160 results on '"le Gac, G"'
Search Results
2. 1258P MET exon14 skipping in non-small cell lung cancer: Clinicopathological characteristics, treatments, and efficacy of crizotinib according to functional analysis: AFonMET - GFPC study
3. Factors influencing disease phenotype and penetrance in HFE haemochromatosis
4. A new case of Kaufman Oculocerebrofacial Syndrome caused by two new splicing variants in UBE3B
5. Analyse FONctionnelle des mutations identifiées au voisinage de l’exon 14 du gène MET et efficacité du crizotinib chez des patients atteints d’un carcinome broncho-pulmonaire non à petites cellules de stade avancé (CBNPC) : étude GFPC-AFonMET
6. Role of bioclimate conditions on cerebral aneurysm rupture in the Brittany region of France
7. TYPE I HEREDITARY HEMOCHROMATOSIS: ROLE OF BODY MASS INDEX ON THE PHENOTYPIC EXPRESSION OF THE C282Y/C282 AND C282Y/H63D GENOTYPES: P-511
8. HEREDITARY HEMOCHROMATOSIS: THE HAPTOGLOBIN 2-2 TYPE DISPLAYS A SIGNIFICANT BUT MODERATE INFLUENCE ON PHENOTYPIC EXPRESSION OF THE PREDOMINANT C282Y HOMOZYGOUS GENOTYPE: P-192
9. Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descent
10. Mucormycose hépatique à Rhizopus microsporus : description d’un cas
11. Intérêt de l’ADN tumoral circulant dans le cancer pulmonaire : à propos d’un cas
12. Extracorporeal circuit for Panton-Valentine leukocidin-producing Staphylococcus aureus necrotizing pneumonia
13. An Accurate Expression for the Noise Figure of Bipolar Transistors Including Crowding Effect
14. SABRINA-RT, a distributed DBMS for telecommunications
15. Traitement par ECMO d'une pneumopathie nécrosante à Staphylococcus aureus producteur de la leucocidine de Panton-Valentine [Extracorporeal circuit for Panton-Valentine leukocidin-producing Staphylococcus aureus necrotizing pneumonia]
16. Scanning of the whole HFE coding region in HC probands with an incomplete HFE genotype by use of Denaturing High Performance Liquid Chromatography (DHPLC)
17. Genotypic and clinical characteristics of a cohort of 144 haemochromatosis patients in western Brittany, France
18. Molecular diagnosis and cascade screening modify the epidemiology of hereditary haemochromatosis
19. Nramp2 ANALYSIS IN HEMOCHROMATOSIS PROBANDS
20. Analysis of the transcriptional regulation of the human HFE gene
21. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
22. Structural and optical investigations of AlGaN MQWs grown on a relaxed AlGaN buffer on AlN templates for emission at 280nm
23. Étude multicentrique sur les patients admis dans un protocole de SAignées Itératives à l’EFS - protocole EMSAI : fin des inclusions et premières observations
24. AlGaN-based MQWs grown on a thick relaxed AlGaN buffer on AlN templates emitting at 285 nm
25. Octomut, étude observationnelle rétrospective multicentrique épidémiologique des patients de 80ans et plus avec un CBNPC muté EGFR et traités par EGFR-TKI
26. A novel missense mutation SLC40A1 results in resistance to hepcidin and confirms phenotypic heterogeneity of the ferroportin disease
27. Multicentric, retrospective study evaluating the epidemiologic characteristics and outcomes of patients aged 80years or older with non-small-cell lung cancer (NSCLC) harboring egfr mutations treated by EGFR-TKI
28. Les anesthésiques locaux inhibent la croissance des cellules humaines de carcinome hépatocellulaire
29. 646: Predicting colon cancer occurrence from transcriptomic, splicing and genomic data in colon adenomas
30. Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients
31. Extraordinary blueshift of a photonic crystal nanocavity by reducing its mode volume with an opaque microtip
32. Hémochromatose HFE : influence d’une alimentation riche en fer sur le temps de traitement par saignées des patients C282Y/C282Y
33. Extraordinary blueshift of a photonic crystal nanocavity by reducing its mode volume with an opaque microtip
34. 1* Comparison of bioinformatics, reporter minigene and mRNA study to analyse the effect of unclassified variants on CFTR mRNA splicing
35. Homozygous deletion of HFE is the common cause of hemochromatosis in Sardinia
36. Tuning of an active photonic crystal cavity by an hybrid silica/silicon near-field probe
37. Early-onset haemochromatosis caused by a novel combination of TFR2 mutations(p.R396X/c.1538-2 A>G) in a woman of Italian descent
38. Phenotypic and functional data confirm causality of the recently identified hemojuvelin p.r176c missense mutation
39. The recently identified type 2A juvenile haemochromatosis gene (HJV), a second candidate modifier of the C282Y homozygous phenotype
40. Multicentric, retrospective study evaluating the epidemiologic characteristics and outcomes of patients aged 80 years or older with non-small-cell lung cancer (NSCLC) harboring egfr mutations treated by EGFR-TKI
41. AlGaN-based MQWs emitting at 280nm for vertical cavity surface emitting lasers
42. Fabrication of an interposer with FIB-etched nanovias for molecular electronics
43. Analysis of the effects of current crowding on noise of transistors with a circular geometry. Application to transistor with any given geometry
44. Influence de la nature distribuée de la base sur le facteur de bruit des transistors bipolaires
45. Experimental study of the effects of current crowding on noise of bipolar transistors at intermediate frequencies
46. Active near-field optical microscopy.
47. Influence of a NSOM probe shape on a photonic crystal microcavity mode coupling.
48. Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis
49. The dual loss and gain of function of the FPN1 iron exporter results in the ferroportin disease phenotype.
50. Targeted RNAseq from patients' urinary cells to validate pathogenic noncoding variants in autosomal dominant polycystic kidney disease genes: a proof of concept.
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