37 results on '"Lemckert, Frances A."'
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2. A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centre
3. Standardized practices for RNA diagnostics using clinically accessible specimens reclassifies 75% of putative splicing variants
4. Unimpaired Autoreactive T-Cell Traffic Within the Central Nervous System During Tumor Necrosis Factor Receptor-Mediated inhibition of Experimental Autoimmune Encephalomyelitis
5. Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy
6. Oxidative stress and pathology in muscular dystrophies: focus on protein thiol oxidation and dysferlinopathies
7. Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy
8. Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch
9. Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy
10. The Murine Stanniocalcin 2 Gene Is a Negative Regulator of Postnatal Growth
11. Characterisation of a P140K mutant O6-methylguanine-DNA-methyltransferase (MGMT)-expressing transgenic mouse line with drug-selectable bone marrow
12. An α-actinin-3 Knockout Mouse Suffers Increased Sarcomeric Damage from Eccentric Exercise: 1111: 9:00 AM – 9:15 AM
13. Modification of the tropomyosin isoform composition of actin filaments in the brain by deletion of an alternatively spliced exon
14. Generation of Splenic Follicular Structure and B Cell Movement in Tumor Necrosis Factor-deficient Mice
15. Challenging Cytokine Redundancy: Inflammatory Cell Movement and Clinical Course of Experimental Autoimmune Encephalomyelitis Are Normal in Lymphotoxin-deficient, but Not Tumor Necrosis Factor-deficient, Mice
16. Critical Points of Tumor Necrosis Factor Action in Central Nervous System Autoimmune Inflammation Defined by Gene Targeting
17. Microglia Induce CD4 T Lymphocyte Final Effector Function and Death
18. Enzymatic cleavage of myoferlin releases a dual C2-domain module linked to ERK signalling
19. Lack of MG53 in human heart precludes utility as a biomarker of myocardial injury or endogenous cardioprotective factor
20. Calpains, Cleaved Mini-DysferlinC72, and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair
21. Functional identity of the Gamma Tropomyosin gene
22. New aspects of tropomyosin-regulated neuritogenesis revealed by the deletion of Tm5NM1 and 2
23. Male Calling Sites in Two Species of Australian Toadlets (Anura: Myobatrachidae: Uperoleia) at Two Ponds in New South Wales
24. Negative Autoregulation of GTF2IRD1 in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism
25. Divergent Regulation of the Sarcomere and the Cytoskeleton
26. Loss of ACTN3 gene function alters mouse muscle metabolism and shows evidence of positive selection in humans
27. Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development
28. Characterisation of a P140K mutantO6-methylguanine-DNA-methyltransferase (MGMT)-expressing transgenic mouse line with drug-selectable bone marrow
29. Membrane lymphotoxin contributes to anti-leishmanial immunity by controlling structural integrity of lymphoid organs
30. Challenging Cytokine Redundancy: Inflammatory Cell Movement and Clinical Course of Experimental Autoimmune Encephalomyelitis Are Normal in Lymphotoxin-deficient, but Not Tumor Necrosis Factor–deficient, Mice
31. Distinct roles for lymphotoxin-α and tumor necrosis factor in organogenesis and spatial organization of lymphoid tissue
32. Tumor necrosis factor blockade in actively induced experimental autoimmune encephalomyelitis prevents clinical disease despite activated T cell infiltration to the central nervous system
33. Calpains, Cleaved Mini-DysferlinC72, and L-Type Channels Underpin Calcium-Dependent Muscle Membrane Repair.
34. Characterisation of a P140K mutant O6-methylguanine-DNA-methyltransferase (MGMT)-expressing transgenic mouse line with drug-selectable bone marrow.
35. Gene targeting in C57BL16 ES cells. Successful germ line transmission using recipient BALB/c blastocysts developmentally matured in vitro.
36. Negative Autoregulation of GTF2IRD1 in Williams-Beuren Syndrome via a Novel DNA Binding Mechanism.
37. Loss of calpains-1 and -2 prevents repair of plasma membrane scrape injuries, but not small pores, and induces a severe muscular dystrophy.
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