J Bonaventure
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Explore the profile of J Bonaventure including associated specialties, affiliations and a list of published articles.
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Articles
80
Citations
1986
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Recent Articles
1.
Larue L, Luciani F, Kumasaka M, Champeval D, Demirkan N, Bonaventure J, et al.
Pathol Biol (Paris)
. 2009 Feb;
57(7-8):543-7.
PMID: 19201106
The Wnt/beta-catenin signaling pathway plays a key role in several cellular functions during embryonic development and adult homeostasis. The deregulation of this pathway may lead to the development of cancer,...
2.
Julien S, Puig I, Caretti E, Bonaventure J, Nelles L, VAN Roy F, et al.
Oncogene
. 2007 Jun;
26(53):7445-56.
PMID: 17563753
Carcinoma progression is associated with the loss of epithelial features, and the acquisition of mesenchymal characteristics and invasive properties by tumour cells. The loss of cell-cell contacts may be the...
3.
Krahn M, Julia S, Sigaudy S, Liprandi A, Bernard R, Gonnet K, et al.
Clin Genet
. 2005 Nov;
68(6):558-60.
PMID: 16283889
No abstract available.
4.
Gonzales M, Heuertz S, Martinovic J, Delahaye S, Bazin A, Loget P, et al.
Clin Genet
. 2005 Jul;
68(2):179-81.
PMID: 15996217
No abstract available.
5.
Legeai-Mallet L, Benoist-Lasselin C, Munnich A, Bonaventure J
Bone
. 2004 Jan;
34(1):26-36.
PMID: 14751560
Achondroplasia (ACH) and thanatophoric dysplasia (TD) are human skeletal disorders of increasing severity accounted for by mutations in the fibroblast growth factor receptor 3 (FGFR3). Attempts to elucidate the molecular...
6.
Francannet C, Le Merrer M, Munnich A, Bonaventure J, Legeai-Mallet L
J Med Genet
. 2001 Jul;
38(7):430-4.
PMID: 11432960
Hereditary multiple exostoses (HME) is a genetically heterogeneous autosomal dominant disorder characterised by the development of bony protuberances mainly located on the long bones. Three HME loci have been mapped...
7.
Billerey C, Chopin D, Aubriot-Lorton M, Ricol D, Gil Diez de Medina S, van Rhijn B, et al.
Am J Pathol
. 2001 Jun;
158(6):1955-9.
PMID: 11395371
We recently identified activating mutations of fibroblast growth factor receptor 3 (FGFR3) in bladder carcinoma. In this study we assessed the incidence of FGFR3 mutations in a series of 132...
8.
El Ghouzzi V, Legeai-Mallet L, Benoist-Lasselin C, Lajeunie E, Renier D, Munnich A, et al.
FEBS Lett
. 2001 Mar;
492(1-2):112-8.
PMID: 11248247
Saethre-Chotzen syndrome is an autosomal dominant skull disorder resulting from premature fusion of coronal sutures (craniosynostosis). It is caused by mutations in the TWIST gene encoding a basic Helix-Loop-Helix transcription...
9.
Megarbane A, Melki I, Souraty N, Gerbaka J, El Ghouzzi V, Bonaventure J, et al.
Clin Dysmorphol
. 2000 Oct;
9(4):303-5.
PMID: 11045594
We report a male patient with craniosysnostosis, bilateral radial and ulnar hypoplasia, absent thumbs, poikiloderma, and short stature. His parents are first cousins. Although this patient was originally diagnosed as...
10.
Legeai-Mallet L, Rossi A, Benoist-Lasselin C, Piazza R, Mallet J, Delezoide A, et al.
J Bone Miner Res
. 2000 Aug;
15(8):1489-500.
PMID: 10934647
Hereditary multiple exostoses (HME), an autosomal skeletal disorder characterized by cartilage-capped excrescences, has been ascribed to mutations in EXT 1 and EXT 2, two tumor suppressor-related genes encoding glycosyltransferases involved...