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1. Variable outcomes of human heart attack recapitulated in genetically diverse mice.

2. Gene Expression Networks in the Murine Pulmonary Myocardium Provide Insight into the Pathobiology of Atrial Fibrillation.

3. Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin

4. Duchenne muscular dystrophy and dystrophin: pathogenesis and opportunities for treatment

5. TPM3 Deletions Cause a Hypercontractile Congenital Muscle Stiffness Phenotype

7. Rescue of skeletal muscle alpha-actin-null mice by cardiac (fetal) alpha-actin.

9. Nemaline myopathy caused by absence of alpha-skeletal muscle actin.

10. Novel mutation in the myelin protein zero gene in a family with intermediate hereditary motor and sensory neuropathy.

12. Fatal hypertrophic cardiomyopathy and nemaline myopathy associated with ACTA1 K336E mutation

13. "Uninsurable because of a genetic test": a qualitative study of consumer views about the use of genetic test results in Australian life insurance.

14. Combined population genomic screening for three high-risk conditions in Australia: a modelling study.

15. Generation of an induced pluripotent stem cell line from a 3-month-old nemaline myopathy patient with a heterozygous dominant c.515C > A (p.Ala172Glu) variant in the ACTA1 gene.

16. Generation of two isogenic induced pluripotent stem cell lines from a 1-month-old nemaline myopathy patient harbouring a homozygous recessive c.121C > T (p.Arg39Ter) variant in the ACTA1 gene.

17. Pilot study of universal screening of children and child-parent cascade testing for familial hypercholesterolaemia in Australia.

18. Generation of two isogenic induced pluripotent stem cell lines from a 10-year-old typical nemaline myopathy patient with a heterozygous dominant c.541G>A (p.Asp179Asn) pathogenic variant in the ACTA1 gene.

19. Descriptive epidemiological study of rare, less common and common cancers in Western Australia.

20. Generation of two isogenic induced pluripotent stem cell lines from a 4-month-old severe nemaline myopathy patient with a heterozygous dominant c.553C > A (p.Arg183Ser) variant in the ACTA1 gene.

21. Safety of daily low-dose aspirin use during pregnancy in low-income and middle-income countries.

22. Neonatal deaths in infants born weighing ≥ 2500 g in low and middle-income countries.

23. Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy.

24. Targeted gene panel use in 2249 neuromuscular patients: the Australasian referral center experience.

25. Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb.

26. Systemic AAV8-mediated delivery of a functional copy of muscle glycogen phosphorylase (Pygm) ameliorates disease in a murine model of McArdle disease.

27. Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus.

28. Genomic Testing for Human Health and Disease Across the Life Cycle: Applications and Ethical, Legal, and Social Challenges.

29. Optimizing Precision Medicine for Public Health.

30. Variable outcomes of human heart attack recapitulated in genetically diverse mice.

31. Recent advances in understanding congenital myopathies.

32. Molecular Consequences of the Myopathy-Related D286G Mutation on Actin Function.

33. The Evolution of Public Health Genomics: Exploring Its Past, Present, and Future.

34. L-tyrosine supplementation does not ameliorate skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy.

37. CUGC for Duchenne muscular dystrophy (DMD).

38. Clinical utility gene card for McArdle disease.

39. Incidental inequity.

40. Myostatin inhibition using mRK35 produces skeletal muscle growth and tubular aggregate formation in wild type and TgACTA1D286G nemaline myopathy mice.

41. Is balance performance reduced after mild traumatic brain injury?: Interim analysis from chronic effects of neurotrauma consortium (CENC) multi-centre study.

42. Variable cardiac α-actin (Actc1) expression in early adult skeletal muscle correlates with promoter methylation.

43. Gene Expression Networks in the Murine Pulmonary Myocardium Provide Insight into the Pathobiology of Atrial Fibrillation.

44. Variants in the Oxidoreductase PYROXD1 Cause Early-Onset Myopathy with Internalized Nuclei and Myofibrillar Disorganization.

45. Effects of virus infection on pollen production and pollen performance: Implications for the spread of resistance alleles.

46. X-ray recordings reveal how a human disease-linked skeletal muscle α-actin mutation leads to contractile dysfunction.

47. Muscle weakness in TPM3-myopathy is due to reduced Ca2+-sensitivity and impaired acto-myosin cross-bridge cycling in slow fibres.

48. Clinical utility gene card for: Nemaline myopathy - update 2015.

49. Zebrafish models for nemaline myopathy reveal a spectrum of nemaline bodies contributing to reduced muscle function.

50. Nebulin interactions with actin and tropomyosin are altered by disease-causing mutations.

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