDF, 1.18 MB

english, 2011

3

BMP antagonists enhance myogenic differentiation and ameliorate the dystrophic phenotype in a DMD mouse model

SongTing Shi, Willem M.H. Hoogaars, David J.J. de Gorter, Sandra H. van Heiningen, Herbert Y. Lin, Charles C. Hong, Dwi U. Kemaladewi, Annemieke Aartsma-Rus, Peter ten Dijke, Peter A.C. 't Hoen

Journal:

Neurobiology of Disease

Year:

2011

Language:

english

File:

PDF, 1.28 MB

english, 2011

4

T.P.1.04 Dual exon skipping in myostatin and dystrophin as a potential therapy for Duchenne muscular dystrophy

D.U. Kemaladewi, W.M.H. Hoogaars, S.H. van Heiningen, J.C.T. van Deutekom, J.T. den Dunnen, G.J.B. van Ommen, A.R. Aartsma-Rus, P. ten Dijke, P.A.C. ’t Hoen

Journal:

Neuromuscular Disorders

Year:

2009

Language:

english

File:

PDF, 39 KB

english, 2009

5

O.10 Effect of combined treatment with soluble activin receptor IIB and AAV-U7-mediated dystrophin exon skipping on muscle function in mdx mice

W.M.H. Hoogaars, E. Mouisel, K. Relizani, A. Pasternack, C. Hourde, G. Precigout, A. Ferry, L. Garcia, D.U. Kemaladewi, A. Aartsma-Rus, O. Ritvos, P.A.C. ’t Hoen, H. Amthor

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 49 KB

english, 2011

6

O.13 Interference of myostatin and TGF-beta signaling by antisense-mediated exon skipping in ALK4/5 receptors

D.U. Kemaladewi, S.H. van Heiningen, A. Aartsma-Rus, G.J.B. van Ommen, P. ten Dijke, P.A.C. ’t Hoen, W.M.H. Hoogaars

Journal:

Neuromuscular Disorders

Year:

2011

Language:

english

File:

PDF, 49 KB

english, 2011

7

G.O.6

Yoon, G., Malam, Z., Paton, T., Marshall, C., Hyatt, E., Ivakine, Z., Kemaladewi, D., Forge, C., Lee, K.S., Hawkins, C., Cohn, R.D.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 45 KB

english, 2014

8

Cell-type specific regulation of myostatin signaling

Kemaladewi, D. U., de Gorter, D. J. J., Aartsma-Rus, A., van Ommen, G.-J., ten Dijke, P., 't Hoen, P. A. C., Hoogaars, W. M.

Journal:

The FASEB Journal

Year:

2012

Language:

english

File:

PDF, 1.13 MB

english, 2012

9

Targeting TGF-β Signaling by Antisense Oligonucleotide-mediated Knockdown of TGF-β Type I Receptor

Kemaladewi, Dwi U, Pasteuning, Svitlana, van der Meulen, Joke W, van Heiningen, Sandra H, van Ommen, Gert-Jan, ten Dijke, Peter, Aartsma-Rus, Annemieke, ‘t Hoen, Peter AC, Hoogaars, Willem M

Journal:

Molecular Therapy — Nucleic Acids

Year:

2014

Language:

english

File:

PDF, 770 KB

english, 2014

10

Novel Ex Vivo Culture Method for the Study of Dupuytren’s Disease: Effects of TGFβ Type 1 Receptor Modulation by Antisense Oligonucleotides

Karkampouna, Sofia, Kruithof, Boudewijn PT, Kloen, Peter, Obdeijn, Miryam C, van der Laan, Annelies MA, Tanke, Hans J, Kemaladewi, Dwi U, Hoogaars, Willem MH, ‘t Hoen, Peter AC, Aartsma-Rus, Annemieke

Journal:

Molecular Therapy — Nucleic Acids

Year:

2014

Language:

english

File:

PDF, 1.47 MB

english, 2014

11

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

Wojtal, Daria, Kemaladewi, Dwi U., Malam, Zeenat, Abdullah, Sarah, Wong, Tatianna W.Y., Hyatt, Elzbieta, Baghestani, Zahra, Pereira, Sergio, Stavropoulos, James, Mouly, Vincent, Mamchaoui, Kamel, Munt

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 1.32 MB

english, 2015

12

Exon Snipping in Duchenne Muscular Dystrophy

Kemaladewi, Dwi U., Cohn, Ronald D.

Journal:

Trends in Molecular Medicine

Year:

2016

Language:

english

File:

PDF, 498 KB

english, 2016

13

559. Spell Checking Nature: A Therapeutic Use of the CRISPR/Cas9 System in Duchenne Muscular Dystrophy

Wojtal, Daria, Kemaladewi, Dwi U., Malam, Zeenat, Abdullah, Sarah, Hyatt, Elzbieta, Huang, Victoria, Mouly, Vincent, Voit, Thomas, Muntoni, Francesco, Ivakine, Evgueni A., Cohn, Ronald D.

Journal:

Molecular Therapy

Year:

2015

Language:

english

File:

PDF, 336 KB

english, 2015

14

TGF-β signaling in Duchenne muscular dystrophy

Kemaladewi, Dwi U, ‘t Hoen, Peter A, ten Dijke, Peter, van Ommen, Gert Jan, Hoogaars, Willem M

Journal:

Future Neurology

Year:

2012

Language:

english

File:

PDF, 4.49 MB

english, 2012

15

Correction of a splicing defect in a mouse model of congenital muscular dystrophy type 1A using a homology-directed-repair-independent mechanism

Kemaladewi, Dwi U, Maino, Eleonora, Hyatt, Elzbieta, Hou, Huayun, Ding, Maylynn, Place, Kara M, Zhu, Xinyi, Bassi, Prabhpreet, Baghestani, Zahra, Deshwar, Amit G, Merico, Daniele, Xiong, Hui Y, Frey,

Journal:

Nature Medicine

Year:

2017

Language:

english

File:

PDF, 3.25 MB

english, 2017

16

Increased polyamines as protective disease modifiers in Congenital Muscular Dystrophy

Kemaladewi, D U, Benjamin, J S, Hyatt, E, Ivakine, E A, Cohn, R D

Journal:

Human Molecular Genetics

Year:

2018

Language:

english

File:

PDF, 1.02 MB

english, 2018

17

Antisense-Oligonucleotide Mediated Exon Skipping in Activin-Receptor-Like Kinase 2: Inhibiting the Receptor That Is Overactive in Fibrodysplasia Ossificans Progressiva

Shi, SongTing, Cai, Jie, de Gorter, David J. J., Sanchez-Duffhues, Gonzalo, Kemaladewi, Dwi U., Hoogaars, Willem M. H., Aartsma-Rus, Annemieke, ’t Hoen, Peter A. C., ten Dijke, Peter, Shi, Wei

Journal:

Year:

2013

Language:

english

File:

PDF, 1016 KB

english, 2013

18

NEW THERAPEUTIC APPROACHES AND THEIR READOUT

Kemaladewi, D., Bassi, P., Lindsay, K., Erwood, S., Hyatt, E., Place, K., Marks, R., Gawlik, K., Durbeej, M., Ivakine, E., Cohn, R.

Journal:

Neuromuscular Disorders

Year:

2018

File:

PDF, 63 KB

2018

19

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

Kemaladewi, Dwi U., Bassi, Prabhpreet S., Erwood, Steven, Al-Basha, Dhekra, Gawlik, Kinga I., Lindsay, Kyle, Hyatt, Elzbieta, Kember, Rebekah, Place, Kara M., Marks, Ryan M., Durbeej, Madeleine, Presc

Journal:

Year:

2019

File:

PDF, 45.77 MB

2019

20

LATE BREAKING NEWS E-POSTER PRESENTATION

Kemaladewi, Dwi, Arockiaraj, Annie, Cheng-Zhang, Jia Qi, Daghlas, Salah, Kim, Caleb

Journal:

Neuromuscular Disorders

Year:

2020

File:

PDF, 62 KB

2020