Published in Comp Biochem Physiol B Biochem Mol Biol on March 01, 2000
Evidence for the involvement of pathogenic bacteria in summer mortalities of the Pacific oyster Crassostrea gigas. Microb Ecol (2007) 1.18
Transcriptome profiling of selectively bred Pacific oyster Crassostrea gigas families that differ in tolerance of heat shock. Mar Biotechnol (NY) (2009) 0.97
DNA methylation is crucial for the early development in the Oyster C. gigas. Mar Biotechnol (NY) (2013) 0.97
Gametogenesis in the Pacific oyster Crassostrea gigas: a microarrays-based analysis identifies sex and stage specific genes. PLoS One (2012) 0.89
Microarray-based identification of gonad transcripts differentially expressed between lines of Pacific oyster selected to be resistant or susceptible to summer mortality. Mar Biotechnol (NY) (2009) 0.89
Genome-wide profiling of DNA methylation and gene expression in Crassostrea gigas male gametes. Front Physiol (2014) 0.89
Metabolomic investigations of American oysters using H-NMR spectroscopy. Mar Drugs (2010) 0.86
Identification of molecular and physiological responses to chronic environmental challenge in an invasive species: the Pacific oyster, Crassostrea gigas. Ecol Evol (2013) 0.81
Shotgun proteomics reveals physiological response to ocean acidification in Crassostrea gigas. BMC Genomics (2014) 0.80
Comparative bioaccumulation of trace metals using six filter feeder organisms in a coastal lagoon ecosystem (of the central-east Gulf of California). Environ Monit Assess (2012) 0.79
Regulation of a truncated isoform of AMP-activated protein kinase α (AMPKα) in response to hypoxia in the muscle of Pacific oyster Crassostrea gigas. J Comp Physiol B (2013) 0.77
Expression Characterization of Stress Genes Under High and Low Temperature Stresses in the Pacific Oyster, Crassostrea gigas. Mar Biotechnol (NY) (2016) 0.76
Genetic parameters of resistance to Vibrio aestuarianus, and OsHV-1 infections in the Pacific oyster, Crassostrea gigas, at three different life stages. Genet Sel Evol (2017) 0.75
Exposure to the Paralytic Shellfish Toxin Producer Alexandrium catenella Increases the Susceptibility of the Oyster Crassostrea gigas to Pathogenic Vibrios. Toxins (Basel) (2016) 0.75
The Kinome of Pacific Oyster Crassostrea gigas, Its Expression during Development and in Response to Environmental Factors. PLoS One (2016) 0.75
PfIRR Interacts with HrIGF-I and Activates the MAP-kinase and PI3-kinase Signaling Pathways to Regulate Glycogen Metabolism in Pinctada fucata. Sci Rep (2016) 0.75
Metal contamination in harbours impacts life-history traits and metallothionein levels in snails. PLoS One (2017) 0.75
Crystal structure of the RNA-dependent RNA polymerase of hepatitis C virus. Proc Natl Acad Sci U S A (1999) 3.77
Glucocorticoid receptor alpha and beta in glucocorticoid dependent asthma. Am J Respir Crit Care Med (2000) 2.36
Specific binding sites in the alcR and alcA promoters of the ethanol regulon for the CREA repressor mediating carbon catabolite repression in Aspergillus nidulans. Mol Microbiol (1993) 2.13
Dengue virus type 1 nonstructural glycoprotein NS1 is secreted from mammalian cells as a soluble hexamer in a glycosylation-dependent fashion. J Virol (1999) 2.07
Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients. Clin Chim Acta (1998) 1.81
Genotypic and phenotypic spectrum in tricho-rhino-phalangeal syndrome types I and III. Am J Hum Genet (2000) 1.80
The mouse dystonia musculorum gene is a neural isoform of bullous pemphigoid antigen 1. Nat Genet (1995) 1.60
Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1. Hum Mol Genet (1997) 1.59
Structure of the Sec7 domain of the Arf exchange factor ARNO. Nature (1998) 1.57
Crystal structure of enoyl-coenzyme A (CoA) hydratase at 2.5 angstroms resolution: a spiral fold defines the CoA-binding pocket. EMBO J (1996) 1.55
Expression of the Sonic hedgehog (SHH ) gene during early human development and phenotypic expression of new mutations causing holoprosencephaly. Hum Mol Genet (1999) 1.53
Homogentisic acid determined in biological fluids by HPLC. Clin Chem (1989) 1.50
Cell cycle-dependent recruitment of HDAC-1 correlates with deacetylation of histone H4 on an Rb-E2F target promoter. EMBO Rep (2001) 1.47
Gene transfer to human rheumatoid synovial tissue engrafted in SCID mice. J Rheumatol (1997) 1.43
[Home chemotherapy for lung cancer: a five year retrospective study]. Rev Mal Respir (2003) 1.40
Environmental regulation of Bacillus subtilis sigma(D)-dependent gene expression. J Bacteriol (2000) 1.39
Molecular analysis of pericentrin gene (PCNT) in a series of 24 Seckel/microcephalic osteodysplastic primordial dwarfism type II (MOPD II) families. J Med Genet (2009) 1.38
Structural basis for human monoglyceride lipase inhibition. J Mol Biol (2009) 1.32
Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts. Biochim Biophys Acta (1993) 1.24
N-terminal arm exchange is observed in the 2.15 A crystal structure of oxidized nitrite reductase from Pseudomonas aeruginosa. Structure (1997) 1.14
Regulation of alcR, the positive regulatory gene of the ethanol utilization regulon of Aspergillus nidulans. Mol Microbiol (1987) 1.09
[Organization and computerization of a cell bank (proceedings)]. Ann Biol Clin (Paris) (1978) 1.07
Identification of the promoter region involved in the autoregulation of the transcriptional activator ALCR in Aspergillus nidulans. Mol Cell Biol (1992) 1.06
Titre and combination of ICA and autoantibodies to glutamic acid decarboxylase discriminate two clinically distinct types of latent autoimmune diabetes in adults (LADA). Diabetologia (2001) 1.06
[Biological diagnosis of hereditary metabolic diseases. From selective screening to the mutant-cell bank]. Ann Biol Clin (Paris) (1988) 1.06
Dystonin-deficient mice exhibit an intrinsic muscle weakness and an instability of skeletal muscle cytoarchitecture. Dev Biol (1999) 1.05
International Federation of Clinical Chemistry, Scientific Division Committee on Enzymes: approved recommendation on IFCC methods for the measurement of catalytic concentration of enzymes. Part 7. IFCC method for creatine kinase (ATP: creatine N-phosphotransferase, EC 2.7.3.2). Eur J Clin Chem Clin Biochem (1991) 1.05
Dystonin is essential for maintaining neuronal cytoskeleton organization. Mol Cell Neurosci (1998) 1.04
Antibody inhibition of the transcriptase activity of the rotavirus DLP: a structural view. J Mol Biol (2001) 1.03
Specific binding sites for the activator protein, ALCR, in the alcA promoter of the ethanol regulon of Aspergillus nidulans. J Biol Chem (1992) 1.01
Use of a synthetic peptide antigen to generate antisera reactive with a proteolytic processing site in native human proinsulin: demonstration of cleavage within clathrin-coated (pro)secretory vesicles. Proc Natl Acad Sci U S A (1987) 1.01
[Total Condylar arthroplasty of the knee (author's transl)]. Chirurgie (1981) 1.01
40 kilobase deletion (CF 40 kb del 4-10) removes exons 4 to 10 of the Cystic Fibrosis Transmembrane Conductance Regulator gene. Hum Mutat (1998) 1.01
The inborn errors of mitochondrial fatty acid oxidation. J Inherit Metab Dis (1987) 1.00
SHOX point mutations in dyschondrosteosis. J Med Genet (2001) 1.00
The crystal structures of TrkA and TrkB suggest key regions for achieving selective inhibition. J Mol Biol (2012) 0.99
Crystallization and preliminary X-Ray analysis of rotavirus protein VP6. J Virol (1998) 0.98
Different expression of endothelin in the bronchoalveolar lavage in patients with pulmonary diseases. Lung (2002) 0.98
Microdeletion at chromosome 4q21 defines a new emerging syndrome with marked growth restriction, mental retardation and absent or severely delayed speech. J Med Genet (2010) 0.98
Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia. Eur J Pediatr (1993) 0.98
Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins. Genomics (1996) 0.97
Protein engineering with monomeric triosephosphate isomerase (monoTIM): the modelling and structure verification of a seven-residue loop. Protein Eng (1997) 0.97
Mutation analysis in 600 French cystic fibrosis patients. J Med Genet (1994) 0.97
Cloning and characterization of the neural isoforms of human dystonin. Genomics (1995) 0.96
Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice. Mol Cell Neurosci (1995) 0.96
Correct intron splicing generates a new type of a putative zinc-binding domain in a transcriptional activator of Aspergillus nidulans. FEBS Lett (1991) 0.96
Prenatal diagnosis of mitochondrial fatty acid oxidation defects. Prenat Diagn (1996) 0.96
IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign. Mol Syndromol (2010) 0.95
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome. Hum Genet (2013) 0.94
Renal insufficiency, a frequent complication with age in oral-facial-digital syndrome type I. Clin Genet (2009) 0.93
The ethanol regulon in Aspergillus nidulans: characterization and sequence of the positive regulatory gene alcR. Gene (1988) 0.93
[Heterogeneity of glycogenosis type VI. Study of leukocyte phosphorylase activity in 2 families]. Arch Fr Pediatr (1972) 0.93
The use of peritoneoscopy in the detection of liver metastases. Cancer (1978) 0.93
Land user participation in developing a computerised decision support system for combating desertification. Environ Monit Assess (2004) 0.93
A gene for Holt-Oram syndrome maps to the distal long arm of chromosome 12. Nat Genet (1994) 0.92
2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new case. J Inherit Metab Dis (1993) 0.91
Determination of total fatty acids in plasma: cis-5-tetradecenoic acid (C14:1 omega-9) in the diagnosis of long-chain fatty acid oxidation defects. J Inherit Metab Dis (1999) 0.90
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xq12-q21). Am J Hum Genet (1993) 0.90
Transcriptional potencies of inhaled glucocorticoids. Am J Respir Crit Care Med (2000) 0.90
Dystonin is an essential component of the Schwann cell cytoskeleton at the time of myelination. Development (1998) 0.90
Demonstration of the recurrence of Marfan-like skeletal and cardiovascular manifestations due to germline mosaicism for an FBN1 mutation. Am J Hum Genet (1999) 0.89
Complexation of two proteic insect inhibitors to the active site of chymotrypsin suggests decoupled roles for binding and selectivity. J Biol Chem (2001) 0.89
The crystal structure of human CskSH3: structural diversity near the RT-Src and n-Src loop. FEBS Lett (1994) 0.88
Hunter syndrome: gene deletions and rearrangements. Hum Mutat (1993) 0.88
Juvenile metachromatic leukodystrophy: neurological outcome two years after bone marrow transplantation. J Inherit Metab Dis (1995) 0.88
First trimester prenatal diagnosis of glycogen storage disease type III. J Inherit Metab Dis (1989) 0.88
Diagnosis of alcaptonuria: rapid analysis of homogentisic acid by HPLC. Clin Chim Acta (1990) 0.88
Structured learning in teaching therapists social skills training: acquisition, maintenance, and impact on client outcome. J Consult Clin Psychol (1980) 0.87
Comparison of red cell transfusion and polyethylene glycol-modified adenosine deaminase therapy in an adenosine deaminase-deficient child: measurement of erythrocyte deoxyadenosine triphosphate as a useful tool. Pediatr Res (1990) 0.87
[Our experience of 2 years oferythrocyte enzymology in pediatrics. Apropos of 250 cases]. Ann Biol Clin (Paris) (1968) 0.87
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2. Am J Hum Genet (1992) 0.86
Effects of five natural gonadotropin-releasing hormones on cell suspensions of marine bivalve gonad: stimulation of gonial DNA synthesis. Gen Comp Endocrinol (1999) 0.86
Regulation of the aldehyde dehydrogenase gene (aldA) and its role in the control of the coinducer level necessary for induction of the ethanol utilization pathway in Aspergillus nidulans. J Biol Chem (2000) 0.86
Pain after total hip arthroplasty: a psychiatric point of view. Int Orthop (2007) 0.86
[Accidents caused by arteritis after fracture or tibial osteotomy]. Rev Chir Orthop Reparatrice Appar Mot (1987) 0.86
Characterization of a cDNA encoding a 72 kDa heat shock cognate protein (Hsc72) from the Pacific oyster, Crassostrea gigas. DNA Seq (2000) 0.85
Stable transfection of the estrogen receptor cDNA into Hela cells induces estrogen responsiveness of endogenous cathepsin D gene but not of cell growth. Biochem Biophys Res Commun (1990) 0.85
[Chronic diarrhea due to pancreatic lipase deficiency]. Pediatrie (1970) 0.85
Diagnosis of mucopolysaccharidoses in a clinically selected population by urinary glycosaminoglycan analysis: a study of 2,000 urine samples. Clin Chim Acta (1993) 0.85
Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts. Clin Chim Acta (1992) 0.85
A 45,X male with an X;Y translocation: implications for the mapping of the genes responsible for Turner syndrome and X-linked chondrodysplasia punctata. Hum Mol Genet (1993) 0.84
A target-orientated algorithm for regional citrate-calcium anticoagulation in extracorporeal therapies. Blood Purif (2011) 0.84
Diagnosis of inborn errors of metabolism by acylcarnitine profiling in blood using tandem mass spectrometry. J Inherit Metab Dis (1997) 0.84
FGF3 from Xenopus laevis. EMBO J (1993) 0.84
Lumping Juberg-Marsidi syndrome and X-linked alpha-thalassemia/mental retardation syndrome? Am J Med Genet (1995) 0.84
Insulin-like system and growth regulation in the Pacific oyster Crassostrea gigas: hrIGF-1 effect on protein synthesis of mantle edge cells and expression of an homologous insulin receptor-related receptor. Gen Comp Endocrinol (2003) 0.84
Structure and expression of mGDF, a new member of the transforming growth factor-beta superfamily in the bivalve mollusc Crassostrea gigas. Eur J Biochem (2000) 0.84
[Still's disease in adults and Wissler-Fanconi syndrome]. Rev Rhum Mal Osteoartic (1973) 0.84
Mycobacterium kansasii infection in a Paris suburb: comparison of disease presentation and outcome according to human immunodeficiency virus status. Groupe dEtude Des Mycobactéries de la Seine-Saint-Denis. Int J Tuberc Lung Dis (1999) 0.83
Processing of iduronate 2-sulphatase in human fibroblasts. Biochem J (1995) 0.83
The risks of tracheal intubation. Acta Anaesthesiol Belg (1978) 0.83
Tropomyosin inhibits the glutaraldehyde-induced cross-link between the central 48-kDa fragment of myosin head and segment 48-67 in actin subdomain 2. Biochemistry (1994) 0.83
Recurrence of pulmonary embolism during anticoagulant treatment: a prospective study. Thorax (1987) 0.83
Correlation between different gene expression assays designed to measure trans-activation potencies of systemic glucocorticoids. Steroids (2001) 0.83
A nonsense mutation in exon 4 of the cystic fibrosis gene frequent among the population of the Reunion Island. Hum Mol Genet (1992) 0.83
Regulation of fatty acid synthetase ribonucleic acid in the human endometrium during the menstrual cycle. J Clin Endocrinol Metab (1990) 0.83
A comparison of celiprolol and atenolol in the treatment of hypertension: a placebo controlled double blind study. Br J Clin Pract Suppl (1985) 0.82
[Information for patients about hospital infections in psychiatry: An assessment of healthcare professionals' knowledge, opinion and attitude]. Encephale (2009) 0.82
["Enzymology" commission. Current enzymology in clinical chemistry and recommendations for the measurement of catalytic activities in the serum at 30 degrees C]. Ann Biol Clin (Paris) (1977) 0.82