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Fengqing Xiang

Showing results (1-10 of 7) with videos related to

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Prion|November 27, 2013
Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutationMartin Paucar, Fengqing Xiang, Richard Moore, et al.
The Open Neurology Journal|September 2, 2016
No Association Between rs7077361 in ITGA8 and Parkinson's Disease in SwedenCaroline Ran, Rawand Naiel Mehdi, Camilla Fardell, et al.
Parkinson'S Disease|May 26, 2017
Genetic Variations and mRNA Expression of NRF2 in Parkinson's DiseaseCaroline Ran, Karin Wirdefeldt, Lovisa Brodin, et al.
Science (New York, N.Y.)|April 2, 2005
The kinase domain of titin controls muscle gene expression and protein turnoverStephan Lange, Fengqing Xiang, Andrey Yakovenko, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Prion|November 27, 2013
Genotype-phenotype analysis in inherited prion disease with eight octapeptide repeat insertional mutationMartin Paucar, Fengqing Xiang, Richard Moore, et al.
The Open Neurology Journal|September 2, 2016
No Association Between rs7077361 in ITGA8 and Parkinson's Disease in SwedenCaroline Ran, Rawand Naiel Mehdi, Camilla Fardell, et al.
Parkinson'S Disease|May 26, 2017
Genetic Variations and mRNA Expression of NRF2 in Parkinson's DiseaseCaroline Ran, Karin Wirdefeldt, Lovisa Brodin, et al.
Science (New York, N.Y.)|April 2, 2005
The kinase domain of titin controls muscle gene expression and protein turnoverStephan Lange, Fengqing Xiang, Andrey Yakovenko, et al.
Neurobiology of Aging|June 4, 2016
Strong association between glucocerebrosidase mutations and Parkinson's disease in SwedenCaroline Ran, Lovisa Brodin, Lars Forsgren, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 23, 2013
Hereditary myopathy with early respiratory failure: occurrence in various populationsJohanna Palmio, Anni Evilä, Françoise Chapon, et al.
Nature Communications|March 29, 2019
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusionsMontse Olivé, Martin Engvall, Gianina Ravenscroft, et al.
Pageof 1