Hepatitis C virus prevalence and genotype distribution in Pakistan: Comprehensive review of recent data.
World journal of gastroenterology | 2016-01-28 | PMID 26819533
Umer Muhammad, Iqbal Mazhar
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 6773 of 10600
Influence of Genetic Variants of the N-Methyl-D-Aspartate Receptor on Emotion and Social Behavior in Adolescents.
Neural plasticity | 2016-01-01 | PMID 26819771
Lee Li-Ching, Cho Ying-Chun, Lin Pei-Jung and 3 more
Genes: GRIN1
Modeling the effect of pathogenic mutations on the conformational landscape of protein kinases.
Current opinion in structural biology | 2016-04-01 | PMID 26820051
Saladino Giorgio, Gervasio Francesco Luigi
Cardiovascular malformations caused by NOTCH1 mutations do not keep left: data on 428 probands with left-sided CHD and their families.
Genetics in medicine : official journal of the American College of Medical Genetics | 2016-09-01 | PMID 26820064
Kerstjens-Frederikse Wilhelmina S, van de Laar Ingrid M B H, Vos Yvonne J and 15 more
Genes: NOTCH1
Evidence for an association between infant mortality and homozygosity for the arctic variant of carnitine palmitoyltransferase 1A.
Genetics in medicine : official journal of the American College of Medical Genetics | 2016-09-01 | PMID 26820065
Gessner Bradford D, Wood Thalia, Johnson Monique A and 2 more
Hypomorphic mutations identified in the candidate Leber congenital amaurosis gene CLUAP1.
Genetics in medicine : official journal of the American College of Medical Genetics | 2016-10-01 | PMID 26820066
Soens Zachry T, Li Yuanyuan, Zhao Li and 10 more
Genes: CLUAP1
Strømme Syndrome Is a Ciliary Disorder Caused by Mutations in CENPF.
Human mutation | 2016-04-01 | PMID 26820108
Filges Isabel, Bruder Elisabeth, Brandal Kristin and 16 more
Genes: CENPF
The prognostic implication of SRSF2 mutations in Chinese patients with acute myeloid leukemia.
Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine | 2016-08-01 | PMID 26820131
Yang Jing, Yao Dong-Ming, Ma Ji-Chun and 7 more
Genes: SRSF2
Co-expression network analysis reveals transcription factors associated to cell wall biosynthesis in sugarcane.
Plant molecular biology | 2016-05-01 | PMID 26820137
Ferreira Savio Siqueira, Hotta Carlos Takeshi, Poelking Viviane Guzzo de Carli and 6 more
Functional Investigation of a Non-coding Variant Associated with Adolescent Idiopathic Scoliosis in Zebrafish: Elevated Expression of the Ladybird Homeobox Gene Causes Body Axis Deformation.
PLoS genetics | 2016-01-01 | PMID 26820155
Guo Long, Yamashita Hiroshi, Kou Ikuyo and 10 more
Genes: LBX1, GATA2
HistoMosaic Detecting KRAS G12V Mutation Across Colorectal Cancer Tissue Slices through in Situ PCR.
Analytical chemistry | 2016-03-01 | PMID 26820161
Raub Christopher B, Lee Chen-Chung, Shibata Darryl and 2 more
Genes: KRAS
Suicide gene-modified killer cells as an allogeneic alternative to autologous cytokine-induced killer cell immunotherapy of hepatocellular carcinoma.
Molecular medicine reports | 2016-03-01 | PMID 26820174
Wu Tao, Leboeuf Céline, Durand Sarah and 6 more
[Neuhauser syndrome: the facial dysmorphic phenotype].
Revista medica del Instituto Mexicano del Seguro Social | 2000-01-01 | PMID 26820212
Aviña-Fierro Jorge Arturo, Hernández-Aviña Daniel Alejandro
Effectiveness of antiepileptic therapy in patients with PCDH19 mutations.
Seizure | 2016-02-01 | PMID 26820223
Lotte Jan, Bast Thomas, Borusiak Peter and 30 more
Genes: PCDH19
Association between XPG polymorphisms and stomach cancer susceptibility in a Chinese population.
Journal of cellular and molecular medicine | 2016-05-01 | PMID 26820236
Chen Yun-Zhi, Guo Fang, Sun Hong-Wei and 6 more
Characterization of malolactic bacteria isolated from Aosta Valley wines and evidence of psychrotrophy in some strains.
Journal of applied microbiology | 2016-04-01 | PMID 26820246
Vigentini I, Praz A, Domeneghetti D and 4 more
Genes: IMPACT
Re-infection of the prion from the scrapie‑infected cell line SMB-S15 in three strains of mice, CD1, C57BL/6 and Balb/c.
International journal of molecular medicine | 2016-03-01 | PMID 26820255
Xiao Kang, Zhang Bao-Yun, Zhang Xiao-Mei and 6 more
Genes: PRNP
Targeted Next-Generation Sequencing Identifies a Recurrent Mutation in MCPH1 Associating with Hereditary Breast Cancer Susceptibility.
PLoS genetics | 2016-01-01 | PMID 26820313
Mantere Tuomo, Winqvist Robert, Kauppila Saila and 5 more
Genes: MCPH1
Constitutive production and efficient secretion of soluble full-length streptavidin by an Escherichia coli 'leaky mutant'.
Journal of biotechnology | 2016-03-10 | PMID 26820322
Müller Jakob Michael, Wetzel David, Flaschel Erwin and 2 more
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type I.
International journal of cardiology | 2016-03-15 | PMID 26820365
Daumy Xavier, Amarouch Mohamed-Yassine, Lindenbaum Pierre and 18 more
Genes: TRPM4, GJA5, LMNA
A Bioinformatics Approach to the Identification of Variants Associated with Type 1 and Type 2 Diabetes Mellitus that Reside in Functionally Validated miRNAs Binding Sites.
Biochemical genetics | 2016-06-01 | PMID 26820452
Ghaedi Hamid, Bastami Milad, Jahani Mohammad Mehdi and 8 more
A stop-codon of the phosphodiesterase 11A gene is associated with elevated blood pressure and measures of obesity.
Journal of hypertension | 2016-03-01 | PMID 26820475
Ohlsson Therese, Lindgren Arne, Engström Gunnar and 2 more
Genes: DBP
Sirtuins 1 and 2 Are Universal Histone Deacetylases.
ACS chemical biology | 2016-03-18 | PMID 26820517
Hsu Willie W, Wu Bo, Liu Wenshe R
Genes: SIRT1, SIRT2
Individual species affect plant traits structure in their surroundings: evidence of functional mechanisms of assembly.
Oecologia | 2016-04-01 | PMID 26820565
Chacón-Labella Julia, de la Cruz Marcelino, Pescador David S and 1 more
A novel mutation in the SCN5A gene contributes to arrhythmogenic characteristics of early repolarization syndrome.
International journal of molecular medicine | 2016-03-01 | PMID 26820605
Guo Qi, Ren Lan, Chen Xuhua and 4 more
Common Variants in CLDN2 and MORC4 Genes Confer Disease Susceptibility in Patients with Chronic Pancreatitis.
PloS one | 2016-01-01 | PMID 26820620
Giri Anil K, Midha Shallu, Banerjee Priyanka and 13 more
Genes: MORC4, CLDN2, PRSS1, PRSS2, SAMD12
LDLR and PCSK9 Are Associated with the Presence of Antiphospholipid Antibodies and the Development of Thrombosis in aPLA Carriers.
PloS one | 2016-01-01 | PMID 26820623
Ochoa Eguzkine, Iriondo Mikel, Manzano Carmen and 5 more
Genes: LDLR, PCSK9, APOH
Molecular Genetics External Quality Assessment Pilot Scheme for Irinotecan-Related UGT1A1 Genotyping in China.
PloS one | 2016-01-01 | PMID 26820647
Yi Lang, Lin Guigao, Zhang Kuo and 4 more
Implication of sortase-dependent proteins of Streptococcus thermophilus in adhesion to human intestinal epithelial cell lines and bile salt tolerance.
Applied microbiology and biotechnology | 2016-04-01 | PMID 26820650
Kebouchi Mounira, Galia Wessam, Genay Magali and 7 more
Diffuse large B-cell lymphoma with MYC gene rearrangements: Current perspective on treatment of diffuse large B-cell lymphoma with MYC gene rearrangements; case series and review of the literature.
European journal of cancer (Oxford, England : 1990) | 2016-03-01 | PMID 26820684
de Jonge A V, Roosma T J A, Houtenbos I and 12 more
Genes: MYC
Molecular Characteristics of Influenza Virus Type B Lineages Circulating in Poland.
Advances in experimental medicine and biology | 2016-01-01 | PMID 26820730
Bednarska K, Hallmann-Szelińska E, Kondratiuk K and 2 more
Craniometaphyseal dysplasia with obvious biochemical abnormality and rickets-like features.
Clinica chimica acta; international journal of clinical chemistry | 2016-05-01 | PMID 26820766
Wu Bo, Jiang Yan, Wang Ou and 3 more
Genes: ANKH, PTH
Sequencing of FTO and ALKBH5 in men undergoing infertility work-up identifies an infertility-associated variant and two missense mutations.
Fertility and sterility | 2016-05-01 | PMID 26820768
Landfors Miriam, Nakken Sigve, Fusser Markus and 3 more
Genes: FTO, ALKBH5
A multi-locus genetic risk score for abdominal aortic aneurysm.
Atherosclerosis | 2016-03-01 | PMID 26820802
Ye Zi, Austin Erin, Schaid Daniel J and 1 more
Multiple microRNA regulation of lipoprotein lipase gene abolished by 3'UTR polymorphisms in a triglyceride-lowering haplotype harboring p.Ser474Ter.
Atherosclerosis | 2016-03-01 | PMID 26820803
Caussy Cyrielle, Charrière Sybil, Meirhaeghe Aline and 11 more
Genes: LPL
Genetic loci for serum lipid fractions and intracerebral hemorrhage.
Atherosclerosis | 2016-03-01 | PMID 26820804
Akoudad Saloua, Ikram M Arfan, Portegies Marileen L P and 8 more
Report of novel genetic variation in NPHS2 gene associated with idiopathic nephrotic syndrome in South Indian children.
Clinical and experimental nephrology | 2017-02-01 | PMID 26820844
Dhandapani Mohanapriya Chinambedu, Venkatesan Vettriselvi, Rengaswamy Nammalwar Bollam and 4 more
Genes: NPHS2, INS
Evaluating Baculovirus Infection Using Green Fluorescent Protein and Variants.
Methods in molecular biology (Clifton, N.J.) | 2016-01-01 | PMID 26820872
Wu Hsuan-Chen, Cha Hyung Joon, Bentley William E
Cytomegalovirus Infection Minimally Affects the Frequencies of B-Cell Phenotypes in Peripheral Blood of Younger and Older Adults.
Gerontology | 2016-01-01 | PMID 26820888
Goldeck David, Oettinger Lilly, Janssen Nicole and 3 more
IFNL4 ss469415590 polymorphism contributes to treatment decisions in patients with chronic hepatitis C virus genotype 1b, but not 2a, infection.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2016-04-01 | PMID 26820907
Wu Ruihong, Chi Xiumei, Wang Xiaomei and 12 more
Distribution of cytokine gene polymorphisms in six Orang Asli subgroups in Peninsular Malaysia.
Human immunology | 2016-04-01 | PMID 26820937
Norhalifah Hanim K, Syafawati Wan U Wan, Che Mat Nor F and 2 more
High Frequency of Pulmonary Hypertension-Causing Gene Mutation in Chinese Patients with Chronic Thromboembolic Pulmonary Hypertension.
PloS one | 2016-01-01 | PMID 26820968
Xi Qunying, Liu Zhihong, Zhao Zhihui and 2 more
Genes: PAH, ACVRL1, BMPR2, CAV1, CBLN2, ENG, KCNK3, SMAD9
Scope for genetic rescue of an endangered subspecies though re-establishing natural gene flow with another subspecies.
Molecular ecology | 2016-03-01 | PMID 26820991
Harrisson Katherine A, Pavlova Alexandra, Gonçalves da Silva Anders and 8 more
Detecting β-Casein Variation in Bovine Milk.
Molecules (Basel, Switzerland) | 2016-01-25 | PMID 26821001
Caroli Anna Maria, Savino Salvatore, Bulgari Omar and 1 more
HPV Population Profiling in Healthy Men by Next-Generation Deep Sequencing Coupled with HPV-QUEST.
Viruses | 2016-01-25 | PMID 26821041
Yin Li, Yao Jin, Chang Kaifen and 4 more
The Story of a Hitchhiker: Population Genetic Patterns in the Invasive Barnacle Balanus(Amphibalanus) improvisus Darwin 1854.
PloS one | 2016-01-01 | PMID 26821161
Wrange Anna-Lisa, Charrier Gregory, Thonig Anne and 5 more
Glucocorticoid Receptor (NR3C1) Variants Associate with the Muscle Strength and Size Response to Resistance Training.
PloS one | 2016-01-01 | PMID 26821164
Ash Garrett I, Kostek Matthew A, Lee Harold and 12 more
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children.
Journal of psychiatric research | 2016-04-01 | PMID 26821215
Salatino-Oliveira Angélica, Akutagava-Martins Glaucia C, Bruxel Estela M and 13 more
Genes: NOS1, SNAP25
The Bioinformatics Report of Mutation Outcome on NADPH Flavin Oxidoreductase Protein Sequence in Clinical Isolates of H. pylori.
Current microbiology | 2016-05-01 | PMID 26821239
Mirzaei Nasrin, Poursina Farkhondeh, Moghim Sharareh and 2 more
Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.
The Journal of physiology | 2016-08-15 | PMID 26821241
Perkins Emma, Suminaite Daumante, Jackson Mandy
Genes: SPTBN2
Genetic variations in GPSM3 associated with protection from rheumatoid arthritis affect its transcript abundance.
Genes and immunity | 2016-03-01 | PMID 26821282
Gall B J, Wilson A, Schroer A B and 5 more
Genes: GPSM3, CCL21
The SLE variant Ala71Thr of BLK severely decreases protein abundance and binding to BANK1 through impairment of the SH3 domain function.
Genes and immunity | 2016-03-01 | PMID 26821283
Díaz-Barreiro A, Bernal-Quirós M, Georg I and 3 more
Genes: BLK
TALEN-mediated enhancer knockout influences TNFAIP3 gene expression and mimics a molecular phenotype associated with systemic lupus erythematosus.
Genes and immunity | 2016-04-01 | PMID 26821284
Wang S, Wen F, Tessneer K L and 1 more
Genes: TNFAIP3
Genetic loci on chromosome 5 are associated with circulating levels of interleukin-5 and eosinophil count in a European population with high risk for cardiovascular disease.
Cytokine | 2016-05-01 | PMID 26821299
McLeod Olga, Silveira Angela, Valdes-Marquez Elsa and 19 more
Genes: RAD50, CAD
Interleukin-6 promoter polymorphism interacts with pain and life stress influencing depression phenotypes.
Journal of neural transmission (Vienna, Austria : 1996) | 2016-05-01 | PMID 26821321
Kovacs David, Eszlari Nora, Petschner Peter and 6 more
Genetic Burden Analyses of Phenotypes Relevant to Aging in the Berlin Aging Study II (BASE-II).
Gerontology | 2016-01-01 | PMID 26821332
Lill Christina M, Liu Tian, Norman Kristina and 4 more
Genes: AKAP11, FTO, MEPE, SMG6
Targeting the mTOR Complex by Everolimus in NRAS Mutant Neuroblastoma.
PloS one | 2016-01-01 | PMID 26821351
Kiessling Michael K, Curioni-Fontecedro Alessandra, Samaras Panagiotis and 6 more
Genes: NRAS
Gene regulation and chromatin organization: relevance of cohesin mutations to human disease.
Current opinion in genetics & development | 2016-04-01 | PMID 26821365
Watrin Erwan, Kaiser Frank J, Wendt Kerstin S
Characterization of genes encoding proteins containing HD-related output domain in Xanthomonas campestris pv. campestris.
Antonie van Leeuwenhoek | 2016-04-01 | PMID 26821378
Lee Hsien-Ming, Liao Chao-Tsai, Chiang Ying-Chuan and 4 more
Glycine and Folate Ameliorate Models of Congenital Sideroblastic Anemia.
PLoS genetics | 2016-01-01 | PMID 26821380
Fernández-Murray J Pedro, Prykhozhij Sergey V, Dufay J Noelia and 8 more
[Development of a Forensic Multiplex Amplification STR Kit for 15 Autosomal STR Loci and 10 Y-STR Loci].
Fa yi xue za zhi | 2015-10-01 | PMID 26821481
Dong Yan, Lin Shuang-shuang, Cao Yu and 7 more
[RESISTANCE OF HCV TO NEW DIRECT ACTING ANTIVIRALS].
Harefuah | 2015-11-01 | PMID 26821497
Gozlan Yael, Mendelson Ella, Ben-Ari Ziv and 1 more
Epileptic Encephalopathy in Childhood: A Stepwise Approach for Identification of Underlying Genetic Causes.
Indian journal of pediatrics | 2016-10-01 | PMID 26821542
Patel Jaina, Mercimek-Mahmutoglu Saadet
Very-low and low-density lipoproteins induce neutral lipid accumulation and impair migration in monocyte subsets.
Scientific reports | 2016-01-29 | PMID 26821597
Jackson William D, Weinrich Tobias W, Woollard Kevin J
Genes: RHOA
Causal Assessment of Serum Urate Levels in Cardiometabolic Diseases Through a Mendelian Randomization Study.
Journal of the American College of Cardiology | 2016-02-02 | PMID 26821629
Keenan Tanya, Zhao Wei, Rasheed Asif and 54 more
Genome-wide association study on stem rust resistance in Kazakh spring barley lines.
BMC plant biology | 2016-01-27 | PMID 26821649
Turuspekov Yerlan, Ormanbekova Danara, Rsaliev Aralbek and 1 more
Biomarkers in psoriatic arthritis: a systematic literature review.
Expert review of clinical immunology | 2016-06-01 | PMID 26821681
Generali Elena, Scirè Carlo A, Favalli Ennio G and 1 more
Genes: TNF
Long non-coding RNAs display higher natural expression variation than protein-coding genes in healthy humans.
Genome biology | 2016-01-29 | PMID 26821746
Kornienko Aleksandra E, Dotter Christoph P, Guenzl Philipp M and 6 more
Promoter polymorphism at the tumour necrosis factor/lymphotoxin-alpha locus is associated with type of diabetes but not with susceptibility to sight-threatening diabetic retinopathy.
Diabetes & vascular disease research | 2016-03-01 | PMID 26821796
Kaidonis Georgia, Craig Jamie E, Gillies Mark C and 9 more
Genes: LTA, TNF
A two-phase procedure for non-normal quantitative trait genetic association study.
BMC bioinformatics | 2016-01-28 | PMID 26821800
Zhang Wei, Li Huiyun, Li Zhaohai and 1 more
Genes: DNAH9
Identification of new heading date determinants in wheat 5B chromosome.
BMC plant biology | 2016-01-27 | PMID 26821813
Kiseleva Antonina A, Shcherban Andrey B, Leonova Irina N and 2 more
Genes: ERF, FAR1
Successful cardiac transplantation in a patient with congenital generalized lipodystrophy.
Pediatric transplantation | 2016-03-01 | PMID 26821845
Marcos-Alonso Sonia, Bautista-Hernandez Víctor, Portela Torrón Francisco
Severe sensory neuropathy in patients with adult-onset multiple acyl-CoA dehydrogenase deficiency.
Neuromuscular disorders : NMD | 2016-02-01 | PMID 26821934
Wang Zhaoxia, Hong Daojun, Zhang Wei and 6 more
Genes: MADD, ETFDH
Comparison of SNP and CAPS markers application in genetic research in wheat and barley.
BMC plant biology | 2016-01-27 | PMID 26821936
Shavrukov Yuri
Genes: CAPS
Pioglitazone-Incorporated Nanoparticles Prevent Plaque Destabilization and Rupture by Regulating Monocyte/Macrophage Differentiation in ApoE-/- Mice.
Arteriosclerosis, thrombosis, and vascular biology | 2016-03-01 | PMID 26821947
Nakashiro Soichi, Matoba Tetsuya, Umezu Ryuta and 6 more
Interaction Between ALK1 Signaling and Connexin40 in the Development of Arteriovenous Malformations.
Arteriosclerosis, thrombosis, and vascular biology | 2016-04-01 | PMID 26821948
Gkatzis Konstantinos, Thalgott Jérémy, Dos-Santos-Luis Damien and 12 more
Genes: GJA5
Evidence That Cingulin Regulates Endothelial Barrier Function In Vitro and In Vivo.
Arteriosclerosis, thrombosis, and vascular biology | 2016-04-01 | PMID 26821949
Schossleitner Klaudia, Rauscher Sabine, Gröger Marion and 8 more
Aminoacyl-Transfer RNA Synthetase Deficiency Promotes Angiogenesis via the Unfolded Protein Response Pathway.
Arteriosclerosis, thrombosis, and vascular biology | 2016-04-01 | PMID 26821951
Castranova Daniel, Davis Andrew E, Lo Brigid D and 9 more
Genome-wide association analysis to predict optimal antipsychotic dosage in schizophrenia: a pilot study.
Journal of neural transmission (Vienna, Austria : 1996) | 2016-03-01 | PMID 26821981
Koga Arthur T, Strauss John, Zai Clement and 2 more
First-generation HapMap in Cajanus spp. reveals untapped variations in parental lines of mapping populations.
Plant biotechnology journal | 2016-08-01 | PMID 26821983
Kumar Vinay, Khan Aamir W, Saxena Rachit K and 2 more
The Effect of the Canine ABCB1-1Δ Mutation on Sedation after Intravenous Administration of Acepromazine.
Journal of veterinary internal medicine | 2000-01-01 | PMID 26822006
Deshpande D, Hill K E, Mealey K L and 2 more
Genes: ABCB1
Daclatasvir, sofosbuvir, and ribavirin for hepatitis C virus genotype 3 and advanced liver disease: A randomized phase III study (ALLY-3+).
Hepatology (Baltimore, Md.) | 2016-05-01 | PMID 26822022
Leroy Vincent, Angus Peter, Bronowicki Jean-Pierre and 10 more
Novel exonic mutation inducing aberrant splicing in the IL10RA gene and resulting in infantile-onset inflammatory bowel disease: a case report.
BMC gastroenterology | 2016-01-28 | PMID 26822028
Yanagi Tadahiro, Mizuochi Tatsuki, Takaki Yugo and 9 more
Exome sequencing identifies a mutation in TMC1 as a novel cause of autosomal recessive nonsyndromic hearing loss.
Journal of translational medicine | 2016-01-28 | PMID 26822030
Hu Jiongjiong, Liu Fei, Xia Wenjun and 6 more
Genes: TMC1
Inactivation of nuclear GSK3β by Ser(389) phosphorylation promotes lymphocyte fitness during DNA double-strand break response.
Nature communications | 2016-01-29 | PMID 26822034
Thornton Tina M, Delgado Pilar, Chen Liang and 10 more
Genes: ATM
Bicaudal D Family of Motor Adaptors: Linking Dynein Motility to Cargo Binding.
Trends in cell biology | 2016-05-01 | PMID 26822037
Hoogenraad Casper C, Akhmanova Anna
Whole genome re-sequencing reveals genome-wide variations among parental lines of 16 mapping populations in chickpea (Cicer arietinum L.).
BMC plant biology | 2016-01-27 | PMID 26822060
Thudi Mahendar, Khan Aamir W, Kumar Vinay and 6 more
HLA-DRB1*15:01-DQA1*01:02-DQB1*06:02 Haplotype Protects Autoantibody-Positive Relatives From Type 1 Diabetes Throughout the Stages of Disease Progression.
Diabetes | 2016-04-01 | PMID 26822082
Pugliese Alberto, Boulware David, Yu Liping and 12 more
Deficiency in Apoptosis-Inducing Factor Recapitulates Chronic Kidney Disease via Aberrant Mitochondrial Homeostasis.
Diabetes | 2016-04-01 | PMID 26822084
Coughlan Melinda T, Higgins Gavin C, Nguyen Tuong-Vi and 30 more
Genes: AIFM1
Diabetes-Associated Variation in TCF7L2 Is Not Associated With Hepatic or Extrahepatic Insulin Resistance.
Diabetes | 2016-04-01 | PMID 26822092
Varghese Ron T, Viegas Ivan, Barosa Cristina and 5 more
Serotonergic Modulation as Effective Treatment for Dravet Syndrome in a Zebrafish Mutant Model.
ACS chemical neuroscience | 2016-05-18 | PMID 26822114
Sourbron Jo, Schneider Henning, Kecskés Angéla and 5 more
Segmental basal cell naevus syndrome caused by an activating mutation in smoothened.
The British journal of dermatology | 2016-07-01 | PMID 26822128
Khamaysi Z, Bochner R, Indelman M and 5 more
Genes: SMO, PTCH1
A trehalase from Zunongwangia sp.: characterization and improving catalytic efficiency by directed evolution.
BMC biotechnology | 2016-01-29 | PMID 26822136
Cheng Qipeng, Gao Haofeng, Hu Nan
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease.
Nature communications | 2016-01-29 | PMID 26822151
Hartiala Jaana A, Tang W H Wilson, Wang Zeneng and 8 more
Genes: CAD, CPS1
Novel alleles of the VERNALIZATION1 genes in wheat are associated with modulation of DNA curvature and flexibility in the promoter region.
BMC plant biology | 2016-01-27 | PMID 26822192
Muterko Alexandr, Kalendar Ruslan, Salina Elena
Frequent variations in cancer-related genes may play prognostic role in treatment of patients with chronic myeloid leukemia.
BMC genetics | 2016-01-27 | PMID 26822197
Lavrov Alexander V, Chelysheva Ekaterina Y, Smirnikhina Svetlana A and 4 more
Genes: DNAH9, MAGEC1, PTCRA, THSD1, TOX3
Technetium Tc 99m sulfur colloid phenotypic probe for the pharmacokinetics and pharmacodynamics of PEGylated liposomal doxorubicin in women with ovarian cancer.
Cancer chemotherapy and pharmacology | 2016-03-01 | PMID 26822231
Giovinazzo Hugh, Kumar Parag, Sheikh Arif and 14 more
Diverse impacts of the rs58542926 E167K variant in TM6SF2 on viral and metabolic liver disease phenotypes.
Hepatology (Baltimore, Md.) | 2016-07-01 | PMID 26822232
Eslam Mohammed, Mangia Alessandra, Berg Thomas and 25 more
Successful switch from insulin to oral sulfonylurea therapy in HNF1A-MODY Tunisian patient with the P291fsinsC mutation.
Diabetes research and clinical practice | 2016-05-01 | PMID 26822262
Khelifa Souhaïra Ben, Dendana Azza, Barboura Ilhem and 4 more
Genetic determinants of pig birth weight variability.
BMC genetics | 2016-01-27 | PMID 26822294
Wang Xuemin, Liu Xiaolei, Deng Dadong and 2 more
Genes: AACS, APOB, OSBPL10