The domestication and evolutionary ecology of apples.
Trends in genetics : TIG | 2014-02-01 | PMID 24290193
Cornille Amandine, Giraud Tatiana, Smulders Marinus J M and 2 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 5809 of 10600
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
The Journal of allergy and clinical immunology | 2014-04-01 | PMID 24290284
Lee Yu Nee, Frugoni Francesco, Dobbs Kerry and 26 more
Genes: RAG1
Pituitary gland development and disease: from stem cell to hormone production.
Current topics in developmental biology | 2013-01-01 | PMID 24290346
Davis Shannon W, Ellsworth Buffy S, Peréz Millan María Inés and 6 more
Mechanisms of thyroid development and dysgenesis: an analysis based on developmental stages and concurrent embryonic anatomy.
Current topics in developmental biology | 2013-01-01 | PMID 24290349
Nilsson Mikael, Fagman Henrik
A germline oncogenic MITF mutation and tumor susceptibility.
European journal of cell biology | 2000-01-01 | PMID 24290354
Paillerets Brigitte Bressac-de, Lesueur Fabienne, Bertolotto Corine
Genes: MITF
Isogenic human iPSC Parkinson's model shows nitrosative stress-induced dysfunction in MEF2-PGC1α transcription.
Cell | 2013-12-05 | PMID 24290359
Ryan Scott D, Dolatabadi Nima, Chan Shing Fai and 23 more
SAMS, a syndrome of short stature, auditory-canal atresia, mandibular hypoplasia, and skeletal abnormalities is a unique neurocristopathy caused by mutations in Goosecoid.
American journal of human genetics | 2013-12-05 | PMID 24290375
Parry David A, Logan Clare V, Stegmann Alexander P A and 11 more
Genes: GSC
Disruption of autoregulatory feedback by a mutation in a remote, ultraconserved PAX6 enhancer causes aniridia.
American journal of human genetics | 2013-12-05 | PMID 24290376
Bhatia Shipra, Bengani Hemant, Fish Margaret and 7 more
Genes: PAX6
Whole-exome sequencing of 2,000 Danish individuals and the role of rare coding variants in type 2 diabetes.
American journal of human genetics | 2013-12-05 | PMID 24290377
Lohmueller Kirk E, Sparsø Thomas, Li Qibin and 23 more
Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.
American journal of human genetics | 2013-12-05 | PMID 24290378
Meyer Kerstin B, O'Reilly Martin, Michailidou Kyriaki and 197 more
Genes: FGFR2, FOXA1
Recessive mutations in SLC38A8 cause foveal hypoplasia and optic nerve misrouting without albinism.
American journal of human genetics | 2013-12-05 | PMID 24290379
Poulter James A, Al-Araimi Musallam, Conte Ivan and 26 more
Contribution of long noncoding RNAs to autism spectrum disorder risk.
International review of neurobiology | 2013-01-01 | PMID 24290382
Wilkinson Brent, Campbell Daniel B
MET receptor tyrosine kinase as an autism genetic risk factor.
International review of neurobiology | 2013-01-01 | PMID 24290385
Peng Yun, Huentelman Matthew, Smith Christopher and 1 more
Genes: MET
Autism susceptibility genes and the transcriptional landscape of the human brain.
International review of neurobiology | 2013-01-01 | PMID 24290390
Miyauchi Shingo, Voineagu Irina
Chronic inflammatory state in sickle cell anemia patients is associated with HBB(*)S haplotype.
Cytokine | 2014-02-01 | PMID 24290434
Bandeira Izabel C J, Rocha Lillianne B S, Barbosa Maritza C and 4 more
Genes: HBB, TNF
The association of IL-8-251T/A polymorphism with complicated malaria in Karbi Anglong district of Assam.
Cytokine | 2014-02-01 | PMID 24290435
Mahanta Anusree, Kakati Sanjeeb, Baruah Shashi
Catechol-O-methyltransferase Val158Met polymorphism (rs4680) is associated with pain in multiple sclerosis.
The journal of pain | 2013-12-01 | PMID 24290452
Fernández-de-las-Peñas César, Ambite-Quesada Silvia, Ortíz-Gutiérrez Rosa and 3 more
Mutations in NSCLC and their link with lung cancer-associated thrombosis: a case-control study.
Thrombosis research | 2014-01-01 | PMID 24290524
Corrales-Rodriguez Luis, Soulières Denis, Weng Xiaoduan and 3 more
Genes: KRAS, EGFR
Genetically modified mice related to schizophrenia and other psychoses: seeking phenotypic insights into the pathobiology and treatment of negative symptoms.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology | 2014-05-01 | PMID 24290531
O'Tuathaigh Colm M P, Desbonnet Lieve, Waddington John L
Molecular characterization and antibiotic susceptibility of Vibrio vulnificus in retail shrimps in Hangzhou, People's Republic of China.
Journal of food protection | 2013-12-01 | PMID 24290683
Pan Junhang, Zhang Yanjun, Jin Dazhi and 5 more
Staphylococcal poisoning foodborne outbreak: epidemiological investigation and strain genotyping.
Journal of food protection | 2013-12-01 | PMID 24290688
Gallina S, Bianchi D M, Bellio A and 6 more
Genes: SEA
WWC1 genotype modulates age-related decline in episodic memory function across the adult life span.
Biological psychiatry | 2014-05-01 | PMID 24290728
Muse John, Emery Matthew, Sambataro Fabio and 8 more
Genes: WWC1
Crystal structure of Prp5p reveals interdomain interactions that impact spliceosome assembly.
Cell reports | 2013-12-12 | PMID 24290758
Zhang Zhi-Min, Yang Fei, Zhang Jinru and 5 more
RIM1α SUMOylation is required for fast synaptic vesicle exocytosis.
Cell reports | 2013-12-12 | PMID 24290762
Girach Fatima, Craig Tim J, Rocca Daniel L and 1 more
Fecal carriage of multi-drug resistant and extended spectrum β-lactamases producing E. coli in household pigeons, Bangladesh.
Veterinary microbiology | 2014-01-10 | PMID 24290770
Hasan Badrul, Islam Kamrul, Ahsan Murshidul and 6 more
Genetic susceptibility, dietary antioxidants, and long-term incidence of age-related macular degeneration in two populations.
Ophthalmology | 2014-03-01 | PMID 24290803
Wang Jie Jin, Buitendijk Gabriëlle H S, Rochtchina Elena and 17 more
Genes: ARMS2, CFH
Short communication: Genetic parameters of individual fatty acids in milk of Canadian Holsteins.
Journal of dairy science | 2014-02-01 | PMID 24290819
Bilal G, Cue R I, Mustafa A F and 1 more
Short communication: Genetic characterization of antimicrobial resistance in Acinetobacter isolates recovered from bulk tank milk.
Journal of dairy science | 2014-02-01 | PMID 24290825
Tamang M D, Gurung M, Nam H M and 4 more
Axonal excitability in X-linked dominant Charcot Marie Tooth disease.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology | 2014-06-01 | PMID 24290847
Liang Christina, Howells James, Kennerson Marina and 3 more
Immunohistochemical analysis of metaplastic non-goblet columnar lined oesophagus shows phenotypic similarities to Barrett's oesophagus: a study in an Asian population.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver | 2014-02-01 | PMID 24290871
Srivastava Supriya, Liew Mei Shan, McKeon Frank and 4 more
Genes: MUC4
Exploring intermolecular interactions of a substrate binding protein using a riboswitch-based sensor.
Chemistry & biology | 2013-12-19 | PMID 24290881
Fowler Casey C, Sugiman-Marangos Seiji, Junop Murray S and 2 more
The assessment of positive dimension of the psychosis phenotype in college students.
Comprehensive psychiatry | 2014-04-01 | PMID 24290885
Fonseca-Pedrero Eduardo, Paino Mercedes, Ortuño-Sierra Javier and 2 more
Support vector machine algorithms in the search of KIR gene associations with disease.
Computers in biology and medicine | 2013-12-01 | PMID 24290921
Cuevas Tello Juan C, Hernández-Ramírez Daniel, García-Sepúlveda Christian A
Should evolutionary geneticists worry about higher-order epistasis?
Current opinion in genetics & development | 2013-12-01 | PMID 24290990
Weinreich Daniel M, Lan Yinghong, Wylie C Scott and 1 more
Trehalose 6-phosphate phosphatase is required for development, virulence and mycotoxin biosynthesis apart from trehalose biosynthesis in Fusarium graminearum.
Fungal genetics and biology : FG & B | 2014-02-01 | PMID 24291007
Song Xiu-Shi, Li He-Ping, Zhang Jing-Bo and 8 more
Phylogenetic analysis of the polyprotein coding region of an infectious South African bursal disease virus (IBDV) strain.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-01-01 | PMID 24291011
Vukea Phillia R, Willows-Munro Sandi, Horner Roger F and 1 more
Genome-wide scan for analysis of simple and imperfect microsatellites in diverse carlaviruses.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-01-01 | PMID 24291012
Alam Chaudhary Mashhood, Singh Avadhesh Kumar, Sharfuddin Choudhary and 1 more
Genes: GAA
Phenotypic and functional heterogeneity of CD169⁺ and CD163⁺ macrophages from porcine lymph nodes and spleen.
Developmental and comparative immunology | 2014-05-01 | PMID 24291017
Alvarez Belén, Martínez Paloma, Yuste María and 5 more
Genes: SLA, TLR2, TLR4
Association analysis of ERBB2 amplicon genetic polymorphisms and STARD3 expression with risk of gastric cancer in the Chinese population.
Gene | 2014-02-10 | PMID 24291029
Qiu Yue, Zhang Zuo-Yang, Du Wei-Dong and 12 more
Genes: STARD3, ERBB2, IKZF3, TCAP
Association of APOE, GCPII and MMP9 polymorphisms with common diseases and lipid levels in an older adult/elderly cohort.
Gene | 2014-02-10 | PMID 24291031
Mazzotti Diego Robles, Singulane Cristiane Carvalho, Ota Vanessa Kiyomi and 9 more
Genes: APOE, MMP9
Cytoplasmic p21(CIP1/WAF1), ERK1/2 activation, and cytoskeletal remodeling are associated with the senescence-like phenotype after airborne particulate matter (PM(10)) exposure in lung cells.
Toxicology letters | 2014-02-10 | PMID 24291038
Sánchez-Pérez Yesennia, Chirino Yolanda I, Osornio-Vargas Álvaro Román and 6 more
Molecular analysis of chylomicronemia in a clinical laboratory setting: diagnosis of 13 cases of lipoprotein lipase deficiency.
Clinica chimica acta; international journal of clinical chemistry | 2014-02-15 | PMID 24291057
Martín-Campos Jesús M, Julve Josep, Roig Rosa and 6 more
Genes: LPL, APOA5, APOC2, GPIHBP1
NOS2A promoter (CCTTT)n association with TB lacks independent functional correlation amongst Indians.
Tuberculosis (Edinburgh, Scotland) | 2014-01-01 | PMID 24291065
Jena Mamata, Srivastava Amit Kumar, Singh Rajnish Kumar and 3 more
Inhibition mechanism exploration of investigational drug TAK-441 as inhibitor against Vismodegib-resistant Smoothened mutant.
European journal of pharmacology | 2014-01-15 | PMID 24291104
Ishii Tsuyoshi, Shimizu Yuji, Nakashima Kosuke and 4 more
Novel insight into the natural history of short QT syndrome.
Journal of the American College of Cardiology | 2014-04-08 | PMID 24291113
Mazzanti Andrea, Kanthan Ajita, Monteforte Nicola and 12 more
Genetic susceptibility to multicase hypersensitivity pneumonitis is associated with the TNF-238 GG genotype of the promoter region and HLA-DRB1*04 bearing HLA haplotypes.
Respiratory medicine | 2014-01-01 | PMID 24291122
Falfán-Valencia Ramcés, Camarena Angel, Pineda César Landa and 10 more
Genes: TNF
Rapid detection of duck hepatitis A virus genotype C using reverse transcription loop-mediated isothermal amplification.
Journal of virological methods | 2014-02-01 | PMID 24291148
Li Chuanfeng, Chen Zongyan, Meng Chunchun and 1 more
Chromosome 10q26 locus and age-related macular degeneration: a progress update.
Experimental eye research | 2014-02-01 | PMID 24291204
Wang Gaofeng
Genes: ARMS2, HTRA1, PLEKHA1
Universality and predictability in molecular quantitative genetics.
Current opinion in genetics & development | 2013-12-01 | PMID 24291213
Nourmohammad Armita, Held Torsten, Lässig Michael
The genetic basis of DOORS syndrome: an exome-sequencing study.
The Lancet. Neurology | 2014-01-01 | PMID 24291220
Campeau Philippe M, Kasperaviciute Dalia, Lu James T and 38 more
Genetic diversity of ORF3 and spike genes of porcine epidemic diarrhea virus in Thailand.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-01-01 | PMID 24291225
Temeeyasen Gun, Srijangwad Anchalee, Tripipat Thitima and 6 more
Comparative genomics of oral isolates of Streptococcus mutans by in silico genome subtraction does not reveal accessory DNA associated with severe early childhood caries.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-01-01 | PMID 24291226
Argimón Silvia, Konganti Kranti, Chen Hao and 3 more
Genomic diversity of human papillomaviruses (HPV) and clinical implications: an overview in adulthood and childhood.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-01-01 | PMID 24291228
Mammas Ioannis N, Spandidos Demetrios A, Sourvinos George
Hypoxic preconditioning-induced mitochondrial protection is not disrupted in a cell model of mtDNA T8993G mutation-induced F1F0-ATP synthase defect: the role of mitochondrial permeability transition.
Free radical biology & medicine | 2014-02-01 | PMID 24291231
Huang Wen-Yi, Jou Mei-Jie, Peng Tsung-I
Extended duration therapy with pegylated interferon and ribavirin for patients with genotype 3 hepatitis C and advanced fibrosis: final results from the STEPS trial.
Journal of hepatology | 2014-04-01 | PMID 24291239
Shoeb D, Dearden J, Weatherall A and 11 more
An oxalyl-CoA synthetase is important for oxalate metabolism in Saccharomyces cerevisiae.
FEBS letters | 2014-01-03 | PMID 24291261
Foster Justin, Nakata Paul A
Dynamic recruitment of active proteasomes into polyglutamine initiated inclusion bodies.
FEBS letters | 2014-01-03 | PMID 24291262
Schipper-Krom Sabine, Juenemann Katrin, Jansen Anne H and 8 more
First case of peritoneal cystic echinococcosis in a domestic cat caused by Echinococcus granulosus sensu stricto (genotype 1) associated to feline immunodeficiency virus infection.
Parasitology international | 2014-04-01 | PMID 24291289
Armua-Fernandez Maria Teresa, Castro Oscar F, Crampet Alejandro and 4 more
Pretreatment of e-waste and mutation of alkali-tolerant cyanogenic bacteria promote gold biorecovery.
Bioresource technology | 2014-01-01 | PMID 24291311
Natarajan Gayathri, Ting Yen-Peng
A His6-SUMO-eXact tag for producing human prepro-urocortin 2 in Escherichia coli for raising monoclonal antibodies.
Journal of immunological methods | 2014-01-31 | PMID 24291344
Liew Oi Wah, Ang Cui Xia, Peh Yu Pei and 7 more
Polymorphisms of endothelin 1 (G5665T and T-1370G) and endothelin receptor type A (C+70G and G-231A) in Graves' disease.
International immunopharmacology | 2014-01-01 | PMID 24291390
Aydın A Fatih, Develi-İş Seval, Doğru-Abbasoğlu Semra and 4 more
Genes: EDN1, EDNRA, TPO
KRIT1 loss of function causes a ROS-dependent upregulation of c-Jun.
Free radical biology & medicine | 2014-03-01 | PMID 24291398
Goitre Luca, De Luca Elisa, Braggion Stefano and 7 more
Hsa-miR-196a2 polymorphism increases the risk of acute lymphoblastic leukemia in Chinese children.
Mutation research | 2014-01-01 | PMID 24291415
Tong Na, Xu Bin, Shi Danni and 9 more
Genes: HOXC8
Sexual dimorphic effect in the genetic association of monoamine oxidase A (MAOA) markers with autism spectrum disorder.
Progress in neuro-psychopharmacology & biological psychiatry | 2014-04-03 | PMID 24291416
Verma Deepak, Chakraborti Barnali, Karmakar Arijit and 8 more
Genes: MAOA, SRY
Characterization of elements involved in allosteric light regulation of phosphodiesterase activity by comparison of different functional BlrP1 states.
Journal of molecular biology | 2014-02-20 | PMID 24291457
Winkler Andreas, Udvarhelyi Anikó, Hartmann Elisabeth and 4 more
Astroglial mGlu3 receptors promote alpha-secretase-mediated amyloid precursor protein cleavage.
Neuropharmacology | 2014-04-01 | PMID 24291464
Durand Daniela, Carniglia Lila, Beauquis Juan and 3 more
Genes: APP
The role of the brain-derived neurotrophic factor SNP rs2883187 in the phenotypic expression of obsessive-compulsive disorder.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia | 2014-05-01 | PMID 24291483
Tükel Raşit, Ozata Berna, Oztürk Nalan and 3 more
Genes: BDNF
Disrupted cross-laminar cortical processing in β amyloid pathology precedes cell death.
Neurobiology of disease | 2014-03-01 | PMID 24291517
Lison H, Happel M F K, Schneider F and 14 more
Drosophila Myc, a novel modifier suppresses the poly(Q) toxicity by modulating the level of CREB binding protein and histone acetylation.
Neurobiology of disease | 2014-03-01 | PMID 24291519
Singh M Dhruba, Raj Kritika, Sarkar Surajit
Pharmacoperones and the calcium sensing receptor: exogenous and endogenous regulators.
Pharmacological research | 2014-05-01 | PMID 24291533
Breitwieser Gerda E
The isolation and molecular characterization of Leishmania spp. from patients with American tegumentary leishmaniasis in northwest Argentina.
Acta tropica | 2014-03-01 | PMID 24291551
Locatelli Fabricio M, Cajal S Pamela, Barroso Paola A and 8 more
Kras gene codon 12 mutation detection enabled by gold nanoparticles conducted in a nanobioarray chip.
Analytical biochemistry | 2014-03-01 | PMID 24291640
Sedighi Abootaleb, Li Paul C H
Fluorescence-based temperature control for polymerase chain reaction.
Analytical biochemistry | 2014-03-01 | PMID 24291705
Sanford Lindsay N, Wittwer Carl T
Abnormal differentiation of dopaminergic neurons in zebrafish trpm7 mutant larvae impairs development of the motor pattern.
Developmental biology | 2014-02-15 | PMID 24291744
Decker Amanda R, McNeill Matthew S, Lambert Aaron M and 11 more
Genes: TRPM7
Emerging insights into resistance to BRAF inhibitors in melanoma.
Biochemical pharmacology | 2014-02-01 | PMID 24291778
Bucheit Amanda D, Davies Michael A
Genes: BRAF
Role of Tet1 in erasure of genomic imprinting.
Nature | 2013-12-19 | PMID 24291790
Yamaguchi Shinpei, Shen Li, Liu Yuting and 2 more
Genes: PGC
Potential mechanisms of aberrant DNA hypomethylation on the x chromosome in uterine leiomyomas.
The Journal of reproduction and development | 2014-03-07 | PMID 24291816
Sato Shun, Maekawa Ryo, Yamagata Yoshiaki and 6 more
Genes: TSPYL2, SATB1, HNRNPU, MED12, SMCHD1
Alignment-free phylogenetics and population genetics.
Briefings in bioinformatics | 2014-05-01 | PMID 24291823
Haubold Bernhard
Multiple divergent haplotypes express completely distinct sets of class I MHC genes in zebrafish.
Immunogenetics | 2014-03-01 | PMID 24291825
McConnell Sean C, Restaino Anthony C, de Jong Jill L O
[Gene mutations; up date].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291829
Nakagawa Masanori
[MicroRNA in neurodegenerative disorders].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291840
Sobue Gen
[Inclusion body myopathy with Paget's disease of bone and frontotemporal dementia].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291843
Hayashi Yukiko
Genes: VCP, GNE
[ALS disease modeling and drug screening using patient-specific iPS cells].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291866
Egawa Naohiro, Inoue Haruhisa
[Clinical aspects of corticobasal syndrome].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291867
Shimohata Takayoshi, Nishizawa Masatoyo
Genes: CBS
[Genetic background of corticobasal syndrome].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291868
Doi Hiroshi, Tanaka Fumiaki
Genes: CBS, MAPT, FUS, GRN, TARDBP
[Molecular pathogenesis of ALS in TDP43 era].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291884
Onodera Osamu
Genes: GEM
[Amyotrophic lateral sclerosis (ALS) with the mutations in the fused in sarcoma/translocated in liposarcoma gene].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291885
Aoki Masashi
Genes: FUS
[Dysfunction of dynactin 1 in motor neuron degeneration].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291886
Katsuno Masahisa, Ikenaka Kensuke, Kawai Kaori and 1 more
[Myofibrillar myopaathy].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291893
Hayashi Yukiko
Genes: TTN, BAG3, CRYAB, DES, DNAJB6, FHL1, FLNC, MYOT
[New congenital muscular dystrophy due to CHKB mutations].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291895
Nishino Ichizo
Genes: CHKB, PINK1
[Hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) is caused by a mutation in TFG].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291930
Ishiura Hiroyuki, Tsuji Shoji
Genes: TFG
[Overview -- exploring molecular basis of sporadic neurologic disorders].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291977
Tsuji Shoji
[Toward identification of susceptible genes for sporadic neurodegenerative disease].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291979
Mitsui Jun
[Epigenome: what we learned from Rett syndrome, a neurological disease caused by mutation of a methyl-CpG binding protein].
Rinsho shinkeigaku = Clinical neurology | 2013-01-01 | PMID 24291980
Kubota Takeo
The novel MAPT mutation K298E: mechanisms of mutant tau toxicity, brain pathology and tau expression in induced fibroblast-derived neurons.
Acta neuropathologica | 2014-02-01 | PMID 24292008
Iovino Mariangela, Pfisterer Ulrich, Holton Janice L and 9 more
Genes: MAPT
Der1 promotes movement of misfolded proteins through the endoplasmic reticulum membrane.
Nature cell biology | 2014-01-01 | PMID 24292014
Mehnert Martin, Sommer Thomas, Jarosch Ernst
Do the placental barrier, parasite genotype and Toll-like receptor polymorphisms contribute to the course of primary infection with various Toxoplasma gondii genotypes in pregnant women?
European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology | 2014-05-01 | PMID 24292064
Wujcicka W, Wilczyński J, Nowakowska D
Genes: TLR2, TLR4
Evolutionary epidemiology of Neisseria meningitidis strains in Belarus compared to other European countries.
Acta microbiologica et immunologica Hungarica | 2013-12-01 | PMID 24292084
Titov Leonid P, Siniuk Kanstantsin V, Wollenberg Kurt K and 9 more
Fli1 deficiency contributes to the suppression of endothelial CXCL5 expression in systemic sclerosis.
Archives of dermatological research | 2014-05-01 | PMID 24292093
Ichimura Yohei, Asano Yoshihide, Akamata Kaname and 12 more
Genes: CXCL5
Epidemiological analysis of hereditary endometrial cancer in a large study population.
Archives of gynecology and obstetrics | 2014-05-01 | PMID 24292105
Svampane Liana, Strumfa Ilze, Berzina Dace and 3 more
Genes: MLH1, MSH2, MSH6