Results
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4041.
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Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial. [electronic resource] by
- Maguire, Albert M
- High, Katherine A
- Auricchio, Alberto
- Wright, J Fraser
- Pierce, Eric A
- Testa, Francesco
- Mingozzi, Federico
- Bennicelli, Jeannette L
- Ying, Gui-shuang
- Rossi, Settimio
- Fulton, Ann
- Marshall, Kathleen A
- Banfi, Sandro
- Chung, Daniel C
- Morgan, Jessica I W
- Hauck, Bernd
- Zelenaia, Olga
- Zhu, Xiaosong
- Raffini, Leslie
- Coppieters, Frauke
- De Baere, Elfride
- Shindler, Kenneth S
- Volpe, Nicholas J
- Surace, Enrico M
- Acerra, Carmela
- Lyubarsky, Arkady
- Redmond, T Michael
- Stone, Edwin
- Sun, Junwei
- McDonnell, Jennifer Wellman
- Leroy, Bart P
- Simonelli, Francesca
- Bennett, Jean
Producer: 20091123
In:
Lancet (London, England) vol. 374
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4042.
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4043.
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4044.
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4045.
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Real-time PCR based on SYBR-Green I fluorescence: an alternative to the TaqMan assay for a relative quantification of gene rearrangements, gene amplifications and micro gene deletions. [electronic resource] by
- Ponchel, Frederique
- Toomes, Carmel
- Bransfield, Kieran
- Leong, Fong T
- Douglas, Susan H
- Field, Sarah L
- Bell, Sandra M
- Combaret, Valerie
- Puisieux, Alain
- Mighell, Alan J
- Robinson, Philip A
- Inglehearn, Chris F
- Isaacs, John D
- Markham, Alex F
Producer: 20040621
In:
BMC biotechnology vol. 3
Availability: No items available.
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4046.
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4047.
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4048.
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4049.
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4050.
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4051.
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4052.
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4053.
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4054.
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Mitochondrial DNA background modulates the assembly kinetics of OXPHOS complexes in a cellular model of mitochondrial disease. [electronic resource] by
- Pello, Rosa
- Martín, Miguel A
- Carelli, Valerio
- Nijtmans, Leo G
- Achilli, Alessandro
- Pala, Maria
- Torroni, Antonio
- Gómez-Durán, Aurora
- Ruiz-Pesini, Eduardo
- Martinuzzi, Andrea
- Smeitink, Jan A
- Arenas, Joaquín
- Ugalde, Cristina
Producer: 20090716
In:
Human molecular genetics vol. 17
Availability: No items available.
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4055.
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A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy. [electronic resource] by
- Alavi, Marcel V
- Bette, Stefanie
- Schimpf, Simone
- Schuettauf, Frank
- Schraermeyer, Ulrich
- Wehrl, Hans F
- Ruttiger, Lukas
- Beck, Susanne C
- Tonagel, Felix
- Pichler, Bernd J
- Knipper, Marlies
- Peters, Thomas
- Laufs, Juergen
- Wissinger, Bernd
Producer: 20070530
In:
Brain : a journal of neurology vol. 130
Availability: No items available.
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4056.
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4057.
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4058.
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4059.
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4060.
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OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. [electronic resource] by
- Reynier, P
- Amati-Bonneau, P
- Verny, C
- Olichon, A
- Simard, G
- Guichet, A
- Bonnemains, C
- Malecaze, F
- Malinge, M C
- Pelletier, J B
- Calvas, P
- Dollfus, H
- Belenguer, P
- Malthièry, Y
- Lenaers, G
- Bonneau, D
Producer: 20050505
In:
Journal of medical genetics vol. 41
Availability: No items available.
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