C Bidaud
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Explore the profile of C Bidaud including associated specialties, affiliations and a list of published articles.
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Articles
12
Citations
336
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Recent Articles
1.
Bidaud C, Berling D, Jamon D, Gamet E, Neveu S, Royer F, et al.
Sci Rep
. 2021 Mar;
11(1):5075.
PMID: 33658579
This paper is aimed at investigating the process of photocrosslinking under Deep-UV irradiation of nanocomposite thin films doped with cobalt ferrite magnetic nanoparticles (MNPs). This material is composed of a...
2.
Albin A, Fayolle C, Bidaud C, Gire P, Sagne A
Soins Gerontol
. 2001 Apr;
(27):23-6.
PMID: 11309893
No abstract available.
3.
Albin A, Bidaud C, Fayolle C, Gire P, Gonthier R, Jirtanner C, et al.
Soins Gerontol
. 2001 Apr;
(25):40-2.
PMID: 11309863
No abstract available.
4.
Bordeaux M, Forcet C, Granger L, Corset V, Bidaud C, Billaud M, et al.
EMBO J
. 2000 Aug;
19(15):4056-63.
PMID: 10921886
The RET (rearranged during transfection) proto-oncogene encodes a tyrosine kinase receptor involved in both multiple endocrine neoplasia type 2 (MEN 2), an inherited cancer syndrome, and Hirschsprung disease (HSCR), a...
5.
Geneste O, Bidaud C, De Vita G, Hofstra R, Tartare-Deckert S, Buys C, et al.
Hum Mol Genet
. 1999 Sep;
8(11):1989-99.
PMID: 10484767
The RET gene codes for a transmembrane tyrosine kinase which is a subunit of a multimeric complex that acts as a receptor for four structurally related molecules: the glial cell...
6.
Bidaud C, Salomon R, Van Camp G, Pelet A, Attie T, Eng C, et al.
Eur J Hum Genet
. 1997 Jul;
5(4):247-51.
PMID: 9359047
Hirschsprung disease (HSCR, aganglionic megacolon) is a frequent congenital malformation regarded as a multigenic neurocristopathy. Four susceptibility genes have recently been identified in HSCR, namely the RET proto-oncogene, the glial...
7.
Bidaud C, Salomon R, Edery P, Van Camp G, Pelet A, Bonduelle M, et al.
Gastroenterol Clin Biol
. 1997 Jan;
21(8-9):548-54.
PMID: 9587491
Aims And Methods: Hirschsprung's disease is a frequent congenital malformation regarded as a multigenic neurocristopathy. Three susceptibility genes have been identified in Hirschsprung's disease, namely the RET proto-oncogene, the Glial...
8.
Salomon R, Attie T, Pelet A, Bidaud C, Eng C, Amiel J, et al.
Nat Genet
. 1996 Nov;
14(3):345-7.
PMID: 8896569
Hirschsprung disease (HSCR, aganglionic megacolon) is a common congenital malformation leading to bowel obstruction, with an incidence of 1/5,000 live births. It is characterized by the absence of intrinsic ganglion...
9.
Edery P, Attie T, Amiel J, Pelet A, Eng C, Hofstra R, et al.
Nat Genet
. 1996 Apr;
12(4):442-4.
PMID: 8630502
Hirschsprung disease (HSCR) and Waardenburg sundrome (WS) are congenital malformations regarded as neurocristopathies since both disorders involve neural crest-derived cells. The WS-HSCR association (Shah-Waardenburg syndrome) is a rare autosomal recessive...
10.
Amiel J, Attie T, Jan D, Pelet A, Edery P, Bidaud C, et al.
Hum Mol Genet
. 1996 Mar;
5(3):355-7.
PMID: 8852660
Hirschsprung disease (HSCR, aganglionic megacolon) is a frequent congenital malformation regarded as a multigenic neurocristopathy. Two susceptibility genes have been recently identified in HSCR, namely the RET proto-oncogene and the...