» Authors » F Fouquet

F Fouquet

Explore the profile of F Fouquet including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 8
Citations 100
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Sevin C, Verot L, Benraiss A, van Dam D, Bonnin D, Nagels G, et al.
Gene Ther . 2006 Nov; 14(5):405-14. PMID: 17093507
Metachromatic leukodystrophy (MLD) is a lysosomal storage disease caused by genetic deficiency of arylsulfatase A (ARSA) enzyme. Failure in catalyzing the degradation of its major substrate, sulfatide (Sulf), in oligodendrocytes...
2.
Morin J, Fouquet F, Monteil C, Le Prieur E, Vaz E, Dionnet F
Cell Biol Toxicol . 1999 Dec; 15(3):143-52. PMID: 10580547
The purpose of this study was the development of a new incubation system that can allow continuous exposure of lung tissue to complex atmospheres as a tool for the assessment...
3.
Doerflinger N, Metzger E, Fouquet F, Mandel J, Aubourg P
Eur J Cell Biol . 1998 May; 75(3):254-64. PMID: 9587057
The adrenoleukodystrophy and adrenoleukodystrophy related proteins belong to a new family of half ATP-binding cassette transporters which are localized within the peroxisomal membrane and whose functions are still unknown. They...
4.
Fouquet F, Zhou J, Ralston E, Murray K, Troalen F, Magal E, et al.
Neurobiol Dis . 1997 Jan; 3(4):271-85. PMID: 9173925
The gene mutated in X-linked adrenoleukodystrophy (ALD), a progressive demyelinating disease, codes for a protein (ALDP) involved in very-long-chain fatty acid (VLCFA) transport. The expression of ALDP and of two...
5.
Meddeb M, Valent A, Danglot G, Nguyen V, Duverger A, Fouquet F, et al.
Cytogenet Cell Genet . 1996 Jan; 73(4):325-30. PMID: 8751388
This report describes a case of rhabdomyosarcoma associated with a 2;13 translocation and multiple double minute chromosomes. The origin of the amplified DNA was identified using comparative genomic hybridization, which...
6.
Telvi L, Bernheim A, Ion A, Fouquet F, Le Bouc Y, Chaussain J
Am J Med Genet . 1995 Jul; 57(4):598-600. PMID: 7573136
We report on a girl with syndromal gonadal dysgenesis and a de novo del(18p). Genetic factors controlling gonadal development are located not only on the X chromosome, but also on...
7.
Goguel A, Fouquet F, Duverger A, Arvelo F, Jacrot M, Poupon M, et al.
Cancer Genet Cytogenet . 1995 Mar; 80(1):47-54. PMID: 7697632
Two small cell lung cancer (SCLC) cell lines were established from metastases of a patient during the course of the disease. SCLC 74A was derived from biopsy material obtained at...
8.
Bernheim A, Duverger A, Fouquet F, Bayle C, Oberlin O
Leukemia . 1995 Jan; 9(1):107-8. PMID: 7845003
A t(8;21)(q22;q22) translocation without blood and bone marrow invasion by immature myeloid precursors was suspected in a conventional karyotype and confirmed by fluorescence in situ hybridization (FISH) with chromosome 8...