Molecular basi of superoxide dismutase alterations in Spirometry proven bronchial asthma.
JPMA. The Journal of the Pakistan Medical Association | 2017-09-01 | PMID 28924281
Hassan Syed Hafeezul, Ghani Rubina, Sarwar Muhammad
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 7495 of 10600
Molecular biology of glioblastoma: Classification and mutational locations.
JPMA. The Journal of the Pakistan Medical Association | 2017-09-01 | PMID 28924284
Soomro Shahid Hussain, Ting Li Rui, Qing Yang Yi and 1 more
Functional Analysis of a Novel FOXL2 Indel Mutation in Chinese Families with Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I.
International journal of biological sciences | 2017-01-01 | PMID 28924383
Chai Peiwei, Li Fang, Fan Jiayan and 3 more
Genes: FOXL2
Super-Resolution High Content Screening and Analysis.
Methods in molecular biology (Clifton, N.J.) | 2017-01-01 | PMID 28924673
Soliman K
Comprehensive annotation and evolutionary insights into the canine (Canis lupus familiaris) antigen receptor loci.
Immunogenetics | 2018-04-01 | PMID 28924718
Martin Jolyon, Ponstingl Hannes, Lefranc Marie-Paule and 3 more
Genes: IGK
Overexpression of the transcription factor NF-YC9 confers abscisic acid hypersensitivity in Arabidopsis.
Plant molecular biology | 2017-11-01 | PMID 28924726
Bi Chao, Ma Yu, Wang Xiao-Fang and 1 more
Diversity of family GH46 chitosanases in Kitasatospora setae KM-6054.
Applied microbiology and biotechnology | 2017-11-01 | PMID 28924834
Zitouni Mina, Viens Pascal, Ghinet Mariana G and 1 more
Diagnostic approach to neurotransmitter monoamine disorders: experience from clinical, biochemical, and genetic profiles.
Journal of inherited metabolic disease | 2018-01-01 | PMID 28924877
Kuster Alice, Arnoux Jean-Baptiste, Barth Magalie and 17 more
Genes: ACSF3, ADAR, CASK, DDC, EXOSC3, FOLR1, FOXG1, KCNQ2
The association between MICA/MICB polymorphism and respiratory syncytial virus infection in children.
International journal of immunogenetics | 2017-12-01 | PMID 28925058
Luo Q, Guo X, Peng S and 4 more
Genes: MICA, MICB
The ontogeny of developmental buffering in lizard head shape.
Evolution & development | 2017-11-01 | PMID 28925092
Lazić Marko M, Rödder Dennis, Kaliontzopoulou Antigoni
Generation of an induced pluripotent stem cell line from a patient with hereditary multiple endocrine neoplasia 2B (MEN2B) syndrome with "highest risk" RET mutation.
Stem cell research | 2017-08-01 | PMID 28925363
Bennaceur-Griscelli A, Hadoux J, Féraud O and 6 more
Genes: RET
Generation of an induced pluripotent stem cell (iPSC) line from a patient with maturity-onset diabetes of the young type 13 (MODY13) with a the potassium inwardly-rectifying channel, subfamily J, member 11 (KCNJ11) mutation.
Stem cell research | 2017-08-01 | PMID 28925365
Griscelli Frank, Feraud Olivier, Ernault Tony and 5 more
Genes: KCNJ11
Establishment of a human iPSC line (IISHDOi001-A) from a patient with McArdle disease.
Stem cell research | 2017-08-01 | PMID 28925366
Ortuño-Costela María Del Carmen, Rodríguez-Mancera Nathalie, García-López Marta and 6 more
Genes: PYGM
A Marfan syndrome human induced pluripotent stem cell line with a heterozygous FBN1 c.4082G>A mutation, ISMMSi002-B, for disease modeling.
Stem cell research | 2017-08-01 | PMID 28925368
Klein Sandra, Dvornik Jill L, Yarrabothula Akshitha R and 1 more
Genes: FBN1
Generation of a gene-corrected isogenic control iPSC line from cystic fibrosis patient-specific iPSCs homozygous for p.Phe508del mutation mediated by TALENs and ssODN.
Stem cell research | 2017-08-01 | PMID 28925369
Merkert Sylvia, Bednarski Christien, Göhring Gudrun and 2 more
Genes: CFTR
A vital sugar code for ricin toxicity.
Cell research | 2017-11-01 | PMID 28925387
Taubenschmid Jasmin, Stadlmann Johannes, Jost Markus and 13 more
Contrasting effects of an Mdm2 functional polymorphism on tumor phenotypes.
Oncogene | 2018-01-18 | PMID 28925402
Ortiz G J, Li Y, Post S M and 6 more
Genes: MDM2
Detection of hereditary hearing loss gene by DNA microarray.
European review for medical and pharmacological sciences | 2017-08-01 | PMID 28925492
Han G-Y, Xu Z, Li Q-S and 3 more
Genes: GJB2, GJB3
Grandmaternal smoking increases asthma risk in grandchildren: A nationwide Swedish cohort.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology | 2018-02-01 | PMID 28925522
Lodge C J, Bråbäck L, Lowe A J and 3 more
One gene, two proteins: coordinated production of a copper chaperone by differential transcript formation and translational frameshifting in Escherichia coli.
Molecular microbiology | 2017-11-01 | PMID 28925527
Drees Steffen L, Klinkert Birgit, Helling Stefan and 4 more
The role of a cytoplasmic loop of MotA in load-dependent assembly and disassembly dynamics of the MotA/B stator complex in the bacterial flagellar motor.
Molecular microbiology | 2017-11-01 | PMID 28925530
Pourjaberi Seyedeh Noorolhoda Shajari, Terahara Naoya, Namba Keiichi and 1 more
Interaction analysis between BLK rs13277113 polymorphism and BANK1 rs3733197 polymorphism, MMEL1/TNFRSF14 rs3890745 polymorphism in determining susceptibility to rheumatoid arthritis.
Autoimmunity | 2017-11-01 | PMID 28925718
Huang Hua, Huang Si-Chao, Hua Dong-Jin and 3 more
Genes: BLK, MMEL1, TNFRSF14
The effect of lomitapide on cardiovascular outcome measures in homozygous familial hypercholesterolemia: A modelling analysis.
European journal of preventive cardiology | 2017-11-01 | PMID 28925748
Leipold Robert, Raal Frederick, Ishak Jack and 2 more
Transcription-driven DNA methylation setting on the mouse Peg3 locus.
Epigenetics | 2017-01-01 | PMID 28925797
Bretz Corey L, Kim Joomyeong
New Insights into the Genome Organization of Yeast Killer Viruses Based on "Atypical" Killer Strains Characterized by High-Throughput Sequencing.
Toxins | 2017-09-19 | PMID 28925975
Ramírez Manuel, Velázquez Rocío, López-Piñeiro Antonio and 3 more
The BDNF Val66Met polymorphism regulates glucocorticoid-induced corticohippocampal remodeling and behavioral despair.
Translational psychiatry | 2017-09-19 | PMID 28926000
Notaras M, Du X, Gogos J and 2 more
Genes: CORT, BDNF, FST, PSD
Polygenic loading for major depression is associated with specific medical comorbidity.
Translational psychiatry | 2017-09-19 | PMID 28926002
McCoy T H, Castro V M, Snapper L and 4 more
Common variants in DLG1 locus are associated with non-syndromic cleft lip with or without cleft palate.
Clinical genetics | 2018-04-01 | PMID 28926086
Mostowska A, Gaczkowska A, Żukowski K and 13 more
Genes: DLG1
Distinct mechanisms of regulation of the ITGA6 and ITGB4 genes by RUNX1 in myeloid cells.
Journal of cellular physiology | 2018-04-01 | PMID 28926098
Phillips Jessica L, Taberlay Phillippa C, Woodworth Alexandra M and 4 more
Genes: RUNX1, ITGB4, ITGA6
Glecaprevir/pibrentasvir for hepatitis C virus genotype 3 patients with cirrhosis and/or prior treatment experience: A partially randomized phase 3 clinical trial.
Hepatology (Baltimore, Md.) | 2018-02-01 | PMID 28926120
Wyles David, Poordad Fred, Wang Stanley and 15 more
Early genetic aberrations in patients with sporadic colorectal cancer.
Molecular carcinogenesis | 2018-01-01 | PMID 28926134
Druliner Brooke R, Ruan Xiaoyang, Sicotte Hugues and 4 more
Genes: APC, BRAF, CTNNB1, DCC, SMAD4
The synonymous nucleotide substitution RHD 1056C>G alters mRNA splicing associated with serologically weak D phenotype.
Journal of clinical laboratory analysis | 2018-05-01 | PMID 28926139
Chun Sejong, Yun Jae Won, Park Geon and 1 more
Genes: RHD
Characterization of TP53 mutations in low-grade myelodysplastic syndromes and myelodysplastic syndromes with a non-complex karyotype.
European journal of haematology | 2017-12-01 | PMID 28926144
Wang Wei, Routbort Mark J, Tang Zhenya and 6 more
Comparative and population genomic landscape of Phellinus noxius: A hypervariable fungus causing root rot in trees.
Molecular ecology | 2017-11-01 | PMID 28926153
Chung Chia-Lin, Lee Tracy J, Akiba Mitsuteru and 18 more
Selection on a behaviour-related gene during the first stages of the biological invasion pathway.
Molecular ecology | 2017-11-01 | PMID 28926158
Mueller Jakob C, Edelaar Pim, Baños-Villalba Adrián and 5 more
Genes: DRD4
Adult plasticity in African cichlids: Rapid changes in opsin expression in response to environmental light differences.
Molecular ecology | 2017-11-01 | PMID 28926160
Nandamuri Sri Pratima, Yourick Miranda R, Carleton Karen L
Association between CFH, CFB, ARMS2, SERPINF1, VEGFR1 and VEGF polymorphisms and anatomical and functional response to ranibizumab treatment in neovascular age-related macular degeneration.
Acta ophthalmologica | 2018-03-01 | PMID 28926193
Cobos Estefania, Recalde Sergio, Anter Jaouad and 11 more
Genes: CFB, CFH, SERPINF1, ARMS2, VEGFA
Retinal dysfunction characterizes subtypes of dominant optic atrophy.
Acta ophthalmologica | 2018-03-01 | PMID 28926202
Cascavilla Maria Lucia, Parisi Vincenzo, Triolo Giacinto and 11 more
Genes: OPA1
Structure-Function Studies of Artemisia tridentata Farnesyl Diphosphate Synthase and Chrysanthemyl Diphosphate Synthase by Site-Directed Mutagenesis and Morphogenesis.
Journal of the American Chemical Society | 2017-10-18 | PMID 28926242
Lee J Scott, Pan Jian-Jung, Ramamoorthy Gurusankar and 1 more
Genes: IPP, LPP
Synthesis and Analysis of Bacterial Folate Metabolism Intermediates and Antifolates.
Organic letters | 2017-10-06 | PMID 28926267
Dawadi Surendra, Kordus Shannon L, Baughn Anthony D and 1 more
VEGF Polymorphisms Among Neovascular Age-Related Macular Degenerative Subjects in a Multiethnic Population.
Genetic testing and molecular biomarkers | 2017-10-01 | PMID 28926292
Mohamad Nur Afiqah, Ramachandran Vasudevan, Ismail Patimah and 7 more
Vitamin D status, serum lipid concentrations, and vitamin D receptor (VDR) gene polymorphisms in Familial Mediterranean fever.
Bosnian journal of basic medical sciences | 2018-02-20 | PMID 28926322
Turhan Turan, Doğan Halef Okan, Boğdaycioğlu Nihal and 5 more
Genes: VDR
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G.
Acta medica portuguesa | 2017-08-31 | PMID 28926334
Alves Daniela, Calmeiro Maria Eufémia, Macário Carmo and 1 more
Time to first positive HIV-1 DNA PCR may differ with antiretroviral regimen in infants infected with non-B subtype HIV-1.
AIDS (London, England) | 2017-11-28 | PMID 28926397
Balasubramanian Raji, Fowler Mary Glenn, Dominguez Kenneth and 11 more
Ontogeny and function of murine epidermal Langerhans cells.
Nature immunology | 2017-09-19 | PMID 28926543
Kaplan Daniel H
A SNP panel and online tool for checking genotype concordance through comparing QR codes.
PloS one | 2017-01-01 | PMID 28926565
Du Yonghong, Martin Joshua S, McGee John and 8 more
Genes: ABO
Whole-genome sequencing illuminates the evolution and spread of multidrug-resistant tuberculosis in Southwest Nigeria.
PloS one | 2017-01-01 | PMID 28926571
Senghore Madikay, Otu Jacob, Witney Adam and 12 more
Functional characterization of zebrafish orthologs of the human Beta 3-Glucosyltransferase B3GLCT gene mutated in Peters Plus Syndrome.
PloS one | 2017-01-01 | PMID 28926587
Weh Eric, Takeuchi Hideyuki, Muheisen Sanaa and 2 more
Assessment of common somatic mutations of EGFR, KRAS, BRAF, NRAS in pulmonary non-small cell carcinoma using iPLEX® HS, a new highly sensitive assay for the MassARRAY® System.
PloS one | 2017-01-01 | PMID 28926605
Sutton Bobbie C, Birse Ryan T, Maggert Kevin and 10 more
Genes: BRAF, EGFR, KRAS, NRAS
Risk analysis of inter-species reassortment through a Rift Valley fever phlebovirus MP-12 vaccine strain.
PloS one | 2017-01-01 | PMID 28926632
Ly Hoai J, Lokugamage Nandadeva, Nishiyama Shoko and 1 more
Association between X-ray repair cross-complementing group 1(XRCC1) Arg399Gln polymorphism and endometriosis: A systematic review and meta-analysis.
European journal of obstetrics, gynecology, and reproductive biology | 2017-11-01 | PMID 28926725
Lv Mo-Qi, Wang Jin, Yu Xiao-Qing and 4 more
Genes: XRCC1
A Distinctive Ictal Amplitude-Integrated Electroencephalography Pattern in Newborns with Neonatal Epilepsy Associated with KCNQ2 Mutations.
Neonatology | 2017-01-01 | PMID 28926830
Vilan Ana, Mendes Ribeiro José, Striano Pasquale and 5 more
Genes: KCNQ2
Multiparameter Investigation of a 46,XX/46,XY Tetragametic Chimeric Phenotypical Male Patient with Bilateral Scrotal Ovotestes and Ovulatory Activity.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation | 2018-01-01 | PMID 28926831
van Bever Yolande, Wolffenbuttel Katja P, Brüggenwirth Hennie T and 11 more
Heme Oxygenase Activity and Heme Binding in a Neonatal Mouse Model.
Neonatology | 2017-01-01 | PMID 28926834
Kourula Stephanie, Ang Joyce, Zhao Hui and 5 more
The Genetic Basis of Delayed Puberty.
Neuroendocrinology | 2018-01-01 | PMID 28926843
Howard Sasha R, Dunkel Leo
[Parsonage-Turner Syndrome - Case Report].
Zeitschrift fur Orthopadie und Unfallchirurgie | 2017-12-01 | PMID 28926848
Katzer Alexander, Niedermauntel Wolf-Peter, Rump Jörg
Polycystic Ovary Syndrome (PCOS) in Juvenile and Adult Type 1 Diabetes in a German/Austrian Cohort.
Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association | 2017-11-01 | PMID 28926868
Reinauer Christina, Bollow Esther, Fröhlich-Reiterer Elke and 11 more
Genes: SDS
Mini-Review: The Contribution of Intermediate Phenotypes to GxE Effects on Disorders of Body Composition in the New OMICS Era.
International journal of environmental research and public health | 2017-09-17 | PMID 28926971
Nava-Gonzalez Edna J, Gallegos-Cabriales Esther C, Leal-Berumen Irene and 1 more
Frequency and Clinicopathologic Features of RUNX1 Mutations in Patients With Acute Myeloid Leukemia Not Otherwise Specified.
American journal of clinical pathology | 2017-07-01 | PMID 28927163
You Eunkyoung, Cho Young-Uk, Jang Seongsoo and 10 more
Genes: RUNX1, ASXL1, FLT3, NPM1, TET2
The intricate interplay between MSI and polymorphisms of DNA repair enzymes in gastric cancer H.pylori associated.
Mutagenesis | 2017-07-01 | PMID 28927196
Silva-Fernandes Isabelle Joyce de Lima, Oliveira Emanuele Silva de, Santos Juliana Carvalho and 5 more
Genes: ERCC1, XRCC3, MGMT, RAD51
Female ClockΔ19/Δ19 mice are protected from the development of age-dependent cardiomyopathy.
Cardiovascular research | 2018-02-01 | PMID 28927226
Alibhai Faisal J, Reitz Cristine J, Peppler Willem T and 5 more
Genes: CLOCK
Multi-azole-resistant strains of Cryptococcus neoformans var. grubii isolated from a FLZ-resistant strain by culturing in medium containing voriconazole.
Medical mycology | 2017-11-01 | PMID 28927230
Kano Rui, Okubo Miki, Hasegawa Atsuhiko and 1 more
Metabolic Profiling of Central Nervous System Disease in Trypanosoma brucei rhodesiense Infection.
The Journal of infectious diseases | 2017-12-05 | PMID 28927234
Lamour Sabrina D, Alibu Vincent P, Holmes Elaine and 1 more
Comparison of allele-specific PCR, created restriction-site PCR, and PCR with primer-introduced restriction analysis methods used for screening complex vertebral malformation carriers in Holstein cattle.
Journal of veterinary science | 2017-12-31 | PMID 28927256
Avanus Kozet, Altınel Ahmet
HDAC11 Inhibits Myoblast Differentiation through Repression of MyoD-Dependent Transcription.
Molecules and cells | 2017-09-30 | PMID 28927261
Byun Sang Kyung, An Tae Hyeon, Son Min Jeong and 8 more
Genes: HDAC11, MYOG
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report.
BMC medical genetics | 2017-09-19 | PMID 28927399
Bánfai Zsolt, Hadzsiev Kinga, Pál Endre and 4 more
Genes: MYH7
The Arg282Ser missense mutation in APOA5 gene determines a reduction of triglyceride and LDL-cholesterol in children, together with low serum levels of apolipoprotein A-V.
Lipids in health and disease | 2017-09-19 | PMID 28927406
Bertoccini Laura, Sentinelli Federica, Incani Michela and 8 more
Genes: APOA5
A systematic review and integrative approach to decode the common molecular link between levodopa response and Parkinson's disease.
BMC medical genomics | 2017-09-19 | PMID 28927418
Guin Debleena, Mishra Manish Kumar, Talwar Puneet and 4 more
Genes: COMT, DRD2, FYN, HOMER1, MTHFR, SNCA, SRC, UBC
First molecular detection and characterization of zoonotic Bartonella species in fleas infesting domestic animals in Tunisia.
Parasites & vectors | 2017-09-19 | PMID 28927427
Zouari Saba, Khrouf Fatma, M'ghirbi Youmna and 1 more
Current status of insecticide resistance among malaria vectors in Kenya.
Parasites & vectors | 2017-09-19 | PMID 28927428
Ondeto Benyl M, Nyundo Christopher, Kamau Luna and 6 more
Neurochemical and behavioral characterization of neuronal glutamate transporter EAAT3 heterozygous mice.
Biological research | 2017-09-19 | PMID 28927446
González Luis F, Henríquez-Belmar Francisca, Delgado-Acevedo Claudia and 5 more
Genetic diversity of Haemonchus contortus isolated from sympatric wild blue sheep (Pseudois nayaur) and sheep in Helan Mountains, China.
Parasites & vectors | 2017-09-19 | PMID 28927469
Shen Dong-Dong, Wang Ji-Fei, Zhang Dan-Yu and 6 more
A vascular endothelial growth factor A genetic variant is associated with improved ventricular function and transplant-free survival after surgery for non-syndromic CHD.
Cardiology in the young | 2018-01-01 | PMID 28927471
Mavroudis Constantine D, Seung Kim Daniel, Burnham Nancy and 15 more
Genes: VEGFA, SOD2
Alpha-1-antitrypsin deficiency: Genetic variations, clinical manifestations and therapeutic interventions.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927525
Hazari Younis Mohammad, Bashir Arif, Habib Mudasir and 7 more
Putative biomarkers for cervical cancer: SNVs, methylation and expression profiles.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927526
Cardoso Maria de Fátima Senra, Castelletti Carlos Henrique Madeiros, Lima-Filho José Luiz de and 2 more
Genes: APC, CDH1, CDH13, FHIT, MLH1, PTEN, TERT, WIF1
DNA mismatch repair and its many roles in eukaryotic cells.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927527
Liu Dekang, Keijzers Guido, Rasmussen Lene Juel
Genes: EXO1
Discriminating RNA variants with single-molecule allele-specific FISH.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927531
Urbanek Martyna O, Krzyzosiak Wlodzimierz J
From sperm to offspring: Assessing the heritable genetic consequences of paternal smoking and potential public health impacts.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927533
Beal Marc A, Yauk Carole L, Marchetti Francesco
Alternative RNA splicing and gastric cancer.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927534
Li Ying, Yuan Yuan
Advances in ligase chain reaction and ligation-based amplifications for genotyping assays: Detection and applications.
Mutation research. Reviews in mutation research | 2017-07-01 | PMID 28927538
Gibriel Abdullah A, Adel Ola
Comparative study of clinical presentation and hematological indices in hospitalized sickle cell patients with severe Plasmodium falciparum malaria.
Journal of infection and public health | 2000-01-01 | PMID 28927555
Purohit Prasanta, Mohanty Pradeep K, Patel Siris and 3 more
CACNA1A-related early-onset encephalopathy with myoclonic epilepsy: A case report.
Brain & development | 2018-02-01 | PMID 28927557
Hayashida Takuya, Saito Yoshiaki, Ishii Atsushi and 6 more
A pilot study to expand treatment of chronic hepatitis C in resource-limited settings.
Antiviral research | 2017-10-01 | PMID 28927676
Mathur Poonam, Comstock Emily, McSweegan Edward and 3 more
Extended-spectrum β-lactamase-producing Escherichia coli bacteremia: Comparison of pediatric and adult populations.
Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi | 2018-12-01 | PMID 28927684
Tsai Wan-Lin, Hung Chih-Hsin, Chen Hui-An and 7 more
Temporal Trends in the Levels of Peripherally Circulating Leukocyte Subtypes in the Hours after Ischemic Stroke.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association | 2018-01-01 | PMID 28927686
Gill Dipender, Sivakumaran Prasanthi, Aravind Adarsh and 3 more
Comparative genomics of four Mycoplasma species of the human urogenital tract: Analysis of their core genomes and virulence genes.
International journal of medical microbiology : IJMM | 2017-12-01 | PMID 28927691
Roachford Orville St E, Nelson Karen E, Mohapatra Bidyut R
Apolipoprotein M gene single nucleotide polymorphisms discovery in patients with chronic obstructive pulmonary disease and determined by the base-quenched probe technique.
Gene | 2017-12-30 | PMID 28927745
Yu Yang, Zhang Jun, Qiao Yingying and 7 more
Protein kinase CK2 inhibition suppresses neointima formation via a proline-rich homeodomain-dependent mechanism.
Vascular pharmacology | 2017-12-01 | PMID 28927755
Wadey K S, Brown B A, Sala-Newby G B and 3 more
A novel role for ciliary function in atopy: ADGRV1 and DNAH5 interactions.
The Journal of allergy and clinical immunology | 2018-05-01 | PMID 28927820
Sugier Pierre-Emmanuel, Brossard Myriam, Sarnowski Chloé and 11 more
Genes: ADGRV1, DNAH5
TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2018-01-01 | PMID 28927886
Blaschek Astrid, V Kries Rüdiger, Lohse Peter and 6 more
Genes: MEFV
The Effect of Water Hardness on Surfactant Deposition after Washing and Subsequent Skin Irritation in Atopic Dermatitis Patients and Healthy Control Subjects.
The Journal of investigative dermatology | 2018-01-01 | PMID 28927888
Danby Simon G, Brown Kirsty, Wigley Andrew M and 4 more
Genes: FLG
Association of ACVRL1 Genetic Polymorphisms with Arteriovenous Malformations: A Case-Control Study and Meta-Analysis.
World neurosurgery | 2017-12-01 | PMID 28927913
Ge Mingxu, Du Chigang, Li Zhaona and 4 more
Genes: ACVRL1
The interaction of polymorphisms in extracellular matrix genes and underlying miRNA motifs that modulate susceptibility to anterior cruciate ligament rupture.
Journal of science and medicine in sport | 2018-01-01 | PMID 28927971
Willard Kyle, Mannion Sasha, Saunders Colleen J and 2 more
Genes: BGN, DCN
Infiltration of polarized macrophages associated with liver fibrosis in infants with biliary atresia.
Journal of pediatric surgery | 2017-12-01 | PMID 28927974
Yang Yifan, Dong Rui, Zheng Chao and 2 more
Identification of susceptible genes for complex chronic diseases based on disease risk functional SNPs and interaction networks.
Journal of biomedical informatics | 2017-10-01 | PMID 28927989
Li Wan, Zhu Lina, Huang Hao and 5 more
Dendritic Homeostasis Disruption in a Novel Frontotemporal Dementia Mouse Model Expressing Cytoplasmic Fused in Sarcoma.
EBioMedicine | 2017-10-01 | PMID 28928015
Shiihashi Gen, Ito Daisuke, Arai Itaru and 7 more
Genes: FUS
Electrophysiological analyses of transgenic mice overexpressing KCNJ8 with S422L mutation in cardiomyocytes.
Journal of pharmacological sciences | 2017-09-01 | PMID 28928055
Watanabe Yasuhiro, Matsumoto Akio, Miki Takashi and 3 more
Genes: KCNJ8
miR-338-3p confers 5-fluorouracil resistance in p53 mutant colon cancer cells by targeting the mammalian target of rapamycin.
Experimental cell research | 2017-11-15 | PMID 28928082
Han Jia, Li Jie, Tang Kaijie and 4 more
PDZ domain containing protein 1 (PDZK1), a modulator of membrane proteins, is regulated by the nuclear receptor THRβ.
Molecular and cellular endocrinology | 2018-02-05 | PMID 28928085
Ferreira Celio, Prestin Katharina, Hussner Janine and 2 more
Genes: PDZK1
Complement factor H in AMD: Bridging genetic associations and pathobiology.
Progress in retinal and eye research | 2018-01-01 | PMID 28928087
Toomey Christopher B, Johnson Lincoln V, Bowes Rickman Catherine
Genes: CFH, RPE