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Consequences of MEGF10 deficiency on myoblast function and Notch1 interactions. [electronic resource] by
- Saha, Madhurima
- Mitsuhashi, Satomi
- Jones, Michael D
- Manko, Kelsey
- Reddy, Hemakumar M
- Bruels, Christine C
- Cho, Kyung-Ah
- Pacak, Christina A
- Draper, Isabelle
- Kang, Peter B
Producer: 20180108
In:
Human molecular genetics vol. 26
Availability: No items available.
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9.
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RNA helicase, DDX27 regulates skeletal muscle growth and regeneration by modulation of translational processes. [electronic resource] by
- Bennett, Alexis H
- O'Donohue, Marie-Francoise
- Gundry, Stacey R
- Chan, Aye T
- Widrick, Jeffrey
- Draper, Isabelle
- Chakraborty, Anirban
- Zhou, Yi
- Zon, Leonard I
- Gleizes, Pierre-Emmanuel
- Beggs, Alan H
- Gupta, Vandana A
Producer: 20180710
In:
PLoS genetics vol. 14
Availability: No items available.
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10.
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Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy. [electronic resource] by
- Saha, Madhurima
- Rizzo, Skylar A
- Ramanathan, Manashwi
- Hightower, Rylie M
- Santostefano, Katherine E
- Terada, Naohiro
- Finkel, Richard S
- Berg, Jonathan S
- Chahin, Nizar
- Pacak, Christina A
- Wagner, Richard E
- Alexander, Matthew S
- Draper, Isabelle
- Kang, Peter B
Producer: 20200312
In:
Human molecular genetics vol. 28
Availability: No items available.
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11.
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Identification of a pathogenic mutation in ATP2A1 via in silico analysis of exome data for cryptic aberrant splice sites. [electronic resource] by
- Bruels, Christine C
- Li, Chengcheng
- Mendoza, Tonatiuh
- Khan, Jamillah
- Reddy, Hemakumar M
- Estrella, Elicia A
- Ghosh, Partha S
- Darras, Basil T
- Lidov, Hart G W
- Pacak, Christina A
- Kunkel, Louis M
- Modave, François
- Draper, Isabelle
- Kang, Peter B
Producer: 20190508
In:
Molecular genetics & genomic medicine vol. 7
Availability: No items available.
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12.
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Formin homology 2 domain containing 3 variants associated with hypertrophic cardiomyopathy. [electronic resource] by
- Wooten, Eric C
- Hebl, Virginia B
- Wolf, Matthew J
- Greytak, Sarah R
- Orr, Nicole M
- Draper, Isabelle
- Calvino, Jenna E
- Kapur, Navin K
- Maron, Martin S
- Kullo, Iftikhar J
- Ommen, Steve R
- Bos, J Martijn
- Ackerman, Michael J
- Huggins, Gordon S
Producer: 20130819
In:
Circulation. Cardiovascular genetics vol. 6
Availability: No items available.
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Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan. [electronic resource] by
- Saha, Madhurima
- Reddy, Hemakumar M
- Salih, Mustafa A
- Estrella, Elicia
- Jones, Michael D
- Mitsuhashi, Satomi
- Cho, Kyung-Ah
- Suzuki-Hatano, Silveli
- Rizzo, Skylar A
- Hamad, Muddathir H
- Mukhtar, Maowia M
- Hamed, Ahlam A
- Elseed, Maha A
- Lek, Monkol
- Valkanas, Elise
- MacArthur, Daniel G
- Kunkel, Louis M
- Pacak, Christina A
- Draper, Isabelle
- Kang, Peter B
Producer: 20190917
In:
Physiological genomics vol. 50
Availability: No items available.
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