X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
alanyl-trna synthetase (30) 30
biochemistry & molecular biology (30) 30
index medicus (20) 20
escherichia-coli (15) 15
transfer rna (15) 15
ligases (14) 14
animals (13) 13
humans (12) 12
microbiology (11) 11
rats (10) 10
transfer-rna-synthetase (10) 10
beta-alanyl-l-histidinato zinc (9) 9
pharmacology & pharmacy (9) 9
proteins (9) 9
β-alanyl-l-histidinato zinc (9) 9
escherichia coli (8) 8
protein-synthesis (8) 8
tissue-culture (8) 8
trna (8) 8
alanine-trna ligase - metabolism (7) 7
bacterial proteins - metabolism (7) 7
biophysics (7) 7
l-histidinato zinc (7) 7
mice (7) 7
molecular sequence data (7) 7
mutation (7) 7
alanine-trna ligase - chemistry (6) 6
amino acid sequence (6) 6
aminoacyl-trna synthetase (6) 6
aminoacylation (6) 6
analysis (6) 6
bacteria (6) 6
crystal-structure (6) 6
endocrinology & metabolism (6) 6
growth (6) 6
kinetics (6) 6
male (6) 6
molecular conformation (6) 6
organometallic compounds - pharmacology (6) 6
transfer-rna synthetase (6) 6
zinc (6) 6
β-alanyl- l-histidinato zinc (6) 6
alanine (5) 5
article (5) 5
binding sites (5) 5
biosynthesis (5) 5
bombyx-mori (5) 5
carnosine - analogs & derivatives (5) 5
enzymes (5) 5
escherichia coli - enzymology (5) 5
female (5) 5
genetic aspects (5) 5
leukodystrophy (5) 5
neurosciences (5) 5
research (5) 5
sequence (5) 5
staphylococcus-aureus (5) 5
substrate specificity (5) 5
alanine - metabolism (4) 4
aminoacyl-trna synthetases (4) 4
bacterial proteins - chemistry (4) 4
bacterial proteins - genetics (4) 4
biochemistry, general (4) 4
carnosine - pharmacology (4) 4
chelating agents - pharmacology (4) 4
chemistry, multidisciplinary (4) 4
crystal structure (4) 4
dipeptides - pharmacology (4) 4
domain (4) 4
escherichia coli - genetics (4) 4
family (4) 4
genes (4) 4
glycyl-trna synthetase (4) 4
inhibitors (4) 4
life sciences (4) 4
membrane (4) 4
mutations (4) 4
peptidoglycan (4) 4
phospholipids (4) 4
physiological aspects (4) 4
quaternary structure (4) 4
recognition (4) 4
ultracentrifugation (4) 4
zinc - pharmacology (4) 4
zinc compounds (4) 4
zinc compounds - pharmacology (4) 4
5'-o-[n-sulfamoyl]adenosine (3) 3
aars (3) 3
adult (3) 3
alanine-trna ligase - genetics (3) 3
alanyl-lipoteichoic acid (3) 3
alanyl-phosphatidylglycerol (3) 3
alanyl-transfer rna (3) 3
amino acyl-trna synthetases - genetics (3) 3
anti-bacterial agents - pharmacology (3) 3
antimicrobial peptides (3) 3
base sequence (3) 3
beta (3) 3
biochemical research methods (3) 3
biotechnology & applied microbiology (3) 3
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Fertility and Sterility, ISSN 0015-0282, 09/2019, Volume 112, Issue 3, pp. 569 - 576.e2
To explore the candidate pathogenic gene in a premature ovarian insufficiency (POI) proband from a consanguineous marriage and detect the potential effects of... 
AARS2 | alanyl-tRNA synthetase | whole exome sequencing | Primary ovarian insufficiency | LEUKODYSTROPHY | TRANSCRIPTION | MITOCHONDRIAL-DNA | TRANSLATION | FAILURE | OBSTETRICS & GYNECOLOGY | PERRAULT SYNDROME | HEARING-LOSS | REPRODUCTIVE BIOLOGY | OVARIOLEUKODYSTROPHY | GENETICS | DYSGENESIS | Family | Genetic aspects | Nucleotide sequencing | Ligases | Transfer RNA | DNA sequencing
Journal Article
Genes, ISSN 2073-4425, 10/2018, Volume 9, Issue 10, pp. 1. - 16
Journal Article
by Zhao, XX and Han, JM and Zhu, L and Xiao, Y and Wang, CH and Hong, F and Jiang, PP and Guan, MX
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, ISSN 1449-2288, 2018, Volume 14, Issue 11, pp. 1437 - 1444
Mutations of mitochondrial transfer RNAs (mt-tRNAs) play a major role in a wide range of mitochondrial diseases because of the vital role of these molecules in... 
PHENOTYPIC MANIFESTATION | DOMAIN | TRNA(ILE) | cybrid | HUMAN-CELLS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CARDIOMYOPATHY | oxidative phosphorylation | mitochondrial tRNA | PEPTIDES | BIOGENESIS | mitochondrial alanyl-tRNA synthetase | ALTERS | AMINOACYLATION | HYPERTENSION
Journal Article
International Journal of Biological Sciences, ISSN 1449-2288, 08/2018, Volume 14, Issue 11, pp. 1437 - 1444
Mutations of mitochondrial transfer RNAs (mt-tRNAs) play a major role in a wide range of mitochondrial diseases because of the vital role of these molecules in... 
Mitochondrial alanyl-tRNA synthetase | Oxidative phosphorylation | Cybrid | Mitochondrial tRNA | Translation | Phosphorylation | Aminoacylation | Cybrids | tRNA | Pathogenesis | Superoxide | Mitochondrial DNA | Defects | Mitochondria | Alanine-tRNA ligase | Membrane potential | Mutation | Electron transport
Journal Article
Cardiology in the Young, ISSN 1047-9511, 07/2017, Volume 27, Issue 5, pp. 936 - 944
Cardiomyopathy is a common manifestation in neonates and infants with mitochondrial disorders. In this study, we report two cases manifesting with fatal... 
mitochondrial cardiomyopathy | Alanyl-tRNA synthetase 2 | ragged red fibres | leucoencephalopathy | thymidine kinase 2 | DEFECTS | CARDIAC & CARDIOVASCULAR SYSTEMS | HUMAN-DISEASE | CARDIAC MANIFESTATIONS | CLINICAL SPECTRUM | DNA DEPLETION SYNDROMES | TK2 GENE | MYOPATHIC FORM | PEDIATRICS | MUTATIONS | RESPIRATORY-CHAIN DEFICIENCIES | ONSET | Mitochondrial Diseases - genetics | Cardiomyopathy, Hypertrophic - genetics | Echocardiography | Thymidine Kinase - genetics | Humans | Infant | Magnetic Resonance Imaging | White Matter - diagnostic imaging | DNA, Mitochondrial - genetics | Alanine-tRNA Ligase - genetics | Autopsy | Fatal Outcome | Female | Alanine-tRNA Ligase - deficiency | Mutation | Cardiomyopathy, Hypertrophic - diagnostic imaging | Thymidine Kinase - deficiency | Infant, Newborn | Cytochrome | Heart | Cerebellum | Neonates | Dehydrogenases | Cardiomyopathy | Genes | Disorders | Oxidase | Cytochrome-c oxidase | Infants | Genomes | Mitochondrial DNA | Thymidine | Motor task performance | Eutrophication | Electron transport chain | Literature reviews | Parents & parenting | Fatty liver | Fibre | Degeneration | Heart diseases | Deoxyribonucleic acid--DNA | Age | Thymidine kinase | tRNA | Case reports | Regression analysis | Steatosis | Neurology | Ostomy | Hospitals | Alanine-tRNA ligase | Biopsy | Medical prognosis | Fatalities | Electron transport | Adenosine triphosphatase | Myopathy
Journal Article
Journal Article
BIOMOLECULAR NMR ASSIGNMENTS, ISSN 1874-2718, 10/2014, Volume 8, Issue 2, pp. 415 - 418
A gene encoding a protein classified as alanyl-tRNA synthetase (AlaRS) was found in the genome of the psychrophilic bacteria Bizionia argentinensis. The enzyme... 
NMR | BIOPHYSICS | Alanyl-tRNA synthetase | FAMILY FLAVOBACTERIACEAE | SPECTROSCOPY | Bizionia argentinensis sp nov | Psychrophilic bacterium | EMENDED DESCRIPTION | WATER | PLUS
Journal Article
Biomolecular NMR Assignments, ISSN 1874-2718, 10/2014, Volume 8, Issue 2, pp. 415 - 418
A gene encoding a protein classified as alanyl-tRNA synthetase (AlaRS) was found in the genome of the psychrophilic bacteria Bizionia argentinensis. The enzyme... 
Polymer Sciences | Biochemistry, general | NMR | Alanyl-tRNA synthetase | Bizionia argentinensis sp. nov | Biophysics and Biological Physics | Psychrophilic bacterium | Physics | Bacteria | Ligases | Genomics | Transfer RNA
Journal Article
Progress in Biochemistry and Biophysics, ISSN 1000-3282, 06/2007, Volume 34, Issue 6, pp. 562 - 566
Journal Article
by Zhu, B and Wang, ED
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS, ISSN 1000-3282, 2007, Volume 34, Issue 6, pp. 562 - 566
Aminoacyl-tRNA synthetases (AARSs) catalyze aminoacylation of their tRNAs for protein biosynthesis. As belong to one of the most ancient and conserved enzyme... 
ANGIOGENESIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | neurodegeneration | CYTOKINE | alanyl-tRNA synthetase | PROTEIN-SYNTHESIS | tyrosyl-tRNA synthetase | 2D | NEUROPATHY | BIOPHYSICS | aminoacyl-tRNA synthetase | Charcot-Marie-Tooth disease | GROWTH | FRAGMENT | glycyl-tRNA synthetase | Purkinje cell | MUTATIONS
Journal Article
Brain and Behavior, ISSN 2162-3279, 07/2019, Volume 9, Issue 7, pp. e01313 - n/a
Introduction Leukodystrophy is a group of hereditary leukoencephalopathies predominantly affecting the white matter. Multiple genes and mutations have been... 
leukoencephalopathy | mutation | leukodystrophy | AARS2 | alanyl‐tRNA synthetase | CLASSIFICATION | BEHAVIORAL SCIENCES | alanyl-tRNA synthetase | NEUROSCIENCES | Genetic aspects | Nucleotide sequencing | Ligases | Analysis | Transfer RNA | DNA sequencing | Proteins | Hospitals | Nuclear magnetic resonance--NMR | Cardiomyopathy | Spectrum analysis | Families & family life | Mutation | Patients
Journal Article
Journal Article
Ukrain'skyi Biokhimichnyi Zhurnal, ISSN 0201-8470, 2008, Volume 80, Issue 6, pp. 52 - 59
Journal Article
Journal of Biomolecular Screening, ISSN 1087-0571, 8/2016, Volume 21, Issue 7, pp. 722 - 728
Journal Article
ACTA NEUROPATHOLOGICA COMMUNICATIONS, ISSN 2051-5960, 11/2019, Volume 7, Issue 1, pp. 1 - 11
Swedish type Hereditary Diffuse Leukoencephalopathy with Spheroids (HDLS-S) is a severe adult-onset leukoencephalopathy with the histopathological hallmark of... 
HDLS | LEUKODYSTROPHY | ADULT-ONSET LEUKOENCEPHALOPATHY | Swedish type hereditary diffuse Leukoencephalopathy with spheroids | GENETIC-CHARACTERIZATION | NEUROSCIENCES | FAMILY | AXONAL SPHEROIDS | TRANSFER-RNA SYNTHETASE | MUTATION | DISEASE | FRAMEWORK | Alanyl tRNA synthetase | AARS
Journal Article