Instituto Universitario de Investigación en Neuroquímica
Zentrum/Institut
University of Birmingham
Birmingham, Reino UnidoPublikationen in Zusammenarbeit mit Forschern von University of Birmingham (10)
2022
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A Dual Role for FADD in Human Precursor T-Cell Neoplasms
International Journal of Molecular Sciences, Vol. 23, Núm. 23
2021
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Association of Variants in the SPTLC1 Gene with Juvenile Amyotrophic Lateral Sclerosis
JAMA Neurology, Vol. 78, Núm. 10, pp. 1236-1248
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
Autophagy, Vol. 17, Núm. 1, pp. 1-382
2016
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CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
Nature Communications, Vol. 7
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Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356
Autophagy
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Autophagy, Vol. 12, Núm. 1, pp. 1-222
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NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Nature Genetics, Vol. 48, Núm. 9, pp. 1037-1042
2014
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DREAM controls the on/off switch of specific activity-dependent transcription pathways
Molecular and Cellular Biology, Vol. 34, Núm. 5, pp. 877-887
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Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
Neuron, Vol. 84, Núm. 2, pp. 324-331
2012
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Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544