Extracellular matrix directs phenotypic heterogeneity of activated fibroblasts.
Matrix biology : journal of the International Society for Matrix Biology | 2018-04-01 | PMID 29248556
Avery Diana, Govindaraju Priya, Jacob Michele and 3 more
Genes: FAP
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 7600 of 10600
EL20, a potent antiarrhythmic compound, selectively inhibits calmodulin-deficient ryanodine receptor type 2.
Heart rhythm | 2018-04-01 | PMID 29248564
Klipp Robert C, Li Na, Wang Qiongling and 5 more
Genetic profile of patients with early onset inflammatory bowel disease.
Gene | 2018-03-01 | PMID 29248579
Girardelli Martina, Basaldella Federica, Paolera Sara Della and 5 more
Genes: NOD2, XIAP
Exome sequencing of a large family identifies potential candidate genes contributing risk to bipolar disorder.
Gene | 2018-03-01 | PMID 29248581
Zhang Tianxiao, Hou Liping, Chen David T and 3 more
Genes: GRID1
Association between vitamin D receptor polymorphisms and hepatitis B virus infection susceptibility: A meta-analysis study.
Gene | 2018-03-01 | PMID 29248582
He Qiao, Huang Yecai, Zhang Li and 4 more
Genes: VDR, VIP
GmPLP1, a PAS/LOV protein, functions as a possible new type of blue light photoreceptor in soybean.
Gene | 2018-03-01 | PMID 29248583
Li Yongguang, Zhang Yanzheng, Li Mengting and 6 more
Genes: CRY1, CRY2
Human protective monoclonal antibodies against the HA stem of group 2 HAs derived from an H3N2 virus-infected human.
The Journal of infection | 2018-02-01 | PMID 29248585
Yamayoshi Seiya, Ito Mutsumi, Uraki Ryuta and 3 more
A vicious interplay between genetic and environmental insults in the etiology of blood cancers.
Experimental hematology | 2018-03-01 | PMID 29248611
Migliaccio Anna Rita
Genes: TNF, TET2
Significant association between catechol-O-methyltransferase (COMT) Val158/108Met polymorphism and cognitive function in veterans with PTSD.
Neuroscience letters | 2018-02-14 | PMID 29248614
Havelka Mestrovic Ana, Tudor Lucija, Nikolac Perkovic Matea and 5 more
Genes: COMT
Vectors of diversity: Genome wide diversity across the geographic range of the Chagas disease vector Triatoma dimidiata sensu lato (Hemiptera: Reduviidae).
Molecular phylogenetics and evolution | 2018-03-01 | PMID 29248626
Justi Silvia A, Cahan Sara, Stevens Lori and 3 more
A case of a primary lung cancer comprised of adenocarcinoma and atypical carcinoid tumor with both components harboring BRAF p.V600E mutation.
Experimental and molecular pathology | 2018-02-01 | PMID 29248665
Olofson Andrea M, Tafe Laura J
Genes: BRAF
The association of Salmonella enterica from aquatic environmental and clinical samples in Taiwan.
The Science of the total environment | 2018-05-15 | PMID 29248701
Ho Ying-Ning, Tsai Hsin-Chi, Hsu Bing-Mu and 1 more
Genetic variant repressing ADH1A expression confers susceptibility to esophageal squamous-cell carcinoma.
Cancer letters | 2018-05-01 | PMID 29248712
Cui Qionghua, Peng Linna, Wei Lixuan and 13 more
Genes: ADH5, ALDH2
Maf1 phenotypes and cell physiology.
Biochimica et biophysica acta. Gene regulatory mechanisms | 2018-04-01 | PMID 29248739
Willis Ian M
Increased mutability to fosfomycin resistance in Proteus mirabilis clinical isolates.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2018-03-01 | PMID 29248795
Fonseca Marina R B, Sato Juliana L, Lima-Noronha Marco A and 3 more
Multiple introductions of reassorted highly pathogenic avian influenza viruses (H5N8) clade 2.3.4.4b causing outbreaks in wild birds and poultry in Egypt.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2018-03-01 | PMID 29248796
Yehia Nahed, Naguib Mahmoud M, Li Ruiyun and 9 more
Molecular epidemiology of Mycobacterium tuberculosis strains from prison populations in Santa Catarina, Southern Brazil.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases | 2018-03-01 | PMID 29248797
Medeiros Taiane Freitas, Nogueira Christiane Lourenço, Prim Rodrigo Ivan and 6 more
Catechol-O-methyltransferase (COMT) genotype affects cognitive control during total sleep deprivation.
Cortex; a journal devoted to the study of the nervous system and behavior | 2018-02-01 | PMID 29248857
Satterfield Brieann C, Hinson John M, Whitney Paul and 3 more
Genes: COMT
Genetics and genomics of breast fibroadenomas.
Journal of clinical pathology | 2018-05-01 | PMID 29248888
Loke Benjamin Nathanael, Md Nasir Nur Diyana, Thike Aye Aye and 4 more
Genes: MED12
Whole-Genome Analysis of an Extensive Drug-Resistant Acinetobacter Baumannii ST195 Isolate from a Recipient After DCD Renal Transplantation in China.
Kidney & blood pressure research | 2017-01-01 | PMID 29248914
Jiang Hong, Cao Luxi, Shen Qixia and 17 more
Genes: DCD
Issues in Identification and Assessment of Children with Autism and a Proposed Resource Toolkit for Speech-Language Pathologists.
Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP) | 2017-01-01 | PMID 29248918
Hus Yvette
Familial X/Y Translocation Encompassing ARSE in Two Moroccan Siblings with Sensorineural Deafness.
Cytogenetic and genome research | 2017-01-01 | PMID 29248929
Amasdl Saadia, Smaili Wiam, Natiq Abdelhafid and 5 more
Genes: SHOX
Patients with Coexistence of Circulating Hepatitis B Surface Antigen and Its Antibody May Have a Strong Predisposition to Virus Reactivation During Immunosuppressive Therapy: A Hypothesis.
Medical science monitor : international medical journal of experimental and clinical research | 2017-12-17 | PMID 29248936
Chen Yu-Lan, Mo Ying-Qian, Zheng Dong-Hui and 3 more
Ancestry inference of 96 population samples using microhaplotypes.
International journal of legal medicine | 2018-05-01 | PMID 29248957
Bulbul Ozlem, Pakstis Andrew J, Soundararajan Usha and 13 more
Species A rotaviruses isolated from hospitalized patients over 5 years of age in Kolkata, India, in 2012/13.
Archives of virology | 2018-03-01 | PMID 29248967
Nayak Mukti Kant, De Papiya, Manna Byomkesh and 3 more
Somatic embryogenesis of muskmelon (Cucumis melo L.) and genetic stability assessment of regenerants using flow cytometry and ISSR markers.
Protoplasma | 2018-05-01 | PMID 29248969
Raji Mohammad Reza, Lotfi Mahmoud, Tohidfar Masoud and 4 more
Application of modified JDP-DGGE-based molecular genotyping method to predict Acanthamoeba genotype and to analyse community diversity in aquatic environments.
Parasitology research | 2018-02-01 | PMID 29248979
Hsu Tsui-Kang, Chen Jung-Sheng, Hsu Bing-Mu and 5 more
Different Cerebellar Ataxia Phenotypes Associated with Mutations of the PNPLA6 Gene in Brazilian Patients with Recessive Ataxias.
Cerebellum (London, England) | 2018-06-01 | PMID 29248984
Teive Hélio Afonso Ghizoni, Camargo Carlos Henrique F, Sato Mario Teruo and 6 more
Genes: PNPLA6
Transthyretin familial amyloid polyneuropathy: an update.
Journal of neurology | 2018-04-01 | PMID 29249054
Plante-Bordeneuve Violaine
Genes: TTR, FAP
Serum 25-hydroxyvitamin D levels in children with recurrent wheezing and relation to the phenotypes and frequency of wheezing.
European annals of allergy and clinical immunology | 2017-11-01 | PMID 29249133
Dogru M, Seren L P
Palatal Tremor Revisited: Disorder with Nosological Diversity and Etiological Heterogeneity.
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques | 2018-03-01 | PMID 29249217
Nagappa Madhu, Bindu Parayil S, Sinha Sanjib and 5 more
Genes: NDUFS8, POLG, EEF2, TENM4
DRD3 Ser9Gly Polymorphism and Its Influence on Risperidone Response in Autistic Children.
Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques | 2017-01-01 | PMID 29249220
Firouzabadi Negar, Nazariat Anna, Zomorrodian Kamiar
Genes: DRD3
NG2 and GFAP co-expression after differentiation in cells transfected with mutant GFAP and in undifferentiated glioma cells.
Neurologia | 2020-09-01 | PMID 29249301
Gómez-Pinedo U, Sirerol-Piquer S, Durán-Moreno M and 4 more
Genes: GFAP
Outcomes in patients with non-small-cell lung cancer and acquired Thr790Met mutation treated with osimertinib: a genomic study.
The Lancet. Respiratory medicine | 2018-02-01 | PMID 29249325
Lin Chia-Chi, Shih Jin-Yuan, Yu Chong-Jen and 11 more
Genes: EGFR, BRAF, KRAS
A novel mutation in ETFDH manifesting as severe neonatal-onset multiple acyl-CoA dehydrogenase deficiency.
Journal of the neurological sciences | 2018-01-15 | PMID 29249369
van der Westhuizen Francois H, Smuts Izelle, Honey Engela and 4 more
Genes: MADD, ETFDH, SDS
Barth Syndrome: Different Approaches to Diagnosis.
The Journal of pediatrics | 2018-02-01 | PMID 29249525
Imai-Okazaki Atsuko, Kishita Yoshihito, Kohda Masakazu and 16 more
Liver Angiomyolipomas in Tuberous Sclerosis Complex-Their Incidence and Course.
Pediatric neurology | 2018-01-01 | PMID 29249553
Jóźwiak Sergiusz, Sadowski Krzysztof, Borkowska Julita and 8 more
Genes: TSC2
Selectively Modulating Conformational States of USP7 Catalytic Domain for Activation.
Structure (London, England : 1993) | 2018-01-02 | PMID 29249604
Özen Ayşegül, Rougé Lionel, Bashore Charlene and 3 more
Genes: USP7
Differential Expression of NF2 in Neuroepithelial Compartments Is Necessary for Mammalian Eye Development.
Developmental cell | 2018-01-08 | PMID 29249622
Moon Kyeong Hwan, Kim Hyoung-Tai, Lee Dahye and 4 more
Genes: RPE
Genetic short stature.
Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society | 2018-02-01 | PMID 29249624
Grunauer Michelle, Jorge Alexander A L
Genes: SDS
Congenital central hypoventilation syndrome: An overview of etiopathogenesis, associated pathologies, clinical presentation, and management.
Autonomic neuroscience : basic & clinical | 2018-03-01 | PMID 29249648
Zaidi Saher, Gandhi Jason, Vatsia Sohrab and 2 more
Patterns of Genomic Variation in the Opportunistic Pathogen Candida glabrata Suggest the Existence of Mating and a Secondary Association with Humans.
Current biology : CB | 2018-01-08 | PMID 29249661
Carreté Laia, Ksiezopolska Ewa, Pegueroles Cinta and 7 more
Impaired IFNγ-Signaling and Mycobacterial Clearance in IFNγR1-Deficient Human iPSC-Derived Macrophages.
Stem cell reports | 2018-01-09 | PMID 29249666
Neehus Anna-Lena, Lam Jenny, Haake Kathrin and 17 more
Genes: STAT1
Dopaminergic polymorphisms associated with medication responsiveness of gait in Parkinson's disease.
Parkinsonism & related disorders | 2018-03-01 | PMID 29249680
Miller Nathaniel S, Chou Kelvin L, Bohnen Nicolaas I and 2 more
Genes: DRD2, BDNF, COMT
Dual Targeting of Oncogenic Activation and Inflammatory Signaling Increases Therapeutic Efficacy in Myeloproliferative Neoplasms.
Cancer cell | 2018-01-08 | PMID 29249691
Kleppe Maria, Koche Richard, Zou Lihua and 21 more
SETD2-mediated crosstalk between H3K36me3 and H3K79me2 in MLL-rearranged leukemia.
Leukemia | 2018-04-01 | PMID 29249820
Bu J, Chen A, Yan X and 13 more
Genes: SETD2, ASXL1, ERG
Associations of genetic determinants of serum vitamin B12 and folate concentrations with hay fever and asthma: a Mendelian randomization meta-analysis.
European journal of clinical nutrition | 2018-02-01 | PMID 29249824
Skaaby Tea, Taylor Amy E, Jacobsen Rikke K and 14 more
Gene expression associated with PTSD in World Trade Center responders: An RNA sequencing study.
Translational psychiatry | 2017-12-18 | PMID 29249826
Kuan Pei-Fen, Waszczuk Monika A, Kotov Roman and 8 more
Genes: FKBP5
Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data.
Translational psychiatry | 2017-12-18 | PMID 29249828
Polushina Tatiana, Giddaluru Sudheer, Bettella Francesco and 9 more
Genes: PGC
A polygenic score for schizophrenia predicts glycemic control.
Translational psychiatry | 2017-12-18 | PMID 29249829
Cao Han, Chen Junfang, Meyer-Lindenberg Andreas and 1 more
Human Primary Epithelial Cells Acquire an Epithelial-Mesenchymal-Transition Phenotype during Long-Term Infection by the Oral Opportunistic Pathogen, Porphyromonas gingivalis.
Frontiers in cellular and infection microbiology | 2017-01-01 | PMID 29250491
Lee Jungnam, Roberts JoAnn S, Atanasova Kalina R and 3 more
Identifying Human Phenotype Terms by Combining Machine Learning and Validation Rules.
BioMed research international | 2017-01-01 | PMID 29250549
Lobo Manuel, Lamurias Andre, Couto Francisco M
Genes: GSC
Angelman Syndrome Due to UBE3A Gene Mutation.
Indian journal of pediatrics | 2018-05-01 | PMID 29250725
Goswami Jyotindra Narayan, Sahu Jitendra Kumar, Singhi Pratibha
Nonredundant functions of Arabidopsis LecRK-V.2 and LecRK-VII.1 in controlling stomatal immunity and jasmonate-mediated stomatal closure.
The New phytologist | 2018-04-01 | PMID 29250804
Yekondi Shweta, Liang Fu-Chun, Okuma Eiji and 8 more
ABCB1 and CYP2D6 polymorphisms and treatment response of psychotic patients in a naturalistic setting.
Human psychopharmacology | 2018-01-01 | PMID 29250824
Papazisis Georgios, Goulas Antonios, Sarrigiannidis Alexios and 6 more
Genes: ABCB1
Structural and sequence variants in patients with Silver-Russell syndrome or similar features-Curation of a disease database.
Human mutation | 2018-03-01 | PMID 29250858
Tümer Zeynep, López-Hernández Julia Angélica, Netchine Irène and 6 more
Genes: IGF2
Uric acid and cardiovascular risk: What genes can say.
International journal of clinical practice | 2018-01-01 | PMID 29250870
Kei Anastazia, Koutsouka Freideriki, Makri Andromachi and 1 more
Atypical Hemolytic Uremic Syndrome: A Meta-Analysis of Case Reports Confirms the Prevalence of Genetic Mutations and the Shift of Treatment Regimens.
Therapeutic apheresis and dialysis : official peer-reviewed journal of the International Society for Apheresis, the Japanese Society for Apheresis, the Japanese Society for Dialysis Therapy | 2018-04-01 | PMID 29250893
Krishnappa Vinod, Gupta Mohit, Elrifai Mohamed and 5 more
Genes: CFH, CFHR1, CFI
Protein identification before and after glyphosate exposure in Lolium multiflorum genotypes.
Pest management science | 2018-05-01 | PMID 29250898
Barroso Arthur Am, de S Costa Marilia G, Neto Nelson J and 4 more
Longitudinal interplays of estrogen receptor alpha gene rs9340799 with social-environmental factors on post-traumatic stress disorder in Chinese Han adolescents after Wenchuan earthquake.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2018-04-01 | PMID 29250928
Feng Yue, Su Mi, Si Yan Jun and 6 more
Genes: ESR1
Microencapsulated macrophages releases conditioned medium able to prevent epithelial to mesenchymal transition.
Drug delivery | 2018-11-01 | PMID 29250977
Sola Anna, Saenz Del Burgo Laura, Ciriza Jesús and 6 more
Coinheritance of α- and β-Thalassemia with a Novel Mutation (HBB: c.268_281delAGTGAGCTGCACTG) in a Chinese Family.
Hemoglobin | 2000-01-01 | PMID 29251005
Cheng Chuyun, Peng Qi, Li Siping and 4 more
Genes: HBB, SEA
Prevalence of Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency in Newborns and Adults at the Ramathibodi Hospital, Bangkok, Thailand.
Hemoglobin | 2000-01-01 | PMID 29251006
Banyatsuppasin Wansa, Jindadamrongwech Sumalee, Limrungsikul Anchalee and 1 more
Genes: HBB
First Report of the Rare IVS-II-705 (T>G) β-Thalassemia Mutation in a Chinese Family.
Hemoglobin | 2000-01-01 | PMID 29251008
Jiang Fan, Chen Gui-Lan, Zhou Jian-Ying and 1 more
Genes: HBB
Fully Dedifferentiated Chondrocytes Expanded in Specific Mesenchymal Stem Cell Growth Medium with FGF2 Obtains Mesenchymal Stem Cell Phenotype In Vitro but Retains Chondrocyte Phenotype In Vivo.
Cell transplantation | 2017-10-01 | PMID 29251111
Lee Jungsun, Lee Jin-Yeon, Chae Byung-Chul and 3 more
Genes: FGF2, MSC
Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population.
The International journal of neuroscience | 2018-08-01 | PMID 29251119
Zhou Xin, Wang Chunrong, Chen Zhao and 8 more
Genes: TNF, MAF
The clinical significance of FLT3 ITD mutation on the prognosis of adult acute promyelocytic leukemia.
Hematology (Amsterdam, Netherlands) | 2018-08-01 | PMID 29251252
Fan Yingchao, Cao Yanan, Bai Xiaosong and 1 more
Genes: FLT3
Effects of genetic factors to inhaled corticosteroid response in children with asthma: a literature review.
The Journal of international medical research | 2017-12-01 | PMID 29251255
Duong-Thi-Ly Huong, Nguyen-Thi-Thu Ha, Nguyen-Hoang Long and 3 more
Genes: CRHR1, DUSP1, FCER2, GLCCI1, ORMDL3, STIP1, TBX21
Genome-Wide Expression Profiles Drive Discovery of Novel Compounds that Reduce Binge Drinking in Mice.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology | 2018-05-01 | PMID 29251283
Ferguson Laura B, Ozburn Angela R, Ponomarev Igor and 5 more
Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review .
Oncology nursing forum | 2018-01-01 | PMID 29251290
Fournier Danielle M, Bazzell Angela F, Dains Joyce E
Epigenetic and Transcriptional Variability Shape Phenotypic Plasticity.
BioEssays : news and reviews in molecular, cellular and developmental biology | 2018-02-01 | PMID 29251357
Ecker Simone, Pancaldi Vera, Valencia Alfonso and 2 more
Association of polymorphism in the VEGFA gene 3'-UTR +936T/C with susceptibility to biliary atresia in a Southern Chinese Han population.
Journal of clinical laboratory analysis | 2018-05-01 | PMID 29251369
Liu Fei, Zeng Jixiao, Zhu Deli and 6 more
Genes: VEGFA
Serological, genetic and clinical associations with increased health-care resource utilization in inflammatory bowel disease.
Journal of digestive diseases | 2018-01-01 | PMID 29251413
Gu Phillip, Kapur Anshika, Li Dalin and 8 more
Specific T Cell Responses against Minor Histocompatibility Antigens Cannot Generally Be Explained by Absence of Their Allelic Counterparts on the Cell Surface.
Proteomics | 2018-06-01 | PMID 29251415
Bijen Helena M, Hassan Chopie, Kester Michel G D and 10 more
[The role of micro-RNA in the regulation of signal pathways in gliomas].
Biomeditsinskaia khimiia | 2017-11-01 | PMID 29251609
Kit O I, Vodolazhsky D I, Rostorguev E E and 2 more
Genes: EGFR, IDH1
[Bacterial TEM-type serine beta-lactamases: structure and analysis of mutations].
Biomeditsinskaia khimiia | 2017-11-01 | PMID 29251610
Grigorenko V G, Rubtsova M Yu, Uporov I V and 5 more
[The association of the mitochondrial DNA oriB variants with metabolic syndrome].
Biomeditsinskaia khimiia | 2017-11-01 | PMID 29251615
Skuratovskaia D A, Sofronova J K, Zatolokin P A and 3 more
[The influence of chorionic gonadotropin on phenotype conversion and hTERT gene expression by T-lymphocytes of different degrees of differentiation].
Biomeditsinskaia khimiia | 2017-11-01 | PMID 29251616
Rayev M B, Zamorina S A, Litvinova L S and 6 more
PBX transcription factors drive pulmonary vascular adaptation to birth.
The Journal of clinical investigation | 2018-02-01 | PMID 29251627
McCulley David J, Wienhold Mark D, Hines Elizabeth A and 7 more
Erythrocyte efferocytosis modulates macrophages towards recovery after intracerebral hemorrhage.
The Journal of clinical investigation | 2018-02-01 | PMID 29251628
Chang Che-Feng, Goods Brittany A, Askenase Michael H and 17 more
Genes: AXL, MERTK
A novel factor X mutation Cys81 by Arg and a reported factor VII polymorphism Arg353 replaced by Gln co-occured in a patient.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis | 2018-01-01 | PMID 29251640
Jin Yanhui, Cheng Xiaoli, Zheng Jiayong and 3 more
De novo variants in KLF7 are a potential novel cause of developmental delay/intellectual disability, neuromuscular and psychiatric symptoms.
Clinical genetics | 2018-05-01 | PMID 29251763
Powis Z, Petrik I, Cohen J S and 12 more
Genes: KLF7
The physical spacing between the von Willebrand factor D'D3 and A1 domains regulates platelet adhesion in vitro and in vivo.
Journal of thrombosis and haemostasis : JTH | 2018-03-01 | PMID 29251812
Zhang C, Kelkar A, Nasirikenari M and 5 more
Genes: VWF
Dual drive coexistence of EML4-ALK and TPM3-ROS1 fusion in advanced lung adenocarcinoma.
Thoracic cancer | 2018-02-01 | PMID 29251824
Zhu You-Cai, Liao Xing-Hui, Wang Wen-Xian and 4 more
Genes: ALK, ROS1, EML4, TPM3, EGFR
Hierarchical investigation of genetic influences on response inhibition in healthy young adults.
Experimental and clinical psychopharmacology | 2017-12-01 | PMID 29251981
Weafer Jessica, Gray Joshua C, Hernandez Kyle and 3 more
Advances in the treatment of HIV/HCV coinfection in adults.
Expert opinion on pharmacotherapy | 2018-01-01 | PMID 29252031
Schlabe Stefan, Rockstroh Jürgen K
Risk factors for abnormal hepatic enzyme elevation by methotrexate treatment in patients with rheumatoid arthritis: A hospital based-cohort study.
Modern rheumatology | 2018-07-01 | PMID 29252093
Hakamata Jun, Hashiguchi Masayuki, Kaneko Yuko and 5 more
Genes: ABCB1, ATIC
HLA-E*0101/0103X is Associated with Susceptibility to Pemphigus Vulgaris: A Case-control Study.
Acta dermatovenerologica Croatica : ADC | 2017-10-01 | PMID 29252170
Altun Ece, Yayli Savas, Toraman Bayram and 4 more
Quiescence unveils a novel mutational force in fission yeast.
eLife | 2017-12-18 | PMID 29252184
Gangloff Serge, Achaz Guillaume, Francesconi Stefania and 4 more
Role of CYP4F2, CYP2C19, and CYP1A2 polymorphisms on acenocoumarol pharmacogenomic algorithm accuracy improvement in the Greek population: need for sub-phenotype analysis.
Drug metabolism and personalized therapy | 2017-12-20 | PMID 29252193
Ragia Georgia, Karantza Ioanna-Maria, Kelli-Kota Eleni and 8 more
Genes: VKORC1
Vaginal bleeding and a giant ovarian cyst in an infant with 21-hydroxylase deficiency.
Journal of pediatric endocrinology & metabolism : JPEM | 2018-01-26 | PMID 29252197
Şahin Nursel Muratoğlu, Bayramoğlu Elvan, Çetinkaya Semra and 4 more
Molecular basis and clinical presentation of classic galactosemia in a Croatian population.
Journal of pediatric endocrinology & metabolism : JPEM | 2018-01-26 | PMID 29252199
Ramadža Danijela Petković, Sarnavka Vladimir, Vuković Jurica and 9 more
Genes: GALT
Microglia ablation alleviates myelin-associated catatonic signs in mice.
The Journal of clinical investigation | 2018-02-01 | PMID 29252214
Janova Hana, Arinrad Sahab, Balmuth Evan and 20 more
Genes: CNP, CSF1
Setting the Threshold for Surgical Prevention in Women at Increased Risk of Ovarian Cancer.
International journal of gynecological cancer : official journal of the International Gynecological Cancer Society | 2018-01-01 | PMID 29252925
Manchanda Ranjit, Menon Usha
Genes: BRCA1, BRCA2, BRIP1
Genetic and antigenic divergence in the influenza A(H3N2) virus circulating between 2016 and 2017 in Thailand.
PloS one | 2017-01-01 | PMID 29252990
Suntronwong Nungruthai, Klinfueng Sirapa, Vichiwattana Preeyaporn and 4 more
Aedes aegypti resistance development to commonly used insecticides in Jakarta, Indonesia.
PloS one | 2017-01-01 | PMID 29253003
Hamid Penny Humaidah, Prastowo Joko, Ghiffari Ahmad and 2 more
Association between osteoprotegerin gene T950C polymorphism and osteoporosis risk in the Chinese population: Evidence via meta-analysis.
PloS one | 2017-01-01 | PMID 29253005
Li Shouyi, Jiang Huiqiang, Du Ningke
Phenotypic characterization of adenomyosis occurring at the inner and outer myometrium.
PloS one | 2017-01-01 | PMID 29253010
Kishi Yohei, Shimada Keiji, Fujii Tomomi and 5 more
Genetic variability of environmental sensitivity revealed by phenotypic variation in body weight and (its) correlations to physiological and behavioral traits.
PloS one | 2017-01-01 | PMID 29253015
Lallias Delphine, Quillet Edwige, Bégout Marie-Laure and 8 more
Complementarity determining regions and frameworks contribute to the disulfide bond independent folding of intrinsically stable scFv.
PloS one | 2017-01-01 | PMID 29253024
Gąciarz Anna, Ruddock Lloyd W