Noer AS - Search Results

1

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. Among authors: noer as. Am J Hum Genet. 1992 Sep;51(3):457-68. Am J Hum Genet. 1992. PMID: 1323207 Free PMC article.

2

The association of the autoantigens of primary biliary cirrhosis with the mitochondrial H+-ATPase--a reassessment.

Sudoyo H, Noer AS, Mackay IR, Marzuki S. Sudoyo H, et al. Among authors: noer as. Biochem Int. 1989 May;18(5):951-60. Biochem Int. 1989. PMID: 2528956

3

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.

4

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. Among authors: noer as. Hum Genet. 1991 Dec;88(2):139-45. doi: 10.1007/BF00206061. Hum Genet. 1991. PMID: 1757091

5

Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathy.

Lertrit P, Noer AS, Byrne E, Marzuki S. Lertrit P, et al. Among authors: noer as. Hum Genet. 1992 Nov;90(3):251-4. doi: 10.1007/BF00220072. Hum Genet. 1992. PMID: 1487239

6

Antipeptide antibodies to the carboxy terminal and the DCCD binding region of the human mitochondrial ATP synthase beta-subunit.

Noer AS, Marzuki S, Allison WS. Noer AS, et al. Biochim Biophys Acta. 1992 Feb 21;1099(2):123-30. Biochim Biophys Acta. 1992. PMID: 1371933

7

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. Among authors: noer as. Hum Mol Genet. 1994 Nov;3(11):1973-81. doi: 10.1093/hmg/3.11.1973. Hum Mol Genet. 1994. PMID: 7874114

8

mtDNA in congenital myotonic dystrophy.

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

9

The M2 autoantigens of primary biliary cirrhosis are not subunits of the mitochondrial H+-ATPase.

Marzuki S, Mackay IR, Sudoyo H, Noer AS. Marzuki S, et al. Among authors: noer as. Hepatology. 1988 Sep-Oct;8(5):1180-1. doi: 10.1002/hep.1840080546. Hepatology. 1988. PMID: 2971016 No abstract available.

10

Mitochondrial DNA deletion in encephalomyopathy.

Noer AS, Marzuki S, Trounce I, Byrne E. Noer AS, et al. Lancet. 1988 Nov 26;2(8622):1253-4. doi: 10.1016/s0140-6736(88)90847-1. Lancet. 1988. PMID: 2903984 No abstract available.

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