Proteomics: Applications and Advances References 493
Part C | 18
J. Peragón: Proteomics in the liver of gilthead sea
bream (Sparus aurata) to elucidate the cellular
response induced by the intake of maslinic acid,
Proteomics 11(16), 3312–3325 (2011)
18.50
M. Fernández-Navarro, J. Peragón, F.J. Esteban,
M. De La Higuera, J.A. Lupiáñez: Maslinic acid
as a feed additive to stimulate growth and
hepatic protein-turnover rates in rainbow trout
(Onchorhynchus mykiss), Comp. Biochem. Physiol. Toxicol. Pharmacol. 144(2), 130–140 (2006)
18.51
A. Ibarz, R. Costa, A.P. Harrison, D.M. Power: Dietary keto-acid feed-back on pituitary activity in
gilthead sea bream: Effects of oral doses of AKG,
A proteomic Approach. Gen. Comp. Endocrinol.
169(3), 284–292 (2010)
18.52
M.F. Addis, R. Cappuccinelli, V. Tedde, D. Pagnozzi, M.C. Porcu, E. Bonaglini, T. Roggio, S. Uzzau: Proteomic analysis of muscle tissue from
gilthead sea bream (Sparus aurata, L.) farmed
in offshore floating cages, Aquaculture 309(1–4),
245–252 (2010)
18.53
M.A. Sewell, S. Eriksen, M.J. Middleditch: Identification of protein components from the mature
ovary of the sea urchin Evechinus chloroticus
(Echinodermata: Echinoidea), Proteomics 8(12),
2531–2542 (2008)
18.54
K.K.W. Wong, A.C. Lane, P.T.Y. Leung, V. Thiyagarajan: Response of larval barnacle proteome to CO 2 -
driven seawater acidification, Comp. Biochem.
Physiol. Part D 6(3), 310–321 (2011)
18.55
F. Silvestre, V. Gillardin, J. Dorts: Proteomics
to assess the role of phenotypic plasticity in
aquatic organisms exposed to pollution and
global warming, Integr. Comp. Biol. 52(5), 681–
694 (2012)
18.56
M. Byrne, N. Soars, P. Selvakumaraswamy,
S.A. Dworjanyn, A.R. Davis: Sea urchin fertilization in a warm, acidified and high pCO 2 ocean
across a range of sperm densities, Mar. Environ.
Res. 69(4), 234–239 (2010)
18.57
V. Thiyagarajan: A review on the role of chemical cues in habitat selection by barnacles: New
insights from larval proteomics, J. Exp. Mar. Biol.
Ecol. 392(1/2), 22–36 (2010)
18.58
L. Tomanek, M.J. Zuzow, A.V. Ivanina, E. Beniash, I.M. Sokolova: Proteomic response to elevated PCO 2 level in eastern oysters, Crassostrea
virginica: Evidence for oxidative stress, J. Exp.
Biol. 214(11), 1836–1844 (2011)
18.59
L. Tomanek, M.J. Zuzow: The proteomic response
of the mussel congeners Mytilus galloprovincialis
and M. trossulus to acute heat stress: Implications
for thermal tolerance limits and metabolic costs
of thermal stress, J. Exp. Biol. 213(20), 3559–3574
(2010)
18.60
P.A. Fields, M.J. Zuzow, L. Tomanek: Proteomic
responses of blue mussel (Mytilus) congeners
to temperature acclimation, J. Exp. Biol. 215(7),
1106–1116 (2012)
18.61
V. Matranga, A. Pinsino, D. Randazzo, A. Giallongo, P. Dubois: Long-term environmental exposure to metals (Cu, Cd, Pb, Zn) activates the
immune cell stress response in the common European sea star (Asterias rubens), Mar. Environ. Res.
76, 122–127 (2012)
18.62
N. Veldhoen, M.G. Ikonomou, C.C. Helbing:
Molecular profiling of marine fauna: Integration
of omics with environmental assessment of the
world’s oceans, Ecotoxicol. Environ. Saf. 76(2), 23–
38 (2012)
18.63
F. Liu, D.-Z. Wang, W.-X. Wang: Cadmiuminduced changes in trace element bioaccumulation and proteomics perspective in four marine bivalves, Environ. Toxicol. Chem./SETAC 31(6),
1292–1300 (2012)
18.64
A. Campos, S. Tedesco, V. Vasconcelos, S. Cristobal: Proteomic research in bivalves: Towards the
identification of molecular markers of aquatic
pollution, J. Proteomics 75(14), 4346–4359 (2012)
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H. Amelina, I. Apraiz, W. Sun, S. Cristobal:
Proteomics-based method for the assessment of
marine pollution using liquid chromatography
coupled with two-dimensional electrophoresis,
J. Proteome Res. 6(6), 2094–2104 (2007)
18.66
P.T.Y. Leung, Y. Wang, S.S.T. Mak, W.C. Ng,
K.M.Y. Leung: Differential proteomic responses
in hepatopancreas and adductor muscles of the
green-lipped mussel Perna viridis to stresses
induced by cadmium and hydrogen peroxide,
Aquatic Toxicol. 105(1/2), 49–61 (2011)
18.67
A. Romero-Ruiz, M. Carrascal, J. Alhama,
J.L. Gómez-Ariza, J. Abian, J. López-Barea:
Utility of proteomics to assess pollutant response
of clams from the Doñana bank of Guadalquivir
Estuary (SW Spain), Proteomics 6(Suppl. 1),
S245–255 (2006)
18.68
K. Berg, P. Puntervoll, S. Valdersnes, A. Goksøyr: Responses in the brain proteome of Atlantic
cod (Gadus morhua) exposed to methylmercury,
Aquat. Toxicol. 100(1), 51–65 (2010)
18.69
D.C. Evers, M.A. Turnquist, D.G. Buck: Patterns
of global seafood mercury concentrations and
their relationship with human health, version 3.
BRI (Science, Communications Series, (Biodiversity Research Institute, Gorham 2012) pp. 1–12
18.70
J. Zhou, Z.-H. Cai, L. Li, Y.-F. Gao, T.H. Hutchinson: A proteomics based approach to assessing
the toxicity of bisphenol A and diallyl phthalate
to the abalone (Haliotis diversicolor supertexta),
Chemosphere 79(5), 595–604 (2010)
18.71
International Programme on Chemical Safety
(2002) Global assessment of the state-ofthe-science of endocrine disruptors. In:
WHO/PCS/EDC/02.2.
http://www.who.int/ipcs/
publications/new_issues/endocrine_disruptors/
en/
18.72
C. Gestal, P. Roch, T. Renault, A. Pallavicini,
C. Paillard, B. Novoa, R. Oubella, P. Venier,
Part C | 18
J. Peragón: Proteomics in the liver of gilthead sea
bream (Sparus aurata) to elucidate the cellular
response induced by the intake of maslinic acid,
Proteomics 11(16), 3312–3325 (2011)
18.50
M. Fernández-Navarro, J. Peragón, F.J. Esteban,
M. De La Higuera, J.A. Lupiáñez: Maslinic acid
as a feed additive to stimulate growth and
hepatic protein-turnover rates in rainbow trout
(Onchorhynchus mykiss), Comp. Biochem. Physiol. Toxicol. Pharmacol. 144(2), 130–140 (2006)
18.51
A. Ibarz, R. Costa, A.P. Harrison, D.M. Power: Dietary keto-acid feed-back on pituitary activity in
gilthead sea bream: Effects of oral doses of AKG,
A proteomic Approach. Gen. Comp. Endocrinol.
169(3), 284–292 (2010)
18.52
M.F. Addis, R. Cappuccinelli, V. Tedde, D. Pagnozzi, M.C. Porcu, E. Bonaglini, T. Roggio, S. Uzzau: Proteomic analysis of muscle tissue from
gilthead sea bream (Sparus aurata, L.) farmed
in offshore floating cages, Aquaculture 309(1–4),
245–252 (2010)
18.53
M.A. Sewell, S. Eriksen, M.J. Middleditch: Identification of protein components from the mature
ovary of the sea urchin Evechinus chloroticus
(Echinodermata: Echinoidea), Proteomics 8(12),
2531–2542 (2008)
18.54
K.K.W. Wong, A.C. Lane, P.T.Y. Leung, V. Thiyagarajan: Response of larval barnacle proteome to CO 2 -
driven seawater acidification, Comp. Biochem.
Physiol. Part D 6(3), 310–321 (2011)
18.55
F. Silvestre, V. Gillardin, J. Dorts: Proteomics
to assess the role of phenotypic plasticity in
aquatic organisms exposed to pollution and
global warming, Integr. Comp. Biol. 52(5), 681–
694 (2012)
18.56
M. Byrne, N. Soars, P. Selvakumaraswamy,
S.A. Dworjanyn, A.R. Davis: Sea urchin fertilization in a warm, acidified and high pCO 2 ocean
across a range of sperm densities, Mar. Environ.
Res. 69(4), 234–239 (2010)
18.57
V. Thiyagarajan: A review on the role of chemical cues in habitat selection by barnacles: New
insights from larval proteomics, J. Exp. Mar. Biol.
Ecol. 392(1/2), 22–36 (2010)
18.58
L. Tomanek, M.J. Zuzow, A.V. Ivanina, E. Beniash, I.M. Sokolova: Proteomic response to elevated PCO 2 level in eastern oysters, Crassostrea
virginica: Evidence for oxidative stress, J. Exp.
Biol. 214(11), 1836–1844 (2011)
18.59
L. Tomanek, M.J. Zuzow: The proteomic response
of the mussel congeners Mytilus galloprovincialis
and M. trossulus to acute heat stress: Implications
for thermal tolerance limits and metabolic costs
of thermal stress, J. Exp. Biol. 213(20), 3559–3574
(2010)
18.60
P.A. Fields, M.J. Zuzow, L. Tomanek: Proteomic
responses of blue mussel (Mytilus) congeners
to temperature acclimation, J. Exp. Biol. 215(7),
1106–1116 (2012)
18.61
V. Matranga, A. Pinsino, D. Randazzo, A. Giallongo, P. Dubois: Long-term environmental exposure to metals (Cu, Cd, Pb, Zn) activates the
immune cell stress response in the common European sea star (Asterias rubens), Mar. Environ. Res.
76, 122–127 (2012)
18.62
N. Veldhoen, M.G. Ikonomou, C.C. Helbing:
Molecular profiling of marine fauna: Integration
of omics with environmental assessment of the
world’s oceans, Ecotoxicol. Environ. Saf. 76(2), 23–
38 (2012)
18.63
F. Liu, D.-Z. Wang, W.-X. Wang: Cadmiuminduced changes in trace element bioaccumulation and proteomics perspective in four marine bivalves, Environ. Toxicol. Chem./SETAC 31(6),
1292–1300 (2012)
18.64
A. Campos, S. Tedesco, V. Vasconcelos, S. Cristobal: Proteomic research in bivalves: Towards the
identification of molecular markers of aquatic
pollution, J. Proteomics 75(14), 4346–4359 (2012)
18.65
H. Amelina, I. Apraiz, W. Sun, S. Cristobal:
Proteomics-based method for the assessment of
marine pollution using liquid chromatography
coupled with two-dimensional electrophoresis,
J. Proteome Res. 6(6), 2094–2104 (2007)
18.66
P.T.Y. Leung, Y. Wang, S.S.T. Mak, W.C. Ng,
K.M.Y. Leung: Differential proteomic responses
in hepatopancreas and adductor muscles of the
green-lipped mussel Perna viridis to stresses
induced by cadmium and hydrogen peroxide,
Aquatic Toxicol. 105(1/2), 49–61 (2011)
18.67
A. Romero-Ruiz, M. Carrascal, J. Alhama,
J.L. Gómez-Ariza, J. Abian, J. López-Barea:
Utility of proteomics to assess pollutant response
of clams from the Doñana bank of Guadalquivir
Estuary (SW Spain), Proteomics 6(Suppl. 1),
S245–255 (2006)
18.68
K. Berg, P. Puntervoll, S. Valdersnes, A. Goksøyr: Responses in the brain proteome of Atlantic
cod (Gadus morhua) exposed to methylmercury,
Aquat. Toxicol. 100(1), 51–65 (2010)
18.69
D.C. Evers, M.A. Turnquist, D.G. Buck: Patterns
of global seafood mercury concentrations and
their relationship with human health, version 3.
BRI (Science, Communications Series, (Biodiversity Research Institute, Gorham 2012) pp. 1–12
18.70
J. Zhou, Z.-H. Cai, L. Li, Y.-F. Gao, T.H. Hutchinson: A proteomics based approach to assessing
the toxicity of bisphenol A and diallyl phthalate
to the abalone (Haliotis diversicolor supertexta),
Chemosphere 79(5), 595–604 (2010)
18.71
International Programme on Chemical Safety
(2002) Global assessment of the state-ofthe-science of endocrine disruptors. In:
WHO/PCS/EDC/02.2.
http://www.who.int/ipcs/
publications/new_issues/endocrine_disruptors/
en/
18.72
C. Gestal, P. Roch, T. Renault, A. Pallavicini,
C. Paillard, B. Novoa, R. Oubella, P. Venier,