Parfait B - Search Results

1

Severe Phenotype in Patients with Large Deletions of NF1.

Pacot L, Vidaud D, Sabbagh A, Laurendeau I, Briand-Suleau A, Coustier A, Maillard T, Barbance C, Morice-Picard F, Sigaudy S, Glazunova OO, Damaj L, Layet V, Quelin C, Gilbert-Dussardier B, Audic F, Dollfus H, Guerrot AM, Lespinasse J, Julia S, Vantyghem MC, Drouard M, Lackmy M, Leheup B, Alembik Y, Lemaire A, Nitschké P, Petit F, Dieux Coeslier A, Mutez E, Taieb A, Fradin M, Capri Y, Nasser H, Ruaud L, Dauriat B, Bourthoumieu S, Geneviève D, Audebert-Bellanger S, Nizon M, Stoeva R, Hickman G, Nicolas G, Mazereeuw-Hautier J, Jannic A, Ferkal S, Parfait B, Vidaud M, Members Of The Nf France Network, Wolkenstein P, Pasmant E. Pacot L, et al. Among authors: parfait b. Cancers (Basel). 2021 Jun 13;13(12):2963. doi: 10.3390/cancers13122963. Cancers (Basel). 2021. PMID: 34199217 Free PMC article.

2

Human TIP49b/RUVBL2 gene: genomic structure, expression pattern, physical link to the human CGB/LHB gene cluster on chromosome 19q13.3.

Parfait B, Giovangrandi Y, Asheuer M, Laurendeau I, Olivi M, Vodovar N, Vidaud D, Vidaud M, Bièche I. Parfait B, et al. Ann Genet. 2000 Apr-Jun;43(2):69-74. doi: 10.1016/s0003-3995(00)01016-9. Ann Genet. 2000. PMID: 10998447

3

The CGA gene as new predictor of the response to endocrine therapy in ER alpha-positive postmenopausal breast cancer patients.

Bièche I, Parfait B, Noguès C, Andrieu C, Vidaud D, Spyratos F, Lidereau R, Vidaud M. Bièche I, et al. Among authors: parfait b. Oncogene. 2001 Oct 18;20(47):6955-9. doi: 10.1038/sj.onc.1204739. Oncogene. 2001. PMID: 11687975 Clinical Trial.

4

Quantification of estrogen receptor alpha and beta expression in sporadic breast cancer.

Bièche I, Parfait B, Laurendeau I, Girault I, Vidaud M, Lidereau R. Bièche I, et al. Among authors: parfait b. Oncogene. 2001 Dec 6;20(56):8109-15. doi: 10.1038/sj.onc.1204917. Oncogene. 2001. PMID: 11781824

5

CGA gene (coding for the alpha subunit of glycoprotein hormones) overexpression in ER alpha-positive prostate tumors.

Bièche I, Latil A, Parfait B, Vidaud D, Laurendeau I, Lidereau R, Cussenot O, Vidaud M. Bièche I, et al. Among authors: parfait b. Eur Urol. 2002 Mar;41(3):335-41. doi: 10.1016/s0302-2838(02)00020-9. Eur Urol. 2002. PMID: 12180238

6

Molecular profiles of neurofibromatosis type 1-associated plexiform neurofibromas: identification of a gene expression signature of poor prognosis.

Lévy P, Bièche I, Leroy K, Parfait B, Wechsler J, Laurendeau I, Wolkenstein P, Vidaud M, Vidaud D. Lévy P, et al. Among authors: parfait b. Clin Cancer Res. 2004 Jun 1;10(11):3763-71. doi: 10.1158/1078-0432.CCR-03-0712. Clin Cancer Res. 2004. PMID: 15173083

7

Molecular profiling of malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1, based on large-scale real-time RT-PCR.

Lévy P, Vidaud D, Leroy K, Laurendeau I, Wechsler J, Bolasco G, Parfait B, Wolkenstein P, Vidaud M, Bièche I. Lévy P, et al. Among authors: parfait b. Mol Cancer. 2004 Jul 15;3:20. doi: 10.1186/1476-4598-3-20. Mol Cancer. 2004. PMID: 15255999 Free PMC article.

8

Noonan syndrome type I with PTPN11 3 bp deletion: structure-function implications.

Lee WH, Raas-Rotschild A, Miteva MA, Bolasco G, Rein A, Gillis D, Vidaud D, Vidaud M, Villoutreix BO, Parfait B. Lee WH, et al. Among authors: parfait b. Proteins. 2005 Jan 1;58(1):7-13. doi: 10.1002/prot.20296. Proteins. 2005. PMID: 15521065

9

Noonan syndrome: relationships between genotype, growth, and growth factors.

Limal JM, Parfait B, Cabrol S, Bonnet D, Leheup B, Lyonnet S, Vidaud M, Le Bouc Y. Limal JM, et al. Among authors: parfait b. J Clin Endocrinol Metab. 2006 Jan;91(1):300-6. doi: 10.1210/jc.2005-0983. Epub 2005 Nov 1. J Clin Endocrinol Metab. 2006. PMID: 16263833

10

[Mutation mechanisms and their consequences].

Hanna N, Parfait B, Vidaud D, Vidaud M. Hanna N, et al. Among authors: parfait b. Med Sci (Paris). 2005 Nov;21(11):969-80. doi: 10.1051/medsci/20052111969. Med Sci (Paris). 2005. PMID: 16274649 Free article. Review. French.

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