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Distinct roles of Hand2 in initiating polarity and posterior Shh expression during the onset of mouse limb bud development.
PLoS Genet. 2010 Apr 8;6(4):e1000901. doi: 10.1371/journal.pgen.1000901.
PLoS Genet. 2010.
PMID: 20386744
Free PMC article.
GLI3 constrains digit number by controlling both progenitor proliferation and BMP-dependent exit to chondrogenesis.
Lopez-Rios J, Speziale D, Robay D, Scotti M, Osterwalder M, Nusspaumer G, Galli A, Holländer GA, Kmita M, Zeller R.
Lopez-Rios J, et al. Among authors: robay d.
Dev Cell. 2012 Apr 17;22(4):837-48. doi: 10.1016/j.devcel.2012.01.006. Epub 2012 Mar 29.
Dev Cell. 2012.
PMID: 22465667
Free PMC article.
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Dual Inhibition of the Lactate Transporters MCT1 and MCT4 Is Synthetic Lethal with Metformin due to NAD+ Depletion in Cancer Cells.
Benjamin D, Robay D, Hindupur SK, Pohlmann J, Colombi M, El-Shemerly MY, Maira SM, Moroni C, Lane HA, Hall MN.
Benjamin D, et al. Among authors: robay d.
Cell Rep. 2018 Dec 11;25(11):3047-3058.e4. doi: 10.1016/j.celrep.2018.11.043.
Cell Rep. 2018.
PMID: 30540938
Free PMC article.
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NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels.
Haefeli RH, Erb M, Gemperli AC, Robay D, Courdier Fruh I, Anklin C, Dallmann R, Gueven N.
Haefeli RH, et al. Among authors: robay d.
PLoS One. 2011 Mar 31;6(3):e17963. doi: 10.1371/journal.pone.0017963.
PLoS One. 2011.
PMID: 21483849
Free PMC article.
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Idebenone protects against retinal damage and loss of vision in a mouse model of Leber's hereditary optic neuropathy.
Heitz FD, Erb M, Anklin C, Robay D, Pernet V, Gueven N.
Heitz FD, et al. Among authors: robay d.
PLoS One. 2012;7(9):e45182. doi: 10.1371/journal.pone.0045182. Epub 2012 Sep 18.
PLoS One. 2012.
PMID: 23028832
Free PMC article.
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Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons.
Robay D, Patel H, Simpson MA, Brown NA, Crosby AH.
Robay D, et al.
Exp Cell Res. 2006 Sep 10;312(15):2764-77. doi: 10.1016/j.yexcr.2006.05.003. Epub 2006 May 13.
Exp Cell Res. 2006.
PMID: 16781711
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A novel NIPA1 mutation associated with a pure form of autosomal dominant hereditary spastic paraplegia.
Reed JA, Wilkinson PA, Patel H, Simpson MA, Chatonnet A, Robay D, Patton MA, Crosby AH, Warner TT.
Reed JA, et al. Among authors: robay d.
Neurogenetics. 2005 May;6(2):79-84. doi: 10.1007/s10048-004-0209-9. Epub 2005 Feb 12.
Neurogenetics. 2005.
PMID: 15711826
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Disruption of Doppel prevents neurodegeneration in mice with extensive Prnp deletions.
Genoud N, Behrens A, Miele G, Robay D, Heppner FL, Freigang S, Aguzzi A.
Genoud N, et al. Among authors: robay d.
Proc Natl Acad Sci U S A. 2004 Mar 23;101(12):4198-203. doi: 10.1073/pnas.0400131101. Epub 2004 Mar 8.
Proc Natl Acad Sci U S A. 2004.
PMID: 15007175
Free PMC article.
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