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Journal Article
AVIAN PATHOLOGY, ISSN 0307-9457, 2011, Volume 40, Issue 1, pp. 1 - 13
Fowl typhoid and pullorum disease are two distinct septicaemic diseases largely specific to avian species and caused by Salmonella Gallinarum and Salmonella... 
INTESTINAL COLONIZATION | HOST-SPECIFICITY | VETERINARY SCIENCES | ENTERICA SEROVAR GALLINARUM | SALMONELLA SEROTYPE GALLINARUM | LAYING HENS | HORIZONTAL TRANSMISSION | ENTERITIDIS-IMMUNE LYMPHOKINES | PHENOTYPIC-EXPRESSION | COMMERCIAL LAYER FLOCKS | III SECRETION SYSTEM
Journal Article
Modern Pathology, ISSN 0893-3952, 04/2019, Volume 32, Issue 4, pp. 568 - 575
A subtype of intestinal-type adenocarcinoma of the stomach, characterized by low-grade cytological atypia and anastomosing glands, has been described in... 
HETEROGENEITY | PATHOLOGY | PHENOTYPIC-EXPRESSION | CARRIERS | DIFFUSE GASTRIC-CANCER | Adenocarcinoma | Stomach | Dysplasia | Next-generation sequencing | CDH1 protein | Intestine | p53 Protein | Glands | Reverse transcription | RhoA protein | Mutation | Tumors
Journal Article
International Journal of Cardiology, ISSN 0167-5273, 07/2019, Volume 286, pp. 92 - 98
Background: Danon disease (DD) is a rare X-linked autophagic vacuolar myopathy, characterized by high penetrance and severe cardiomyopathy. Because of its... 
Hypertrophic cardiomyopathy | Danon disease | Gender | Genetic testing | Dilated cardiomyopathy | LAMP2 mutation | DIAGNOSIS | CARDIAC & CARDIOVASCULAR SYSTEMS | TASK-FORCE | AUTOPHAGIC VACUOLES | PHENOTYPIC-EXPRESSION
Journal Article
by Li, RH and Guan, MX
MOLECULAR AND CELLULAR BIOLOGY, ISSN 0270-7306, 05/2010, Volume 30, Issue 9, pp. 2147 - 2154
Mutations in mitochondrial tRNA genes are associated with a wide spectrum of human diseases. In particular, the tRNA(Leu(UUR)) A3243G mutation causes... 
CELLS | DEFECTS | A1555G MUTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENE-EXPRESSION | DEAFNESS | MELAS | RIBOSOMAL-RNA | AMINOACYLATION | PROTEIN-SYNTHESIS | PHENOTYPIC-EXPRESSION | CELL BIOLOGY
Journal Article
Trends in Genetics, ISSN 0168-9525, 08/2018, Volume 34, Issue 8, pp. 578 - 586
Journal Article
Nature Reviews Cardiology, ISSN 1759-5002, 11/2016, Volume 13, Issue 11, pp. 651 - 675
Journal Article
ONCOTARGET, ISSN 1949-2553, 11/2017, Volume 8, Issue 56, pp. 96351 - 96358
The prevalence of PCOS was investigated in many studies in different continents. However, there is no established prevalence of PCOS for distinct ethnic... 
GENETIC ANCESTRY | POPULATION | ethnicity | REPORTED ETHNICITY | systematic review | PHENOTYPIC-EXPRESSION | INDIAN WOMEN | polycystic ovary syndrome | STUDENTS | CELL BIOLOGY | prevalence | INSULIN-RESISTANCE | SYNDROME PCOS | DIAGNOSTIC-CRITERIA | REVISED 2003 CONSENSUS
Journal Article
by Chen, DN and Zhang, ZM and Chen, C and Yao, SH and Yang, QX and Li, F and He, X and Ai, C and Wang, M and Guan, MX
NUCLEIC ACIDS RESEARCH, ISSN 0305-1048, 06/2019, Volume 47, Issue 10, pp. 5341 - 5355
GTPBP3 is a highly conserved tRNA modifying enzyme for the biosynthesis of m(5)U at the wobble position of mitochondrial tRNA(Glu), tRNA(Gln), tRNA(Lys),... 
RESPIRATORY-CHAIN DEFICIENCY | NATRIURETIC-PEPTIDE | COMPLEX I | WOBBLE URIDINE | MG37 MODIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LACTIC-ACIDOSIS | POSTTRANSCRIPTIONAL MODIFICATIONS | TRANSLATION | PHENOTYPIC-EXPRESSION | MUTATION ALTERS | RNA and RNA-protein complexes
Journal Article
Scientific Reports, ISSN 2045-2322, 07/2016, Volume 6, Issue 1, p. 29621
Aminoglycosides are ototoxic to the cochlear hair cells, and mitochondrial dysfunction is one of the major mechanisms behind ototoxic drug-induced hair cell... 
APOPTOSIS | OXIDATIVE STRESS | INHIBITION | MULTIDISCIPLINARY SCIENCES | MODIFIER GENE | OTOTOXICITY | TRANSFER-RNA | MUTATIONS | MITOCHONDRIAL-DNA | PHENOTYPIC-EXPRESSION | GENTAMICIN
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 9, pp. 3321 - 3334
The 1555A→G mutation in mitochondrial 12S rRNA has been associated with aminoglycoside-induced and non-syndromic deafness in many individuals worldwide.... 
Molecular Bases of Disease | modifier factors | transfer RNA (tRNA) | ribosomal ribonucleic acid (rRNA) (ribosomal RNA) | reactive oxygen species (ROS) | maternal inheritance | mitochondrial disease | phenotypic expression | mutation | genetics | mitochondrial DNA (mtDNA) | pathophysiology | translation | hearing | ATP | respiratory chain
Journal Article
NUCLEIC ACIDS RESEARCH, ISSN 0305-1048, 12/2016, Volume 44, Issue 22, pp. 10974 - 10985
In this report, we investigated the pathogenic mechanism underlying the deafness-associated mitochondrial(mt) tRNA(Asp) 7551A > G mutation. The m.7551A > G... 
INHERITED HEARING-LOSS | OXIDATIVE STRESS | DNA MUTATION | TRANSFER-RNA MODIFICATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRNA(SER(UCN)) GENE | NON-SYNDROMIC DEAFNESS | HAN CHINESE FAMILIES | HEREDITARY OPTIC NEUROPATHY | NONSYNDROMIC DEAFNESS | PHENOTYPIC-EXPRESSION
Journal Article