F. Samson

发表

Mutations in the MTM1 gene implicated in X-linked myotubular myopathy. ENMC International Consortium on Myotubular Myopathy. European Neuro-Muscular Center.

E. Bertini, C. Wallgren‐Pettersson, J. Mandel, 1997, Human molecular genetics.

Decreased type VI adenylyl cyclase mRNA concentration and Mg(2+)-dependent adenylyl cyclase activities and unchanged type V adenylyl cyclase mRNA concentration and Mn(2+)-dependent adenylyl cyclase activities in the left ventricle of rats with myocardial infarction and longstanding heart failure.

J. Michel, J. Hanoune, E. Pussard, 1999, Cardiovascular research.

Type V, but not type VI, adenylyl cyclase mRNA accumulates in the rat heart during ontogenic development. Correlation with increased global adenylyl cyclase activity.

J. Hanoune, F. Samson, N. Defer, 1995, Journal of molecular and cellular cardiology.

Human cardiac troponin T: cloning and expression of new isoforms in the normal and failing heart.

S. Diriong, S. Taviaux, D. Logeart, 1995, Circulation research.

Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis.

B. Trask, J. Gilbert, P. D. de Jong, 1992, Genomics.

Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA

J. Gilbert, W. Hung, A. Roses, 1990, Journal of Neuroscience Research.

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

J. Gilbert, A. Roses, J. Vance, 1992, American journal of human genetics.

Molecular cloning and developmental expression of human cardiac troponin T

F. Samson, J. Mercadier, J. Neveux, 1993, FEBS letters.

Mitochondrial creatine kinase isoform expression does not correlate with its mode of action.

P. Mateo, V. Saks, V. Veksler, 1997, The Biochemical journal.

Troponin T mRNA and protein isoforms in the human left ventricle: pattern of expression in failing and control hearts.

G. Butler-Browne, P. Allen, D. Logeart, 1997, Journal of molecular and cellular cardiology.

A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene.

J. Gilbert, A. Roses, F. Samson, 1994, Biochemical and biophysical research communications.

Polymerase chain reaction in the detection of mRNA transcripts from the slow skeletal troponin T (TNNT1) gene in myotonic dystrophy and normal muscle

B. Dallapiccola, G. Novelli, F. Sangiuolo, 1992, Cell biochemistry and function.

The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.

A. Clarke, C. Wallgren‐Pettersson, V. Dubowitz, 1995, Journal of medical genetics.

Genetic linkage heterogeneity in myotubular myopathy.

C. Junien, J. Mandel, A. Hanauer, 1995, American journal of human genetics.

A mutation in the MTM1 gene invalidates a previous suggestion of nonallelic heterogeneity in X-linked myotubular myopathy.

J. Mandel, J. Laporte, M. Fardeau, 1997, American journal of human genetics.

X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).

A. Poustka, J. Mandel, G. Herman, 1994, Journal of medical genetics.

Left Ventricular Alterations in a Model of Fetal Left Ventricular Overload

A. Serraf, F. Samson, N. Bonnet, 2000, Pediatric Research.

[Oculopharyngeal muscular dystrophy. A census of French families and genealogic study].

M. Fardeau, F. Tomé, F. Samson, 1990, Revue neurologique.

Interactions between endothelin-1 and atrial natriuretic peptide influence cultured chick cardiac myocyte contractility.

D. Longrois, F. Samson, J. Mercadier, 1996, European journal of pharmacology.

Molecular cloning and developmental expression of human cardiac troponin T

F. Samson, J. Mercadier, J. Neveux, 1993 .

[A study of the expression of sarcoplasmic reticulum calcium ATP-ase gene in the left ventricle of the sheep's fetus submitted to chronic increased afterload in utero].

A. Serraf, F. Samson, C. Planché, 1997, Archives des maladies du coeur et des vaisseaux.