Results
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13961.
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13962.
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Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC. [electronic resource] by
- Tingaud-Sequeira, Angèle
- Raldúa, Demetrio
- Lavie, Julie
- Mathieu, Guilaine
- Bordier, Magali
- Knoll-Gellida, Anja
- Rambeau, Pierre
- Coupry, Isabelle
- André, Michèle
- Malm, Eva
- Möller, Claes
- Andreasson, Sten
- Rendtorff, Nanna D
- Tranebjærg, Lisbeth
- Koenig, Michel
- Lacombe, Didier
- Goizet, Cyril
- Babin, Patrick J
Producer: 20180227
In:
Neurobiology of disease vol. 98
Availability: No items available.
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13963.
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13964.
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13965.
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13966.
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13967.
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13968.
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Homozygous hydroxymethylbilane synthase knock-in mice provide pathogenic insights into the severe neurological impairments present in human homozygous dominant acute intermittent porphyria. [electronic resource] by
- Yasuda, Makiko
- Gan, Lin
- Chen, Brenden
- Yu, Chunli
- Zhang, Jinglan
- Gama-Sosa, Miguel A
- Pollak, Daniela D
- Berger, Stefanie
- Phillips, John D
- Edelmann, Winfried
- Desnick, Robert J
Producer: 20200206
In:
Human molecular genetics vol. 28
Availability: No items available.
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13969.
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13970.
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13971.
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The Stem Cell Factor Sox2 Is a Positive Timer of Oligodendrocyte Development in the Postnatal Murine Spinal Cord. [electronic resource] by
- Zhang, Sheng
- Rasai, Abeer
- Wang, Yan
- Xu, Jie
- Bannerman, Peter
- Erol, Daffcar
- Tsegaye, Danayit
- Wang, Aijun
- Soulika, Athena
- Zhan, Xiangjiang
- Guo, Fuzheng
Producer: 20190118
In:
Molecular neurobiology vol. 55
Availability: No items available.
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13972.
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13973.
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13974.
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13975.
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13976.
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13977.
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13978.
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13979.
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13980.
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