J. Demaille

C. Ferraz, A. Viari, F. Boyer, 2008, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

Comparative Genomic Analysis of Three Strains of Ehrlichia ruminantium Reveals an Active Process of Genome Size Plasticity

C. Ferraz, A. Viari, R. Frutos, 2006, Journal of bacteriology.

Implications for cAMP-dependent protein kinase in the maintenance of the interphase state.

J. Cavadore, A. Fernandez, J. Demaille, 1995, Progress in cell cycle research.

Reduced MEFV messenger RNA expression in patients with familial Mediterranean fever.

I. Touitou, J. Demaille, C. Notarnicola, 2002, Arthritis and rheumatism.

Enhanced cytokine mRNA levels in attack-free patients with familial Mediterranean fever

I. Touitou, J. Demaille, C. Notarnicola, 2002, Genes and Immunity.

Familial Mediterranean fever in the ‘Chuetas’ of Mallorca: a question of Jewish origin or genetic heterogeneity

E. Ben-Chetrit, I. Touitou, S. Ozen, 2000, European Journal of Human Genetics.

Spatial and temporal expression of the cystathionine beta-synthase gene during early human development.

P. Kamoun, J. Demaille, J. Dufier, 1999, Biochemical and biophysical research communications.

Linkage disequilibrium between the M470V variant and the IVS8 polyT alleles of the CFTR gene in CBAVD.

M Claustres, M. Claustres, J. Demaille, 1998, Journal of medical genetics.

Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutations

M. Claustres, J. Demaille, C. Guittard, 1998 .

Terbium binding to octopus calmodulin provides the complete sequence of ion binding

J. Demaille, M. Kilhoffer, D. Gérard, 1980, FEBS letters.

Multiplex fluorescent RT-PCR to quantify leukemic fusion transcripts.

J. Rossi, T. Lavabre‐Bertrand, J. Demaille, 2002, BioTechniques.

Phenotype-genotype correlation in Jewish patients suffering from familial Mediterranean fever (FMF)

A. Bernot, E. Ben-Chetrit, I. Touitou, 1998, European Journal of Human Genetics.

Muscular parvalbumins: preparative and analytical methods of general applicability.

J. Demaille, J. Capony, J. Péchère, 1971, Biochimica et biophysica acta.

The QT interval: a predictor of the plasma and myocardial concentrations of amiodarone.

A. Camm, J. Demaille, R. Bexton, 1984, British heart journal.

The protein truncation test (PTT) as a method of detection for choroideremia mutations.

M. Claustres, C. Bareil, J. Demaille, 1997, Experimental eye research.

A complex allele (1064delTC and IVS2 + 22ins7) in the peripherin/RDS gene in retinitis pigmentosa with macular dystrophy.

M. Claustres, C. Bareil, J. Demaille, 1997, Ophthalmic genetics.

Localization of human cell cycle regulatory genes CDC25C to 5q31 and WEE1 to 11p15.3-11p15.1 by fluorescence in situ hybridization.

S. Taviaux, J. Demaille, 1993, Genomics.

Stimulation of endogenous protein phosphorylation in oocytes of Sabellaria alveolata (polychaete annelid) at meiosis reinitiation induced by protease, fertilization, or ionophore A 23187

M. Dorée, G. Peaucellier, J. Demaille, 1982 .

Calcium-mediated transduction of the hormonal message in meiosis reinitiation of starfish oocytes: modulation following injection of cholera toxin and cAMP-dependent protein kinase.

M. Dorée, C. Le Peuch, T. Kishimoto, 1981, Experimental cell research.

Amino-acid sequence of an alpha-parvalbumin, pI = 4.88, from frog skeletal muscle.

G. Briand, J. Demaille, C. Richet, 1982, European journal of biochemistry.

Evolutionary Aspects of the Structure of Muscular Parvalbumins

J. Demaille, J. Capony, J. Péchère, 1973 .

Isolation and characterization of a rat skin parvalbumin-like calcium-binding protein.

C. Ferraz, J. Haiech, J. Derancourt, 1982, Biochemistry.

Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes.

J. Demaille, F. Pellestor, C. Humeau, 2002, Human reproduction.

Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens

M. Claustres, J. Demaille, J. Culard, 1994, Human Genetics.

Rapid detection of single nucleotide deletions: application to the β 6 (-A) mutation of the β-globin gene and to cystic fibrosis

M. Claustres, J. Demaille, P. Aguilar-Martinez, 1993, Human Genetics.

Complex allele [-102T>A+S549R(T>G)] is associated with milder forms of cystic fibrosis than allele S549R(T>G) alone

M. Patton, M. Claustres, D. Bozon, 1999, Human Genetics.

Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies

B. Echenne, M. Claustres, J. Demaille, 1991, Human Genetics.

Research Repor t Multiplex Fluorescent RT-PCR to Quantif y Leukemic Fusion Transcript s

T. Lavabre‐Bertrand, J. Demaille, A. Goldsborough, 2002 .

Simple variant t(8;21) acute myeloid leukemias harbor insertions of the AML1 or ETO genes

F. Birg, S. Taviaux, J. Demaille, 1999, Genes, chromosomes & cancer.

A case/control study of the association between primary liver cancer and hepatitis b infection in senegal

W. Szmuness, J. Demaille, A. Prince, 1975, International journal of cancer.

The distribution of parvalbumins in muscle and in other tissues

J. Demaille, G. Baron, E. Dutruge, 1975, FEBS letters.

Octopus calmodulin. The trimethyllysyl residue is not required for myosin light chain kinase activation.

C. Ferraz, J. Demaille, A. Molla, 1981, The Journal of biological chemistry.

Evidence for aggregation of endothelin 1 in water

F. Heitz, R. Bennes, J. Demaille, 1990, FEBS letters.

Mapping and identification of essential gene functions on the X chromosome of Drosophila

B. Barrell, M. Ashburner, L. Pachter, 2002, EMBO reports.

BIGH3 (TGFBI) Arg124 mutations influence the amyloid conversion of related peptides in vitro.

À. Argilés, J. Demaille, A. Chavanieu, 2002, European journal of biochemistry.

Analysis of the 27 exons and flanking regions of the cystic fibrosis gene: 40 different mutations account for 91.2% of the mutant alleles in southern France.

M. Claustres, J. Demaille, J. Culard, 1993, Human molecular genetics.

Amino acid sequence of the heat-stable inhibitor of the cAMP-dependent protein kinase from rabbit skeletal muscle.

E. Krebs, J. Scott, E. Fischer, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Identification ofaninhibitory region oftheheat-stable protein inhibitor ofthecAMP-dependent protein kinase

John E. Scott, J. Demaille, E. Krebs, 1985 .

Terbium as luminescent probe of calmodulin calcium‐binding sites

J. Demaille, M. Kilhoffer, D. Gérard, 1980, FEBS letters.

Prenatal diagnosis for cystic fibrosis using SSCP analysis

M. Claustres, M. Rolland, G. Lefort, 1993, Prenatal diagnosis.

Sequence of two phosphorylated sites in the catalytic subunit of bovine cardiac muscle adenosine 3':5'-monophosphate-dependent protein kinase.

K. Titani, E. Fischer, J. Demaille, 1979, The Journal of biological chemistry.

Protein truncation test: Analysis of two novel point mutations at the carboxy‐terminus of the human dystrophin gene associated with mental retardation

M. Claustres, J. Demaille, S. Tuffery, 1995, Human mutation.

A reappraisal of the relationship of phosphate-acceptor protein to parvalbumins.

E. Fischer, J. Demaille, G. Baron, 1975, Biochemical and biophysical research communications.

The amino-acid sequence of the most acidic major parvalbumin from frog muscle.

J. Demaille, J. Capony, J. Péchère, 1975, European journal of biochemistry.

The primary structure of the major parvalbumin from hake muscle. Overlapping peptides obtained with chemical and enzymatic methods. The complete amino-acid sequence.

J. Demaille, L. Rydén, J. Capony, 1973, European journal of biochemistry.

The pure inhibitor of cAMP-dependent protein kinase initiates Xenopus laevis meiotic maturation A 4-step scheme for meiotic maturation

E. Fischer, J. Demaille, D. Huchon, 1981, Molecular and Cellular Endocrinology.

Calcium and cyclic nucleotide dependent regulatory mechanisms during development of chick embryo skeletal muscle.

C. Le Peuch, C. Ferraz, E. Fischer, 1979, Biochemistry.

The protein inhibitor of adenosine 3':5'-monophosphate-dependent protein kinases. Isolation and characterization of three isoinhibitors.

C. Ferraz, E. Fischer, J. Demaille, 1979, Biochimie.

Evolution of Ca2+- and cAMP-dependent regulatory mechanisms during ram spermatogenesis.

J. Demaille, M. Lanneau, C. Pariset, 1983, Developmental biology.

Absence of dystrophin and utrophin in a boy with severe muscular dystrophy.

B. Echenne, J. Demaille, M. Chevron, 1994, The New England journal of medicine.

Regulation of calcium accumulation and efflux from platelet vesicles. Possible role for cyclic-AMP-dependent phosphorylation and calmodulin.

C. Le Peuch, J. Demaille, M. Hincke, 1983, Biochimica et biophysica acta.

Germinal mosaicism from grand-paternal origin in a family with Duchenne muscular dystrophy

M. Claustres, J. Demaille, H. Bellet, 1990, Human Genetics.

SESSION 3: “Hot Topics: Insulin Receptor Phosphatases, Vanadium and Diabetes”

J. Demaille, 1990 .

Phospholamban phosphorylation in the perfused rat heart is not solely dependent on β‐adrenergic stimulation

C. Le Peuch, J. Demaille, J. Guilleux, 1980, FEBS letters.

Purification and characterization of bovine cardiac calmodulin-dependent myosin light chain kinase.

B. Vallet, J. Demaille, M. Walsh, 1979, The Journal of biological chemistry.

The variable surface glycoproteins of Trypanosoma equiperdum are phosphorylated.

T. Baltz, J. Demaille, C. Giroud, 1982, The EMBO journal.

Protein phosphatase-1 is involved in Xenopus oocyte maturation

J. Demaille, D. Huchon, R. Ozon, 1981, Nature.

Calmodulin from neurospora crassa. General properties and conformational changes.

J. Cox, C. Ferraz, D. Marmé, 1982, The Journal of biological chemistry.

Large-scale purification and characterization of calmodulin from ram testis: its metal-ion-dependent conformers.

J. Cavadore, C. Ferraz, J. Demaille, 1980, Biochimica et biophysica acta.

Potential co‐existence of haemophilia A and B carrier status in two sisters

J. Gris, J. Demaille, J. Schved, 1992, Prenatal diagnosis.

Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting.

J. Demaille, F. Pellestor, J. P. Soulié, 2003, Molecular human reproduction.

A candidate gene for familial Mediterranean fever

Jacques Demaille, Isabelle Touitou, Delphine Samson, 1997, Nature Genetics.

Tyrosine fluorescence of ram testis and octopus calmodulins. Effects of calcium, magnesium, and ionic strength.

J. Demaille, M. Kilhoffer, D. Gérard, 1981, Biochemistry.

Ion binding to calmodulin

J. Haiech, J. Demaille, M. Kilhoffer, 2004, Molecular and Cellular Biochemistry.

Calmodulin during development and metamorphosis in urodelan amphibians.

D. Rainteau, J. Demaille, M. Guyot, 1984, Developmental biology.

Role of Calmodulin in the Regulation of Muscle Contraction

J. Demaille, A. Molla, S. Katz, 1985 .

Phosphorylation and the control of calcium fluxes.

J. Haiech, J. Demaille, 1983, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

The epinephrine‐induced activation of the cardiac slow Ca2+ channel is mediated by the cAMP‐dependent phosphorylation of calciductin, a 23 000 M r sarcolemmal protein

C. Le Peuch, J. Demaille, M. Rinaldi, 1981, FEBS letters.

Acute adaptative changes to unilateral nephrectomy in humans.

J. Cavadore, À. Argilés, J. Haiech, 1987, Kidney international.

Analytical subcellular distribution of cAMP‐dependent protein kinase activity in bull sperm

F. Iftode, J. Demaille, M. Guyot, 1984 .

Expression and subcellular localization of dystrophin in skeletal, cardiac and smooth muscles during the human development

M. Claustres, J. Demaille, F. Girard, 1994, Neuromuscular Disorders.

INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutations

Manuel Ruiz, Cyril Sarrauste de Menthière, Stéphane Terrière, 2003, Nucleic Acids Res..

Lattice corneal dystrophy.

M. Claustres, À. Argilés, J. Demaille, 2000, Ophthalmology.

BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.

M. Claustres, À. Argilés, J. Demaille, 2000, Investigative ophthalmology & visual science.

DNA LIBRARIES FOR SEQUENCING THE GENOME OF OSTREOCOCCUS TAURI (CHLOROPHYTA, PRASINOPHYCEAE): THE SMALLEST FREE‐LIVING EUKARYOTIC CELL 1

Hervé Moreau, Richard Cooke, Xavier Sabau, 2002 .

Ligand binding to macromolecules: determination of binding parameters by combined use of ligand buffers and flow dialysis; application to calcium-binding proteins.

J. Haiech, B. Vallet, J. Demaille, 1980, Analytical biochemistry.

Adenosine 3':5'-monophosphate dependent protein kinase from bovine heart. Characterization of the catalytic subunit.

E. Fischer, J. Demaille, K. Peters, 1977, Biochemistry.

A rapid microdetermination of phosphoserine, phosphothreonine, and phosphotyrosine in proteins by automatic cation exchange on a conventional amino acid analyzer.

J. Demaille, J. Capony, 1983, Analytical biochemistry.

Xenopus laevis oocyte calmodulin in the process of meiotic maturation.

J. Haiech, J. Demaille, M. Walsh, 1980, The Journal of biological chemistry.

Calmodulin is involved in the first step of oocyte maturation: effects of the antipsychotic drug fluphenazine and of anticalmodulin antibodies on the progesterone-induced maturation of xenopus laevis oocyte.

J. Demaille, D. Huchon, R. Ozon, 1981, Cell differentiation.

Calmodulin antagonists and hormonal control of meiosis in starfish oocytes.

J. Cavadore, A. Picard, M. Dorée, 1982, Experimental cell research.

Calmodulin intracelluar concentration and cAMP-dependent protein kinase activity in human sperm samples in relation to sperm motphlogy and motlity

J. Demaille, C. Pariset, S. Weinman, 1983 .

High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferens.

J. Lafitte, M. Claustres, J. Demaille, 1993, The New England journal of medicine.

The protein inhibitor of adenosine 3',5'-monophosphate-dependent protein kinases. The NH2-terminal portion of the peptide chain contains the inhibitory site.

C. Ferraz, E. Fischer, J. Demaille, 1979, Biochimica et biophysica acta.

Concerted regulation of cardiac sarcoplasmic reticulum calcium transport by cyclic adenosine monophosphate dependent and calcium--calmodulin-dependent phosphorylations.

C. Le Peuch, J. Haiech, J. Demaille, 1979, Biochemistry.

Specific detection of deleted and non-deleted dystrophin exons together with gender assignment in preimplantation genetic diagnosis of Duchenne muscular dystrophy.

M. Claustres, J. Demaille, S. Hamamah, 2003, Molecular human reproduction.

Comparison of the protein and DNA approaches for the characterization of a β-globin chain variant, hemoglobin Cocody [β21 (B3) Asp- → Asn], in a Caucasian patient

J. Gris, M. Claustres, Y. Blouquit, 1993, Annals of Hematology.

A genomic region encompassing a cluster of olfactory receptor genes and a myosin light chain kinase (MYLK) gene is duplicated on human chromosome regions 3q13-q21 and 3p13.

B. Trask, H. Massa, P. D. de Jong, 1999, Genomics.

Distribution of olfactory receptor genes in the human genome

B. Trask, S. Taviaux, J. Demaille, 1998, Nature Genetics.

Distribution of olfactory receptor genes in the human genome

B. Trask, S. Taviaux, J. Demaille, 1998, Nature Genetics.

Segregation of a mutation in CNGB1 encoding the β-subunit of the rod cGMP-gated channel in a family with autosomal recessive retinitis pigmentosa

M. Claustres, C. Bareil, J. Demaille, 2001, Human Genetics.

A single olfactory receptor specifically binds a set of odorant molecules

Patrice Mollard, Jacques Demaille, Sylvain Richard, 2002, The European journal of neuroscience.

Sequence, structure, and evolution of a complete human olfactory receptor gene cluster.

G Glusman, D. Lancet, S. Clifton, 2000, Genomics.

Comparative Genomics of Three Strains of Ehrlichia ruminantium

C. Ferraz, A. Viari, F. Boyer, 2006, Annals of the New York Academy of Sciences.

Troponins C from reptile and fish muscles and their relation to muscular parvalbumins

E. Eisenberg, J. Demaille, J. Capony, 1974, FEBS letters.

The cyclic AMP-dependent modulation of cardiac sarcolemmal slow calcium channels.

J. Demaille, J. Capony, M. Rinaldi, 1982, Journal of molecular and cellular cardiology.

Porcine odorant-binding protein selectively binds to a human olfactory receptor.

Jacques Demaille, M. Crowe, J. Demaille, 2002, Chemical senses.

The myosin light chain kinase gene is not duplicated in mouse: partial structure and chromosomal localization of Mylk.

C. Ferraz, M. Mattei, J. Demaille, 2001, Genomics.

Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation

G. Lefort, J. Demaille, F. Pellestor, 2001, Journal of medical genetics.

Comparative genomics of the SOX9 region in human and Fugu rubripes: conservation of short regulatory sequence elements within large intergenic regions.

C. Ferraz, J. Demaille, G. Scherer, 2001, Genomics.

Genomic sequencing reveals the structure of the Kcnk6 and Map3k11 genes and their close vicinity to the Sipa1 gene on mouse chromosome 19

C. Ferraz, A. Roux, J. Demaille, 2000, Cytogenetic and Genome Research.

Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test

B. Echenne, M. Claustres, C. Bareil, 1998, Human Genetics.

From first base: the sequence of the tip of the X chromosome of Drosophila melanogaster, a comparison of two sequencing strategies.

B. Barrell, M. Ashburner, L. Pachter, 2001, Genome research.

Chapter 4 – Calmodulin and Calcium-Binding Proteins: Evolutionary Diversification of Structure and Function

J. Demaille, 1982 .

Homologous calcium-binding proteins in the activation of skeletal, cardiac, and smooth muscle myosin light chain kinases.

J. Cavadore, B. Vallet, J. Demaille, 1980, The Journal of biological chemistry.

Evolution of the Gypsy endogenous retrovirus in the Drosophila melanogaster subgroup.

C. Ferraz, A. Bucheton, C. Terzian, 2000, Molecular biology and evolution.

Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes

J. Demaille, F. Pellestor, C. Humeau, 2003, Human Genetics.

Cystic fibrosis in Lebanon: distribution of CFTR mutations among Arab communities

A. Mégarbané, J. Loiselet, M. Claustres, 1997, Human Genetics.

First preimplantation genetic diagnosis of hereditary retinoblastoma using informative microsatellite markers.

M. Claustres, J. Demaille, S. Hamamah, 2003, Molecular human reproduction.

Complete amino acid sequence of the catalytic subunit of bovine cardiac muscle cyclic AMP-dependent protein kinase.

R. D. Wade, K. Titani, D. Parmelee, 1981, Proceedings of the National Academy of Sciences of the United States of America.

Fast multicolor primed in situ protocol for chromosome identification in isolated cells may be used for human oocytes and polar bodies.

J. Demaille, F. Pellestor, J. P. Soulié, 2004, Fertility and sterility.

Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion.

F. Rivier, G. Lefort, J. Demaille, 2002, American journal of medical genetics. Part A.

The early adaptive evolution of calmodulin.

M. Baba, M. Goodman, G. Matsuda, 1984, Molecular biology and evolution.

Mode of stimulation by injection of cyclic AMP and external acidification of the sodium efflux in barnacle muscle fibres.

E. Fischer, J. Demaille, E. Bittar, 1979, The Journal of physiology.

Non-founder mutations in the MEFV gene establish this gene as the cause of familial Mediterranean fever (FMF).

J. Weissenbach, A. Bernot, C. Cruaud, 1998, Human molecular genetics.

Beta 2 microglobulin isoforms in healthy individuals and in amyloid deposits.

À. Argilés, J. Derancourt, J. Demaille, 1995, Kidney international.

Infevers: An evolving mutation database for auto‐inflammatory syndromes

J. Hugot, H. Waterham, S. Lesage, 2004, Human mutation.

Transcriptome analysis of monocytic leukemia cell differentiation.

L. Manchon, C. Ferraz, J. Elalouf, 2002, Genomics.

Genome-wide identification of in vivo Drosophila Engrailed-binding DNA fragments and related target genes

David Martin, B. Jacq, C. Ferraz, 2003, Development.

Analysis of 30 known cystic fibrosis mutations: 10 mutations account for 27% of non-ΔF508 chromosomes in Southern France

M. Claustres, J. Demaille, M. Desgeorges, 1992, Human Genetics.

Heterotaxia syndrome and autosomal dominant inheritance.

S. Taviaux, M. Pierpont, I. Dähnert, 1995, American journal of medical genetics.

Identification of an autosomal recessive mode of inheritance in paediatric Behçet's families by segregation analysis

J. Daurès, I. Touitou, R. Manna, 2003, American journal of medical genetics. Part A.

A detailed linkage map of subtelomeric murine Chromosome 12 region including the situs inversus mutation locus IV

J. Demaille, P. Bouvagnet, A. Meeus, 2004, Mammalian Genome.

Transcript analysis of CFTR frameshift mutations in lymphocytes using the reverse transcription-polymerase chain reaction technique and the protein truncation test

M. Claustres, T. Bienvenu, J. Demaille, 1996, Human Genetics.

Identification of variable length polyadenosine tract at the dystrophin locus

M. Claustres, J. Demaille, S. Tuffery, 1995, Human Genetics.

Binding of serum response factor to cystic fibrosis transmembrane conductance regulator CArG-like elements, as a new potential CFTR transcriptional regulation pathway

M. Claustres, J. Demaille, M. Taulan, 2005, Nucleic acids research.

Identification of a 6 bp deletion (3195del6) in exon 17a of the cystic fibrosis (CFTR) gene.

M. Claustres, J. Demaille, M. Desgeorges, 1994, Human Molecular Genetics.

Familial Mediterranean fever clinical and genetic features in Druzes and in Iraqi Jews: a preliminary study.

E. Ben-Chetrit, I. Touitou, J. Demaille, 1998, The Journal of rheumatology.

Genotypic diagnosis of familial Mediterranean fever (FMF) using new microsatellite markers: example of two extensive non-Ashkenazi Jewish pedigrees.

I. Touitou, C. Clépet, M. Delpech, 1997, Journal of medical genetics.

Calmodulin stimulation of adenylate cyclase of intestinal epithelium.

J. Demaille, M. Laburthe, B. Amiranoff, 2005, European journal of biochemistry.

Calmodulin regulation of the ATP-dependent calcium uptake by inverted vesicles prepared from rabbit synaptosomal plasma membranes.

J. Demaille, M. Hincke, 1984, Biochimica et biophysica acta.

The MICA region determines the first modifier locus in familial Mediterranean fever.

M. Picot, I. Touitou, J. Demaille, 2001, Arthritis and rheumatism.

Supramolecular Organization of Regulatory Proteins into Calcisomes: A Model of the Concerted Regulation by Calcium Ions and Cyclic Adenosine 3′:5′-Monophosphate in Eukaryotic Cells

J. Haiech, J. Demaille, 1981 .

Renal Toxicogenomic Response to Chronic Uranyl Nitrate Insult in Mice

J. Demaille, M. Taulan, M. Romey, 2004, Environmental health perspectives.

Isolation and properties of the rabbit skeletal muscle protein inhibitor of adenosine 3',5'-monophosphate dependent protein kinases.

E. Fischer, J. Demaille, K. Peters, 1977, Biochemistry.

A new large-scale purification procedure for muscular parvalbumins.

J. Haiech, J. Derancourt, J. Demaille, 1979, Biochimie.

Characterization and partial purification of cardiac sarcoplasmic reticulum phospholamban kinase.

J. Demaille, A. Molla, 1986, Biochemistry.

The First Green Lineage cdc25 Dual-Specificity Phosphatase

Y. Peer, C. Ferraz, H. Moreau, 2004, Cell cycle.

Identification of an inhibitory region of the heat-stable protein inhibitor of the cAMP-dependent protein kinase.

E. Krebs, J. Scott, E. Fischer, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Comprehensive analysis of the renal transcriptional response to acute uranyl nitrate exposure

À. Argilés, J. Demaille, M. Taulan, 2006, BMC Genomics.

A Naturally Occurring Sequence Variation That Creates a YY1 Element Is Associated with Increased Cystic Fibrosis Transmembrane Conductance Regulator Gene Expression*

A. Mangé, M. Claustres, N. Pallares-Ruiz, 2000, The Journal of Biological Chemistry.

The amino acid sequence of the major parvalbumin from hake muscle.

J. Demaille, L. Rydén, J. Capony, 1971, Biochemical and biophysical research communications.

An isolated cardiac conduction disease maps to chromosome 19q.

J. Weissenbach, J. Loiselet, J. Demaille, 1995, Circulation research.

Subcellular localization of myosin light chain kinase in skeletal, cardiac, and smooth muscles.

J. Cavadore, J. Demaille, M. Harricane, 1982, Proceedings of the National Academy of Sciences of the United States of America.

Screening for cystic fibrosis mutations in Southern France: Identification of a frameshift mutation and two missense variations

M. Claustres, M. Dean, J. Demaille, 1992, Human mutation.

Covalent regulation of the cardiac sarcoplasmic reticulum calcium pump. Review article.

C. Le Peuch, J. Demaille, 1989, Cell calcium.

Covalent regulation of the cardiac sarcoplasmic reticulum calcium pump: purification and properties of phospholamban, a substrate of cAMP-dependent protein kinase and Ca2+-calmodulin-dependent phospholamban kinase.

C. Le Peuch, J. Demaille, D. A. Le Peuch, 1983, Methods in enzymology.

Isolation of cardiac membrane proteolipids by high pressure liquid chromatography. A comparison of reticular and sarcolemmal proteolipids, phospholamban and calciductin.

J. Demaille, J. Capony, M. Rinaldi, 1983, Biochimica et biophysica acta.

Ca2+/CALMODULIN‐DEPENDENT PHOSPHOLAMBAN KINASE FROM CARDIAC SARCOPLASMIC RETICULUM IS DISTINCT FROM PHOSPHORYLASE KINASE AND FORMS A REGULATORY COMPLEX WITH PHOSPHOLAMBAN AND THE Ca2+‐ATPase *

C. L. Peuch, J. Demaille, Danielle A.‐M. Le Peuch, 1982, Annals of the New York Academy of Sciences.

Cardiac sarcoplasmic-reticulum calmodulin-binding proteins. Modulation of calmodulin binding to phospholamban by phosphorylation.

J. Demaille, A. Molla, J. Capony, 1985, The Biochemical journal.

Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness.

M. Claustres, N. Pallares-Ruiz, A. Roux, 2001, Genetic testing.

Evolutionary diversification of structure and function in the family of intracellular calcium-binding proteins

M. Goodman, J. Haiech, J. Demaille, 1979, Journal of Molecular Evolution.

A healthy male with compound and double heterozygosities for delta F508, F508C, and M47OV in exon 10 of the cystic fibrosis gene.

M. Claustres, J. Demaille, M. Desgeorges, 1994, American journal of human genetics.

Cyclic AMP- and Ca2+-dependent protein kinases and their concerted effects on Ca2+ fluxes.

J. Demaille, 1981, Biochemical Society Transactions.

W179R: A novel missense mutation in the peripherin/RDS gene in a family with autosomal dominant retinitis pigmentosa

M. Claustres, C. Bareil, J. Demaille, 2000, Human Mutation.

Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4.

M. Claustres, N. Pallares-Ruiz, C. Bareil, 1999, Ophthalmic genetics.

Direct carrier testing of haemophilia B by SSCP.

J. Gris, M. Claustres, J. Demaille, 2008, Clinical and laboratory haematology.

A novel mutation (Val‐373 to Glu) in the catalytic domain of factor IX, resulting in moderately/severe hemophilia B in a Southern French patient

J. Gris, M. Claustres, J. Demaille, 1994, Human Mutation.

Point mutations in the dystrophin gene: Evidence for frequent use of cryptic splice sites as a result of splicing defects

M. Claustres, J. Demaille, S. Tuffery-Giraud, 1999, Human mutation.

Cells surrounding haemodialysis-associated amyloid deposits are mainly macrophages.

P. Kerr, À. Argilés, J. Demaille, 1994, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Four Novel Dystrophin Point Mutations: Detection by Protein Truncation Test and Transcript Analysis in Lymphocytes from Duchenne Muscular Dystrophy Patients

M. Claustres, C. Bareil, J. Demaille, 1996, European journal of human genetics : EJHG.

Severe pulmonary and digestive disease in a cystic fibrosis child homozygous for G542X.

M. Claustres, J. Demaille, M. Desgeorges, 1994, Journal of medical genetics.

First putative sequence alterations in the minimal CFTR promoter region

M. Claustres, J. Demaille, M. Romey, 1999, Journal of medical genetics.

Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype

M. Claustres, J. Demaille, M. Rodier, 1995, Human Genetics.

Novel missense mutation in the first transmembrane segment of the CFTR gene (Q98R) identified in a male adult

M. Claustres, P. Godard, J. Demaille, 1995, Human mutation.

Base substitutions in the human dystrophin gene: Detection by using the single‐strand conformation polymorphism (SSCP) technique

M. Claustres, J. Demaille, S. Tuffery, 1993, Human mutation.