About: Florence Coulet

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Coulet, Florence Coulet, Florence
preferred label	Coulet, Florence
name	Florence Coulet
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	0000000430898763
Given name	Florence
familyName	Coulet
has biographical i...tion (Deprecated)	Auteur d'une thèse de doctorat en Sciences de la vie et de la santé soutenue en 2004 à l'Université de Paris 6 Docteur en pharmacie (thèse d'exercice et mémoire de Diplôme d'Etudes Spécialisées, Paris 11, 1998)
Scopus ID	6603635528
is sameAs of	Coulet, Florence Coulet, Florence
is Author of	http://www.sudoc.fr/089059670/id http://www.sudoc.fr/049495844/id Régulation transcriptionnelle du gène de la ENOS et des facteurs de transcription DEC1 et DEC2 par l'hypoxie dans la cellule endothéliale Discordance between immunochemistry of mismatch repair proteins and molecular testing of microsatellite instability in colorectal cancer Full in-frame exon 3 skipping of BRCA2 confers high risk of breast and/or ovarian cancer Abstract P6-08-12: Feasibility of a nation-wide family-based study to assess cancer risks in families with a predicted pathogenic variant identified through hereditary breast and ovary multi-gene panel testing: The TUMOSPEC study Proteomic analysis of BRCA1-depleted cell line reveals a putative role for replication protein A2 up-regulation in BRCA1 breast tumor development Overcoming the challenges associated with universal screening for Lynch syndrome in colorectal and endometrial cancer Absence of influence of gender and BMPR2 mutation type on clinical phenotypes of pulmonary arterial hypertension. Droplet digital PCR of circulating tumor cells from colorectal cancer patients can predict KRAS mutations before surgery Constitutional mismatch repair deficiency syndrome: clinical description in a French cohort The contribution of germline rearrangements to the spectrum of BRCA2 mutations Significant Contribution of Germline BRCA2 Rearrangements in Male Breast Cancer Families Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France Utility of a mainstreamed genetic testing pathway in breast and ovarian cancer patients during the COVID-19 pandemic Comprehensive RNA and protein functional assessments contribute to the clinical interpretation of MSH2 variants causing in-frame splicing alterations Clinical Cancer Genetics : a guide for the pathologist TUMOSPEC: A Nation-Wide Study of Hereditary Breast and Ovarian Cancer Families with a Predicted Pathogenic Variant Identified through Multigene Panel Testing Lynch syndrome: What is new? No evidence for point mutations of the calcium-sensing receptor in familial idiopathic hypercalciuria Intraductal Papillary Mucinous Carcinoma Versus Conventional Pancreatic Ductal Adenocarcinoma: A Comprehensive Review of Clinical-Pathological Features, Outcomes, and Molecular Insights Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension Clinical implications of CTNNA1 germline mutations in asymptomatic carriers Endoglin germline mutation in a patient with hereditary haemorrhagic telangiectasia and dexfenfluramine associated pulmonary arterial hypertension Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer HSP110 T17 simplifies and improves the microsatellite instability testing in patients with colorectal cancer http://www.sudoc.fr/246821582/id Widening the landscape of heritable pulmonary hypertension mutations in pediatric and adult cases BRCA Share: A Collection of Clinical BRCA Gene Variants Genomic variations integrated database for MUTYH -associated adenomatous polyposis Novel diagnostic tool for prediction of variant spliceogenicity derived from a set of 395 combined in silico/in vitro studies: an international collaborative effort [MUTYH-associated polyposis: Review and update of the French recommendations established in 2012 under the auspices of the National Cancer Institute (INCa)]. Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach In Vitro fertilization failure of normozoospermic men: search for a lack of testicular isozyme of angiotensin-converting enzyme Standardisation of pathogenicity classification for somatic alterations in solid tumours and haematologic malignancies https://serval.unil.ch/notice/serval:BIB_849EB160E92A#id
is primary topic of	http://www.idref.fr/089059905
is Opponent of	http://www.sudoc.fr/25511592X/id http://www.sudoc.fr/25511236X/id Caractérisation fonctionnelle de variations splicéogéniques à l'origine d'anomalies d'épissage en phase dans des gènes de prédisposition aux cancers, implications en génétique médicale
is Thesis referee of	http://www.sudoc.fr/260127035/id

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