Arabidopsis RhoGDIs Are Critical for Cellular Homeostasis of Pollen Tubes.
Plant physiology | 2016-02-01 | PMID 26662604
Feng Qiang-Nan, Kang Hui, Song Shi-Jian and 5 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.
Semantic proximity supports literature exploration. It does not establish scientific or clinical evidence.
Publications
Page 6717 of 10600
Changes in the Salmonella enterica Enteritidis phenotypes in presence of acyl homoserine lactone quorum sensing signals.
Journal of basic microbiology | 2016-05-01 | PMID 26662614
Campos-Galvão Maria Emilene Martino, Ribon Andrea Oliveira Barros, Araújo Elza Fernandes and 1 more
Novel genetic tools facilitate the study of cortical neuron migration.
Mammalian genome : official journal of the International Mammalian Genome Society | 2016-02-01 | PMID 26662625
Cionni Megan, Menke Chelsea, Stottmann Rolf W
Natural variation involving deletion alleles of FRIGIDA modulate temperature-sensitive flowering responses in Arabidopsis thaliana.
Plant, cell & environment | 2016-06-01 | PMID 26662639
Sanchez-Bermejo Eduardo, Balasubramanian Sureshkumar
The genetics and pathogenesis of thoracic aortic aneurysm disorder and dissections.
Clinical genetics | 2016-06-01 | PMID 26662674
Zhang L, Wang H-H
Whole Exome Sequencing Identifies Rare Protein-Coding Variants in Behçet's Disease.
Arthritis & rheumatology (Hoboken, N.J.) | 2016-05-01 | PMID 26662719
Ognenovski Mikhail, Renauer Paul, Gensterblum Elizabeth and 8 more
Genes: LIMK2, NEIL1
Apolipoprotein E genotyping in Egyptian diabetic nephropathy patients.
IUBMB life | 2016-01-01 | PMID 26662731
Atta Mohamed I, Abo Gabal Khadiga, El-Hadidi Khalid and 3 more
Population differentiation in a Mediterranean relict shrub: the potential role of local adaptation for coping with climate change.
Oecologia | 2016-04-01 | PMID 26662734
Lázaro-Nogal Ana, Matesanz Silvia, Hallik Lea and 3 more
Genes: RGR
Response of Soybean Genotypes Challenged by a Stink Bug Complex (Hemiptera: Pentatomidae).
Journal of economic entomology | 2016-04-01 | PMID 26662735
Souza E S, Silva J P G F, Baldin E L L and 5 more
Candidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in Drosophila.
Human molecular genetics | 2016-02-15 | PMID 26662796
Chow Clement Y, Kelsey Keegan J P, Wolfner Mariana F and 1 more
Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL).
Human molecular genetics | 2016-02-15 | PMID 26662797
Morrison Jean, Laurie Cathy C, Marazita Mary L and 13 more
Genes: BMP7, NAMPT
FIG4 regulates lysosome membrane homeostasis independent of phosphatase function.
Human molecular genetics | 2016-02-15 | PMID 26662798
Bharadwaj Rajnish, Cunningham Kathleen M, Zhang Ke and 1 more
Genes: FIG4
Influence of BCL2-938 C>A promoter polymorphism and BCL2 gene expression on the progression of breast cancer.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-05-01 | PMID 26662799
Bhushann Meka Phanni, Jarjapu Sarika, Vishwakarma Sandeep Kumar and 6 more
Genes: BCL2
NKp46(+) natural killer cells attenuate metabolism-induced hepatic fibrosis by regulating macrophage activation in mice.
Hepatology (Baltimore, Md.) | 2016-03-01 | PMID 26662852
Tosello-Trampont Annie-Carole, Krueger Peter, Narayanan Sowmya and 3 more
Genetic determinants of cytochrome P450 2A6 activity and biomarkers of tobacco smoke exposure in relation to risk of lung cancer development in the Shanghai cohort study.
International journal of cancer | 2016-05-01 | PMID 26662855
Yuan Jian-Min, Nelson Heather H, Butler Lesley M and 7 more
[Phenotypic variability of the 1q21.1 microdeletion syndrome in members of the same family: relevance of detection of neuropsychiatric disorders for diagnosis of genetic syndromes].
Revista de neurologia | 2015-12-16 | PMID 26662873
Natera-De Benito Daniel, Vidal-Esteban Arantxa, Sanchez-Del Pozo Jaime and 4 more
Dimerization of glycoprotein Ibα is not sufficient to induce platelet clearance.
Journal of thrombosis and haemostasis : JTH | 2016-02-01 | PMID 26662889
Liang X, Syed A K, Russell S R and 2 more
Genotype/allelic combinations as potential predictors of myocardial infarction.
Molecular biology reports | 2016-01-01 | PMID 26662939
Nasibullin Timur R, Timasheva Yanina R, Sadikova Regina I and 6 more
Genes: CCL2, DDAH1, VEGFA, NOS3, PECAM1, SELE, VCAM1, ICAM1
The knowns and unknowns of phosphorus loading into grains, and implications for phosphorus efficiency in cropping systems.
Journal of experimental botany | 2016-03-01 | PMID 26662950
Wang Fanmiao, Rose Terry, Jeong Kwanho and 2 more
Effect of CD44 gene polymorphisms on risk of transitional cell carcinoma of the urinary bladder in Taiwan.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-05-01 | PMID 26662954
Weng Wei-Chun, Huang Yu-Hui, Yang Shun-Fa and 5 more
Distinct prognostic values of four-Notch-receptor mRNA expression in ovarian cancer.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-05-01 | PMID 26662955
Zhou Xinling, Teng Lingling, Wang Min
An immortalized rat pancreatic stellate cell line RP-2 as a new cell model for evaluating pancreatic fibrosis, inflammation and immunity.
Hepatobiliary & pancreatic diseases international : HBPD INT | 2015-12-01 | PMID 26663014
Piao Rong-Li, Xiu Ming, Brigstock David R and 1 more
Genes: TLR4, MIP, TNF
Pigmented well-differentiated hepatocellular neoplasm with beta-catenin mutation.
Hepatobiliary & pancreatic diseases international : HBPD INT | 2015-12-01 | PMID 26663015
Souza Lara Neves, de Martino Rodrigo Bronze, Thompson Richard and 3 more
Genetic variations in interleukin-12B in allergic rhinitis.
Immunologic research | 2016-02-01 | PMID 26663019
Wei Ping, Kou Wei, Zhang Cheng and 4 more
Spectrum of urorectal septum malformation sequence.
Congenital anomalies | 2016-05-01 | PMID 26663027
Shah Krupa, Nayak Shalini S, Shukla Anju and 1 more
[Germline mutations of TP53 gene among Chinese families with high risk for breast cancer].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663043
Yang Xiaochen, Hu Zhen, Wu Jiong and 8 more
[Combined hearing and deafness gene mutation screening of 11,046 Chinese newborns].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663044
Sun Xuejing, Xi Zuoming, Zhang Jing and 4 more
Genes: GJB2
[Establishment of a novel HLA genotyping method for preimplantation genetic diagnonis using multiple displacement amplification-polymerase chain reaction-sequencing based technique].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663045
Zhang Yinfeng, Luo Haining, Zhang Yunshan
Genes: PGD
[Genetic and clinical analysis in a Parkinson's disease family caused by expansion of SCA2].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663046
Zhang Ying, Lu Xingjiao, Cen Zhidong and 4 more
Genes: ATXN2
[Construction of CYP1B1 gene haplotypes predisposing to primary congenital glaucoma through allele-specific PCR/restriction fragment length polymorphism analysis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663047
Zhang Aiping, Li Shengjie, Ouyang Qi and 4 more
[Analysis of molecular pathogenesis and clinical phenotypes in 10 probands with inherited fibrinogen deficiency].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663050
Zhu Liqing, Zhao Misheng, Lin Jie and 5 more
Genes: FGG
[Behavioral phenotypes of autism spectrum disorder patients and their parents].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663051
Situ Mingjing, Hu Xiao, Cai Jia and 2 more
[Influence of interleukin-1 beta gene polymorphism and childhood maltreatment on antidepressant treatment].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663052
Chen Ying, Zhang Zhijun, Xu Zhi and 2 more
[Analysis of nuclear localization and signal function of MITF protein predisposing to Warrdenburg syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663053
Zhang Hua, Feng Juan, Chen Hongsheng and 3 more
Genes: MITF, TYR
[Clinical classification and genetic mutation study of two pedigrees with type II Waardenburg syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663054
Chen Yong, Yang Fuwei, Zheng Hexin and 3 more
Genes: MITF, PAX3, SNAI2, SOX10
[Application of chromosome microarray analysis for prenatal diagnosis of a fetus with partial duplication of 1p and uniparental disomy of chromosome 6].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663056
Zhu Ruifang, Zhu Xiangyu, Wang Yaping and 3 more
[Phenotypic and genetic analysis of a girl with multiple congenital deformities due to 2p15-p16.1 microdeletion syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663057
Wu Dong, Wang Hongdan, Zhang Hui and 6 more
[Prenatal diagnosis for a women with a suspected birth history of Angelman syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663058
Guo Caiqin, Xiao Jianping, Wang Junfeng and 2 more
[Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663059
Wu Jianzhu, Xie Yingjun, Chen Baojiang
[Study of a case with homozygous 35C>T and 658C>T mutations of FUT1 gene leading to a para-Bombay phenotype].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663060
Lin Fengqiu, Sun Changping, Wang Hui and 2 more
Genes: FUT1, ABO
[Molecular genetic analysis of an Ax13B phenotype of ABO subtype].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663061
Zhang Xu, Li Jianping
Genes: ABO
[Association of rs13405728 polymorphism of LHR gene with slow ovarian response].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663062
Yin Qianqian, Li Yu, Huang Jia and 1 more
[Association of ADAMTS-1 gene polymorphisms with ischemic stroke caused by large artery atherosclerosis].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663063
Lyu Chenling, Chen Yawen, Zhu Min and 9 more
[Association of inflammatory bowel disease with the polymorphisms and haplotypes of fucosyltransferase 3 gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663064
Guo Maodong, Min Xiaoyan, Xia Xuanping and 5 more
Genes: FUT3
[Effect of mitochondrial DNA 5178 C/A polymorphism on risks for type 2 diabetes mellitus and its complications].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663065
Yang Xunjun, Zhang Yuning, Ma Yin and 2 more
[Association of thyroperoxidase gene polymorphisms with dyshormonogenesis in congenital hypothyroidism].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663066
Su Yueqing, Wang Jing, Zhou Jinfu and 7 more
Genes: TPO
[Association of SPO11 and GST gene polymorphisms with idiopathic male infertility in ethnic Han Chinese].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663067
Feng Zhanqi, Jing Zhian, Liu Hongyan and 6 more
Genes: SPO11, GSTP1, GSTM1, GSTT1
[Association of CYP2C19 gene polymorphisms with long-term recurrent risk of ischemic stroke among ethnic Han Chinese from Fujian].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663068
Fang Ling, Zhao Yuting, Wang Ning and 3 more
[Association of vitamin D receptor gene polymorphisms with mild cognitive impairment among elderly ethnic Uygurs].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663069
Zhou Xiaohui, Zhu Meisheng, Ma Li and 1 more
Genes: VDR
[Polymorphisms of SLC17A1 gene and their interaction with alcohol drinking among Uygur patients with hyperuricemia].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663070
Wang Tingting, Su Yinxia, Wang Zhiqiang and 2 more
[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663071
Zeng Sheng, Tang Beisha, Wang Junling
Genes: NOP56
[Advances in research on the genetics of peripheral arterial disease].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics | 2015-12-01 | PMID 26663072
Yin Li, Han Qi, Li Xueyang and 1 more
Regulation of Acetate Metabolism and Acetyl Co-a Synthetase 1 (ACS1) Expression by Methanol Expression Regulator 1 (Mxr1p) in the Methylotrophic Yeast Pichia pastoris.
The Journal of biological chemistry | 2016-02-12 | PMID 26663080
Sahu Umakant, Rangarajan Pundi N
The EF-hand Ca2+ Binding Domain Is Not Required for Cytosolic Ca2+ Activation of the Cardiac Ryanodine Receptor.
The Journal of biological chemistry | 2016-01-29 | PMID 26663082
Guo Wenting, Sun Bo, Xiao Zhichao and 5 more
Deficiency of Neuronal p38α MAPK Attenuates Amyloid Pathology in Alzheimer Disease Mouse and Cell Models through Facilitating Lysosomal Degradation of BACE1.
The Journal of biological chemistry | 2016-01-29 | PMID 26663083
Schnöder Laura, Hao Wenlin, Qin Yiren and 5 more
Genes: BACE1, ATG5
Recognition of the Cornelia de Lange syndrome phenotype with facial dysmorphology novel analysis.
Clinical genetics | 2016-05-01 | PMID 26663098
Basel-Vanagaite L, Wolf L, Orin M and 4 more
Genes: NIPBL
A single nucleotide polymorphism in the dimethylarginine dimethylaminohydrolase gene is associated with lower risk of pulmonary hypertension in bronchopulmonary dysplasia.
Acta paediatrica (Oslo, Norway : 1992) | 2016-04-01 | PMID 26663142
Trittmann Jennifer K, Gastier-Foster Julie M, Zmuda Erik J and 5 more
Genes: DDAH1, DDAH2
Microdeletions of the 7q32.2 imprinted region are associated with Silver-Russell syndrome features.
American journal of medical genetics. Part A | 2016-03-01 | PMID 26663145
Carrera Ignacio Arroyo, de Zaldívar María Solo, Martín Rebeca and 3 more
Genes: MEST
Phylogeny of the Highly Divergent Echinosteliales (Amoebozoa).
The Journal of eukaryotic microbiology | 2016-07-01 | PMID 26663217
Kretzschmar Martin, Kuhnt Andreas, Bonkowski Michael and 1 more
Desmoid tumor patients carry an elevated risk of familial adenomatous polyposis.
Journal of surgical oncology | 2016-02-01 | PMID 26663236
Koskenvuo Laura, Peltomäki Päivi, Renkonen-Sinisalo Laura and 4 more
Genes: FAP, APC
Shift in interictal relative gamma power as a novel biomarker for drug response in two mouse models of absence epilepsy.
Epilepsia | 2016-01-01 | PMID 26663261
Maheshwari Atul, Marks Rachel L, Yu Katherine M and 1 more
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.
Arthritis & rheumatology (Hoboken, N.J.) | 2016-05-01 | PMID 26663301
Lessard Christopher J, Sajuthi Satria, Zhao Jian and 36 more
Genes: FCHSD2, TNFAIP3, TNFSF4, WDFY4, BLK, ETS1, HIP1, IKZF1
Rare copy number variants implicated in posterior urethral valves.
American journal of medical genetics. Part A | 2016-03-01 | PMID 26663319
Boghossian Nansi S, Sicko Robert J, Kay Denise M and 13 more
Genes: BMP7, FAT1, FGF12, TBX2, TBX4, TSPAN1
Enhanced B Cell Alloantigen Presentation and Its Epigenetic Dysregulation in Liver Transplant Rejection.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons | 2016-02-01 | PMID 26663361
Ningappa M, Ashokkumar C, Higgs B W and 9 more
Genes: CTCF
Altered Maturation Status and Possible Immune Exhaustion of CD8 T Lymphocytes in the Peripheral Blood of Patients Presenting With Acute Coronary Syndromes.
Arteriosclerosis, thrombosis, and vascular biology | 2016-02-01 | PMID 26663396
Zidar David A, Mudd Joseph C, Juchnowski Steven and 19 more
Inherited variation in OATP1B1 is associated with treatment outcome in acute myeloid leukemia.
Clinical pharmacology and therapeutics | 2016-06-01 | PMID 26663398
Drenberg C D, Paugh S W, Pounds S B and 10 more
Extracellular superoxide dismutase deficiency impairs wound healing in advanced age by reducing neovascularization and fibroblast function.
Experimental dermatology | 2016-03-01 | PMID 26663425
Fujiwara Toshihiro, Duscher Dominik, Rustad Kristine C and 6 more
Genes: SOD3
Protein Quantitative Trait Loci Analysis Identifies Genetic Variation in the Innate Immune Regulator TOLLIP in Post-Lung Transplant Primary Graft Dysfunction Risk.
American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons | 2016-03-01 | PMID 26663441
Cantu E, Suzuki Y, Diamond J M and 26 more
Genes: PGD, TOLLIP
Esrrb-Cre excises loxP-flanked alleles in early four-cell embryos.
Genesis (New York, N.Y. : 2000) | 2016-01-01 | PMID 26663459
Lee Sungeun, Pallerla Srinivas R, Kim Suyeon and 4 more
Development of a sink-source interaction model for the growth of short-rotation coppice willow and in silico exploration of genotype×environment effects.
Journal of experimental botany | 2016-02-01 | PMID 26663471
Cerasuolo M, Richter G M, Richard B and 5 more
Fitness effects of new mutations in Chlamydomonas reinhardtii across two stress gradients.
Journal of evolutionary biology | 2016-03-01 | PMID 26663473
Kraemer S A, Morgan A D, Ness R W and 2 more
Two subpopulations of Crocosphaera watsonii have distinct distributions in the North and South Pacific.
Environmental microbiology | 2016-02-01 | PMID 26663484
Bench Shellie R, Frank Ildiko, Robidart Julie and 1 more
SNEV(Prp19/PSO4) deficiency increases PUVA-induced senescence in mouse skin.
Experimental dermatology | 2016-03-01 | PMID 26663487
Monteforte Rossella, Beilhack Georg F, Grausenburger Reinhard and 8 more
Variability in a three-generation family with Pierre Robin sequence, acampomelic campomelic dysplasia, and intellectual disability due to a novel ∼1 Mb deletion upstream of SOX9, and including KCNJ2 and KCNJ16.
Birth defects research. Part A, Clinical and molecular teratology | 2016-01-01 | PMID 26663529
Castori Marco, Bottillo Irene, Morlino Silvia and 4 more
Genes: SOX9, ACD, KCNJ16, KCNJ2
Genome-wide association study reveals greater polygenic loading for schizophrenia in cases with a family history of illness.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2016-03-01 | PMID 26663532
Bigdeli Tim B, Ripke Stephan, Bacanu Silviu-Alin and 20 more
OsWRKY74, a WRKY transcription factor, modulates tolerance to phosphate starvation in rice.
Journal of experimental botany | 2016-02-01 | PMID 26663563
Dai Xiaoyan, Wang Yuanyuan, Zhang Wen-Hao
The use of proteases complementary to trypsin to probe isoforms and modifications.
Proteomics | 2016-03-01 | PMID 26663565
Trevisiol Stéphane, Ayoub Daniel, Lesur Antoine and 3 more
Genetic structure of the Amur tiger (Panthera tigris altaica) population: Are tigers in Sikhote-Alin and southwest Primorye truly isolated?
Integrative zoology | 2016-01-01 | PMID 26663570
Sorokin Pavel A, Rozhnov Vyatcheslav V, Krasnenko Anna U and 3 more
Temperature stress promotes cell division arrest in Xanthomonas citri subsp. citri.
MicrobiologyOpen | 2016-04-01 | PMID 26663580
Sumares Júlia A P, Morão Luana Galvão, Martins Paula M M and 4 more
MicroRNA-31 is a positive modulator of endothelial-mesenchymal transition and associated secretory phenotype induced by TGF-β.
Genes to cells : devoted to molecular & cellular mechanisms | 2016-01-01 | PMID 26663584
Katsura Akihiro, Suzuki Hiroshi I, Ueno Toshihide and 7 more
Genes: CCL17, CXCL16, TNF, VAV3
Noninvasive genetics provides insights into the population size and genetic diversity of an Amur tiger population in China.
Integrative zoology | 2016-01-01 | PMID 26663614
Wang Dan, Hu Yibo, Ma Tianxiao and 3 more
Combined Use of Molecular Markers and High-Resolution Melting (HRM) to Assess Chromosome Dosage in Potato Hybrids.
The Journal of heredity | 2016-03-01 | PMID 26663623
Villano Clizia, Miraglia Valeria, Iorizzo Massimo and 2 more
Clinical, genetic and neuropathological findings in a series of 138 fetuses with a corpus callosum malformation.
Birth defects research. Part A, Clinical and molecular teratology | 2016-01-01 | PMID 26663670
Alby Caroline, Malan Valérie, Boutaud Lucile and 13 more
Alkaline phosphatases are involved in the response of Aedes aegypti larvae to intoxication with Bacillus thuringiensis subsp. israelensis Cry toxins.
Environmental microbiology | 2016-03-01 | PMID 26663676
Stalinski Renaud, Laporte Frédéric, Després Laurence and 1 more
Breast MRI radiogenomics: Current status and research implications.
Journal of magnetic resonance imaging : JMRI | 2016-06-01 | PMID 26663695
Grimm Lars J
A Primer on the Genetics of Comorbid Eating Disorders and Substance Use Disorders.
European eating disorders review : the journal of the Eating Disorders Association | 2016-03-01 | PMID 26663753
Munn-Chernoff Melissa A, Baker Jessica H
Aldimine Formation Reaction, the First Step of the Maillard Early-phase Reaction, Might be Enhanced in Variant Hemoglobin, Hb Himeji.
Annals of clinical and laboratory science | 2015-01-01 | PMID 26663794
Koga Masafumi, Inada Shinya, Shimizu Sayoko and 3 more
Mechanistic Evaluation for Mixed-field Agglutination in the K562 Cell Study Model with Exon 3 Deletion of A1 Gene.
Annals of clinical and laboratory science | 2015-01-01 | PMID 26663798
Chen Ding-Ping, Tseng Ching-Ping, Lin Chi-Jui and 2 more
Application of PCR and High-Resolution Melting for Rapid Identification of Yeasts Routinely Isolated in a Clinical Microbiology Laboratory.
Annals of clinical and laboratory science | 2015-01-01 | PMID 26663799
Ninghui Guo, Bing Wang, Wei Ren and 5 more
Brief Report: Influence of HLA-DRB1 Susceptibility Alleles on the Clinical Subphenotypes of Systemic Lupus Erythematosus in Koreans.
Arthritis & rheumatology (Hoboken, N.J.) | 2016-05-01 | PMID 26663868
Bang So-Young, Choi Ji-Young, Park Songree and 5 more
Genes: RPE
Role of epidermal growth factor mutational status for distinction between recurrent lung cancer and second primary lung cancer: case report.
The clinical respiratory journal | 2017-11-01 | PMID 26663872
Vaz Daniel, Conde Sara, Tente David and 2 more
Genes: EGFR
MC3R gene polymorphisms are associated with early childhood adiposity gain and infant appetite in an Asian population.
Pediatric obesity | 2016-12-01 | PMID 26663875
Aris I M, Tint M T, Teh A L and 13 more
Structural and functional insights into enzymes of the vitamin K cycle.
Journal of thrombosis and haemostasis : JTH | 2016-02-01 | PMID 26663892
Tie J-K, Stafford D W
Genes: GGCX
A case of maternal-foetal chimerism identified during routine histocompatibility testing for hematopoietic stem cell transplantation.
International journal of immunogenetics | 2016-02-01 | PMID 26663895
Grubic Z, Stingl Jankovic K, Kelecic J and 3 more
Genetic risk clustering increases children's body weight at 2 years of age - the STEPS Study.
Pediatric obesity | 2016-12-01 | PMID 26663901
Mäkelä J, Lagström H, Pitkänen N and 4 more
Genes: SDS
Personalized medicine and stroke prevention: where are we?
Vascular health and risk management | 2015-01-01 | PMID 26664130
Kim Joosup, Thrift Amanda G, Nelson Mark R and 2 more
The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation.
Molecular vision | 2015-01-01 | PMID 26664249
Pak Joseph S, Lee Eun-Jin, Craft Cheryl Mae
Genes: GFAP, GRK1
The Influence of C3435T Polymorphism of the ABCB1 Gene on Genetic Susceptibility to Depression and Treatment Response in Polish Population - Preliminary Report.
International journal of medical sciences | 2015-01-01 | PMID 26664259
Jeleń Agnieszka Maria, Sałagacka Aleksandra, Żebrowska Marta Karolina and 4 more
Genes: ABCB1
Polymorphisms in three genes are associated with hemorrhagic stroke.
Brain and behavior | 2015-11-01 | PMID 26664786
Liu Wenpeng, Ge Shichao, Liu Yan and 5 more
The ANKK1/DRD2 locus is a genomic substrate for affective priming and recognition of angry faces.
Brain and behavior | 2015-11-01 | PMID 26664790
Koeneke Alejandra, Ponce Guillermo, Hoenicka Janet and 1 more
Genes: DRD2