145 results on '"Choquet, Karine"'
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2. Regulators of mitonuclear balance link mitochondrial metabolism to mtDNA expression
3. Magnetic Resonance Acoustic Radiation Force Imaging (MR-ARFI) for the monitoring of High Intensity Focused Ultrasound (HIFU) ablation in anisotropic tissue
4. Genome-wide quantification of RNA flow across subcellular compartments reveals determinants of the mammalian transcript life cycle
5. Intronic small nucleolar RNAs regulate host gene splicing through base pairing with their adjacent intronic sequences
6. Pre-mRNA splicing order is predetermined and maintains splicing fidelity across multi-intronic transcripts
7. A kinetic dichotomy between mitochondrial and nuclear gene expression processes
8. RNA polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation
9. Revealing nascent RNA processing dynamics with nano-COP
10. RNA Polymerase II pausing temporally coordinates cell cycle progression and erythroid differentiation
11. Évaluation de l'efficacité de la saturation du signal de la graisse pour la thermométrie IRM
12. The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesis
13. Sacs R272C missense homozygous mice develop an ataxia phenotype
14. Genome-wide screens for mitonuclear co-regulators uncover links between compartmentalized metabolism and mitochondrial gene expression
15. Regulatory principles of human mitochondrial gene expression revealed by kinetic analysis of the RNA life cycle
16. Monitoring MR-guided high intensity focused ultrasound therapy using transient supersonic shear wave MR-elastography
17. Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia
18. Suivi par IRM de l'évolution des propriétés mécaniques des tissus lors des ablations thermiques par ultrasons focalisés
19. Additional file 1 of Intronic small nucleolar RNAs regulate host gene splicing through base pairing with their adjacent intronic sequences
20. Additional file 3 of Intronic small nucleolar RNAs regulate host gene splicing through base pairing with their adjacent intronic sequences
21. A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability
22. A recessive ataxia diagnosis algorithm for the next generation sequencing era
23. Magnetic Resonance Acoustic Radiation Force Imaging (MR-ARFI) for the estimation of local viscoelasticity and anisotropy
24. Mutations in GALC cause late-onset Krabbe disease with predominant cerebellar ataxia
25. Genome-wide quantification of RNA flow across subcellular compartments reveals determinants of the mammalian transcript life cycle
26. Pre-mRNA splicing order is predetermined and maintains splicing fidelity across multi-intronic transcripts
27. Magnetic Resonance Acoustic Radiation Force Imaging (mr-arfi) For The Monitoring Of Mr-guided Hifu Therapy
28. Recessive mutations in the kinase ZAK cause a congenital myopathy with fibre type disproportion
29. A novel frameshift mutation in FGF14 causes an autosomal dominant episodic ataxia
30. Echo time selection in PRFS MR-thermometry to minimize errors in adipose tissues
31. MR-guided high intensity focused ultrasound therapy monitoring using transient supersonic shear wave MR-elastography
32. Transient Supersonic Shear wave MR-Elastography
33. Évaluation quantitative des propriétés mécaniques des tissus par IRM de la force de radiation ultrasonore (MR-ARFI)
34. Autosomal recessive cerebellar ataxia caused by a homozygous mutation in PMPCA
35. RNA Polymerase III Subunit Mutations in Genetic Diseases
36. IRM de la force de radiation ultrasonore (ARFI) pour la caractérisation de la viscoélasticité des tissus
37. 4H Syndrome With Late-Onset Growth Hormone Deficiency Caused by POLR3A Mutations
38. Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy
39. A Molecular Diagnosis of LGMDR1 Established by RNA Sequencing
40. Channelopathies are a frequent cause of genetic ataxias associated with cerebellar atrophy (1719)
41. A Novel Late-onset Dominant Episodic Ataxia in a Large French Canadian Kindred (1460)
42. Splicing Kinetics and Coordination Revealed by Direct Nascent RNA Sequencing through Nanopores
43. Additional file 1: of The leukodystrophy mutation Polr3b R103H causes homozygote mouse embryonic lethality and impairs RNA polymerase III biogenesis
44. Leukodystrophy-associated POLR3A mutations down-regulate the RNA polymerase III transcript and important regulatory RNA BC200
45. Human co-transcriptional splicing kinetics and coordination revealed by direct nascent RNA sequencing
46. Additional file 1: of Absence of neurological abnormalities in mice homozygous for the Polr3a G672E hypomyelinating leukodystrophy mutation
47. Loss of PRMT5 Promotes PDGFRα Degradation during Oligodendrocyte Differentiation and Myelination
48. A Molecular Diagnosis of LGMDR1 Established by RNA Sequencing
49. Transcriptome profiling of mouse brains with qkI-deficient oligodendrocytes reveals major alternative splicing defects including self-splicing
50. RNA-seq for the diagnosis of inherited myopathies: a pilot study (S54.002)
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