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1. Corrigendum.

2. Morphology of the triangular fibrocartilage complex of the Vietnamese adult: a cadaveric study.

3. Genomic basis for skin phenotype and cold adaptation in the extinct Steller's sea cow

4. Genomic basis for skin phenotype and cold adaptation in the extinct Steller's sea cow.

5. PTEN regulates adipose progenitor cell growth, differentiation, and replicative aging

6. Reduced lipolysis in lipoma phenocopies lipid accumulation in obesity

8. Travelers With Cutaneous Leishmaniasis Cured Without Systemic Therapy

9. Kiwi genome provides insights into evolution of a nocturnal lifestyle

10. Local Effects on Airway Inflammation and Systemic Uptake of 5 nm PEGylated and Citrated Gold Nanoparticles in Asthmatic Mice

11. The G protein-coupled receptor P2Y14 influences insulin release and smooth muscle function in mice

14. Defective Macrophage Migration in Gαi2- but Not Gαi3-Deficient Mice.

16. Suite des dances pour les violons, et hautbois. Qui se joüent ordinairement à tous les bals chez le Roy. Recueillies, mises en ordre, et composées la plus grande partie, par M. Philidor l'aîné, ordinaire de la musique du Roy et garde de tous les livres de sa bibliothèque de musique, l'an 1712

18. Travelers With Cutaneous Leishmaniasis Cured Without Systemic Therapy

20. Screening for Hypophosphatasia in Adult Patients at a Maximum Care Provider-Retrospective Analyses over Fifteen Years.

21. Dominant CST3 variants cause adult onset leukodystrophy without amyloid angiopathy.

22. Dysfunction of the adhesion G protein-coupled receptor latrophilin 1 (ADGRL1/LPHN1) increases the risk of obesity.

23. A chromosome-level genome assembly for the dugong (Dugong dugon).

24. Pten knockout in mouse preosteoblasts leads to changes in bone turnover and strength.

25. Genetic dissection of serum vaspin highlights its causal role in lipid metabolism.

26. Morphology of the triangular fibrocartilage complex of the Vietnamese adult: a cadaveric study.

27. GABRA1-Related Disorders: From Genetic to Functional Pathways.

28. Interactive webtool for analyzing drug sensitivity and resistance associated with genetic signatures of cancer cell lines.

29. Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population.

30. The role of rare genetic variants enrichment in epilepsies of presumed genetic etiology.

31. Phospholipid Scramblase 4 (PLSCR4) Regulates Adipocyte Differentiation via PIP3-Mediated AKT Activation.

32. Altered gene expression profiles impair the nervous system development in individuals with 15q13.3 microdeletion.

33. Small integral membrane protein 10 like 1 downregulation enhances differentiation of adipose progenitor cells.

34. Genomic basis for skin phenotype and cold adaptation in the extinct Steller's sea cow.

35. Improving one-step scarless genome editing in Drosophila melanogaster by combining ovo D co-CRISPR selection with sgRNA target site masking.

36. Prenatal phenotype of PNKP-related primary microcephaly associated with variants affecting both the FHA and phosphatase domain.

37. Phenotype-tissue expression and exploration (PTEE) resource facilitates the choice of tissue for RNA-seq-based clinical genetics studies.

38. ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder.

39. Obesity-An Update on the Basic Pathophysiology and Review of Recent Therapeutic Advances.

40. Ecological Specialization and Evolutionary Reticulation in Extant Hyaenidae.

41. The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals.

42. In cis TP53 and RAD51C pathogenic variants may predispose to sebaceous gland carcinomas.

43. Reduced lipolysis in lipoma phenocopies lipid accumulation in obesity.

44. Germline AGO2 mutations impair RNA interference and human neurological development.

45. Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1 .

46. Childhood Dystonia-Parkinsonism Following Infantile Spasms-Clinical Clue to Diagnosis in Early Beta-Propeller Protein-Associated Neurodegeneration.

47. Novel EXOSC3 pathogenic variant results in a mild course of neurologic disease with cerebellum involvement.

48. Pathogenic WDFY3 variants cause neurodevelopmental disorders and opposing effects on brain size.

49. Ethanol exposed maturing rat cerebellar granule cells show impaired energy metabolism and increased cell death after oxygen-glucose deprivation.

50. A new p.(Ile66Serfs*93) IGF2 variant is associated with pre- and postnatal growth retardation.

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