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3,407 results on '"Institut de Génétique et de Biologie Moléculaire et Cellulaire ( IGBMC )"'

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1. Ghrelin Gene Deletion Alters Pulsatile Growth Hormone Secretion in Adult Female Mice

2. Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition) 1

3. The three-finger toxin fold: a multifunctional structural scaffold able to modulate cholinergic functions

4. French Intensive Care Society, International congress – Réanimation 2016

5. Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks in 188 countries, 1990-2013

6. p27Kip1 Modulates Axonal Transport by Regulating α-Tubulin Acetyltransferase 1 Stability

7. Gearing up to handle the mosaic nature of life in the quest for orthologs

8. Health-Related Quality of Life Is Severely Affected in Primary Orthostatic Tremor

9. Phagocytosis by Sertoli Cells: Analysis of Main Phagocytosis Steps by Confocal and Electron Microscopy

10. Evidence for rRNA 2′-O-methylation plasticity: Control of intrinsic translational capabilities of human ribosomes

11. Global, regional, and national disability-adjusted life years (DALYs) for 306 diseases and injuries and healthy life expectancy (HALE) for 188 countries, 1990-2013

12. FGFR3 Mutational Activation Can Induce Luminal-like Papillary Bladder Tumor Formation and Favors a Male Sex Bias

13. Expanding the Kinome World: A New Protein Kinase Family Widely Conserved in Bacteria

14. Serotonergic 5-HT 2B receptors in mitral valvulopathy: bone marrow mobilization of endothelial progenitors

15. Intragenic FMR1 disease-causing variants: a significant mutational mechanism leading to Fragile-X syndrome

16. Quantification of Detergents Complexed with Membrane Proteins

17. Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

18. L'anxiété et les symptômes dépressifs chez les parents d'enfants atteints de syndrome de Dravet

19. Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

20. GenIDA: an international participatory database to gain knowledge on health issues related to genetic forms of neurodevelopmental disorders

21. Short tandem repeats are important contributors to silencer elements in T cells

22. Study of the mechanisms underlying the type 2 immune response in atopic dermatitis pathogenesis

23. A suppressor locus for MODY3-diabetes

24. A new family with an SLC9A6 mutation expanding the phenotypic spectrum of Christianson syndrome

25. Synthesis and materialization of a reaction-diffusion French flag pattern

26. Validation of a clinical practice-based algorithm for the diagnosis of autosomal recessive cerebellar ataxias based on NGS identified cases

27. Matrix metalloproteinase 11 protects from diabesity and promotes metabolic switch

28. Effet du remodelage de l'hétérochromatine sur le destin cellulaire et le développement préimplantatoire chez la souris

29. Mosaic parental germline mutations causing recurrent forms of malformations of cortical development

30. Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells

31. Medications between psychiatric and addictive disorders

32. A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

33. The effect of constitutive inactivation of the myostatin gene on the gain in muscle strength during postnatal growth in two murine models

34. The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in 14 new patients

35. Tau phosphorylation regulates the interaction between BIN1’s SH3 domain and Tau’s proline-rich domain

36. Heterogeneity of PD-MCI in Candidates to Subthalamic Deep Brain Stimulation: Associated Cortical and Subcortical Modifications

37. Dual role of histone variant H3.3B in spermatogenesis: positive regulation of piRNA transcription and implication in X-chromosome inactivation

38. A novel IRE1 kinase inhibitor for adjuvant glioblastoma treatment

39. Analysis of the P. lividus sea urchin genome highlights contrasting trends of genomic and regulatory evolution in deuterostomes

40. Fast and interpretable unsupervised domain adaptation for FIB-SEM cell segmentation

41. Identification of new candidate drugs for primary Sjögren’s syndrome using a drug repurposing transcriptomic approach

42. A time- and space-resolved nuclear receptor atlas in mouse liver

43. Synthetic polyamines: new compounds specific to actin dynamics for mammalian cell and fission yeast

44. Early adaptive response of the retina to a pro-diabetogenic diet: Impairment of cone response and gene expression changes in high-fructose fed rats

45. DNA Physical Properties and Nucleosome Positions Are Major Determinants of HIV-1 Integrase Selectivity

46. Mutation of SLC9A1, encoding the major Na+/H+ exchanger, causes ataxia-deafness Lichtenstein-Knorr syndrome

47. RFX6 Regulates Insulin Secretion by Modulating Ca2+ Homeostasis in Human β Cells

48. Efficacy of Caffeine in <scp>ADCY5</scp> ‐Related Dyskinesia: A Retrospective Study

49. uPA/PAI-1 et EPClin® : comparaison de leur impact sur la prise en charge des cancers du sein de pronostic intermédiaire

50. Immune-Desert Tumor Microenvironment in Thoracic SMARCA4-Deficient Undifferentiated Tumors with Limited Efficacy of Immune Checkpoint Inhibitors

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