Evidence of constitutional MLH1 epimutation associated to transgenerational inheritance of cancer susceptibility.
- Published in:
- Human Mutation, 2012, v. 33, n. 1, p. 180, doi. 10.1002/humu.21617
- By:
- Publication type:
- Article
Works by Crépin, Michel
Results: 11
1
2
MUC1 Expression in Papillary Thyroid Carcinoma Is Associated with BRAF Mutation and Lymph Node Metastasis; the Latter is the Most Important Risk Factor of Relapse.
- Published in:
- Thyroid, 2014, v. 24, n. 9, p. 1375, doi. 10.1089/thy.2013.0594
- By:
- Publication type:
- Article
3
Identification of a New Mutation on the β-Globin Gene: Codons 8/9 (+AGAA); GAG.AAG.TCT(Glu-Lys-Ser)>GAG. AA AGAAG, in a Patient From the North of France with a Phenotype of β-Thalassemia Minor.
- Published in:
- Hemoglobin, 2010, v. 34, n. 4, p. 389, doi. 10.3109/03630269.2010.500937
- By:
- Publication type:
- Article
4
Diagnosis of mosaic mutations in the MEN1 gene by next generation sequencing.
- Published in:
- European Journal of Endocrinology, 2019, v. 180, n. 2, p. L1, doi. 10.1530/EJE-18-0852
- By:
- Publication type:
- Article
5
Aponecrotic, antiangiogenic and antiproliferative effects of a novel dextran derivative on breast cancer growth in vitro and in vivo.
- Published in:
- British Journal of Pharmacology, 2002, v. 135, n. 8, p. 1859, doi. 10.1038/sj.bjp.0704645
- By:
- Publication type:
- Article
6
The serrated neoplasia pathway of colorectal tumors: Identification of MUC5AC hypomethylation as an early marker of polyps with malignant potential.
- Published in:
- International Journal of Cancer, 2016, v. 138, n. 6, p. 1472, doi. 10.1002/ijc.29891
- By:
- Publication type:
- Article
7
MUC5 AC hypomethylation is a predictor of microsatellite instability independently of clinical factors associated with colorectal cancer.
- Published in:
- International Journal of Cancer, 2015, v. 136, n. 12, p. 2811, doi. 10.1002/ijc.29342
- By:
- Publication type:
- Article
8
Functional Rac-1 and Nck signaling networks are required for FGF-2-induced DNA synthesis in MCF-7 cells.
- Published in:
- Oncogene, 1999, v. 18, n. 47, p. 6425, doi. 10.1038/sj.onc.1203027
- By:
- Publication type:
- Article
9
VHL mosaicism can be detected by clinical next-generation sequencing and is not restricted to patients with a mild phenotype.
- Published in:
- European Journal of Human Genetics, 2014, v. 22, n. 9, p. 1149, doi. 10.1038/ejhg.2013.279
- By:
- Publication type:
- Article
10
Efficient mutation detection in MEN1 gene using a combination of single-strand conformation polymorphism (MDGA™) and heteroduplex analysis.
- Published in:
- Electrophoresis, 2003, v. 24, n. 1/2, p. 26, doi. 10.1002/elps.200390023
- By:
- Publication type:
- Article
11
A Full Phenotype of Paraganglioma Linked to a Germline SDHB Mosaic Mutation.
- Published in:
- 2019
- By:
- Publication type:
- journal article