Characterization of the sterol and phosphatidylinositol 4-phosphate binding properties of Golgi-associated OSBP-related protein 9 (ORP9).
PloS one | 2014-01-01 | PMID 25255026
Liu Xinwei, Ridgway Neale D
Genes: OSBP
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 6174 of 10600
Nipbl and mediator cooperatively regulate gene expression to control limb development.
PLoS genetics | 2014-09-01 | PMID 25255084
Muto Akihiko, Ikeda Shingo, Lopez-Burks Martha E and 4 more
Fringe proteins modulate Notch-ligand cis and trans interactions to specify signaling states.
eLife | 2014-09-25 | PMID 25255098
LeBon Lauren, Lee Tom V, Sprinzak David and 2 more
Requirement for Drosophila SNMP1 for rapid activation and termination of pheromone-induced activity.
PLoS genetics | 2014-09-01 | PMID 25255106
Li Zhengzheng, Ni Jinfei D, Huang Jia and 1 more
Genotypic distribution and phylogenetic characterization of Enterocytozoon bieneusi in diarrheic chickens and pigs in multiple cities, China: potential zoonotic transmission.
PloS one | 2014-01-01 | PMID 25255117
Li Wei, Tao Wei, Jiang Yanxue and 3 more
Human leptospirosis: seroreactivity and genetic susceptibility in the population of São Miguel Island (Azores, Portugal).
PloS one | 2014-01-01 | PMID 25255143
Esteves Lisa M, Bulhões Sara M, Branco Claudia C and 5 more
Genes: CISH, LTA, TLR2, TLR4, TLR9, TNF
How IGF-1 activates its receptor.
eLife | 2014-09-25 | PMID 25255214
Kavran Jennifer M, McCabe Jacqueline M, Byrne Patrick O and 9 more
An evolutionarily conserved role for the aryl hydrocarbon receptor in the regulation of movement.
PLoS genetics | 2014-09-01 | PMID 25255223
Williams Evan G, Mouchiroud Laurent, Frochaux Michael and 4 more
Genes: AHR
Altered behavioral performance and live imaging of circuit-specific neural deficiencies in a zebrafish model for psychomotor retardation.
PLoS genetics | 2014-09-01 | PMID 25255244
Zada David, Tovin Adi, Lerer-Goldshtein Tali and 2 more
Biomarkers in lung adenocarcinoma: a decade of progress.
Archives of pathology & laboratory medicine | 2015-04-01 | PMID 25255293
Sholl Lynette M
Genes: ALK, BRAF, EGFR, ERBB2, KRAS, RET, ROS1
Complex MSH2 and MSH6 mutations in hypermutated microsatellite unstable advanced prostate cancer.
Nature communications | 2014-09-25 | PMID 25255306
Pritchard Colin C, Morrissey Colm, Kumar Akash and 13 more
Genes: MSH2, MSH6, MLH1
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy.
PloS one | 2014-01-01 | PMID 25255310
Moreira Danielle P, Griesi-Oliveira Karina, Bossolani-Martins Ana L and 11 more
Memory and fitness optimization of bacteria under fluctuating environments.
PLoS genetics | 2014-09-01 | PMID 25255314
Lambert Guillaume, Kussell Edo, Kussel Edo
Derlin-1 regulates mutant VCP-linked pathogenesis and endoplasmic reticulum stress-induced apoptosis.
PLoS genetics | 2014-09-01 | PMID 25255315
Liang Cyong-Jhih, Chang Ya-Chu, Chang Henry C and 7 more
Genes: VCP
Characterizing protein interactions employing a genome-wide siRNA cellular phenotyping screen.
PLoS computational biology | 2014-09-01 | PMID 25255318
Suratanee Apichat, Schaefer Martin H, Betts Matthew J and 14 more
Barcoding beetles: a regional survey of 1872 species reveals high identification success and unusually deep interspecific divergences.
PloS one | 2014-01-01 | PMID 25255319
Pentinsaari Mikko, Hebert Paul D N, Mutanen Marko
Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestry.
Genetics in medicine : official journal of the American College of Medical Genetics | 2015-04-01 | PMID 25255364
Venturini Giulia, Koskiniemi-Kuendig Hanna, Harper Shyana and 2 more
Genes: MAK, DHDDS
Mortality of New York children with sickle cell disease identified through newborn screening.
Genetics in medicine : official journal of the American College of Medical Genetics | 2015-06-01 | PMID 25255366
Wang Ying, Liu Gang, Caggana Michele and 7 more
Development of DNA confirmatory and high-risk diagnostic testing for newborns using targeted next-generation DNA sequencing.
Genetics in medicine : official journal of the American College of Medical Genetics | 2015-05-01 | PMID 25255367
Bhattacharjee Arindam, Sokolsky Tanya, Wyman Stacia K and 6 more
Anterograde Activin signaling regulates postsynaptic membrane potential and GluRIIA/B abundance at the Drosophila neuromuscular junction.
PloS one | 2014-01-01 | PMID 25255438
Kim Myung-Jun, O'Connor Michael B
Correlation of the interleukin-29 levels in crevicular fluid and plasma with the genetic polymorphism in chronic and aggressive periodontitis patients.
Archives of oral biology | 2015-01-01 | PMID 25255471
Shivaprasad B M, Pradeep A R
Fitness cost due to herbicide resistance may trigger genetic background evolution.
Evolution; international journal of organic evolution | 2015-01-01 | PMID 25255698
Darmency Henri, Menchari Yosra, Le Corre Valérie and 1 more
Congenital central diabetes insipidus and optic atrophy in a Wolfram newborn: is there a role for WFS1 gene in neurodevelopment?
Italian journal of pediatrics | 2014-09-26 | PMID 25255707
Ghirardello Stefano, Dusi Elisa, Castiglione Bianca and 2 more
Genes: WFS1
Decreased expression of glutamate transporter GLAST in Bergmann glia is associated with the loss of Purkinje neurons in the spinocerebellar ataxia type 1.
Cerebellum (London, England) | 2015-02-01 | PMID 25255716
Cvetanovic Marija
Genes: ATXN1
Monocyte-derived fibrocytes induce an inflammatory phenotype in airway smooth muscle cells.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 2014-11-01 | PMID 25255717
Lin T-Y, Venkatesan N, Nishioka M and 6 more
Molecular mechanisms of disease-related human β-actin mutations p.R183W and p.E364K.
The FEBS journal | 2014-12-01 | PMID 25255767
Hundt Nikolas, Preller Matthias, Swolski Olga and 4 more
Genes: ACTB
A versatile and highly efficient method for scarless genome editing in Escherichia coli and Salmonella enterica.
BMC biotechnology | 2014-09-25 | PMID 25255806
Kim Juhan, Webb Anthony M, Kershner Jamie P and 2 more
Additive interactions between susceptibility single-nucleotide polymorphisms identified in genome-wide association studies and breast cancer risk factors in the Breast and Prostate Cancer Cohort Consortium.
American journal of epidemiology | 2014-11-15 | PMID 25255808
Joshi Amit D, Lindström Sara, Hüsing Anika and 41 more
Genes: RAD51
Variations in CYP78A13 coding region influence grain size and yield in rice.
Plant, cell & environment | 2015-04-01 | PMID 25255828
Xu Fan, Fang Jun, Ou Shujun and 9 more
Role of vascular endothelial growth factor polymorphisms (-2578C>A, -460 T>C, -1154G>A, +405G>C and +936C>T) in endometriosis: a case-control study with Brazilians.
BMC women's health | 2014-09-26 | PMID 25255852
Perini Jamila Alessandra, Cardoso Jessica Vilarinho, Berardo Plínio Tostes and 5 more
The interactions between plant life form and fungal traits of arbuscular mycorrhizal fungi determine the symbiotic community.
Oecologia | 2014-12-01 | PMID 25255855
López-García Álvaro, Azcón-Aguilar Concepción, Barea José M
Enhanced down-regulation of ALCAM/CD166 in African-American Breast Cancer.
BMC cancer | 2014-09-25 | PMID 25255861
Tan Fang, Mosunjac Marina, Adams Amy L and 5 more
Genes: ALCAM
CC chemokine receptor-like 1 functions as a tumour suppressor by impairing CCR7-related chemotaxis in hepatocellular carcinoma.
The Journal of pathology | 2015-03-01 | PMID 25255875
Shi Jie-Yi, Yang Liu-Xiao, Wang Zhi-Chao and 11 more
Genes: CCR7, CCL19, CCL21, ACR
Pseudofolliculitis cutis: a vexing disorder of hair growth.
The British journal of dermatology | 2015-04-01 | PMID 25255890
Jasterzbski T J, Schwartz R A
Cognitive-motor profile, clinical characteristics and diagnosis of CHARGE syndrome: an Italian experience.
American journal of medical genetics. Part A | 2014-12-01 | PMID 25255904
Santoro Lucia, Ficcadenti Anna, Zallocco Federica and 5 more
Impaired thrombin generation in Reelin-deficient mice: a potential role of plasma Reelin in hemostasis.
Journal of thrombosis and haemostasis : JTH | 2014-12-01 | PMID 25255925
Tseng W-L, Chen T-H, Huang C-C and 9 more
Pathogenesis of varicelloviruses in primates.
The Journal of pathology | 2015-01-01 | PMID 25255989
Ouwendijk Werner J D, Verjans Georges M G M
Association between MTHFR C677T polymorphism and congenital heart disease. A family-based meta-analysis.
Herz | 2015-04-01 | PMID 25256053
Li Z, Jun Y, Zhong-Bao R and 2 more
Genes: MTHFR
Genotype-phenotype correlation of xeroderma pigmentosum in a Chinese Han population.
The British journal of dermatology | 2015-04-01 | PMID 25256075
Sun Z, Zhang J, Guo Y and 5 more
Genes: ERCC5, POLH, XPA, XPC
Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study.
Movement disorders : official journal of the Movement Disorder Society | 2014-12-01 | PMID 25256078
Gómez-Garre Pilar, Huertas-Fernández Ismael, Cáceres-Redondo María Teresa and 30 more
Genes: NALCN
Genome-wide exploration identifies sex-specific genetic effects of alleles upstream NPY to increase the risk of severe periodontitis in men.
Journal of clinical periodontology | 2014-12-01 | PMID 25256105
Freitag-Wolf Sandra, Dommisch Henrik, Graetz Christian and 13 more
Genes: NPY
Risk genes and autoantibodies in Egyptian children with type 1 diabetes - low frequency of autoantibodies in carriers of the HLA-DRB1*04:05-DQA1*03-DQB1*02 risk haplotype.
Diabetes/metabolism research and reviews | 2015-03-01 | PMID 25256132
El-Amir Mostafa I, El-Feky Mohamed Ali, Laine Antti-Pekka and 7 more
Genes: INS
Subjective cognitive concerns, episodic memory, and the APOE ε4 allele.
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2014-11-01 | PMID 25256133
Samieri Cécilia, Proust-Lima Cécile, M Glymour Maria and 5 more
Genes: APOE
Interferon lambda 3 genotype predicts hepatitis C virus RNA levels in early acute infection among people who inject drugs: the InC(3) study.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology | 2014-11-01 | PMID 25256151
Hajarizadeh Behzad, Grady Bart, Page Kimberly and 17 more
Genes: IFNL3
Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutation.
Pediatric radiology | 2015-04-01 | PMID 25256152
Tüysüz Beyhan, Yılmaz Saliha, Erener-Ercan Tuğba and 2 more
Genes: KIF22
Mutational profiling of kinases in glioblastoma.
BMC cancer | 2014-09-26 | PMID 25256166
Bleeker Fonnet E, Lamba Simona, Zanon Carlo and 8 more
Genes: IDH1, NRAS, PTEN, BRAF, EGFR, EPHA3, FLT3, IDH2
Leber congenital amaurosis caused by mutations in GUCY2D.
Cold Spring Harbor perspectives in medicine | 2014-09-25 | PMID 25256176
Boye Shannon E
Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7.
Stroke | 2014-11-01 | PMID 25256182
Foroud Tatiana, Lai Dongbing, Koller Daniel and 37 more
Genes: HDAC9
Association study of MICA gene polymorphisms with rheumatoid arthritis susceptibility in south Tunisian population.
International journal of immunogenetics | 2014-12-01 | PMID 25256191
Achour Y, Kammoun A, Ben Hamad M and 7 more
Genes: MICA
Light modulated activity of root alkaline/neutral invertase involves the interaction with 14-3-3 proteins.
The Plant journal : for cell and molecular biology | 2014-12-01 | PMID 25256212
Gao Jing, van Kleeff Paula J M, Oecking Claudia and 5 more
Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene.
Muscle & nerve | 2015-04-01 | PMID 25256213
Ruggiero Lucia, Fiorillo Chiara, Tessa Alessandra and 8 more
Genes: LMNA
Genotype-phenotype relationships in Freeman-Sheldon syndrome.
American journal of medical genetics. Part A | 2014-11-01 | PMID 25256237
Beck Anita E, McMillin Margaret J, Gildersleeve Heidi I S and 3 more
Genes: MYH3
Prevalence of BRCA1 and BRCA2 mutations in unselected breast cancer patients from Peru.
Clinical genetics | 2015-10-01 | PMID 25256238
Abugattas J, Llacuachaqui M, Allende Y Sullcahuaman and 12 more
Genes: BRCA1, BRCA2
Genetic characterization of highly pathogenic H5N1 avian influenza virus from live migratory birds in Bangladesh.
Virus genes | 2014-12-01 | PMID 25256256
Parvin Rokshana, Kamal Abu H M, Haque Md E and 4 more
SOX10 mutations mimic isolated hearing loss.
Clinical genetics | 2015-10-01 | PMID 25256313
Pingault V, Faubert E, Baral V and 9 more
Genes: SOX10
Genetic identification of endangered North African ungulates using noninvasive sampling.
Molecular ecology resources | 2015-05-01 | PMID 25256349
Silva Teresa Luísa, Godinho Raquel, Castro Diana and 3 more
Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus.
Human molecular genetics | 2015-02-01 | PMID 25256354
Acevedo Nathalie, Reinius Lovisa E, Greco Dario and 9 more
Genes: ORMDL3, GSDMB, IKZF3
New susceptibility variants to narcolepsy identified in HLA class II region.
Human molecular genetics | 2015-02-01 | PMID 25256355
Miyagawa Taku, Toyoda Hiromi, Hirataka Akane and 40 more
Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.
Human molecular genetics | 2015-02-01 | PMID 25256356
Lemmers Richard J L F, Goeman Jelle J, van der Vliet Patrick J and 18 more
Genes: SMCHD1, DUX4
Hierarchical population structure and habitat differences in a highly mobile marine species: the Atlantic spotted dolphin.
Molecular ecology | 2014-10-01 | PMID 25256360
Viricel Amélia, Rosel Patricia E
Association of the tumor necrosis factor -308 A/G promoter polymorphism with Tourette syndrome.
International journal of immunogenetics | 2014-12-01 | PMID 25256363
Keszler G, Kruk E, Kenezloi E and 3 more
Genes: TNF
Arabidopsis gulliver1/SUPERROOT2-7 identifies a metabolic basis for auxin and brassinosteroid synergy.
The Plant journal : for cell and molecular biology | 2014-12-01 | PMID 25256367
Maharjan Puna M, Dilkes Brian P, Fujioka Shozo and 5 more
Low-frequency NNRTI-resistant HIV-1 variants and relationship to mutational load in antiretroviral-naïve subjects.
Viruses | 2014-09-16 | PMID 25256391
Gupta Shaili, Lataillade Max, Kyriakides Tassos C and 6 more
The role of the protein tyrosine phosphatase SHP2 in cardiac development and disease.
Seminars in cell & developmental biology | 2015-01-01 | PMID 25256404
Lauriol Jessica, Jaffré Fabrice, Kontaridis Maria I
p.L18P: a novel IDUA mutation that causes a distinct attenuated phenotype in mucopolysaccharidosis type I patients.
Clinical genetics | 2015-10-01 | PMID 25256405
Pasqualim G, Ribeiro M G, da Fonseca G G G and 6 more
Genes: IDUA
High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites.
Carbohydrate polymers | 2014-11-26 | PMID 25256524
Manno N, Sherratt S, Boaretto F and 11 more
Genes: CHIT1
Thrombospondin-1 is part of a Slug-independent motility and metastatic program in cutaneous melanoma, in association with VEGFR-1 and FGF-2.
Pigment cell & melanoma research | 2015-01-01 | PMID 25256553
Borsotti Patrizia, Ghilardi Carmen, Ostano Paola and 14 more
Genes: SNAI2
Adjustments of embryonic photosynthetic activity modulate seed fitness in Arabidopsis thaliana.
The New phytologist | 2015-01-01 | PMID 25256557
Allorent Guillaume, Osorio Sonia, Vu Joseph Ly and 8 more
Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndrome.
American journal of medical genetics. Part A | 2014-12-01 | PMID 25256560
Quintero-Rivera Fabiola, Woo Jennifer S, Bomberg Eric M and 3 more
DNA replication in nurse cell polytene chromosomes of Drosophila melanogaster otu mutants.
Chromosoma | 2015-03-01 | PMID 25256561
Koryakov Dmitry E, Zhimulev Igor F
Isolation by environment.
Molecular ecology | 2014-12-01 | PMID 25256562
Wang Ian J, Bradburd Gideon S
Targeting oncogenic interleukin-7 receptor signalling with N-acetylcysteine in T cell acute lymphoblastic leukaemia.
British journal of haematology | 2015-01-01 | PMID 25256574
Mansour Marc R, Reed Casie, Eisenberg Amy R and 15 more
Next-generation DNA sequencing of a Swedish malignant hyperthermia cohort.
Clinical genetics | 2015-10-01 | PMID 25256590
Broman M, Kleinschnitz I, Bach J E and 3 more
Genes: RYR1
Phenotype and expression profile analysis of Staphylococcus aureus biofilms and planktonic cells in response to licochalcone A.
Applied microbiology and biotechnology | 2015-01-01 | PMID 25256617
Shen Fengge, Tang Xudong, Wang Yang and 10 more
Electrostatic interactions and hydrogen bond dynamics in chloride pumping by halorhodopsin.
Biochimica et biophysica acta | 2014-12-01 | PMID 25256652
Jardón-Valadez Eduardo, Bondar Ana-Nicoleta, Tobias Douglas J
Adaptive divergence between lake and stream populations of an East African cichlid fish.
Molecular ecology | 2014-11-01 | PMID 25256664
Theis Anya, Ronco Fabrizia, Indermaur Adrian and 2 more
CRTC2 and PROM1 expression in non-small cell lung cancer: analysis by Western blot and immunohistochemistry.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2014-12-01 | PMID 25256670
Li Yalun, He Yanqi, Qiu Zhixin and 6 more
Genes: CRTC2, PROM1
Identification of TRIML2, a novel p53 target, that enhances p53 SUMOylation and regulates the transactivation of proapoptotic genes.
Molecular cancer research : MCR | 2015-02-01 | PMID 25256710
Kung Che-Pei, Khaku Sakina, Jennis Matthew and 2 more
Genes: TRIML2, PRODH, SUMO2
Phenotyping structural abnormalities in mouse embryos using high-resolution episcopic microscopy.
Disease models & mechanisms | 2014-10-01 | PMID 25256713
Weninger Wolfgang J, Geyer Stefan H, Martineau Alexandrine and 4 more
Discrepancies in cancer genomic sequencing highlight opportunities for driver mutation discovery.
Cancer research | 2014-11-15 | PMID 25256751
Hudson Andrew M, Yates Tim, Li Yaoyong and 7 more
Genes: PAK4
Genes and the hypothalamic control of metabolism in humans.
Best practice & research. Clinical endocrinology & metabolism | 2014-10-01 | PMID 25256760
Hinney Anke, Volckmar Anna-Lena, Antel Jochen
Delivering a disease-modifying treatment for Huntington's disease.
Drug discovery today | 2015-01-01 | PMID 25256777
Godinho Bruno M D C, Malhotra Meenakshi, O'Driscoll Caitriona M and 1 more
Genes: HTT
Finding chemical drugs for genetic diseases.
Drug discovery today | 2014-12-01 | PMID 25256778
Sun Hui-Yong, Hou Ting-Jun, Zhang Hong-Yu
Role of osteoprotegerin gene variants in early-onset severe pre-eclampsia.
The journal of obstetrics and gynaecology research | 2015-03-01 | PMID 25256810
Yang Yan, Liu Xijing, Jia Jin and 6 more
BRCA1 germline mutations may be associated with reduced ovarian reserve.
Fertility and sterility | 2014-12-01 | PMID 25256924
Wang Erica T, Pisarska Margareta D, Bresee Catherine and 5 more
Genes: AMH, BRCA1, BRCA2
World Endometriosis Research Foundation Endometriosis Phenome and Biobanking Harmonization Project: II. Clinical and covariate phenotype data collection in endometriosis research.
Fertility and sterility | 2014-11-01 | PMID 25256930
Vitonis Allison F, Vincent Katy, Rahmioglu Nilufer and 9 more
Contribution of glucan-binding protein A to firm and stable biofilm formation by Streptococcus mutans.
Molecular oral microbiology | 2015-06-01 | PMID 25256943
Matsumi Y, Fujita K, Takashima Y and 3 more
Evaluation of association of maternal IL-10 polymorphisms with risk of preeclampsia by A meta-analysis.
Journal of cellular and molecular medicine | 2014-12-01 | PMID 25257050
Yang Wenchao, Zhu Zhenmin, Wang Jin and 2 more
Nature of the visual loss in observers with Leber's congenital amaurosis caused by specific mutations in RPE65.
Investigative ophthalmology & visual science | 2014-09-25 | PMID 25257057
Ripamonti Caterina, Henning G Bruce, Ali Robin R and 9 more
Genes: RPE65, RPE
Reaching a CNV milestone.
Nature genetics | 2014-10-01 | PMID 25257083
Beaudet Arthur L
Different stocks of brook lamprey in Spain and their origin from Lampetra fluviatilis at two distinct times and places.
Journal of fish biology | 2014-11-01 | PMID 25257102
Pereira A M, Doadrio I, Robalo J I and 1 more
The role of FGF-2/HGF and fibronectin matrix on pleomorphic adenoma myoepithelial cell morphology and immunophenotype: an in vitro study.
Growth factors (Chur, Switzerland) | 2015-02-01 | PMID 25257141
Silva Carolina Amália Barcellos, Nardello Laura Cristina Leite, Garcia Frederico Windlin and 4 more
Genes: HGF
Inverted duplication with deletion: first interstitial case suggesting a novel undescribed mechanism of formation.
American journal of medical genetics. Part A | 2014-12-01 | PMID 25257167
Milosevic J, El Khattabi L, Roubergue A and 8 more
β-Catenin and NF-κB co-activation triggered by TLR3 stimulation facilitates stem cell-like phenotypes in breast cancer.
Cell death and differentiation | 2015-02-01 | PMID 25257174
Jia D, Yang W, Li L and 7 more
Genes: TLR3
Diffuse melanosis cutis in the setting of BRAF(V600E) metastatic melanoma.
International journal of dermatology | 2014-11-01 | PMID 25257244
Sebaratnam Deshan F, Martin Linda K, Venugopal Supriya S and 7 more
Genes: BRAF
Gene mutations in Mycobacterium tuberculosis: multidrug-resistant TB as an emerging global public health crisis.
Tuberculosis (Edinburgh, Scotland) | 2015-01-01 | PMID 25257261
Mishra Rahul, Shukla Priyanka, Huang Wei and 1 more
Relationship between human LTA4H polymorphisms and extra-pulmonary tuberculosis in an ethnic Han Chinese population in Eastern China.
Tuberculosis (Edinburgh, Scotland) | 2014-12-01 | PMID 25257262
Yang Jinghui, Chen Jin, Yue Jun and 3 more
Clinical multiplexed exome sequencing distinguishes adult oligodendroglial neoplasms from astrocytic and mixed lineage gliomas.
Oncotarget | 2014-09-30 | PMID 25257301
Cryan Jane B, Haidar Sam, Ramkissoon Lori A and 17 more
Genes: ATRX, IDH1
Confirmation of the cellular targets of benomyl and rapamycin using next-generation sequencing of resistant mutants in S. cerevisiae.
Molecular bioSystems | 2014-12-01 | PMID 25257345
Wride Dustin A, Pourmand Nader, Bray Walter M and 8 more
Genes: FPR1
GNE myopathy associated with congenital thrombocytopenia: a report of two siblings.
Neuromuscular disorders : NMD | 2014-12-01 | PMID 25257349
Izumi Rumiko, Niihori Tetsuya, Suzuki Naoki and 17 more
Genes: GNE