XLP: clinical features and molecular etiology due to mutations in SH2D1A encoding SAP.
Journal of clinical immunology | 2014-10-01 | PMID 25085526
Tangye Stuart G
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 6108 of 10600
Presence of fimH, mrkD, and irp2 virulence genes in KPC-2-producing Klebsiella pneumoniae isolates in Recife-PE, Brazil.
Current microbiology | 2014-12-01 | PMID 25085544
de Cássia Andrade Melo Rita, de Barros Emmily Margate Rodrigues, Loureiro Noel Guedes and 3 more
The Amyloid Precursor Protein is rapidly transported from the Golgi apparatus to the lysosome and where it is processed into beta-amyloid.
Molecular brain | 2014-08-01 | PMID 25085554
Tam Joshua H K, Seah Claudia, Pasternak Stephen H
Genes: APP, CFP, LAMP1
Influence of multiple APOE genetic variants on cognitive function in a cohort of older men - results from the Normative Aging Study.
BMC psychiatry | 2014-08-01 | PMID 25085564
Prada Diddier, Colicino Elena, Power Melinda C and 10 more
Genes: APOE
Significant association among the Fas -670 A/G (rs1800682) polymorphism and esophageal cancer, hepatocellular carcinoma, and prostate cancer susceptibility: a meta-analysis.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2014-11-01 | PMID 25085585
Liu Tao, Zuo Li, Li Lin and 8 more
Increased prevalence of hepatitis C virus subtype 6a in China: a comparison between 2004-2007 and 2008-2011.
Archives of virology | 2014-12-01 | PMID 25085624
Rong Xia, Xu Ru, Xiong Huaping and 11 more
How many Coccolithovirus genotypes does it take to terminate an Emiliania huxleyi bloom?
Virology | 2014-10-01 | PMID 25085627
Highfield Andrea, Evans Claire, Walne Anthony and 2 more
Frequency and clinical pattern of vitelliform macular dystrophy caused by mutations of interphotoreceptor matrix IMPG1 and IMPG2 genes.
Ophthalmology | 2014-12-01 | PMID 25085631
Meunier Isabelle, Manes Gaël, Bocquet Béatrice and 11 more
Genes: IMPG1, IMPG2, BEST1, PRPH2, RPE
The promoter mutation c.-259C>T (-3438C>T) is not a common cause of non-syndromic hearing impairment in Austria.
European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery | 2015-01-01 | PMID 25085637
Koenighofer Martin, Lucas Trevor, Parzefall Thomas and 3 more
Genes: GJB2
TUBB4A de novo mutations cause isolated hypomyelination.
Neurology | 2014-09-02 | PMID 25085639
Pizzino Amy, Pierson Tyler Mark, Guo Yiran and 17 more
Genetic analysis of PHOX2B in sudden unexpected death in epilepsy cases.
Neurology | 2014-09-09 | PMID 25085640
Bagnall Richard D, Crompton Douglas E, Cutmore Carina and 4 more
Neuronal loss is an early component of subacute sclerosing panencephalitis.
Neurology | 2014-09-02 | PMID 25085642
Yüksel Deniz, Diren Barış, Ulubay Hakan and 2 more
Current status and future directions of molecularly targeted therapies and immunotherapies for melanoma.
Seminars in cutaneous medicine and surgery | 2014-06-01 | PMID 25085663
Miller David M, Flaherty Keith T, Tsao Hensin
Precision medicine and precision therapeutics: hedgehog signaling pathway, basal cell carcinoma and beyond.
Seminars in cutaneous medicine and surgery | 2014-06-01 | PMID 25085664
Mohan Shalini V, Chang Anne Lynn S
A new Turkish family with homozygous FBXO7 truncating mutation and juvenile atypical parkinsonism.
Parkinsonism & related disorders | 2014-11-01 | PMID 25085748
Yalcin-Cakmakli Gul, Olgiati Simone, Quadri Marialuisa and 4 more
Genes: FBXO7
Identification of FXTAS presenting with SCA 12 like phenotype in India.
Parkinsonism & related disorders | 2014-10-01 | PMID 25085749
Faruq Mohammed, Srivastava Achal K, Suroliya Varun and 4 more
Genes: FMR1
Development and validation of a new algorithm for the reclassification of genetic variants identified in the BRCA1 and BRCA2 genes.
Breast cancer research and treatment | 2014-08-01 | PMID 25085752
Pruss Dmitry, Morris Brian, Hughes Elisha and 9 more
Genes: BRCA1, BRCA2
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.
Neurobiology of aging | 2014-11-01 | PMID 25085782
Lattante Serena, Le Ber Isabelle, Galimberti Daniela and 8 more
Genes: GRN
Differences in protein quality control correlate with phenotype variability in 2 mouse models of familial amyotrophic lateral sclerosis.
Neurobiology of aging | 2015-01-01 | PMID 25085783
Marino Marianna, Papa Simonetta, Crippa Valeria and 11 more
Genes: CRYAB, SOD1
CDKL5 variant in a boy with infantile epileptic encephalopathy: case report.
Brain & development | 2015-04-01 | PMID 25085838
Wong Virginia Chun-Nei, Kwong Anna Ka-Yee
Genes: CDKL5
Up-regulation of urinary-type plasminogen activator correlates with high-risk papillary thyroid carcinoma with BRAF(V600E) mutation and its possible molecular mechanism.
Pathology, research and practice | 2014-11-01 | PMID 25085839
Wakasa Tomoko, Li Yaqiong, Bai Yanhua and 6 more
Genes: BRAF
Advanced onset of puberty after metformin therapy in swine with thrifty genotype.
Experimental physiology | 2014-09-01 | PMID 25085845
Astiz S, Gonzalez-Bulnes A, Astiz I and 3 more
Engineering vascular tissue with functional smooth muscle cells derived from human iPS cells and nanofibrous scaffolds.
Biomaterials | 2014-10-01 | PMID 25085858
Wang Yongyu, Hu Jiang, Jiao Jiao and 7 more
Whole exome sequencing for familial bicuspid aortic valve identifies putative variants.
Circulation. Cardiovascular genetics | 2014-10-01 | PMID 25085919
Martin Lisa J, Pilipenko Valentina, Kaufman Kenneth M and 6 more
A common polymorphism in extracellular superoxide dismutase affects cardiopulmonary disease risk by altering protein distribution.
Circulation. Cardiovascular genetics | 2014-10-01 | PMID 25085920
Hartney John M, Stidham Timothy, Goldstrohm David A and 13 more
Genes: SOD3
Endogenous retrovirus insertion in the KIT oncogene determines white and white spotting in domestic cats.
G3 (Bethesda, Md.) | 2014-08-01 | PMID 25085922
David Victor A, Menotti-Raymond Marilyn, Wallace Andrea Coots and 10 more
Genes: KIT
Psoriasis.
Cold Spring Harbor perspectives in medicine | 2014-08-01 | PMID 25085957
Di Meglio Paola, Villanova Federica, Nestle Frank O
Cardiac-specific suppression of NF-κB signaling prevents diabetic cardiomyopathy via inhibition of the renin-angiotensin system.
American journal of physiology. Heart and circulatory physiology | 2014-10-01 | PMID 25085967
Thomas Candice M, Yong Qian Chen, Rosa Rodolfo M and 7 more
Ptch2 mediates the Shh response in Ptch1-/- cells.
Development (Cambridge, England) | 2014-09-01 | PMID 25085974
Alfaro Astrid C, Roberts Brock, Kwong Lina and 2 more
Ntf3 acts downstream of Sip1 in cortical postmitotic neurons to control progenitor cell fate through feedback signaling.
Development (Cambridge, England) | 2014-09-01 | PMID 25085976
Parthasarathy Srinivas, Srivatsa Swathi, Nityanandam Anjana and 1 more
A Drosophila model of mitochondrial disease caused by a complex I mutation that uncouples proton pumping from electron transfer.
Disease models & mechanisms | 2014-10-01 | PMID 25085991
Burman Jonathon L, Itsara Leslie S, Kayser Ernst-Bernhard and 6 more
Genome-wide SNP analysis reveals population structure and demographic history of the ryukyu islanders in the southern part of the Japanese archipelago.
Molecular biology and evolution | 2014-11-01 | PMID 25086001
Sato Takehiro, Nakagome Shigeki, Watanabe Chiaki and 11 more
Multihost experimental evolution of the pathogen Ralstonia solanacearum unveils genes involved in adaptation to plants.
Molecular biology and evolution | 2014-11-01 | PMID 25086002
Guidot Alice, Jiang Wei, Ferdy Jean-Baptiste and 4 more
The importance of a gatekeeper residue on the aggregation of transthyretin: implications for transthyretin-related amyloidoses.
The Journal of biological chemistry | 2014-10-10 | PMID 25086037
Sant'Anna Ricardo, Braga Carolina, Varejão Nathalia and 7 more
Genes: TTR
Dictyostelium LvsB has a regulatory role in endosomal vesicle fusion.
Journal of cell science | 2014-10-15 | PMID 25086066
Falkenstein Kristin, De Lozanne Arturo
Clinical and immunogenetic factors associated with pneumonia in patients with systemic lupus erythematosus: a case-control study.
The Journal of rheumatology | 2014-09-01 | PMID 25086072
Rúa-Figueroa Iñigo, Nóvoa Javier, García-Laorden María Isabel and 10 more
Genes: ACR
Identification of protein kinase C activation as a novel mechanism for RGS2 protein upregulation through phenotypic screening of natural product extracts.
Molecular pharmacology | 2014-10-01 | PMID 25086086
Raveh Avi, Schultz Pamela J, Aschermann Lauren and 7 more
Genes: RGS2
Signaling through three chemokine receptors triggers the migration of transplanted neural precursor cells in a model of multiple sclerosis.
Stem cell research | 2014-09-01 | PMID 25086214
Cohen Mikhal E, Fainstein Nina, Lavon Iris and 1 more
Genes: CCR2, CXCR4, EGF
Atmospheric-pressure plasma jet induces DNA double-strand breaks that require a Rad51-mediated homologous recombination for repair in Saccharomyces cerevisiae.
Archives of biochemistry and biophysics | 2014-10-15 | PMID 25086216
Lee Yoonna, Kim Kangil, Kang Kyu-Tae and 3 more
Genotyping of α-thalassemias by the colorimetric nanogold probes.
Clinica chimica acta; international journal of clinical chemistry | 2014-11-01 | PMID 25086282
Chomean Sirinart, Wangmaung Nantawan, Sritongkham Pornpimol and 2 more
Genes: SEA
Global epidemiology and genotype distribution of the hepatitis C virus infection.
Journal of hepatology | 2014-11-01 | PMID 25086286
Gower Erin, Estes Chris, Blach Sarah and 2 more
Genetic variation underlying common hereditary hyperbilirubinaemia (Gilbert's syndrome) and respiratory health in the 1946 British birth cohort.
Journal of hepatology | 2014-12-01 | PMID 25086287
Horsfall Laura J, Hardy Rebecca, Wong Andrew and 2 more
Endogenous opioid system influences depressive reactions to socially painful targeted rejection life events.
Psychoneuroendocrinology | 2014-11-01 | PMID 25086307
Slavich George M, Tartter Molly A, Brennan Patricia A and 1 more
Genes: OPRM1
Immune responsiveness of Japanese quail selected for egg yolk testosterone content under severe protein restriction.
Comparative biochemistry and physiology. Part A, Molecular & integrative physiology | 2014-11-01 | PMID 25086332
Kankova Zuzana, Okuliarova Monika, Zeman Michal
Human influence on the dispersal and genetic structure of French Globodera tabacum populations.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2014-10-01 | PMID 25086343
Alenda Charline, Montarry Josselin, Grenier Eric
Oncogenic ras-driven cancer cell vesiculation leads to emission of double-stranded DNA capable of interacting with target cells.
Biochemical and biophysical research communications | 2014-08-22 | PMID 25086355
Lee Tae Hoon, Chennakrishnaiah Shilpa, Audemard Eric and 3 more
Downregulation of cystathionine β-synthase/hydrogen sulfide contributes to rotenone-induced microglia polarization toward M1 type.
Biochemical and biophysical research communications | 2014-08-22 | PMID 25086357
Du Chenchen, Jin Mengmeng, Hong Yu and 8 more
Genes: CBS, TNF
Phen-Gen: combining phenotype and genotype to analyze rare disorders.
Nature methods | 2014-09-01 | PMID 25086502
Javed Asif, Agrawal Saloni, Ng Pauline C
Structural insights into recognition of c-di-AMP by the ydaO riboswitch.
Nature chemical biology | 2014-09-01 | PMID 25086507
Gao Ang, Serganov Alexander
Gene set enrichment analysis for multiple continuous phenotypes.
BMC bioinformatics | 2014-08-03 | PMID 25086605
Wang Xiaoming, Pyne Saumyadipta, Dinu Irina
Genes: LCT
Beyond genotype: serotonin transporter epigenetic modification predicts human brain function.
Nature neuroscience | 2014-09-01 | PMID 25086606
Nikolova Yuliya S, Koenen Karestan C, Galea Sandro and 5 more
Population genetic structure of endangered Mongolian racerunner (Eremias argus) from the Korean Peninsula.
Molecular biology reports | 2014-11-01 | PMID 25086619
Park Han-Chan, Suk Ho Young, Jeong Eu-Jin and 3 more
MicroRNA-9 is associated with epithelial-mesenchymal transition, breast cancer stem cell phenotype, and tumor progression in breast cancer.
Breast cancer research and treatment | 2014-08-01 | PMID 25086633
Gwak Jae Moon, Kim Hyun Jeong, Kim Eun Joo and 5 more
RAD51C germline mutations found in Spanish site-specific breast cancer and breast-ovarian cancer families.
Breast cancer research and treatment | 2014-08-01 | PMID 25086635
Blanco Ana, Gutiérrez-Enríquez Sara, Santamariña Marta and 6 more
Genes: BRCA1, BRCA2
Measuring quantitative autism traits in families: informant effect or intergenerational transmission?
European child & adolescent psychiatry | 2015-04-01 | PMID 25086652
De la Marche Wouter, Noens Ilse, Kuppens Sofie and 3 more
Cellular microparticle and thrombogram phenotypes in the Prospective Observational Multicenter Major Trauma Transfusion (PROMMTT) study: correlation with coagulopathy.
Thrombosis research | 2014-09-01 | PMID 25086657
Matijevic Nena, Wang Yao-Wei W, Wade Charles E and 9 more
Multi-tiered genomic analysis of head and neck cancer ties TP53 mutation to 3p loss.
Nature genetics | 2014-09-01 | PMID 25086664
Gross Andrew M, Orosco Ryan K, Shen John P and 11 more
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
Nature genetics | 2014-09-01 | PMID 25086665
Wolpin Brian M, Rizzato Cosmeri, Kraft Peter and 114 more
Genes: BCAR1, CTRB1, CTRB2, PDX1, TERT, ZNRF3
A framework for the interpretation of de novo mutation in human disease.
Nature genetics | 2014-09-01 | PMID 25086666
Samocha Kaitlin E, Robinson Elise B, Sanders Stephan J and 23 more
Targeted sequencing of a pediatric metabolic bone gene panel using a desktop semiconductor next-generation sequencer.
Calcified tissue international | 2014-10-01 | PMID 25086671
Rauch Frank, Lalic Liljana, Glorieux Francis H and 2 more
Genes: LRP5, PHEX
Association of the ST3GAL4 rs11220462 polymorphism and serum lipid levels in the Mulao and Han populations.
Lipids in health and disease | 2014-08-03 | PMID 25086711
Lin Quan-Zhen, Yin Rui-Xing, Guo Tao and 7 more
Filaggrin loss-of-function mutations are not a predisposing factor for atopic dermatitis in an Ishigaki Island under subtropical climate.
Journal of dermatological science | 2014-10-01 | PMID 25086748
Sasaki Takashi, Furusyo Norihiro, Shiohama Aiko and 11 more
Genes: FLG
Integrating germline and somatic data towards a personalized cancer medicine.
Trends in molecular medicine | 2014-08-01 | PMID 25086750
Pujana Miguel Angel
Phenotypic characteristics in metabolically healthy but obese patients with schizophrenia.
Psychiatry research | 2014-12-15 | PMID 25086765
Sheng Jianhua, Li Chunbo, Wang Jijun and 5 more
ER reorganization is remarkably induced in COS-7 cells accumulating transmembrane protein receptors not competent for export from the endoplasmic reticulum.
The Journal of membrane biology | 2014-11-01 | PMID 25086772
D'Agostino Massimo, Crespi Arianna, Polishchuk Elena and 4 more
Transient, recurrent, white matter lesions in x-linked Charcot-Marie-tooth disease with novel mutation of gap junction protein beta 1 gene in China: a case report.
BMC neurology | 2014-08-03 | PMID 25086786
Zhao Yuan, Xie Yanchen, Zhu Xiaoquan and 3 more
Gene dose effect between a fat mass and obesity-associated polymorphism and body mass index was observed in Korean women with polycystic ovary syndrome but not in control women.
Fertility and sterility | 2014-10-01 | PMID 25086788
Kim Jin Ju, Choi Young Min, Hong Min A and 7 more
Genes: FTO
Platelet-specific collagen receptor glycoprotein VI gene variants affect recurrent pregnancy loss.
Fertility and sterility | 2014-10-01 | PMID 25086789
Siddesh Anjurani, Parveen Farah, Misra Maneesh Kumar and 2 more
Genetic defects in cytolysis in macrophage activation syndrome.
Current rheumatology reports | 2014-01-01 | PMID 25086802
Zhang Mingce, Behrens Edward M, Atkinson T Prescott and 3 more
Variability and prognostic relevance of different phenotypes in amyotrophic lateral sclerosis - data from a population-based registry.
Journal of the neurological sciences | 2014-10-15 | PMID 25086855
Wolf Joachim, Safer Anton, Wöhrle Johannes C and 4 more
Identification and characterization of a novel splice-site mutation in the Wilson disease gene.
Journal of the neurological sciences | 2014-10-15 | PMID 25086856
Diao Sheng-Peng, Hong Ming-Fan, Huang Ye-Qing and 7 more
ALS-Plus syndrome: non-pyramidal features in a large ALS cohort.
Journal of the neurological sciences | 2014-10-15 | PMID 25086858
McCluskey Leo, Vandriel Shannon, Elman Lauren and 8 more
Genes: SOD1, TARDBP, VCP
An evaluation of the RapidHIT(®) system for reliably genotyping reference samples.
Forensic science international. Genetics | 2014-11-01 | PMID 25086874
LaRue Bobby L, Moore Andrea, King Jonathan L and 2 more
Functional characterisation of the R2452W ryanodine receptor variant associated with malignant hyperthermia susceptibility.
Cell calcium | 2014-09-01 | PMID 25086907
Roesl Cornelia, Sato Keisaku, Schiemann Anja and 2 more
Genes: RYR1
Klinefelter syndrome with fabry disease--a case of nondisjunction of the X-chromosome with sex-linked recessive mutation.
Heart, lung & circulation | 2014-12-01 | PMID 25086909
Sadick Victoria J, Fietz Michael J, Tchan Michel C and 3 more
Prediction of miRNA-mRNA associations in Alzheimer's disease mice using network topology.
BMC genomics | 2014-08-03 | PMID 25086961
Noh Haneul, Park Charny, Park Soojun and 3 more
Genes: ARRDC3
High lung shunt fraction in colorectal liver tumors is associated with distant metastasis and decreased survival.
Journal of vascular and interventional radiology : JVIR | 2014-10-01 | PMID 25086965
Deipolyi Amy R, Iafrate A John, Zhu Andrew X and 3 more
The efficacy of EGFR gene mutation testing in various samples from non-small cell lung cancer patients: a multicenter retrospective study.
Journal of cancer research and clinical oncology | 2015-01-01 | PMID 25086987
Krawczyk Paweł, Ramlau Rodryg, Chorostowska-Wynimko Joanna and 23 more
Genes: EGFR, TTF1
A farnesoid X receptor polymorphism predisposes to spontaneous bacterial peritonitis.
Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver | 2014-11-01 | PMID 25086996
Lutz Philipp, Berger Cordula, Langhans Bettina and 9 more
Short communication: Antimicrobial susceptibility profiling and genotyping of Staphylococcus aureus isolates from bovine mastitis in Poland.
Journal of dairy science | 2014-10-01 | PMID 25087034
Jagielski T, Puacz E, Lisowski A and 4 more
Family history of myocardial infarction and cause-specific risk of myocardial infarction and venous thromboembolism: the Tromsø Study.
Circulation. Cardiovascular genetics | 2014-10-01 | PMID 25087051
Lind Caroline, Enga Kristin F, Mathiesen Ellisiv B and 3 more
Genetic diversity in Scots pine populations along a radiation exposure gradient.
The Science of the total environment | 2014-10-15 | PMID 25087063
Geras'kin Stanislav A, Volkova Polina Yu
MET abnormalities in patients with genitourinary malignancies and outcomes with c-MET inhibitors.
Clinical genitourinary cancer | 2015-02-01 | PMID 25087088
Jardim Denis L F, de Melo Gagliato Débora, Falchook Gerald and 14 more
Genes: MET
Hypertrophy of lymphoid organs is a possible phenotypic characteristic of R420W mutation of the cardiac ryanodine receptor gene: a study using a knock-in mouse model.
Legal medicine (Tokyo, Japan) | 2014-11-01 | PMID 25087098
Nishio Hajime, Okudaira Noriyuki, Matsushita Kazufumi and 3 more
Genes: RYR2
[Effect of anticholinergic drugs on cognitive impairment in the elderly].
Revista de psiquiatria y salud mental | 2000-01-01 | PMID 25087132
López-Álvarez Jorge, Zea Sevilla María Ascensión, Agüera Ortiz Luis and 3 more
Founder p.Arg 446* mutation in the PDHX gene explains over half of cases with congenital lactic acidosis in Roma children.
Molecular genetics and metabolism | 2000-01-01 | PMID 25087164
Ivanov Ivan S, Azmanov Dimitar N, Ivanova Mariya B and 26 more
Genes: PDHX
Generation of fertile and fecund F0 XY female mice from XY ES cells.
Transgenic research | 2015-02-01 | PMID 25087174
Kuno Junko, Poueymirou William T, Gong Guochun and 13 more
Hepatitis B virus X protein promotes hepatocellular carcinoma transformation through interleukin-6 activation of microRNA-21 expression.
European journal of cancer (Oxford, England : 1990) | 2014-10-01 | PMID 25087183
Li Chi Han, Xu Feiyue, Chow Sheungching and 4 more
Genes: STAT3
Dynamics differentiate between active and inactive inteins.
European journal of medicinal chemistry | 2015-02-16 | PMID 25087201
Cronin Melissa, Coolbaugh Michael J, Nellis David and 4 more
[Algorithm for the molecular analysis of Bardet-Biedl syndrome in Spain].
Medicina clinica | 2015-08-21 | PMID 25087209
Castro-Sánchez Sheila, Álvarez-Satta María, Pereiro Inés and 2 more
Identification of the novel KIR3DL1*01505 allele from southern Chinese Han individual.
Tissue antigens | 2014-10-01 | PMID 25087463
Wang D, Zhen J, Deng Z
Functional assessment of potential splice site variants in arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Heart rhythm | 2014-11-01 | PMID 25087486
Groeneweg Judith A, Ummels Amber, Mulder Marcel and 13 more
Genes: DSG2, JUP, PKP2, DSC2
Induced and natural variation of promoter length modulates the photoperiodic response of FLOWERING LOCUS T.
Nature communications | 2014-08-04 | PMID 25087553
Liu Liangyu, Adrian Jessika, Pankin Artem and 4 more
[Beneficial effects of 3,4-diaminopyridine in a 26-year-old woman with DOK7 congenital myasthenic syndrome who was originally diagnosed with facioscapulohumeral dystrophy].
Rinsho shinkeigaku = Clinical neurology | 2014-01-01 | PMID 25087557
Nishikawa Atsuko, Mori-Yoshimura Madoka, Okamoto Tomoko and 4 more
Genes: DOK7
Tumour heterogeneity and the evolution of polyclonal drug resistance.
Molecular oncology | 2014-09-12 | PMID 25087573
Burrell Rebecca A, Swanton Charles
PPARα-L162V polymorphism is not associated with schizophrenia risk in a Croatian population.
Prostaglandins, leukotrienes, and essential fatty acids | 2014-11-01 | PMID 25087592
Nadalin S, Giacometti J, Buretić-Tomljanović A
The importance of phenotypic data analysis for genomic prediction - a case study comparing different spatial models in rye.
BMC genomics | 2014-08-04 | PMID 25087599
Bernal-Vasquez Angela-Maria, Möhring Jens, Schmidt Malthe and 3 more
Genes: MET
A promoter mutation in the haemagglutinin segment of influenza A virus generates an effective candidate live attenuated vaccine.
Influenza and other respiratory viruses | 2014-11-01 | PMID 25087607
Harvey Ruth, Johnson Rachel E, MacLellan-Gibson Kirsty and 2 more
Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes.
American journal of human genetics | 2014-08-07 | PMID 25087609
Okada Yukinori, Han Buhm, Tsoi Lam C and 19 more
Genes: MICA
Parental somatic mosaicism is underrecognized and influences recurrence risk of genomic disorders.
American journal of human genetics | 2014-08-07 | PMID 25087610
Campbell Ian M, Yuan Bo, Robberecht Caroline and 25 more