Biological nitrogen removal from landfill leachate using anaerobic-aerobic process: denitritation via organics in raw leachate and intracellular storage polymers of microorganisms.

PubWeight™: 0.77‹?›

🔗 View Article (PMID 23201521)

Published in Bioresour Technol on October 23, 2012

Authors

Rulong Zhu1, Shuying Wang, Jun Li, Kai Wang, Lei Miao, Bin Ma, Yongzhen Peng

Author Affiliations

1: Key Laboratory of Beijing for Water Quality Science and Water Environment Recovery Engineering, Engineering Research Center of Beijing, Beijing University of Technology, Beijing 100124, PR China.

Articles by these authors

(truncated to the top 100)

Initial sequencing and comparative analysis of the mouse genome. Nature (2002) 96.15

The diploid genome sequence of an Asian individual. Nature (2008) 46.29

ZOOM! Zillions of oligos mapped. Bioinformatics (2008) 29.78

Genome sequence of the Brown Norway rat yields insights into mammalian evolution. Nature (2004) 24.40

Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. Nat Genet (2010) 17.38

The sequence and de novo assembly of the giant panda genome. Nature (2009) 15.76

Functional impact of global rare copy number variation in autism spectrum disorders. Nature (2010) 14.66

Rare variants create synthetic genome-wide associations. PLoS Biol (2010) 14.43

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature (2011) 13.23

Genotype, haplotype and copy-number variation in worldwide human populations. Nature (2008) 12.40

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes. Nature (2009) 9.47

The genome of the cucumber, Cucumis sativus L. Nat Genet (2009) 8.19

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nat Genet (2013) 8.02

Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing. Nat Biotechnol (2013) 7.97

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people. Science (2012) 7.94

The Genomes of Oryza sativa: a history of duplications. PLoS Biol (2005) 7.67

Echinococcosis. Lancet (2003) 6.83

The microRNA spectrum in 12 body fluids. Clin Chem (2010) 6.82

Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet (2009) 6.79

A draft sequence for the genome of the domesticated silkworm (Bombyx mori). Science (2004) 6.62

Clinical findings in 111 cases of influenza A (H7N9) virus infection. N Engl J Med (2013) 5.38

A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms. Nature (2004) 5.24

Resequencing of 31 wild and cultivated soybean genomes identifies patterns of genetic diversity and selection. Nat Genet (2010) 5.20

Circular RNAs are abundant, conserved, and associated with ALU repeats. RNA (2012) 5.16

An Aboriginal Australian genome reveals separate human dispersals into Asia. Science (2011) 4.84

Natural malaria infection in Anopheles gambiae is regulated by a single genomic control region. Science (2006) 4.38

Preclinical characterization of the selective JAK1/2 inhibitor INCB018424: therapeutic implications for the treatment of myeloproliferative neoplasms. Blood (2010) 4.33

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications. Am J Psychiatry (2011) 4.29

A critical function for TGF-beta signaling in the development of natural CD4+CD25+Foxp3+ regulatory T cells. Nat Immunol (2008) 4.28

Patternhunter II: highly sensitive and fast homology search. J Bioinform Comput Biol (2004) 4.24

Adjustment of genomic waves in signal intensities from whole-genome SNP genotyping platforms. Nucleic Acids Res (2008) 4.22

Targeted genome modification of crop plants using a CRISPR-Cas system. Nat Biotechnol (2013) 4.19

Variants of DENND1B associated with asthma in children. N Engl J Med (2009) 4.18

KaKs_Calculator: calculating Ka and Ks through model selection and model averaging. Genomics Proteomics Bioinformatics (2006) 4.15

Copy number variation at 1q21.1 associated with neuroblastoma. Nature (2009) 4.10

[Human natural infection of Plasmodium knowlesi]. Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi (2006) 3.99

Mutation of FIG4 causes neurodegeneration in the pale tremor mouse and patients with CMT4J. Nature (2007) 3.91

Common variants at five new loci associated with early-onset inflammatory bowel disease. Nat Genet (2009) 3.82

Detectable clonal mosaicism from birth to old age and its relationship to cancer. Nat Genet (2012) 3.68

Reverse engineering cellular networks. Nat Protoc (2006) 3.67

A gate-latch-lock mechanism for hormone signalling by abscisic acid receptors. Nature (2009) 3.63

Using VAAST to identify an X-linked disorder resulting in lethality in male infants due to N-terminal acetyltransferase deficiency. Am J Hum Genet (2011) 3.43

A genome-wide scan for common alleles affecting risk for autism. Hum Mol Genet (2010) 3.42

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes. PLoS Genet (2009) 3.42

The role of geography in human adaptation. PLoS Genet (2009) 3.41

Evidence for a common mechanism of SIRT1 regulation by allosteric activators. Science (2013) 3.40

Inhibition of lipoprotein-associated phospholipase A2 reduces complex coronary atherosclerotic plaque development. Nat Med (2008) 3.33

Ethics and scientific publication. Adv Physiol Educ (2005) 3.26

Randomized phase III trial of induction chemotherapy with docetaxel, cisplatin, and fluorouracil followed by surgery versus up-front surgery in locally advanced resectable oral squamous cell carcinoma. J Clin Oncol (2012) 3.08

The landscape of recombination in African Americans. Nature (2011) 3.06

Immediate intraportal transplantation of human bone marrow mesenchymal stem cells prevents death from fulminant hepatic failure in pigs. Hepatology (2012) 3.04

Comprehensive Molecular Characterization of Papillary Renal-Cell Carcinoma. N Engl J Med (2015) 3.00

Mouse transcriptome: neutral evolution of 'non-coding' complementary DNAs. Nature (2004) 3.00

From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetes. PLoS Genet (2009) 2.99

A systems biology approach to prediction of oncogenes and molecular perturbation targets in B-cell lymphomas. Mol Syst Biol (2008) 2.99

Validation of candidate causal genes for obesity that affect shared metabolic pathways and networks. Nat Genet (2009) 2.97

A human B-cell interactome identifies MYB and FOXM1 as master regulators of proliferation in germinal centers. Mol Syst Biol (2010) 2.92

Genome-wide measurement of RNA folding energies. Mol Cell (2012) 2.85

DNACompress: fast and effective DNA sequence compression. Bioinformatics (2002) 2.82

A critical role for TLR4 in the pathogenesis of necrotizing enterocolitis by modulating intestinal injury and repair. J Immunol (2007) 2.77

Concepts in immunology and diagnosis of hydatid disease. Clin Microbiol Rev (2003) 2.77

IL-22 and IL-22 binding protein (IL-22BP) regulate fibrosis and cirrhosis in hepatitis C virus and schistosome infections. Hepatology (2015) 2.76

Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. Hum Mol Genet (2008) 2.71

Complete resequencing of 40 genomes reveals domestication events and genes in silkworm (Bombyx). Science (2009) 2.68

Brain anatomical network and intelligence. PLoS Comput Biol (2009) 2.68

Safety and efficacy of warfarin plus aspirin combination therapy for giant coronary artery aneurysm secondary to Kawasaki disease: a meta-analysis. Cardiology (2014) 2.64

Comparative analysis of microarray normalization procedures: effects on reverse engineering gene networks. Bioinformatics (2007) 2.63

Interleukin-17 signaling in inflammatory, Kupffer cells, and hepatic stellate cells exacerbates liver fibrosis in mice. Gastroenterology (2012) 2.58

Surveillance of demographic characteristics and health behaviors among adult cancer survivors--Behavioral Risk Factor Surveillance System, United States, 2009. MMWR Surveill Summ (2012) 2.57

Denoising array-based comparative genomic hybridization data using wavelets. Biostatistics (2005) 2.56

Extracellular microRNA: a new source of biomarkers. Mutat Res (2011) 2.55

Effect of agonal and postmortem factors on gene expression profile: quality control in microarray analyses of postmortem human brain. Biol Psychiatry (2004) 2.53

The polycomb group protein Bmi-1 represses the tumor suppressor PTEN and induces epithelial-mesenchymal transition in human nasopharyngeal epithelial cells. J Clin Invest (2009) 2.52

Hop is an unusual homeobox gene that modulates cardiac development. Cell (2002) 2.52

Molecular mimicry regulates ABA signaling by SnRK2 kinases and PP2C phosphatases. Science (2011) 2.52

Gender-specific gene expression in post-mortem human brain: localization to sex chromosomes. Neuropsychopharmacology (2004) 2.48

Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis. J Clin Invest (2010) 2.45

Open mesh techniques for inguinal hernia repair: a meta-analysis of randomized controlled trials. Ann Surg (2009) 2.44

A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24. J Pediatr (2009) 2.44

LOXL1 mutations are associated with exfoliation syndrome in patients from the midwestern United States. Am J Ophthalmol (2007) 2.43

wANNOVAR: annotating genetic variants for personal genomes via the web. J Med Genet (2012) 2.43

Low fetuin-A levels are associated with cardiovascular death: Impact of variations in the gene encoding fetuin. Kidney Int (2005) 2.42

Photoselective vaporization with the green light laser vs transurethral resection of the prostate for treating benign prostate hyperplasia: a systematic review and meta-analysis. BJU Int (2012) 2.42

Complexity of the microRNA repertoire revealed by next-generation sequencing. RNA (2010) 2.38

PEAKS DB: de novo sequencing assisted database search for sensitive and accurate peptide identification. Mol Cell Proteomics (2011) 2.37

Basis set exchange: a community database for computational sciences. J Chem Inf Model (2007) 2.37

The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMI. Obesity (Silver Spring) (2009) 2.34

Inhibition of the catalytic function of activation-induced cytidine deaminase promotes apoptosis of germinal center B cells in BXD2 mice. Arthritis Rheum (2011) 2.33

Biliary repair and carcinogenesis are mediated by IL-33-dependent cholangiocyte proliferation. J Clin Invest (2014) 2.31

West Nile virus. Lancet Neurol (2007) 2.26

PatternHunter II: highly sensitive and fast homology search. Genome Inform (2003) 2.26

Improved exome prioritization of disease genes through cross-species phenotype comparison. Genome Res (2013) 2.24

Alternative splicing in colon, bladder, and prostate cancer identified by exon array analysis. Mol Cell Proteomics (2008) 2.24

Nociceptors lacking TRPV1 and TRPV2 have normal heat responses. J Neurosci (2004) 2.24

A microsatellite-based, gene-rich linkage map reveals genome structure, function and evolution in Gossypium. Genetics (2007) 2.23

Parathyroid hormone signaling through low-density lipoprotein-related protein 6. Genes Dev (2008) 2.22

The effect of lidocaine on early postoperative cognitive dysfunction after coronary artery bypass surgery. Anesth Analg (2002) 2.20

Proteomic identification of proteins conjugated to ISG15 in mouse and human cells. Biochem Biophys Res Commun (2005) 2.18

A negative feedback loop of transcription factors that controls stem cell pluripotency and self-renewal. FASEB J (2006) 2.17

Prognostic nomogram for intrahepatic cholangiocarcinoma after partial hepatectomy. J Clin Oncol (2013) 2.16