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38 results on '"Genetique et Biotherapies des Maladies Degeneratives et Proliferatives du Systeme Nerveux ( Inserm U745 )"'

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1. Mutational analysis of anal cancers demonstrates frequent PIK3CA mutations associated with poor outcome after salvage abdominoperineal resection

2. The early pregnancy placenta foreshadows dna methylation alterations of solid tumors

3. Likely effect of the 2014 Ebola epidemic on HIV care in Liberia

4. CYP46A1 inhibition, brain cholesterol accumulation and neurodegeneration pave the way for Alzheimer’s disease

5. IFI35, mir-99a and HCV Genotype to Predict Sustained Virological Response to Pegylated-Interferon Plus Ribavirin in Chronic Hepatitis C

6. Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients

7. Vasculature analysis of patient derived tumor xenografts using species-specific PCR assays: evidence of tumor endothelial cells and atypical VEGFA-VEGFR1/2 signalings

8. Targeting VEGFR1 on endothelial progenitors modulates their differentiation potential

9. Mutations in SETD2 cause a novel overgrowth condition

10. Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study

11. MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesis

12. Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephaly

13. NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

14. Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

15. SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype

16. Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy

17. Effect of tyrosine kinase inhibitor STI571 on the kinase activity of wild-type and various mutated c-kit receptors found in mast cell neoplasms

18. CYP46A1 gene therapy deciphers the role of brain cholesterol metabolism in Huntington’s disease

19. Clonally Expanded T Cells Reveal Immunogenicity of Rhabdoid Tumors

20. Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum

21. SHH medulloblastoma in a young adult with a TCF4 germline pathogenic variation

22. UMD-MEN1 database: an overview of the 370 MEN1 variants present in 1,676 patients from the French population

23. Active cell migration is critical for steady-state epithelial turnover in the gut

24. Detection and monitoring of circulating tumor DNA in adrenocortical carcinoma

25. Long Noncoding RNAs as New Architects in Cancer Epigenetics, Prognostic Biomarkers, and Potential Therapeutic Targets

26. Cytidine Deaminase Deficiency Reveals New Therapeutic Opportunities against Cancer

27. Chronic hepatitis E virus infection in a cirrhotic patient

28. CAG repeat size in Huntingtin alleles is associated with cancer prognosis

29. Prognostic value of a newly identified MALAT1 alternatively spliced transcript in breast cancer

30. Rett networked database: An integrated clinical and genetic network of rett syndrome databases

31. First description of ABCB4 gene deletions in familial low phospholipid-associated cholelithiasis and oral contraceptives-induced cholestasis

32. Expression analysis of mitotic spindle checkpoint genes in breast carcinoma: role of NDC80/HEC1 in early breast tumorigenicity, and a two-gene signature for aneuploidy

33. Transarterial chemoembolisation: effect of selectivity on tolerance, tumour response and survival

34. Brain gene therapy for metachromatic leukodystrophy: towards clinical trial

35. CD133, CD15/SSEA-1, CD34 or side populations do not resume tumor-initiating properties of long-term cultured cancer stem cells from human malignant glio-neuronal tumors

36. Pentoxifylline Does Not Decrease Short-term Mortality but Does Reduce Complications in Patients With Advanced Cirrhosis

37. MALDI reveals membrane lipid profile reversion in MDX mice

38. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report

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