Kapsa RMI - Search Results

1

Wired for Success: Probing the Effect of Tissue-Engineered Neural Interface Substrates on Cell Viability.

Nascimento ATD, Mendes AX, Duchi S, Duc D, Aguilar LC, Quigley AF, Kapsa RMI, Nisbet DR, Stoddart PR, Silva SM, Moulton SE. Nascimento ATD, et al. Among authors: kapsa rmi. ACS Biomater Sci Eng. 2024 Jun 10;10(6):3775-3791. doi: 10.1021/acsbiomaterials.4c00111. Epub 2024 May 9. ACS Biomater Sci Eng. 2024. PMID: 38722625

2

Developmental genetics of deleted mtDNA in mitochondrial oculomyopathy.

Marzuki S, Berkovic SF, Saifuddin Noer A, Kapsa RM, Kalnins RM, Byrne E, Sasmono T, Sudoyo H. Marzuki S, et al. J Neurol Sci. 1997 Feb 12;145(2):155-62. doi: 10.1016/s0022-510x(96)00241-9. J Neurol Sci. 1997. PMID: 9094043

3

A novel mtDNA deletion in an infant with Pearson syndrome.

Kapsa R, Thompson GN, Thorburn DR, Dahl HH, Marzuki S, Byrne E, Blok RB. Kapsa R, et al. J Inherit Metab Dis. 1994;17(5):521-6. doi: 10.1007/BF00711584. J Inherit Metab Dis. 1994. PMID: 7837757

4

Leukemia inhibitory factor ameliorates muscle fiber degeneration in the mdx mouse.

Austin L, Bower JJ, Bennett TM, Lynch GS, Kapsa R, White JD, Barnard W, Gregorevic P, Byrne E. Austin L, et al. Muscle Nerve. 2000 Nov;23(11):1700-5. doi: 10.1002/1097-4598(200011)23:11<1700::aid-mus5>3.0.co;2-w. Muscle Nerve. 2000. PMID: 11054748

5

Myostatin, insulin-like growth factor-1, and leukemia inhibitory factor mRNAs are upregulated in chronic human disuse muscle atrophy.

Reardon KA, Davis J, Kapsa RM, Choong P, Byrne E. Reardon KA, et al. Muscle Nerve. 2001 Jul;24(7):893-9. doi: 10.1002/mus.1086. Muscle Nerve. 2001. PMID: 11410916

6

Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction.

Lertrit P, Kapsa RM, Jean-Francois MJ, Thyagarajan D, Noer AS, Marzuki S, Byrne E. Lertrit P, et al. Hum Mol Genet. 1994 Nov;3(11):1973-81. doi: 10.1093/hmg/3.11.1973. Hum Mol Genet. 1994. PMID: 7874114

7

Normal variants of human mitochondrial DNA and translation products: the building of a reference data base.

Marzuki S, Noer AS, Lertrit P, Thyagarajan D, Kapsa R, Utthanaphol P, Byrne E. Marzuki S, et al. Hum Genet. 1991 Dec;88(2):139-45. doi: 10.1007/BF00206061. Hum Genet. 1991. PMID: 1757091

8

A tRNA(Lys) mutation in the mtDNA is the causal genetic lesion underlying myoclonic epilepsy and ragged-red fiber (MERRF) syndrome.

Noer AS, Sudoyo H, Lertrit P, Thyagarajan D, Utthanaphol P, Kapsa R, Byrne E, Marzuki S. Noer AS, et al. Am J Hum Genet. 1991 Oct;49(4):715-22. Am J Hum Genet. 1991. PMID: 1910259 Free PMC article.

9

A new disease-related mutation for mitochondrial encephalopathy lactic acidosis and strokelike episodes (MELAS) syndrome affects the ND4 subunit of the respiratory complex I.

Lertrit P, Noer AS, Jean-Francois MJ, Kapsa R, Dennett X, Thyagarajan D, Lethlean K, Byrne E, Marzuki S. Lertrit P, et al. Am J Hum Genet. 1992 Sep;51(3):457-68. Am J Hum Genet. 1992. PMID: 1323207 Free PMC article.

10

mtDNA in congenital myotonic dystrophy.

Thyagarajan D, Byrne E, Noer AS, Lertrit P, Kapsa R, Marzuki S. Thyagarajan D, et al. Am J Hum Genet. 1993 Jan;52(1):207-10. Am J Hum Genet. 1993. PMID: 8192709 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

96 results

Search Page

Filters