Identification of genetic polymorphisms in FABP3 and FABP4 and putative association with back fat thickness in Korean native cattle.

PubWeight™: 0.89‹?›

🔗 View Article (PMID 18304447)

Published in BMB Rep on January 31, 2008

Authors

Seoae Cho1, Tae Sung Park, Du-Hak Yoon, Hyun Sub Cheong, Sohg Namgoong, Byung Lae Park, Hye Won Lee, Chang Soo Han, Eun Mi Kim, Il-Cheong Cheong, Heebal Kim, Hyoung Doo Shin

Author Affiliations

1: Laboratory of Bioinformatics and Biostatistics, Interdisciplinary Program in Bioinformatics, Department of Statistics, Seoul National University, Seoul, Korea.

Articles by these authors

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. Nat Genet (2008) 9.39

Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat Genet (2009) 6.83

Analyses of pig genomes provide insight into porcine demography and evolution. Nature (2012) 5.58

Multi-platform next-generation sequencing of the domestic turkey (Meleagris gallopavo): genome assembly and analysis. PLoS Biol (2010) 5.39

Discrepancy between the tuberculin skin test and the whole-blood interferon gamma assay for the diagnosis of latent tuberculosis infection in an intermediate tuberculosis-burden country. JAMA (2005) 4.02

A TRPV family ion channel required for hearing in Drosophila. Nature (2003) 3.53

Implication of genetic variants near TCF7L2, SLC30A8, HHEX, CDKAL1, CDKN2A/B, IGF2BP2, and FTO in type 2 diabetes and obesity in 6,719 Asians. Diabetes (2008) 3.45

Yeast Mre11 and Rad1 proteins define a Ku-independent mechanism to repair double-strand breaks lacking overlapping end sequences. Mol Cell Biol (2003) 3.32

A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. Nat Genet (2010) 2.81

Two interdependent TRPV channel subunits, inactive and Nanchung, mediate hearing in Drosophila. J Neurosci (2004) 2.66

Mean platelet volume and mean platelet volume/platelet count ratio in infective endocarditis. Platelets (2013) 2.24

FISH-negative cryptic PML-RARA rearrangement detected by long-distance polymerase chain reaction and sequencing analyses: a case study and review of the literature. Cancer Genet Cytogenet (2010) 1.91

The Chiari Severity Index: a preoperative grading system for Chiari malformation type 1. Neurosurgery (2015) 1.86

Epstein-barr virus-positive gastric carcinoma demonstrates frequent aberrant methylation of multiple genes and constitutes CpG island methylator phenotype-positive gastric carcinoma. Am J Pathol (2002) 1.82

Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations. Gut (2013) 1.79

Safety and effect of adipose tissue-derived stem cell implantation in patients with critical limb ischemia: a pilot study. Circ J (2012) 1.79

Increased mean platelet volume and mean platelet volume/platelet count ratio in Korean patients with deep vein thrombosis. Platelets (2012) 1.76

Usefulness of whole-blood interferon-gamma assay and interferon-gamma enzyme-linked immunospot assay in the diagnosis of active pulmonary tuberculosis. Chest (2007) 1.75

A sequence variant on 17q21 is associated with age at onset and severity of asthma. Eur J Hum Genet (2010) 1.74

Neurosurgical treatment of progressive posthemorrhagic ventricular dilation in preterm infants: a 10-year single-institution study. J Neurosurg Pediatr (2010) 1.63

Effect of selective dorsal rhizotomy in the treatment of children with cerebral palsy. J Neurosurg (2006) 1.60

Long-term outcome in children treated for craniopharyngioma with and without radiotherapy. J Neurosurg Pediatr (2008) 1.59

Estimating rates of alternative splicing in mammals and invertebrates. Nat Genet (2004) 1.57

Genetic effect of CCR3 and IL5RA gene polymorphisms on eosinophilia in asthmatic patients. J Allergy Clin Immunol (2007) 1.57

Time course for inhibition of lipopolysaccharide-induced lung injury by genistein: relationship to alteration in nuclear factor-kappaB activity and inflammatory agents. Crit Care Med (2003) 1.52

Joint identification of multiple genetic variants via elastic-net variable selection in a genome-wide association analysis. Ann Hum Genet (2010) 1.51

Identification of copy number variations and common deletion polymorphisms in cattle. BMC Genomics (2010) 1.46

Regulation of HOXA9 activity by predominant expression of DACH1 against C/EBPα and GATA-1 in myeloid leukemia with MLL-AF9. Biochem Biophys Res Commun (2012) 1.42

Pediatric neurosurgical injuries associated with all-terrain vehicle accidents: a 10-year experience at St. Louis Children's Hospital. J Neurosurg (2006) 1.42

Orthopedic surgery after selective dorsal rhizotomy for spastic diplegia in relation to ambulatory status and age. J Neurosurg (2005) 1.41

Association analysis of UBE3C polymorphisms in Korean aspirin-intolerant asthmatic patients. Ann Allergy Asthma Immunol (2010) 1.41

A genome-wide association study of gestational diabetes mellitus in Korean women. Diabetes (2012) 1.41

Coordinated international action to accelerate genome-to-phenome with FAANG, the Functional Annotation of Animal Genomes project. Genome Biol (2015) 1.40

Association analysis of RGS7BP gene polymorphisms with aspirin intolerance in asthmatic patients. Ann Allergy Asthma Immunol (2011) 1.39

Diagnostic usefulness of genomic breakpoint analysis of various gene rearrangements in acute leukemias: a perspective of long distance- or long distance inverse-PCR-based approaches. Ann Lab Med (2012) 1.39

Clinical influence of early follow-up glycosylated hemoglobin levels on cardiovascular outcomes in diabetic patients with ST-segment elevation myocardial infarction after coronary reperfusion. Coron Artery Dis (2015) 1.39

A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes. PLoS Genet (2010) 1.38

Effects of ultrasound-guided stellate ganglion block on acute pain after arthroscopic shoulder surgery. Pain Physician (2015) 1.38

Inactivation of SMAD4 tumor suppressor gene during gastric carcinoma progression. Clin Cancer Res (2007) 1.35

Association of TNF-alpha promoter polymorphisms with the clearance of hepatitis B virus infection. Hum Mol Genet (2003) 1.31

Ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in Koreans. PLoS Genet (2013) 1.29

Controlled attenuation parameter (CAP) for detection of hepatic steatosis in patients with chronic liver diseases: a prospective study of a native Korean population. Liver Int (2013) 1.27

A novel PML-ADAMTS17-RARA gene rearrangement in a patient with pregnancy-related acute promyelocytic leukemia. Leuk Res (2011) 1.20

Interleukin 10 haplotype associated with increased risk of hepatocellular carcinoma. Hum Mol Genet (2003) 1.20

Preanesthetic dexmedetomidine 1 µg/kg single infusion is a simple, easy, and economic adjuvant for general anesthesia. Korean J Anesthesiol (2013) 1.17

A consensus sequence for binding of SmcR, a Vibrio vulnificus LuxR homologue, and genome-wide identification of the SmcR regulon. J Biol Chem (2008) 1.14

Detection of t(3;5) and NPM1/MLF1 rearrangement in an elderly patient with acute myeloid leukemia: clinical and laboratory study with review of the literature. Cancer Genet Cytogenet (2010) 1.14

Association analysis of cysteinyl-leukotriene receptor 2 (CYSLTR2) polymorphisms with aspirin intolerance in asthmatics. Pharmacogenet Genomics (2005) 1.13

Association analysis of CD40 polymorphisms with asthma and the level of serum total IgE. Am J Respir Crit Care Med (2007) 1.12

Major genetic components underlying alcoholism in Korean population. Hum Mol Genet (2007) 1.12

Validation of an International Classification of Diseases, Ninth Revision Code Algorithm for Identifying Chiari Malformation Type 1 Surgery in Adults. Neurosurgery (2015) 1.12

Hypoxic preconditioning-induced cerebral ischemic tolerance: role of microvascular sphingosine kinase 2. Stroke (2009) 1.11

Continuous fabrication of biocatalyst immobilized microparticles using photopolymerization and immiscible liquids in microfluidic systems. Langmuir (2005) 1.10

Incidence and seroprevalence of hepatitis A virus infections among young Korean soldiers. J Korean Med Sci (2007) 1.08

Hemispherotomy: efficacy and analysis of seizure recurrence. J Neurosurg Pediatr (2009) 1.07

Naturally occurring anti-Jk(a). Transfusion (2005) 1.07

Genetic polymorphisms in peroxisome proliferator-activated receptor delta associated with obesity. Diabetes (2004) 1.07

Re: Acute myeloid leukemia associated with FGFR1 abnormalities. Int J Hematol (2013) 1.06

Association of DNA repair gene XRCC1 polymorphisms with head and neck cancer in Korean population. Int J Cancer (2004) 1.06

Anti-inflammatory effects of Asparagus cochinchinensis extract in acute and chronic cutaneous inflammation. J Ethnopharmacol (2008) 1.05

Association of tumor necrosis factor polymorphisms with asthma and serum total IgE. Hum Mol Genet (2003) 1.05

Association of transforming growth factor-beta1 gene polymorphisms with a hepatocellular carcinoma risk in patients with chronic hepatitis B virus infection. Exp Mol Med (2003) 1.05

CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia. Cancer Genet Cytogenet (2009) 1.05

Melatonin receptor 1 B polymorphisms associated with the risk of gestational diabetes mellitus. BMC Med Genet (2011) 1.05

Genetic diversity, population structure and relationships in indigenous cattle populations of Ethiopia and Korean Hanwoo breeds using SNP markers. Front Genet (2013) 1.04

Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication. Hum Genet (2013) 1.04

Diagnostic standardization of leukemia fusion gene detection system using multiplex reverse transcriptase-polymerase chain reaction in Korea. J Korean Med Sci (2011) 1.03

A genome-wide association study identified new variants associated with the risk of chronic hepatitis B. Hum Mol Genet (2013) 1.02

Common CYP7A1 promoter polymorphism associated with risk of neuromyelitis optica. Neurobiol Dis (2009) 1.02

Neuronal genes for subcutaneous fat thickness in human and pig are identified by local genomic sequencing and combined SNP association study. PLoS One (2011) 1.02

Identification of SNP markers for common CNV regions and association analysis of risk of subarachnoid aneurysmal hemorrhage in Japanese population. Biochem Biophys Res Commun (2008) 1.02

Prevalence of the plasmid-mediated quinolone resistance genes, aac(6')-Ib-cr, qepA, and oqxAB in clinical isolates of extended-spectrum β-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae in Korea. Ann Clin Lab Sci (2012) 1.01

Scanning of genetic effects of alcohol metabolism gene (ADH1B and ADH1C) polymorphisms on the risk of alcoholism. Hum Mutat (2005) 1.01

An approach of orthology detection from homologous sequences under minimum evolution. Nucleic Acids Res (2008) 1.00

Complementary and alternative medicine in the undergraduate medical curriculum: a survey of Korean medical schools. J Altern Complement Med (2012) 1.00

Association of interleukin-18 gene polymorphisms with hepatitis B virus clearance. Dig Dis Sci (2009) 1.00

Replication of the genetic effects of IFN regulatory factor 5 (IRF5) on systemic lupus erythematosus in a Korean population. Arthritis Res Ther (2007) 1.00