Impacts of the Callipyge mutation on ovine plasma metabolites and muscle fibre type.
PloS one | 2014-01-01 | PMID 24937646
Li Juan, Greenwood Paul L, Cockett Noelle E and 6 more
Publication catalog
Biomedical publications with connected research
Browse 1,060,000 source-attributed publications. Article pages show available bibliographic context, indexed concepts and SPECTER2 related publications where supported by the source and graph. Missing metadata is not invented, and source retraction notices remain visible.
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Publications
Page 6052 of 10600
Comprehensive overview of the structure and regulation of the glucocorticoid receptor.
Endocrine reviews | 2014-08-01 | PMID 24937701
Vandevyver Sofie, Dejager Lien, Libert Claude
Identification of genomic features in environmentally induced epigenetic transgenerational inherited sperm epimutations.
PloS one | 2014-01-01 | PMID 24937757
Guerrero-Bosagna Carlos, Weeks Shelby, Skinner Michael K
High mobility group box 1 (HMGB1) phenotypic role revealed with stress.
Molecular medicine (Cambridge, Mass.) | 2014-08-19 | PMID 24937773
Tang Daolin, Kang Rui, Van Houten Bennett and 3 more
Genes: HMGB1
The MTMR9 rs2293855 polymorphism is associated with glucose tolerance, insulin secretion, insulin sensitivity and increased risk of prediabetes.
Gene | 2014-08-10 | PMID 24937802
Tang L, Tong Y, Cao H and 13 more
Genes: MTMR9
Vitiligo--part 1.
Anais brasileiros de dermatologia | 2000-01-01 | PMID 24937821
Tarlé Roberto Gomes, Nascimento Liliane Machado do, Mira Marcelo Távora and 1 more
Genes: DDR1, NLRP1, XBP1
Molecular systematics and diagnosis.
Veterinary parasitology | 2004-10-28 | PMID 24937880
Thompson R C A, Zarlenga D S, La Rosa G and 11 more
Matrix metalloproteinases in coronary artery disease.
Advances in clinical chemistry | 2014-01-01 | PMID 24938016
Mittal Balraj, Mishra Avshesh, Srivastava Anshika and 2 more
Genes: CAD
Vanishing white matter disease presenting as opsoclonus myoclonus syndrome in childhood--a case report and review of the literature.
Pediatric neurology | 2014-07-01 | PMID 24938145
Klingelhoefer Lisa, Misbahuddin Anjum, Jawad Tania and 4 more
Genetic structure and hybridization in the species group of Ficus auriculata: can closely related sympatric Ficus species retain their genetic identity while sharing pollinators?
Molecular ecology | 2014-07-01 | PMID 24938182
Wei Z-D, Kobmoo N, Cruaud A and 1 more
Nuclease delivery: versatile functions of SLX4/FANCP in genome maintenance.
Molecules and cells | 2014-08-01 | PMID 24938228
Kim Yonghwan
Genes: SLX4
Linking genetics to structural biology: complex heterozygosity screening with actin alanine scan alleles identifies functionally related surfaces on yeast actin.
G3 (Bethesda, Md.) | 2014-06-17 | PMID 24938290
DiPrima Stephanie, Haarer Brian, Viggiano Susan and 3 more
Harnessing natural sequence variation to dissect posttranscriptional regulatory networks in yeast.
G3 (Bethesda, Md.) | 2014-06-17 | PMID 24938291
Fazlollahi Mina, Lee Eunjee, Muroff Ivor and 4 more
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.
Scientific reports | 2014-06-18 | PMID 24938310
Nakano Masakazu, Ikeda Yoko, Tokuda Yuichi and 10 more
Genes: LOXL1, PML
AMH in women with diminished ovarian reserve: potential differences by FMR1 CGG repeat level.
Journal of assisted reproduction and genetics | 2014-10-01 | PMID 24938362
Pastore Lisa M, McMurry Timothy L, Williams Christopher D and 2 more
Genes: AMH, FMR1
TOPLESS mediates brassinosteroid-induced transcriptional repression through interaction with BZR1.
Nature communications | 2014-06-18 | PMID 24938363
Oh Eunkyoo, Zhu Jia-Ying, Ryu Hojin and 2 more
Genes: ERF
Methylenetetrahydrofolate reductase (MTHFR) polymorphism susceptibility to schizophrenia and bipolar disorder: an updated meta-analysis.
Journal of neural transmission (Vienna, Austria : 1996) | 2015-02-01 | PMID 24938371
Hu Cai-Yun, Qian Zhen-Zhong, Gong Feng-Feng and 5 more
Genes: MTHFR
Ullrich congenital muscular dystrophy: clinicopathological features, natural history and pathomechanism(s).
Journal of neurology, neurosurgery, and psychiatry | 2015-03-01 | PMID 24938411
Yonekawa Takahiro, Nishino Ichizo
Integrative genomic analyses of secreted protein acidic and rich in cysteine and its role in cancer prediction.
Molecular medicine reports | 2014-09-01 | PMID 24938427
Wang Bo, Chen Kai, Xu Wenming and 3 more
Genes: SPARC
Polymorphisms in the XRCC1 gene are associated with treatment response to platinum chemotherapy in advanced non-small cell lung cancer patients based on meta-analysis.
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938464
Li L, Wan C, Wen F Q
Genes: XRCC1
Inter-retrotransposon-amplified polymorphism markers for germplasm characterization in Manihot esculenta (Euphorbiaceae).
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938466
Oliveira-Silva A M, Silva G F, Dias M C and 2 more
Genetic variants of the endothelial NO synthase gene (eNOS) may confer increased risk of sporadic congenital heart disease.
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938467
Zhou K, Wang Y, Peng W and 3 more
Implication of polymorphisms in DNA repair genes with an increased risk of hepatocellular carcinoma.
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938468
Wu J S, Chen Y P, Wang L C and 5 more
Genes: XRCC1
Association of polymorphisms of the xeroderma pigmentosum complementation group F gene with increased glioma risk.
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938470
Zhou W K, Huang L Y, Hui L and 7 more
Single-nucleotide polymorphisms and reading frame shifts in RNA2 recombinant regions of tobacco rattle virus isolates Slu24 and Deb57.
Archives of virology | 2014-11-01 | PMID 24938482
Yin Zhimin, Pawełkowicz Magdalena, Michalak Krystyna and 2 more
Association of SORL1 gene variants with hippocampal and cerebral atrophy and Alzheimer's disease.
Current Alzheimer research | 2014-01-01 | PMID 24938503
Assareh Amelia A, Piguet Olivier, Lye Tanya C and 5 more
Genes: SORL1
Preoperative GNAS and KRAS testing in the diagnosis of pancreatic mucinous cysts.
Clinical cancer research : an official journal of the American Association for Cancer Research | 2014-08-15 | PMID 24938521
Singhi Aatur D, Nikiforova Marina N, Fasanella Kenneth E and 15 more
Genes: GNAS, KRAS
Association of BRCA2 variants with cardiovascular disease in Saudi Arabia.
Genetics and molecular research : GMR | 2014-05-16 | PMID 24938600
Alanazi M, Reddy N P, Shaik J P and 5 more
Genes: BRCA2, BRCA1
Analysis of cell cycle shortening and developmental interruption in Dictyostelium discoideum allC RNAi mutants.
Genetics and molecular research : GMR | 2014-05-23 | PMID 24938606
Xue D M, Hou L S, Zhang S R and 1 more
Polymorphic microsatellite loci isolated from Cervus unicolor (Cervidae) show inbreeding in a domesticated population of Taiwan Sambar deer.
Genetics and molecular research : GMR | 2014-05-23 | PMID 24938607
Lin D Y, Chiang T Y, Huang C C and 5 more
Quantative trait loci of seed traits for soybean in multiple environments.
Genetics and molecular research : GMR | 2014-05-23 | PMID 24938611
Che J Y, Ding J J, Liu C Y and 4 more
Desmoplakin truncations and arrhythmogenic left ventricular cardiomyopathy: characterizing a phenotype.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology | 2014-12-01 | PMID 24938629
López-Ayala Jose María, Gómez-Milanés Ivan, Sánchez Muñoz Juan José and 8 more
Genes: DSP
Atrial arrhythmias in the young: early onset atrial arrhythmias preceding a diagnosis of a primary muscular dystrophy.
Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology | 2014-12-01 | PMID 24938630
Stoyanov Nik, Winterfield Jeffrey, Varma Niraj and 1 more
Comparison of bivariate and multivariate joint analyses on the selection loss of beef cattle.
Genetics and molecular research : GMR | 2014-05-23 | PMID 24938697
Pedrosa V B, Groeneveld E, Eler J P and 1 more
Quantitative genetic study of age at subsequent rebreeding in Nellore cattle by using survival analysis.
Genetics and molecular research : GMR | 2014-05-30 | PMID 24938699
Van Melis M H, Figueiredo L G G, Oliveira H N and 5 more
Analysis of the genetic variability and structure of Ochlerotatus taeniorhynchus (Diptera: Culicidae) populations from the Colombian Atlantic coast on the basis of random amplified polymorphic DNA markers.
Genetics and molecular research : GMR | 2014-05-30 | PMID 24938703
Bello F J, Segura N A, Ruiz-Garcia M
Identification and authentication of Rosa species through development of species-specific SCAR marker(s).
Genetics and molecular research : GMR | 2014-05-30 | PMID 24938705
Bashir K M I, Awan F S, Khan I A and 2 more
Insulin-like growth factor binding protein-3 (IGFBP-3) genetic variant and the risk of esophageal squamous cell carcinoma in a Chinese population.
Genetics and molecular research : GMR | 2014-05-30 | PMID 24938707
Yang H-P, Liu J-F, Rao J and 4 more
Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.
Human genetics | 2014-10-01 | PMID 24938718
Xu Yan, Guan Liping, Shen Tao and 10 more
Enzyme replacement therapy attenuates disease progression in a canine model of late-infantile neuronal ceroid lipofuscinosis (CLN2 disease).
Journal of neuroscience research | 2014-11-01 | PMID 24938720
Katz Martin L, Coates Joan R, Sibigtroth Christine M and 7 more
Genes: TPP1
Rapid molecular genetic diagnosis of hypertrophic cardiomyopathy by semiconductor sequencing.
Journal of translational medicine | 2014-06-17 | PMID 24938736
Li Zongzhe, Huang Jin, Zhao Jinzhao and 5 more
Analysis of RBFOX1 gene expression in lymphoblastoid cell lines of Italian discordant autism spectrum disorders sib-pairs.
Molecular and cellular probes | 2000-01-01 | PMID 24938762
Prandini Paola, Zusi Chiara, Malerba Giovanni and 3 more
Genes: RBFOX1
Mutations in Ralstonia solanacearum loci involved in lipopolysaccharide biogenesis, phospholipid trafficking and peptidoglycan recycling render bacteriophage infection.
Archives of microbiology | 2014-09-01 | PMID 24938767
Hong Yu-Hau, Huang Chi, Wang Kuan-Chung and 4 more
Light-dependent gravitropism and negative phototropism of inflorescence stems in a dominant Aux/IAA mutant of Arabidopsis thaliana, axr2.
Journal of plant research | 2014-09-01 | PMID 24938853
Sato Atsuko, Sasaki Shu, Matsuzaki Jun and 1 more
Multi-view singular value decomposition for disease subtyping and genetic associations.
BMC genetics | 2014-06-17 | PMID 24938865
Sun Jiangwen, Bi Jinbo, Kranzler Henry R
Combined effects of CYP1A1 MspI and GSTM1 genetic polymorphisms on risk of lung cancer: an updated meta-analysis.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2014-09-01 | PMID 24938875
Li Wen, Song Li-Qiang, Tan Jian
Genes: GSTM1
CRKL amplification is rare as a mechanism for acquired resistance to kinase inhibitors in lung cancers with epidermal growth factor receptor mutation.
Lung cancer (Amsterdam, Netherlands) | 2014-08-01 | PMID 24939008
Suda Kenichi, Mizuuchi Hiroshi, Murakami Isao and 8 more
Genes: EGFR, CRKL, MET
Genomic approaches for the discovery of genes mutated in inherited retinal degeneration.
Cold Spring Harbor perspectives in medicine | 2014-06-17 | PMID 24939053
Siemiatkowska Anna M, Collin Rob W J, den Hollander Anneke I and 1 more
Literome: PubMed-scale genomic knowledge base in the cloud.
Bioinformatics (Oxford, England) | 2014-10-01 | PMID 24939151
Poon Hoifung, Quirk Chris, DeZiel Charlie and 1 more
Inactivation of the phosphoglucomutase gene pgm in Paenibacillus polymyxa leads to overproduction of fusaricidin.
Journal of industrial microbiology & biotechnology | 2014-09-01 | PMID 24939175
Kim Ha-Rim, Park Soo-Young, Kim Seong-Bin and 3 more
Self-incompatibility in Brassicaceae: identification and characterization of SRK-like sequences linked to the S-locus in the tribe Biscutelleae.
G3 (Bethesda, Md.) | 2014-06-17 | PMID 24939184
Leducq Jean-Baptiste, Gosset Célia C, Gries Rita and 4 more
Sex-determination system in the diploid yeast Zygosaccharomyces sapae.
G3 (Bethesda, Md.) | 2014-06-17 | PMID 24939186
Solieri Lisa, Dakal Tikam Chand, Giudici Paolo and 1 more
Genes: SLA2, CBS
'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.
Database : the journal of biological databases and curation | 2014-01-01 | PMID 24939193
Ran Xia, Cai Wei-Jun, Huang Xiu-Feng and 5 more
Therapeutic suppression of premature termination codons: mechanisms and clinical considerations (review).
International journal of molecular medicine | 2014-08-01 | PMID 24939317
Karijolich John, Yu Yi-Tao
CYP1A1 Ile462Val polymorphism and colorectal cancer risk in Polish patients.
Medical oncology (Northwood, London, England) | 2014-07-01 | PMID 24939416
Gil Justyna, Gaj Paweł, Misiak Błażej and 5 more
Genes: ERCC1, NAT2, XPC, XRCC3
Focal and abnormally persistent paralysis associated with congenital paramyotonia.
BMJ case reports | 2014-06-17 | PMID 24939454
Magot Armelle, David Albert, Sternberg Damien and 1 more
Investigating population history using temporal genetic differentiation.
Molecular biology and evolution | 2014-09-01 | PMID 24939468
Skoglund Pontus, Sjödin Per, Skoglund Tobias and 2 more
Elevated O₃ enhances the attraction of whitefly-infested tomato plants to Encarsia formosa.
Scientific reports | 2014-06-18 | PMID 24939561
Cui Hongying, Su Jianwei, Wei Jianing and 2 more
The HLA-DQ2 genotype selects for early intestinal microbiota composition in infants at high risk of developing coeliac disease.
Gut | 2015-03-01 | PMID 24939571
Olivares M, Neef A, Castillejo G and 11 more
A novel KIF5A mutation in an Italian family marked by spastic paraparesis and congenital deafness.
Journal of the neurological sciences | 2014-08-15 | PMID 24939576
Muglia M, Citrigno L, D'Errico E and 10 more
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.
European journal of human genetics : EJHG | 2015-01-01 | PMID 24939585
Fransen Erik, Bonneux Sarah, Corneveaux Jason J and 9 more
Heterozygous germline mutations in A2ML1 are associated with a disorder clinically related to Noonan syndrome.
European journal of human genetics : EJHG | 2015-03-01 | PMID 24939586
Vissers Lisenka E L M, Bonetti Monica, Paardekooper Overman Jeroen and 16 more
Germline PTPN11 and somatic PIK3CA variant in a boy with megalencephaly-capillary malformation syndrome (MCAP)--pure coincidence?
European journal of human genetics : EJHG | 2015-03-01 | PMID 24939587
Döcker Dennis, Schubach Max, Menzel Moritz and 5 more
Genes: PTPN11, AKT3
Linking genotypes database with locus-specific database and genotype-phenotype correlation in phenylketonuria.
European journal of human genetics : EJHG | 2015-03-01 | PMID 24939588
Wettstein Sarah, Underhaug Jarl, Perez Belen and 4 more
Improving accuracy of rare variant imputation with a two-step imputation approach.
European journal of human genetics : EJHG | 2015-03-01 | PMID 24939589
Kreiner-Møller Eskil, Medina-Gomez Carolina, Uitterlinden André G and 2 more
Genes: MAF
Novel mutations in PXDN cause microphthalmia and anterior segment dysgenesis.
European journal of human genetics : EJHG | 2015-03-01 | PMID 24939590
Choi Alex, Lao Richard, Ling-Fung Tang Paul and 7 more
Genes: PXDN
Oncogenic Ras/ERK signaling activates CDCP1 to promote tumor invasion and metastasis.
Molecular cancer research : MCR | 2014-10-01 | PMID 24939643
Uekita Takamasa, Fujii Satoko, Miyazawa Yuri and 8 more
Genes: CDCP1, MMP2, MMP9
The effects of intestinal tract bacterial diversity on mortality following allogeneic hematopoietic stem cell transplantation.
Blood | 2014-08-14 | PMID 24939656
Taur Ying, Jenq Robert R, Perales Miguel-Angel and 12 more
Genome-wide analysis of simple sequence repeats in marine animals-a comparative approach.
Marine biotechnology (New York, N.Y.) | 2014-10-01 | PMID 24939717
Jiang Qun, Li Qi, Yu Hong and 1 more
Altered inhibition of Cx26 hemichannels by pH and Zn2+ in the A40V mutation associated with keratitis-ichthyosis-deafness syndrome.
The Journal of biological chemistry | 2014-08-01 | PMID 24939841
Sanchez Helmuth A, Bienkowski Rick, Slavi Nefeli and 2 more
Locomotor conditioning by amphetamine requires cyclin-dependent kinase 5 signaling in the nucleus accumbens.
Neuropharmacology | 2014-10-01 | PMID 24939858
Singer Bryan F, Neugebauer Nichole M, Forneris Justin and 4 more
piRNA pathway targets active LINE1 elements to establish the repressive H3K9me3 mark in germ cells.
Genes & development | 2014-07-01 | PMID 24939875
Pezic Dubravka, Manakov Sergei A, Sachidanandam Ravi and 1 more
The characterization of RNA viruses in tropical seawater using targeted PCR and metagenomics.
mBio | 2014-06-17 | PMID 24939887
Culley Alexander I, Mueller Jaclyn A, Belcaid Madhi and 3 more
Genetic diversity and population history of the endangered killifish Aphanius baeticus.
The Journal of heredity | 2000-01-01 | PMID 24939890
Gonzalez Elena G, Pedraza-Lara Carlos, Doadrio Ignacio
Molecular analysis of Oryza latifolia Desv. (CCDD genome)-derived introgression lines and identification of value-added traits for rice (O. sativa L.) improvement.
The Journal of heredity | 2000-01-01 | PMID 24939891
Angeles-Shim Rosalyn B, Vinarao Ricky B, Marathi Balram and 1 more
CBP and p300 acetylate PCNA to link its degradation with nucleotide excision repair synthesis.
Nucleic acids research | 2014-07-01 | PMID 24939902
Cazzalini Ornella, Sommatis Sabrina, Tillhon Micol and 9 more
Genes: PCNA
Evidence after imputation for a role of MICA variants in nonprogression and elite control of HIV type 1 infection.
The Journal of infectious diseases | 2014-12-15 | PMID 24939907
Le Clerc Sigrid, Delaneau Olivier, Coulonges Cédric and 9 more
Genes: MICA
16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy.
Human molecular genetics | 2014-11-15 | PMID 24939913
Reinthaler Eva M, Lal Dennis, Lebon Sebastien and 34 more
Growth hormone deficiency in a dopa-responsive dystonia patient with a novel mutation of guanosine triphosphate cyclohydrolase 1 gene.
Journal of child neurology | 2015-05-01 | PMID 24939974
Lin Yu, Wang Dan-Ni, Chen Wan-Jin and 3 more
Genes: GCH1
PDF neuron firing phase-shifts key circadian activity neurons in Drosophila.
eLife | 2014-06-17 | PMID 24939987
Guo Fang, Cerullo Isadora, Chen Xiao and 1 more
Genes: PDF
The yeast deletion collection: a decade of functional genomics.
Genetics | 2014-06-01 | PMID 24939991
Giaever Guri, Nislow Corey
The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells.
EMBO molecular medicine | 2014-07-01 | PMID 24940003
Pepermans Elise, Michel Vincent, Goodyear Richard and 13 more
Genes: PCDH15
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosis.
Molecular vision | 2014-01-01 | PMID 24940029
Siemiatkowska Anna M, van den Born L Ingeborgh, van Genderen Maria M and 12 more
Genes: NMNAT1
Whole exome sequencing identifies a novel splice-site mutation in ADAMTS17 in an Indian family with Weill-Marchesani syndrome.
Molecular vision | 2014-01-01 | PMID 24940034
Shah Mohd Hussain, Bhat Vishwanath, Shetty Jyoti S and 1 more
Genes: ADAMTS17, LTBP2, ADAMTS10, FBN1
Endothelial nitric oxide synthase polymorphisms and susceptibility to high-tension primary open-angle glaucoma in an Egyptian cohort.
Molecular vision | 2014-01-01 | PMID 24940036
Emam Wafaa A, Zidan Haidy E, Abdulhalim Bahaa-Eldin H and 3 more
Genes: NOS3
Novel mutation in FBN1 causes ectopia lentis and varicose great saphenous vein in one Chinese autosomal dominant family.
Molecular vision | 2014-01-01 | PMID 24940037
Fu Qing, Liu Peng, Lu Qingsheng and 7 more
Genes: FBN1
Identification of a novel C-terminal extension mutation in EPHA2 in a family affected with congenital cataract.
Molecular vision | 2014-01-01 | PMID 24940039
Reis Linda M, Tyler Rebecca C, Semina Elena V
Genes: EPHA2, CRYBA2
miR-345 in metastatic colorectal cancer: a non-invasive biomarker for clinical outcome in non-KRAS mutant patients treated with 3rd line cetuximab and irinotecan.
PloS one | 2014-01-01 | PMID 24940606
Schou Jakob V, Rossi Simona, Jensen Benny V and 8 more
Genes: KRAS, BRAF
Interaction of plectin with keratins 5 and 14: dependence on several plectin domains and keratin quaternary structure.
The Journal of investigative dermatology | 2014-11-01 | PMID 24940650
Bouameur Jamal-Eddine, Favre Bertrand, Fontao Lionel and 3 more
Hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiencies: HPRT1 mutations in new Japanese families and PRPP concentration.
Nucleosides, nucleotides & nucleic acids | 2014-01-01 | PMID 24940672
Yamada Yasukazu, Nomura Noriko, Yamada Kenichiro and 11 more
Genes: HPRT1
Identification of a hypouricemia patient with SLC2A9 R380W, a pathogenic mutation for renal hypouricemia type 2.
Nucleosides, nucleotides & nucleic acids | 2014-01-01 | PMID 24940677
Chiba Toshinori, Matsuo Hirotaka, Nagamori Shushi and 10 more
ABCG2 dysfunction increases the risk of renal overload hyperuricemia.
Nucleosides, nucleotides & nucleic acids | 2014-01-01 | PMID 24940678
Matsuo Hirotaka, Takada Tappei, Nakayama Akiyoshi and 11 more
Genes: ABCG2
Mycoplasma pneumoniae thymidine phosphorylase.
Nucleosides, nucleotides & nucleic acids | 2014-01-01 | PMID 24940683
Wang Liya, Schmidl Sebastian R, Stülke Jörg
Gene expression correlations in human cancer cell lines define molecular interaction networks for epithelial phenotype.
PloS one | 2014-01-01 | PMID 24940735
Kohn Kurt W, Zeeberg Barry M, Reinhold William C and 1 more
Genes: ADAP1, EPN3, LLGL2, RAB25, BSPRY, CAMSAP3, CDH1, CGN
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese.
PloS one | 2014-01-01 | PMID 24940741
Chang Su-Wei, Fann Cathy Shen-Jang, Su Wen-Hui and 8 more
Expression of DISC1-interactome members correlates with cognitive phenotypes related to schizophrenia.
PloS one | 2014-01-01 | PMID 24940743
Rampino Antonio, Walker Rosie May, Torrance Helen Scott and 15 more
Genes: DISC1, NDEL1, AKAP9, FEZ1, PCM1
GADD45a promoter regulation by a functional genetic variant associated with acute lung injury.
PloS one | 2014-01-01 | PMID 24940746
Mitra Sumegha, Wade Michael S, Sun Xiaoguang and 6 more
Cannabinoid receptor 2-63 QQ variant is associated with persistently normal aminotransferase serum levels in chronic hepatitis C.
PloS one | 2014-01-01 | PMID 24940753
Coppola Nicola, Zampino Rosa, Sagnelli Caterina and 11 more
Genes: CNR2
[Update on corneal dystrophies: new insights following first publication of the IC3D classification].
Klinische Monatsblatter fur Augenheilkunde | 2014-06-01 | PMID 24940759
Auw-Hädrich C, Reinhard T, Grünauer-Klövekorn C
CTLA-4 SNPs (CT60A/G, -1722T/C, -1661G/A, and -318C/T) and systemic lupus erythematosus: a meta-analysis.
Critical reviews in eukaryotic gene expression | 2014-01-01 | PMID 24940764
Zhu Yun, Wang Jing, Feng Xuebing