Author

Achmad Saefuddin Noer

Observed names: A Noer, A S Noer, A. S. Noer, A.S. Noer, Achmad S. Noer

Institution: Bandung Institute of Technology

Observed institutions: Bandung Institute of Technology, St Vincent's Hospital Melbourne, Monash University

OpenAlex ID: A5113567625

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

1991 · A S Noer, H Sudoyo, et al. · Europe PMC (PubMed Central) · 86

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

1991 · S. Marzuki, A.S. Noer, et al. · Human Genetics · 81

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

1992 · P Lertrit, A S Noer, et al. · Europe PMC (PubMed Central) · 74

Raw starch-degrading α-amylase fromBacillus aquimarisMKSC 6.2: isolation and expression of the gene, bioinformatics and biochemical characterization of the recombinant enzyme

2012 · F. Puspasari, O.K. Radjasa, et al. · Journal of Applied Microbiology · 67

Characteristics of raw starch degrading α‐amylase from Bacillus aquimaris MKSC 6.2 associated with soft coral Sinularia sp.

2011 · Fernita Puspasari, Zeily Nurachman, et al. · Starch - Stärke · 33

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

1992 · P. Lertrit, A.S. Noer, et al. · Human Genetics · 32

Biochemical characterization of a raw starch degrading α-amylase from the Indonesian marine bacterium Bacillus sp. ALSHL3

2009 · Keni Vidilaseris, Karina Hidayat, et al. · Biologia · 23

Novel mutations in katG gene of a clinical isolate of isoniazid-resistant Mycobacterium tuberculosis

2012 · Purkan, Ihsanawati, et al. · Biologia · 10

mtDNA in congenital myotonic dystrophy.

1993 · D Thyagarajan, E Byrne, et al. · Europe PMC (PubMed Central) · 5

Optimization of Neuro-Fuzzy System Using Genetic Algorithm for Chromosome Classification

2013 · M. Sarosa, A. S. Ahmad, et al. · DOAJ (DOAJ: Directory of Open Access Journals) · 4

Identifikasi Mutasi Heteroplasmi A3243g Dna Mitokondria Dan Studi Pewarisan Maternal Pada Pasien Diabetes Melitus Tipe 2

2010 · Iman Permana Maksum, Sriwidodo Sriwidodo, et al. · 4

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

1992 · A.S. Noer, S. Marzuki, et al. · Biochimica et Biophysica Acta (BBA) - Bioenergetics · 3

Optimization of Neuro-Fuzzy System

2007 · M. Sarosa, A. S. Ahmad, et al. · ITB Journal of Information and Communication Technology · 1

Maternally inherited diabetes pPatients from Manado and Jakarta posses A3243G mutation by PCR-Allele's specific amplification

2008 · Iman Permana Maksum, Harwan D. Sasongko, et al.

Study on the interaction between the compounds of Gardenia tubifera and Harmandia mekongensis extracts with Salmonella typhi chromosomal DNA molecule

2002 · Linar Z. Udin, I. Soediro, et al.

Sequencing a 903 nucleotide carA gene of Salmonella typhi obtained through PCR employing Ca-3 and Ca-6 primers

1998 · Ari Rudiretna, A.S. Noer, et al. · Medical Journal of Indonesia

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

1992 · A Noer · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology

Works count: 18

Citation count: 423

H-index: 8

I10-index: 8