-
1
-
-
84922805752
-
Dependence of brown adipose tissue function on CD36-mediated coenzyme Q uptake
-
Anderson, C.M., Kazantzis, M., Wang, J., Venkatraman, S., Goncalves, R.L., Quinlan, C.L., Ng, R., Jastroch, M., Benjamin, D.I., Nie, B., et al. Dependence of brown adipose tissue function on CD36-mediated coenzyme Q uptake. Cell Rep. 10 (2015), 505–515.
-
(2015)
Cell Rep.
, vol.10
, pp. 505-515
-
-
Anderson, C.M.1
Kazantzis, M.2
Wang, J.3
Venkatraman, S.4
Goncalves, R.L.5
Quinlan, C.L.6
Ng, R.7
Jastroch, M.8
Benjamin, D.I.9
Nie, B.10
-
2
-
-
84890038202
-
ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption
-
Ashraf, S., Gee, H.Y., Woerner, S., Xie, L.X., Vega-Warner, V., Lovric, S., Fang, H., Song, X., Cattran, D.C., Avila-Casado, C., et al. ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. J. Clin. Invest. 123 (2013), 5179–5189.
-
(2013)
J. Clin. Invest.
, vol.123
, pp. 5179-5189
-
-
Ashraf, S.1
Gee, H.Y.2
Woerner, S.3
Xie, L.X.4
Vega-Warner, V.5
Lovric, S.6
Fang, H.7
Song, X.8
Cattran, D.C.9
Avila-Casado, C.10
-
3
-
-
4143084862
-
Progression despite replacement of a myopathic form of coenzyme Q10 defect
-
Auré, K., Benoist, J.F., Ogier de Baulny, H., Romero, N.B., Rigal, O., Lombès, A., Progression despite replacement of a myopathic form of coenzyme Q10 defect. Neurology 63 (2004), 727–729.
-
(2004)
Neurology
, vol.63
, pp. 727-729
-
-
Auré, K.1
Benoist, J.F.2
Ogier de Baulny, H.3
Romero, N.B.4
Rigal, O.5
Lombès, A.6
-
4
-
-
84978808789
-
Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3
-
Published online January 27, 2016
-
Barca, E., Musumeci, O., Montagnese, F., Marino, S., Granata, F., Nunnari, D., Peverelli, L., DiMauro, S., Quinzii, C.M., Toscano, A., Cerebellar ataxia and severe muscle CoQ10 deficiency in a patient with a novel mutation in ADCK3. Clin. Genet., 2016, 10.1111/cge.12742 Published online January 27, 2016.
-
(2016)
Clin. Genet.
-
-
Barca, E.1
Musumeci, O.2
Montagnese, F.3
Marino, S.4
Granata, F.5
Nunnari, D.6
Peverelli, L.7
DiMauro, S.8
Quinzii, C.M.9
Toscano, A.10
-
5
-
-
0028341134
-
The glycine-rich sequence of protein kinases: a multifunctional element
-
Bossemeyer, D., The glycine-rich sequence of protein kinases: a multifunctional element. Trends Biochem. Sci. 19 (1994), 201–205.
-
(1994)
Trends Biochem. Sci.
, vol.19
, pp. 201-205
-
-
Bossemeyer, D.1
-
6
-
-
80053465657
-
Functional viability profiles of breast cancer
-
Brough, R., Frankum, J.R., Sims, D., Mackay, A., Mendes-Pereira, A.M., Bajrami, I., Costa-Cabral, S., Rafiq, R., Ahmad, A.S., Cerone, M.A., et al. Functional viability profiles of breast cancer. Cancer Discov. 1 (2011), 260–273.
-
(2011)
Cancer Discov.
, vol.1
, pp. 260-273
-
-
Brough, R.1
Frankum, J.R.2
Sims, D.3
Mackay, A.4
Mendes-Pereira, A.M.5
Bajrami, I.6
Costa-Cabral, S.7
Rafiq, R.8
Ahmad, A.S.9
Cerone, M.A.10
-
7
-
-
0014558891
-
Biosynthesis of ubiquinone in Escherichia coli K-12: location of genes affecting the metabolism of 3-octaprenyl-4-hydroxybenzoic acid and 2-octaprenylphenol
-
Cox, G.B., Young, I.G., McCann, L.M., Gibson, F., Biosynthesis of ubiquinone in Escherichia coli K-12: location of genes affecting the metabolism of 3-octaprenyl-4-hydroxybenzoic acid and 2-octaprenylphenol. J. Bacteriol. 99 (1969), 450–458.
-
(1969)
J. Bacteriol.
, vol.99
, pp. 450-458
-
-
Cox, G.B.1
Young, I.G.2
McCann, L.M.3
Gibson, F.4
-
8
-
-
0001186007
-
Isolation of a quinone from beef heart mitochondria
-
Crane, F.L., Hatefi, Y., Lester, R.L., Widmer, C., Isolation of a quinone from beef heart mitochondria. Biochim. Biophys. Acta 25 (1957), 220–221.
-
(1957)
Biochim. Biophys. Acta
, vol.25
, pp. 220-221
-
-
Crane, F.L.1
Hatefi, Y.2
Lester, R.L.3
Widmer, C.4
-
9
-
-
33749010065
-
Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport
-
Custer, S.K., Garden, G.A., Gill, N., Rueb, U., Libby, R.T., Schultz, C., Guyenet, S.J., Deller, T., Westrum, L.E., Sopher, B.L., La Spada, A.R., Bergmann glia expression of polyglutamine-expanded ataxin-7 produces neurodegeneration by impairing glutamate transport. Nat. Neurosci. 9 (2006), 1302–1311.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 1302-1311
-
-
Custer, S.K.1
Garden, G.A.2
Gill, N.3
Rueb, U.4
Libby, R.T.5
Schultz, C.6
Guyenet, S.J.7
Deller, T.8
Westrum, L.E.9
Sopher, B.L.10
La Spada, A.R.11
-
10
-
-
0035947594
-
A defect in coenzyme Q biosynthesis is responsible for the respiratory deficiency in Saccharomyces cerevisiae abc1 mutants
-
Do, T.Q., Hsu, A.Y., Jonassen, T., Lee, P.T., Clarke, C.F., A defect in coenzyme Q biosynthesis is responsible for the respiratory deficiency in Saccharomyces cerevisiae abc1 mutants. J. Biol. Chem. 276 (2001), 18161–18168.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 18161-18168
-
-
Do, T.Q.1
Hsu, A.Y.2
Jonassen, T.3
Lee, P.T.4
Clarke, C.F.5
-
11
-
-
84870839593
-
ATPase-dependent role of the atypical kinase Rio2 on the evolving pre-40S ribosomal subunit
-
Ferreira-Cerca, S., Sagar, V., Schäfer, T., Diop, M., Wesseling, A.M., Lu, H., Chai, E., Hurt, E., LaRonde-LeBlanc, N., ATPase-dependent role of the atypical kinase Rio2 on the evolving pre-40S ribosomal subunit. Nat. Struct. Mol. Biol. 19 (2012), 1316–1323.
-
(2012)
Nat. Struct. Mol. Biol.
, vol.19
, pp. 1316-1323
-
-
Ferreira-Cerca, S.1
Sagar, V.2
Schäfer, T.3
Diop, M.4
Wesseling, A.M.5
Lu, H.6
Chai, E.7
Hurt, E.8
LaRonde-LeBlanc, N.9
-
12
-
-
84992735863
-
Mitochondrial protein interaction mapping identifies new regulators of respiratory chain function
-
this issue
-
Floyd, B.J., Wilkerson, E.M., Veling, M.T., Minogue, C.E., Xia, C., Beebe, E.T., Wrobel, R.L., Cho, H., Kremer, L.S., Alston, C.L., et al. Mitochondrial protein interaction mapping identifies new regulators of respiratory chain function. Mol. Cell 63 (2016), 621–632 this issue.
-
(2016)
Mol. Cell
, vol.63
, pp. 621-632
-
-
Floyd, B.J.1
Wilkerson, E.M.2
Veling, M.T.3
Minogue, C.E.4
Xia, C.5
Beebe, E.T.6
Wrobel, R.L.7
Cho, H.8
Kremer, L.S.9
Alston, C.L.10
-
13
-
-
77955424107
-
Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy
-
Gerards, M., van den Bosch, B., Calis, C., Schoonderwoerd, K., van Engelen, K., Tijssen, M., de Coo, R., van der Kooi, A., Smeets, H., Nonsense mutations in CABC1/ADCK3 cause progressive cerebellar ataxia and atrophy. Mitochondrion 10 (2010), 510–515.
-
(2010)
Mitochondrion
, vol.10
, pp. 510-515
-
-
Gerards, M.1
van den Bosch, B.2
Calis, C.3
Schoonderwoerd, K.4
van Engelen, K.5
Tijssen, M.6
de Coo, R.7
van der Kooi, A.8
Smeets, H.9
-
14
-
-
0342460538
-
Tonic synaptic inhibition modulates neuronal output pattern and spatiotemporal synaptic integration
-
Häusser, M., Clark, B.A., Tonic synaptic inhibition modulates neuronal output pattern and spatiotemporal synaptic integration. Neuron 19 (1997), 665–678.
-
(1997)
Neuron
, vol.19
, pp. 665-678
-
-
Häusser, M.1
Clark, B.A.2
-
15
-
-
84895725183
-
Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants
-
He, C.H., Xie, L.X., Allan, C.M., Tran, U.C., Clarke, C.F., Coenzyme Q supplementation or over-expression of the yeast Coq8 putative kinase stabilizes multi-subunit Coq polypeptide complexes in yeast coq null mutants. Biochim. Biophys. Acta 1841 (2014), 630–644.
-
(2014)
Biochim. Biophys. Acta
, vol.1841
, pp. 630-644
-
-
He, C.H.1
Xie, L.X.2
Allan, C.M.3
Tran, U.C.4
Clarke, C.F.5
-
16
-
-
0030859238
-
Role of the glycine triad in the ATP-binding site of cAMP-dependent protein kinase
-
Hemmer, W., McGlone, M., Tsigelny, I., Taylor, S.S., Role of the glycine triad in the ATP-binding site of cAMP-dependent protein kinase. J. Biol. Chem. 272 (1997), 16946–16954.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 16946-16954
-
-
Hemmer, W.1
McGlone, M.2
Tsigelny, I.3
Taylor, S.S.4
-
17
-
-
84855616355
-
Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3
-
Horvath, R., Czermin, B., Gulati, S., Demuth, S., Houge, G., Pyle, A., Dineiger, C., Blakely, E.L., Hassani, A., Foley, C., et al. Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3. J. Neurol. Neurosurg. Psychiatry 83 (2012), 174–178.
-
(2012)
J. Neurol. Neurosurg. Psychiatry
, vol.83
, pp. 174-178
-
-
Horvath, R.1
Czermin, B.2
Gulati, S.3
Demuth, S.4
Houge, G.5
Pyle, A.6
Dineiger, C.7
Blakely, E.L.8
Hassani, A.9
Foley, C.10
-
18
-
-
33947226782
-
Structural and functional diversity of the microbial kinome
-
Kannan, N., Taylor, S.S., Zhai, Y., Venter, J.C., Manning, G., Structural and functional diversity of the microbial kinome. PLoS Biol., 5, 2007, e17.
-
(2007)
PLoS Biol.
, vol.5
, pp. e17
-
-
Kannan, N.1
Taylor, S.S.2
Zhai, Y.3
Venter, J.C.4
Manning, G.5
-
19
-
-
0026342401
-
Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase
-
Knighton, D.R., Zheng, J.H., Ten Eyck, L.F., Ashford, V.A., Xuong, N.H., Taylor, S.S., Sowadski, J.M., Crystal structure of the catalytic subunit of cyclic adenosine monophosphate-dependent protein kinase. Science 253 (1991), 407–414.
-
(1991)
Science
, vol.253
, pp. 407-414
-
-
Knighton, D.R.1
Zheng, J.H.2
Ten Eyck, L.F.3
Ashford, V.A.4
Xuong, N.H.5
Taylor, S.S.6
Sowadski, J.M.7
-
20
-
-
33845197964
-
Surface comparison of active and inactive protein kinases identifies a conserved activation mechanism
-
Kornev, A.P., Haste, N.M., Taylor, S.S., Eyck, L.F., Surface comparison of active and inactive protein kinases identifies a conserved activation mechanism. Proc. Natl. Acad. Sci. U S A 103 (2006), 17783–17788.
-
(2006)
Proc. Natl. Acad. Sci. U S A
, vol.103
, pp. 17783-17788
-
-
Kornev, A.P.1
Haste, N.M.2
Taylor, S.S.3
Eyck, L.F.4
-
21
-
-
84953236882
-
Structural basis for the non-catalytic functions of protein kinases
-
Kung, J.E., Jura, N., Structural basis for the non-catalytic functions of protein kinases. Structure 24 (2016), 7–24.
-
(2016)
Structure
, vol.24
, pp. 7-24
-
-
Kung, J.E.1
Jura, N.2
-
22
-
-
41149121580
-
ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency
-
Lagier-Tourenne, C., Tazir, M., López, L.C., Quinzii, C.M., Assoum, M., Drouot, N., Busso, C., Makri, S., Ali-Pacha, L., Benhassine, T., et al. ADCK3, an ancestral kinase, is mutated in a form of recessive ataxia associated with coenzyme Q10 deficiency. Am. J. Hum. Genet. 82 (2008), 661–672.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 661-672
-
-
Lagier-Tourenne, C.1
Tazir, M.2
López, L.C.3
Quinzii, C.M.4
Assoum, M.5
Drouot, N.6
Busso, C.7
Makri, S.8
Ali-Pacha, L.9
Benhassine, T.10
-
23
-
-
0016613913
-
Cell number and cell density in the cerebellar cortex of man and some other mammals
-
Lange, W., Cell number and cell density in the cerebellar cortex of man and some other mammals. Cell Tissue Res. 157 (1975), 115–124.
-
(1975)
Cell Tissue Res.
, vol.157
, pp. 115-124
-
-
Lange, W.1
-
24
-
-
84897045738
-
The molecular genetics of coenzyme Q biosynthesis in health and disease
-
Laredj, L.N., Licitra, F., Puccio, H.M., The molecular genetics of coenzyme Q biosynthesis in health and disease. Biochimie 100 (2014), 78–87.
-
(2014)
Biochimie
, vol.100
, pp. 78-87
-
-
Laredj, L.N.1
Licitra, F.2
Puccio, H.M.3
-
25
-
-
0031722706
-
Novel families of putative protein kinases in bacteria and archaea: evolution of the “eukaryotic” protein kinase superfamily
-
Leonard, C.J., Aravind, L., Koonin, E.V., Novel families of putative protein kinases in bacteria and archaea: evolution of the “eukaryotic” protein kinase superfamily. Genome Res. 8 (1998), 1038–1047.
-
(1998)
Genome Res.
, vol.8
, pp. 1038-1047
-
-
Leonard, C.J.1
Aravind, L.2
Koonin, E.V.3
-
26
-
-
0001553686
-
The natural occurrence of coenzyme Q and related compounds
-
Lester, R.L., Crane, F.L., The natural occurrence of coenzyme Q and related compounds. J. Biol. Chem. 234 (1959), 2169–2175.
-
(1959)
J. Biol. Chem.
, vol.234
, pp. 2169-2175
-
-
Lester, R.L.1
Crane, F.L.2
-
27
-
-
84903980293
-
An overview of current mouse models recapitulating coenzyme q10 deficiency syndrome
-
Licitra, F., Puccio, H., An overview of current mouse models recapitulating coenzyme q10 deficiency syndrome. Mol. Syndromol. 5 (2014), 180–186.
-
(2014)
Mol. Syndromol.
, vol.5
, pp. 180-186
-
-
Licitra, F.1
Puccio, H.2
-
28
-
-
84879475236
-
Loss of plastoglobule kinases ABC1K1 and ABC1K3 causes conditional degreening, modified prenyl-lipids, and recruitment of the jasmonic acid pathway
-
Lundquist, P.K., Poliakov, A., Giacomelli, L., Friso, G., Appel, M., McQuinn, R.P., Krasnoff, S.B., Rowland, E., Ponnala, L., Sun, Q., van Wijk, K.J., Loss of plastoglobule kinases ABC1K1 and ABC1K3 causes conditional degreening, modified prenyl-lipids, and recruitment of the jasmonic acid pathway. Plant Cell 25 (2013), 1818–1839.
-
(2013)
Plant Cell
, vol.25
, pp. 1818-1839
-
-
Lundquist, P.K.1
Poliakov, A.2
Giacomelli, L.3
Friso, G.4
Appel, M.5
McQuinn, R.P.6
Krasnoff, S.B.7
Rowland, E.8
Ponnala, L.9
Sun, Q.10
van Wijk, K.J.11
-
29
-
-
67651154308
-
Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration
-
Maltecca, F., Magnoni, R., Cerri, F., Cox, G.A., Quattrini, A., Casari, G., Haploinsufficiency of AFG3L2, the gene responsible for spinocerebellar ataxia type 28, causes mitochondria-mediated Purkinje cell dark degeneration. J. Neurosci. 29 (2009), 9244–9254.
-
(2009)
J. Neurosci.
, vol.29
, pp. 9244-9254
-
-
Maltecca, F.1
Magnoni, R.2
Cerri, F.3
Cox, G.A.4
Quattrini, A.5
Casari, G.6
-
30
-
-
0037032835
-
The protein kinase complement of the human genome
-
Manning, G., Whyte, D.B., Martinez, R., Hunter, T., Sudarsanam, S., The protein kinase complement of the human genome. Science 298 (2002), 1912–1934.
-
(2002)
Science
, vol.298
, pp. 1912-1934
-
-
Manning, G.1
Whyte, D.B.2
Martinez, R.3
Hunter, T.4
Sudarsanam, S.5
-
31
-
-
84878467141
-
A chloroplast ABC1-like kinase regulates vitamin E metabolism in Arabidopsis
-
Martinis, J., Glauser, G., Valimareanu, S., Kessler, F., A chloroplast ABC1-like kinase regulates vitamin E metabolism in Arabidopsis. Plant Physiol. 162 (2013), 652–662.
-
(2013)
Plant Physiol.
, vol.162
, pp. 652-662
-
-
Martinis, J.1
Glauser, G.2
Valimareanu, S.3
Kessler, F.4
-
32
-
-
84886179220
-
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression
-
Mignot, C., Apartis, E., Durr, A., Marques Lourenço, C., Charles, P., Devos, D., Moreau, C., de Lonlay, P., Drouot, N., Burglen, L., et al. Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression. Orphanet J. Rare Dis., 8, 2013, 173.
-
(2013)
Orphanet J. Rare Dis.
, vol.8
, pp. 173
-
-
Mignot, C.1
Apartis, E.2
Durr, A.3
Marques Lourenço, C.4
Charles, P.5
Devos, D.6
Moreau, C.7
de Lonlay, P.8
Drouot, N.9
Burglen, L.10
-
33
-
-
41149134880
-
CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures
-
Mollet, J., Delahodde, A., Serre, V., Chretien, D., Schlemmer, D., Lombes, A., Boddaert, N., Desguerre, I., de Lonlay, P., de Baulny, H.O., et al. CABC1 gene mutations cause ubiquinone deficiency with cerebellar ataxia and seizures. Am. J. Hum. Genet. 82 (2008), 623–630.
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 623-630
-
-
Mollet, J.1
Delahodde, A.2
Serre, V.3
Chretien, D.4
Schlemmer, D.5
Lombes, A.6
Boddaert, N.7
Desguerre, I.8
de Lonlay, P.9
de Baulny, H.O.10
-
34
-
-
33845803442
-
Ubiquinone
-
Morton, R.A., Ubiquinone. Nature 182 (1958), 1764–1767.
-
(1958)
Nature
, vol.182
, pp. 1764-1767
-
-
Morton, R.A.1
-
35
-
-
84873324400
-
Ubiad1 is an antioxidant enzyme that regulates eNOS activity by CoQ10 synthesis
-
Mugoni, V., Postel, R., Catanzaro, V., De Luca, E., Turco, E., Digilio, G., Silengo, L., Murphy, M.P., Medana, C., Stainier, D.Y., et al. Ubiad1 is an antioxidant enzyme that regulates eNOS activity by CoQ10 synthesis. Cell 152 (2013), 504–518.
-
(2013)
Cell
, vol.152
, pp. 504-518
-
-
Mugoni, V.1
Postel, R.2
Catanzaro, V.3
De Luca, E.4
Turco, E.5
Digilio, G.6
Silengo, L.7
Murphy, M.P.8
Medana, C.9
Stainier, D.Y.10
-
36
-
-
84953840324
-
Identification and classification of small molecule kinases: insights into substrate recognition and specificity
-
Oruganty, K., Talevich, E.E., Neuwald, A.F., Kannan, N., Identification and classification of small molecule kinases: insights into substrate recognition and specificity. BMC Evol. Biol., 16, 2016, 7.
-
(2016)
BMC Evol. Biol.
, vol.16
, pp. 7
-
-
Oruganty, K.1
Talevich, E.E.2
Neuwald, A.F.3
Kannan, N.4
-
37
-
-
46349103594
-
A mitochondrial protein compendium elucidates complex I disease biology
-
Pagliarini, D.J., Calvo, S.E., Chang, B., Sheth, S.A., Vafai, S.B., Ong, S.E., Walford, G.A., Sugiana, C., Boneh, A., Chen, W.K., et al. A mitochondrial protein compendium elucidates complex I disease biology. Cell 134 (2008), 112–123.
-
(2008)
Cell
, vol.134
, pp. 112-123
-
-
Pagliarini, D.J.1
Calvo, S.E.2
Chang, B.3
Sheth, S.A.4
Vafai, S.B.5
Ong, S.E.6
Walford, G.A.7
Sugiana, C.8
Boneh, A.9
Chen, W.K.10
-
38
-
-
77954182740
-
Involvement of mitochondrial ferredoxin and para-aminobenzoic acid in yeast coenzyme Q biosynthesis
-
Pierrel, F., Hamelin, O., Douki, T., Kieffer-Jaquinod, S., Mühlenhoff, U., Ozeir, M., Lill, R., Fontecave, M., Involvement of mitochondrial ferredoxin and para-aminobenzoic acid in yeast coenzyme Q biosynthesis. Chem. Biol. 17 (2010), 449–459.
-
(2010)
Chem. Biol.
, vol.17
, pp. 449-459
-
-
Pierrel, F.1
Hamelin, O.2
Douki, T.3
Kieffer-Jaquinod, S.4
Mühlenhoff, U.5
Ozeir, M.6
Lill, R.7
Fontecave, M.8
-
39
-
-
0033820931
-
Identification of Escherichia coli ubiB, a gene required for the first monooxygenase step in ubiquinone biosynthesis
-
Poon, W.W., Davis, D.E., Ha, H.T., Jonassen, T., Rather, P.N., Clarke, C.F., Identification of Escherichia coli ubiB, a gene required for the first monooxygenase step in ubiquinone biosynthesis. J. Bacteriol. 182 (2000), 5139–5146.
-
(2000)
J. Bacteriol.
, vol.182
, pp. 5139-5146
-
-
Poon, W.W.1
Davis, D.E.2
Ha, H.T.3
Jonassen, T.4
Rather, P.N.5
Clarke, C.F.6
-
41
-
-
84874956967
-
Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging
-
Rhee, H.W., Zou, P., Udeshi, N.D., Martell, J.D., Mootha, V.K., Carr, S.A., Ting, A.Y., Proteomic mapping of mitochondria in living cells via spatially restricted enzymatic tagging. Science 339 (2013), 1328–1331.
-
(2013)
Science
, vol.339
, pp. 1328-1331
-
-
Rhee, H.W.1
Zou, P.2
Udeshi, N.D.3
Martell, J.D.4
Mootha, V.K.5
Carr, S.A.6
Ting, A.Y.7
-
42
-
-
0343559188
-
Distribution of coenzyme Q in rat liver cell fractions
-
Seshadri Sastry, P., Jayaraman, J., Ramasarma, T., Distribution of coenzyme Q in rat liver cell fractions. Nature, 189, 1961, 577.
-
(1961)
Nature
, vol.189
, pp. 577
-
-
Seshadri Sastry, P.1
Jayaraman, J.2
Ramasarma, T.3
-
43
-
-
51049121572
-
Identification of genes that regulate epithelial cell migration using an siRNA screening approach
-
Simpson, K.J., Selfors, L.M., Bui, J., Reynolds, A., Leake, D., Khvorova, A., Brugge, J.S., Identification of genes that regulate epithelial cell migration using an siRNA screening approach. Nat. Cell Biol. 10 (2008), 1027–1038.
-
(2008)
Nat. Cell Biol.
, vol.10
, pp. 1027-1038
-
-
Simpson, K.J.1
Selfors, L.M.2
Bui, J.3
Reynolds, A.4
Leake, D.5
Khvorova, A.6
Brugge, J.S.7
-
44
-
-
77950526211
-
Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes
-
Stankewich, M.C., Gwynn, B., Ardito, T., Ji, L., Kim, J., Robledo, R.F., Lux, S.E., Peters, L.L., Morrow, J.S., Targeted deletion of betaIII spectrin impairs synaptogenesis and generates ataxic and seizure phenotypes. Proc. Natl. Acad. Sci. U S A 107 (2010), 6022–6027.
-
(2010)
Proc. Natl. Acad. Sci. U S A
, vol.107
, pp. 6022-6027
-
-
Stankewich, M.C.1
Gwynn, B.2
Ardito, T.3
Ji, L.4
Kim, J.5
Robledo, R.F.6
Lux, S.E.7
Peters, L.L.8
Morrow, J.S.9
-
45
-
-
84920625908
-
Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis
-
Stefely, J.A., Reidenbach, A.G., Ulbrich, A., Oruganty, K., Floyd, B.J., Jochem, A., Saunders, J.M., Johnson, I.E., Minogue, C.E., Wrobel, R.L., et al. Mitochondrial ADCK3 employs an atypical protein kinase-like fold to enable coenzyme Q biosynthesis. Mol. Cell 57 (2015), 83–94.
-
(2015)
Mol. Cell
, vol.57
, pp. 83-94
-
-
Stefely, J.A.1
Reidenbach, A.G.2
Ulbrich, A.3
Oruganty, K.4
Floyd, B.J.5
Jochem, A.6
Saunders, J.M.7
Johnson, I.E.8
Minogue, C.E.9
Wrobel, R.L.10
-
46
-
-
84946574062
-
Golgi fragmentation in amyotrophic lateral sclerosis, an overview of possible triggers and consequences
-
Sundaramoorthy, V., Sultana, J.M., Atkin, J.D., Golgi fragmentation in amyotrophic lateral sclerosis, an overview of possible triggers and consequences. Front. Neurosci., 9, 2015, 400.
-
(2015)
Front. Neurosci.
, vol.9
, pp. 400
-
-
Sundaramoorthy, V.1
Sultana, J.M.2
Atkin, J.D.3
-
47
-
-
84883411824
-
Mcp1 and Mcp2, two novel proteins involved in mitochondrial lipid homeostasis
-
Tan, T., Ozbalci, C., Brügger, B., Rapaport, D., Dimmer, K.S., Mcp1 and Mcp2, two novel proteins involved in mitochondrial lipid homeostasis. J. Cell Sci. 126 (2013), 3563–3574.
-
(2013)
J. Cell Sci.
, vol.126
, pp. 3563-3574
-
-
Tan, T.1
Ozbalci, C.2
Brügger, B.3
Rapaport, D.4
Dimmer, K.S.5
-
48
-
-
55349084786
-
Ubiquinone biosynthesis in Saccharomyces cerevisiae: the molecular organization of O-methylase Coq3p depends on Abc1p/Coq8p
-
Tauche, A., Krause-Buchholz, U., Rödel, G., Ubiquinone biosynthesis in Saccharomyces cerevisiae: the molecular organization of O-methylase Coq3p depends on Abc1p/Coq8p. FEMS Yeast Res. 8 (2008), 1263–1275.
-
(2008)
FEMS Yeast Res.
, vol.8
, pp. 1263-1275
-
-
Tauche, A.1
Krause-Buchholz, U.2
Rödel, G.3
-
49
-
-
34248195476
-
Endogenous synthesis of coenzyme Q in eukaryotes
-
Tran, U.C., Clarke, C.F., Endogenous synthesis of coenzyme Q in eukaryotes. Mitochondrion 7:Suppl (2007), S62–S71.
-
(2007)
Mitochondrion
, vol.7
, pp. S62-S71
-
-
Tran, U.C.1
Clarke, C.F.2
-
50
-
-
0033581886
-
Structural insights into phosphoinositide 3-kinase catalysis and signalling
-
Walker, E.H., Perisic, O., Ried, C., Stephens, L., Williams, R.L., Structural insights into phosphoinositide 3-kinase catalysis and signalling. Nature 402 (1999), 313–320.
-
(1999)
Nature
, vol.402
, pp. 313-320
-
-
Walker, E.H.1
Perisic, O.2
Ried, C.3
Stephens, L.4
Williams, R.L.5
-
51
-
-
77954929373
-
Pattern of retinoblastoma pathway inactivation dictates response to CDK4/6 inhibition in GBM
-
Wiedemeyer, W.R., Dunn, I.F., Quayle, S.N., Zhang, J., Chheda, M.G., Dunn, G.P., Zhuang, L., Rosenbluh, J., Chen, S., Xiao, Y., et al. Pattern of retinoblastoma pathway inactivation dictates response to CDK4/6 inhibition in GBM. Proc. Natl. Acad. Sci. U S A 107 (2010), 11501–11506.
-
(2010)
Proc. Natl. Acad. Sci. U S A
, vol.107
, pp. 11501-11506
-
-
Wiedemeyer, W.R.1
Dunn, I.F.2
Quayle, S.N.3
Zhang, J.4
Chheda, M.G.5
Dunn, G.P.6
Zhuang, L.7
Rosenbluh, J.8
Chen, S.9
Xiao, Y.10
-
52
-
-
84876826707
-
Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration
-
Wolf, N.I., Koenig, M., Progressive cerebellar atrophy: hereditary ataxias and disorders with spinocerebellar degeneration. Handb. Clin. Neurol. 113 (2013), 1869–1878.
-
(2013)
Handb. Clin. Neurol.
, vol.113
, pp. 1869-1878
-
-
Wolf, N.I.1
Koenig, M.2
-
53
-
-
79953795039
-
Expression of the human atypical kinase ADCK3 rescues coenzyme Q biosynthesis and phosphorylation of Coq polypeptides in yeast coq8 mutants
-
Xie, L.X., Hsieh, E.J., Watanabe, S., Allan, C.M., Chen, J.Y., Tran, U.C., Clarke, C.F., Expression of the human atypical kinase ADCK3 rescues coenzyme Q biosynthesis and phosphorylation of Coq polypeptides in yeast coq8 mutants. Biochim. Biophys. Acta 1811 (2011), 348–360.
-
(2011)
Biochim. Biophys. Acta
, vol.1811
, pp. 348-360
-
-
Xie, L.X.1
Hsieh, E.J.2
Watanabe, S.3
Allan, C.M.4
Chen, J.Y.5
Tran, U.C.6
Clarke, C.F.7
-
54
-
-
78649642175
-
Pseudokinases-remnants of evolution or key allosteric regulators?
-
Zeqiraj, E., van Aalten, D.M., Pseudokinases-remnants of evolution or key allosteric regulators?. Curr. Opin. Struct. Biol. 20 (2010), 772–781.
-
(2010)
Curr. Opin. Struct. Biol.
, vol.20
, pp. 772-781
-
-
Zeqiraj, E.1
van Aalten, D.M.2
|