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1. Complex trait susceptibilities and population diversity in a sample of 4,145 Russians

2. TWINGEN: protocol for an observational clinical biobank recall and biomarker cohort study to identify Finnish individuals with high risk of Alzheimer’s disease

3. Pharmacoepigenetics of hypertension: genome-wide methylation analysis of responsiveness to four classes of antihypertensive drugs using a double-blind crossover study design

4. Recontacting biobank participants to collect lifestyle, behavioural and cognitive information via online questionnaires: lessons from a pilot study within FinnGen

5. Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosa

6. Sleep apnoea is a risk factor for severe COVID-19

7. Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

8. Understanding Complex Trait Susceptibilities and Ethnical Diversity in a Sample of 4,145 Russians Through Analysis of Clinical and Genetic Data

9. New insights into the genetic etiology of Alzheimer's disease and related dementias

10. FinnGen: Unique genetic insights from combining isolated population and national health register data

11. Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene

12. Genetic Loci Associated with Allergic Sensitization in Lithuanians.

13. SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population.

14. SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues

15. Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions

16. CRY2 genetic variants associate with dysthymia.

17. Genomics of asthma, allergy and chronic rhinosinusitis: novel concepts and relevance in airway mucosa

18. PRKCDBP (CAVIN3) and CRY2 associate with major depressive disorder

19. Heme oxygenase-1 repeat polymorphism in septic acute kidney injury

20. Mutation Update: The Spectra of Nebulin Variants and Associated Myopathies

21. CRY1, CRY2 and PRKCDBP genetic variants in metabolic syndrome

22. Replicated evidence for aminoacylase 3 and nephrin gene variations to predict antihypertensive drug responses

23. Genomic Association Analysis of Common Variants Influencing Antihypertensive Response to Hydrochlorothiazide

24. Generalized glucocorticoid resistance caused by a novel two-nucleotide deletion in the hormone-binding domain of the glucocorticoid receptor gene NR3C1

25. CRY1 and CRY2 genetic variants in seasonality: A longitudinal and cross-sectional study

26. PTPRD gene associated with blood pressure response to atenolol and resistant hypertension

27. Common genetic variation of β1- and β2-adrenergic receptor and response to four classes of antihypertensive treatment

28. TET2 and CSMD1 genes affect SBP response to hydrochlorothiazide in never-treated essential hypertensives

29. Pharmacogenomics of hypertension: a genome‐wide, placebo‐controlled cross‐over study, using four classes of antihypertensive drugs

30. Genetic Loci Associated with Allergic Sensitization in Lithuanians

31. Complete genomic structure of the human nebulin gene and identification of alternatively spliced transcripts

32. Mutations in the β-tropomyosin (TPM2) gene – a rare cause of nemaline myopathy

33. Nebulin expression in patients with nemaline myopathy

34. Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

35. CRY2 genetic variants associate with dysthymia

36. Abnormal actin binding of aberrant β-tropomyosins is a molecular cause of muscle weakness in TPM2-related nemaline and cap myopathy

37. CYP2C9 genotype modifies activity of the renin-angiotensin-aldosterone system in hypertensive men

38. Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES study

39. Laboratory tests as predictors of the antihypertensive effects of amlodipine, bisoprolol, hydrochlorothiazide and losartan in men: results from the randomized, double-blind, crossover GENRES Study

40. Identification Of A Founder Mutation In Tpm3 In Nemaline Myopathy Patients Of Turkish Origin

41. SIRT1 Polymorphisms Associate with Seasonal Weight Variation, Depressive Disorders, and Diastolic Blood Pressure in the General Population

42. Identification of 45 novel mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

43. Developmental and muscle-type-specific expression of mouse nebulin exons 127 and 128

44. G.P.7.09 Functional studies of aberrant beta-tropomyosin causing nemaline myopathy and cap myopathy

45. G.P.13.02 Functional study of mutated beta-tropomyosin causing nemaline myopathy, cap myopathy and distal arthrogryposis

46. C.P.1.08 A homozygous deletion of TPM3 causing severe nemaline myopathy in two Turkish sib pairs from separate families

47. C.P.1.12 One causative gene, TPM2, and two congenital myopathies. A functional study

48. Mutations in the nebulin gene can cause severe congenital nemaline myopathy

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