Ich stimme zu, dass diese Seite Cookies verwende. Weitere Informationen finden Sie unter unseren Datenschutzerklärungen .
X
Sapp, Peter C.
390  Ergebnisse:
Personensuche X
?
1

Exome sequencing in amyotrophic lateral sclerosis identifie..:

Cirulli, Elizabeth T. ; Lasseigne, Brittany N. ; Petrovski, Slavé...
Science.  347 (2015)  6229 - p. 1436-1441 , 2015
Link: http://www.jstor.org/sta..
 
?
2

Exome sequencing in amyotrophic lateral sclerosis identifie..:

Cirulli, Elizabeth T. ; Lasseigne, Brittany N. ; Petrovski, Slavé...
Science.  347 (2015)  6229 - p. 1436-1441 , 2015
Link: https://doi.org/10.1126/..
 
?
3

The distinct genetic pattern of ALS in Turkey and novel mut..:

Özoğuz, Aslıhan ; Uyan, Özgün ; Birdal, Güneş...
Neurobiology of Aging.  36 (2015)  4 - p. 1764.e9-1764.e18 , 2015
Link: https://doi.org/10.1016/..
 
?
4

Reply to comment on: A novel dysferlin mutant pseudoexon by..:

Dominov, Janice A. ; Uyan, Özgün ; Sapp, Peter C....
Annals of Clinical and Translational Neurology.  2 (2015)  7 - p. 785-785 , 2015
Link: https://doi.org/10.1002/..
 
?
5

Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci ..:

Peters, Owen M. ; Cabrera, Gabriela Toro ; Tran, Helene...
Neuron.  88 (2015)  5 - p. 902-909 , 2015
Link: https://doi.org/10.1016/..
 
?
6

Exome-wide Rare Variant Analysis Identifies TUBA4A Mutation..:

Smith, Bradley N. ; Ticozzi, Nicola ; Fallini, Claudia...
Neuron.  84 (2014)  2 - p. 324-331 , 2014
Link: https://doi.org/10.1016/..
 
?
7

Identifying diagnostic DNA methylation profiles for faciosc..:

Jones, Takako I ; Yan, Chi ; Sapp, Peter C...
Clinical Epigenetics.  6 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
?
8

A novel dysferlin mutant pseudoexon bypassed with antisense..:

Dominov, Janice A. ; Uyan, Özgün ; Sapp, Peter C....
Annals of Clinical and Translational Neurology.  1 (2014)  9 - p. 703-720 , 2014
Link: https://doi.org/10.1002/..
 
?
9

Mutations in the profilin 1 gene cause familial amyotrophic..:

Wu, Chi-Hong ; Fallini, Claudia ; Ticozzi, Nicola...
Nature.  488 (2012)  7412 - p. 499-503 , 2012
Link: https://doi.org/10.1038/..
 
?
10

Association of UBQLN1 mutation with Brown–Vialetto–Van Laer..:

González-Pérez, Paloma ; Lu, Yubing ; Chian, Ru-Ju...
Neurobiology of Disease.  48 (2012)  3 - p. 391-398 , 2012
Link: https://doi.org/10.1016/..
 
?
11

Novel mutation inVCPgene causes atypical amyotrophic latera..:

González-Pérez, Paloma ; Cirulli, Elizabeth T. ; Drory, Vivian E....
Neurology.  79 (2012)  22 - p. 2201-2208 , 2012
Link: https://doi.org/10.1212/..
 
?
12

Mutational analysis of TARDBP in neurodegenerative diseases:

Ticozzi, Nicola ; LeClerc, Ashley Lyn ; van Blitterswijk, Marka...
Neurobiology of Aging.  32 (2011)  11 - p. 2096-2099 , 2011
Link: https://doi.org/10.1016/..
 
?
13

Paraoxonase gene mutations in amyotrophic lateral sclerosis:

Ticozzi, Nicola ; LeClerc, Ashley Lyn ; Keagle, Pamela J....
Annals of Neurology.  68 (2010)  1 - p. 102-107 , 2010
Link: https://doi.org/10.1002/..
 
?
14

A large genome scan for rare CNVs in amyotrophic lateral sc..:

Blauw, Hylke M. ; Al-Chalabi, Ammar ; Andersen, Peter M....
Human Molecular Genetics.  19 (2010)  20 - p. 4091-4099 , 2010
Link: https://doi.org/10.1093/..
 
?
15

Reduced expression of theKinesin-Associated Protein 3(KIFAP..:

Landers, John E. ; Melki, Judith ; Meininger, Vincent...
Proceedings of the National Academy of Sciences.  106 (2009)  22 - p. 9004-9009 , 2009
Link: https://doi.org/10.1073/..
 
1-15