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5. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression

8. Das Deutsche Netzwerk für mitochondriale Erkrankungen (mitoNET)

12. Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies

13. A common atopy-associated variant in the Th2 cytokine locus control region impacts transcriptional regulation and alters SMAD3 and SP1 binding

24. GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI

25. Genomics of 1 million parent lifespans implicates novel pathways and common diseases and distinguishes survival chances

26. Quantification and discovery of sequence determinants of protein-per-mRNA amount in 29 human tissues

27. Mendelian randomization integrating GWAS and eQTL data reveals genetic determinants of complex and clinical traits

28. Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency

32. Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes

33. A DNA methylation biomarker of alcohol consumption

35. Assessing Mitochondrial Bioenergetics in Isolated Mitochondria from Various Mouse Tissues Using Seahorse XF96 Analyzer

36. Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies

39. Trans-ethnic meta-analysis of white blood cell phenotypes

40. A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

41. Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

42. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

43. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy

44. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

45. A DNA methylation biomarker of alcohol consumption

46. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356

48. NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early Childhood

49. Novel GFM2 variants identified in two cases of early-onset mitochondrial disease cause impaired expression of mtDNA encoded OXPHOS subunits

50. A DNA methylation biomarker of alcohol consumption

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