Cell cycle-independent furrowing triggered by phosphomimetic mutations of the INCENP STD motif requires Plk1.
Journal of cell science | 2019-11-06 | PMID 31601613
Papini Diana, Fant Xavier, Ogawa Hiromi and 7 more
Genes: INCENP, ROCK1
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 7917 of 10600
Contribution of retrotransposition to developmental disorders.
Nature communications | 2019-10-11 | PMID 31604926
Gardner Eugene J, Prigmore Elena, Gallone Giuseppe and 16 more
Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium.
International journal of epidemiology | 2020-02-01 | PMID 31605532
Kapoor Pooja Middha, Lindström Sara, Behrens Sabine and 13 more
Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.
Cell | 2019-10-17 | PMID 31607513
Peterson Roseann E, Kuchenbaecker Karoline, Walters Raymond K and 28 more
Germ-line genetic variation in the immunoglobulin heavy chain creates stroke susceptibility in the spontaneously hypertensive rat.
Physiological genomics | 2019-11-01 | PMID 31608789
Dhande Isha S, Kneedler Sterling C, Joshi Aniket S and 5 more
Genes: FABP4
Polygenic burden in focal and generalized epilepsies.
Brain : a journal of neurology | 2019-11-01 | PMID 31608925
Leu Costin, Stevelink Remi, Smith Alexander W and 17 more
Myxoid glioneuronal tumor, PDGFRA p.K385-mutant: clinical, radiologic, and histopathologic features.
Brain pathology (Zurich, Switzerland) | 2020-05-01 | PMID 31609499
Lucas Calixto-Hope G, Villanueva-Meyer Javier E, Whipple Nicholas and 32 more
Genes: PDGFRA
Novel genetic variants in KIF16B and NEDD4L in the endosome-related genes are associated with nonsmall cell lung cancer survival.
International journal of cancer | 2020-07-15 | PMID 31618441
Yang Sen, Tang Dongfang, Zhao Yu C and 9 more
Genes: KIF16B, NEDD4L
Limited Intrahost Diversity and Background Evolution Accompany 40 Years of Canine Parvovirus Host Adaptation and Spread.
Journal of virology | 2019-12-12 | PMID 31619551
Voorhees Ian E H, Lee Hyunwook, Allison Andrew B and 9 more
Different mutation profiles between epithelium and stroma in endometriosis and normal endometrium.
Human reproduction (Oxford, England) | 2019-10-02 | PMID 31621846
Suda Kazuaki, Nakaoka Hirofumi, Yoshihara Kosuke and 6 more
Genes: KRAS, PIK3CA
TRIM39-RPP21 Variants (∆19InsCCC) Are Not Associated with Juvenile Idiopathic Epilepsy in Egyptian Arabian Horses.
Genes | 2019-10-16 | PMID 31623255
Rivas Victor N, Aleman Monica, Peterson Janel A and 3 more
Genes: TRIM39, RPP21
De novo and recessive forms of congenital heart disease have distinct genetic and phenotypic landscapes.
Nature communications | 2019-10-17 | PMID 31624253
Watkins W Scott, Hernandez E Javier, Wesolowski Sergiusz and 17 more
Sperm morphology and count vary with fine-scale changes in local density in a wild lizard population.
Oecologia | 2019-11-01 | PMID 31624957
Kustra Matthew C, Kahrl Ariel F, Reedy Aaron M and 2 more
Stoichiometric optimization of Gata4, Hand2, Mef2c, and Tbx5 expression for contractile cardiomyocyte reprogramming.
Scientific reports | 2019-10-18 | PMID 31628386
Zhang Zhentao, Zhang Wenhui, Nam Young-Jae
Genetic and genomic studies of pathogenic EXOSC2 mutations in the newly described disease SHRF implicate the autophagy pathway in disease pathogenesis.
Human molecular genetics | 2020-03-13 | PMID 31628467
Yang Xue, Bayat Vafa, DiDonato Nataliya and 10 more
Genes: EXOSC2, MITF
Dual Roles for the TSPYL Family in Mediating Serotonin Transport and the Metabolism of Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.
Clinical pharmacology and therapeutics | 2020-03-01 | PMID 31628858
Qin Sisi, Eugene Andy R, Liu Duan and 6 more
Genes: CYP2C19, TSPYL1, CYP2C9, CYP3A4, SLC6A4
A Comprehensive Resource for Induced Pluripotent Stem Cells from Patients with Primary Tauopathies.
Stem cell reports | 2019-11-12 | PMID 31631020
Karch Celeste M, Kao Aimee W, Karydas Anna and 31 more
Genes: MAPT
Re-programing Chromatin with a Bifunctional LSD1/HDAC Inhibitor Induces Therapeutic Differentiation in DIPG.
Cancer cell | 2019-11-11 | PMID 31631026
Anastas Jamie N, Zee Barry M, Kalin Jay H and 18 more
Genes: KDM1A
Metabolomic profiling identifies pathways associated with minimal residual disease in childhood acute lymphoblastic leukaemia.
EBioMedicine | 2019-10-01 | PMID 31631039
Schraw Jeremy M, Junco Jacob J, Brown Austin L and 3 more
Genes: NAMPT
MIBI-TOF: A multiplexed imaging platform relates cellular phenotypes and tissue structure.
Science advances | 2019-10-01 | PMID 31633026
Keren Leeat, Bosse Marc, Thompson Steve and 16 more
Engineered Reader Proteins for Enhanced Detection of Methylated Lysine on Histones.
ACS chemical biology | 2020-01-17 | PMID 31634430
Albanese Katherine I, Krone Mackenzie W, Petell Christopher J and 4 more
Genes: CBX1
Contribution and Interaction of Shiga Toxin Genes to Escherichia coli O157:H7 Virulence.
Toxins | 2019-10-18 | PMID 31635282
Tarr Gillian A M, Stokowski Taryn, Shringi Smriti and 5 more
Global selective sweep of a highly inbred genome of the cattle parasite Neospora caninum.
Proceedings of the National Academy of Sciences of the United States of America | 2019-11-05 | PMID 31636194
Khan Asis, Fujita Ayako Wendy, Randle Nadine and 16 more
Molecular features of the UNC-45 chaperone critical for binding and folding muscle myosin.
Nature communications | 2019-10-21 | PMID 31636255
Hellerschmied Doris, Lehner Anita, Franicevic Nina and 9 more
Analyses of FGFR3 and PIK3CA mutations in neuroblastomas and the effects of the corresponding inhibitors on neuroblastoma cell lines.
International journal of oncology | 2019-12-01 | PMID 31638167
Kostopoulou Ourania N, Holzhauser Stefan, Lange Birthe K A and 5 more
Whole‑exome sequencing in Russian children with non‑type 1 diabetes mellitus reveals a wide spectrum of genetic variants in MODY‑related and unrelated genes.
Molecular medicine reports | 2019-12-01 | PMID 31638168
Glotov Oleg S, Serebryakova Elena A, Turkunova Mariia E and 27 more
Idiopathic renal hypouricemia: A case report and literature review.
Molecular medicine reports | 2019-12-01 | PMID 31638209
Wang Cuiyu, Wang Jin, Liu Song and 5 more
Dynamic features of liver fibrogenesis and fibrosis resolution in the absence of matrix metalloproteinase‑9.
Molecular medicine reports | 2019-12-01 | PMID 31638220
Wang Quanrongzi, Liu Xisheng, Zhang Jie and 3 more
Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy.
Molecular medicine reports | 2019-12-01 | PMID 31638223
Wang Bo, Wang Jing, Wang Li-Feng and 9 more
Mutations of RAS genes in endometrial polyps.
Oncology reports | 2019-12-01 | PMID 31638232
Takeda Takashi, Banno Kouji, Kobayashi Yusuke and 5 more
Potential function of microRNAs in thoracic aortic aneurysm and thoracic aortic dissection pathogenesis.
Molecular medicine reports | 2019-12-01 | PMID 31638233
Senturk Tugce, Antal Arzu, Gunel Tuba
Novel compound heterozygous PKHD1 mutations cause autosomal recessive polycystic kidney disease in a Han Chinese family.
Molecular medicine reports | 2019-12-01 | PMID 31638247
Wang Jin, Qi Dandan, Yang Jialiang and 4 more
Gene mutation profile and risk stratification in AML1‑ETO‑positive acute myeloid leukemia based on next‑generation sequencing.
Oncology reports | 2019-12-01 | PMID 31638252
Yu Guopan, Yin Changxin, Wu Fuqun and 7 more
Early‑onset epilepsy and microcephaly‑capillary malformation syndrome caused by a novel STAMBP mutation in a Chinese boy.
Molecular medicine reports | 2019-12-01 | PMID 31638258
Wu Fangrui, Dai Ying, Wang Juan and 9 more
Intersected functional zone of transcriptional regulators patterns stemness within stem cell niche of root apical meristem.
Journal of integrative plant biology | 2020-07-01 | PMID 31638324
Xu Meizhi, Gu Xu, Liang Nengsong and 5 more
Arginine- but not alanine-rich carboxy-termini trigger nuclear translocation of mutant keratin 10 in ichthyosis with confetti.
Journal of cellular and molecular medicine | 2019-12-01 | PMID 31638346
Renz Patricia, Imahorn Elias, Spoerri Iris and 8 more
The utility of MODY Probability Calculator in probands of families with early-onset autosomal dominant diabetes from Poland.
Minerva medica | 2019-12-01 | PMID 31638358
Hohendorff Jerzy, Zapala Barbara, Ludwig-Slomczynska Agnieszka H and 6 more
Diagnostics of Hereditary Connective Tissue Disorders by Genetic Next-Generation Sequencing.
Genetic testing and molecular biomarkers | 2019-11-01 | PMID 31638417
Pope Marita Knudsen, Ratajska Aleksandra, Johnsen Hilde and 3 more
A Novel CDH1 Mutation Causing Reduced E-Cadherin Dimerization Is Associated with Nonsyndromic Cleft Lip With or Without Cleft Palate.
Genetic testing and molecular biomarkers | 2019-11-01 | PMID 31638429
Du Shiyue, Yang Yujie, Yi Ping and 13 more
Is ultra wide-field retinal imaging alone appropriate for retinal angioma screening in lower risk subjects attending Von Hippel-Lindau (VHL) clinics?
Ophthalmic genetics | 2019-10-01 | PMID 31638449
Mansfield Smith S, Makam R, Sullivan L and 2 more
Presence of corneal crystals confirms an unusual presentation of Bietti's retinal dystrophy.
Ophthalmic genetics | 2019-10-01 | PMID 31638456
Song Won Kyung, Clouston Penny, MacLaren Robert E
Early nutrition in combination with polymorphisms in fatty acid desaturase gene cluster modulate fatty acid composition of cheek cells' glycerophospholipids in school-age children.
The British journal of nutrition | 2019-09-01 | PMID 31638497
Martínez-Zaldívar Cristina, Azaryah Hatim, García-Santos José A and 6 more
Review of SRD5A3 Disease-Causing Sequence Variants and Ocular Findings in Steroid 5α-Reductase Type 3 Congenital Disorder of Glycosylation, and a Detailed New Case.
Folia biologica | 2019-01-01 | PMID 31638560
Kousal B, Honzík T, Hansíková H and 7 more
Metabolic Tools for Identification of New Mutations of Enzymes Engaged in Purine Synthesis Leading to Neurological Impairment.
Folia biologica | 2019-01-01 | PMID 31638562
Krijt M, Souckova O, Baresova V and 2 more
Hedgehog signaling promotes tumor-associated macrophage polarization to suppress intratumoral CD8+ T cell recruitment.
The Journal of clinical investigation | 2019-12-02 | PMID 31638600
Petty Amy J, Li Ang, Wang Xinyi and 5 more
Hyperuricemia and gout caused by missense mutation in d-lactate dehydrogenase.
The Journal of clinical investigation | 2019-12-02 | PMID 31638601
Drabkin Max, Yogev Yuval, Zeller Lior and 9 more
Paroxysmal nocturnal hemoglobinuria without GPI-anchor deficiency.
The Journal of clinical investigation | 2019-12-02 | PMID 31638602
Brodsky Robert A
Superficial Nodular Fasciitis With Atypical Presentations: Report of 3 Cases and Review of Recent Molecular Genetics.
The American Journal of dermatopathology | 2019-12-01 | PMID 31638603
Maloney Nolan, LeBlanc Robert E, Sriharan Aravindhan and 2 more
Detection and molecular characterization of respiratory viruses that cause acute respiratory infection in the adult population.
Gaceta medica de Mexico | 2019-01-01 | PMID 31638611
Díaz-Chiguer Dylan Lucía, Tirado-Mendoza Rocío, Márquez-Navarro Adrián and 5 more
An in silico Approach for Integrating Phenotypic and Target-based Approaches in Drug Discovery.
Molecular informatics | 2020-01-01 | PMID 31638744
Iwata Hiroaki, Kojima Ryosuke, Okuno Yasushi
New Case Detection by Cascade Testing in Familial Hypercholesterolemia: A Systematic Review of the Literature.
Circulation. Genomic and precision medicine | 2019-11-01 | PMID 31638829
Lee Christopher, Rivera-Valerio Miriannie, Bangash Hana and 2 more
MRAS Variants Cause Cardiomyocyte Hypertrophy in Patient-Specific Induced Pluripotent Stem Cell-Derived Cardiomyocytes: Additional Evidence for MRAS as a Definitive Noonan Syndrome-Susceptibility Gene.
Circulation. Genomic and precision medicine | 2019-11-01 | PMID 31638832
Higgins Erin M, Bos J Martijn, Dotzler Steven M and 2 more
Prevalence and Electronic Health Record-Based Phenotype of Loss-of-Function Genetic Variants in Arrhythmogenic Right Ventricular Cardiomyopathy-Associated Genes.
Circulation. Genomic and precision medicine | 2019-11-01 | PMID 31638835
Carruth Eric D, Young Wilson, Beer Dominik and 14 more
Using imputation-based whole-genome sequencing data to improve the accuracy of genomic prediction for combined populations in pigs.
Genetics, selection, evolution : GSE | 2019-10-21 | PMID 31638889
Song Hailiang, Ye Shaopan, Jiang Yifan and 3 more
A framework for TRIM21-mediated protein depletion in early mouse embryos: recapitulation of Tead4 null phenotype over three days.
BMC genomics | 2019-10-21 | PMID 31638890
Israel Steffen, Casser Ellen, Drexler Hannes C A and 2 more
Genetic diversity and population structure of the sweet leaf herb, Stevia rebaudiana B., cultivated and landraces germplasm assessed by EST-SSRs genotyping and steviol glycosides phenotyping.
BMC plant biology | 2019-10-21 | PMID 31638900
Cosson Patrick, Hastoy Cécile, Errazzu Luis Ernesto and 4 more
Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness - a case report for dual diagnosis.
BMC pediatrics | 2019-10-21 | PMID 31638924
Zhang Yan, Zhang Yi, Zhang Victor Wei and 3 more
MMP-8 C-799 T, Lys460Thr, and Lys87Glu variants are not related to risk of cancer.
BMC medical genetics | 2019-10-21 | PMID 31638929
Zhang Li-Feng, Zhu Li-Jie, Zhang Wei and 6 more
Validation of computational determination of microsatellite status using whole exome sequencing data from colorectal cancer patients.
BMC cancer | 2019-10-21 | PMID 31638937
Johansen Amanda Frydendahl Boll, Kassentoft Christine Gaasdal, Knudsen Michael and 6 more
Phylogenetic characterization of the energy taxis receptor Aer in Pseudomonas and phenotypic characterization in Pseudomonas pseudoalcaligenes KF707.
Microbiology (Reading, England) | 2019-12-01 | PMID 31639075
Booth Sean C, Turner Raymond J
Targetable cellular signaling events mediate vascular pathology in vascular Ehlers-Danlos syndrome.
The Journal of clinical investigation | 2020-02-03 | PMID 31639107
Bowen Caitlin J, Calderón Giadrosic Juan Francisco, Burger Zachary and 6 more
Genotyping and antimicrobial resistance of Streptococcus uberis isolated from bovine clinical mastitis.
PloS one | 2019-01-01 | PMID 31639136
Tomazi Tiago, Freu Gustavo, Alves Bruna Gomes and 3 more
Korean soybean core collection: Genotypic and phenotypic diversity population structure and genome-wide association study.
PloS one | 2019-01-01 | PMID 31639154
Jeong Namhee, Kim Ki-Seung, Jeong Seongmun and 10 more
Allele-specific enhancer interaction at the Peg3 imprinted domain.
PloS one | 2019-01-01 | PMID 31639176
Kim Joomyeong, Frey Wesley D, Sharma Kaustubh and 3 more
Diversification and independent polyploid origins in the disjunct species Alyssum repens from the Southeastern Alps and the Carpathians.
American journal of botany | 2019-11-01 | PMID 31639199
Melichárková Andrea, Španiel Stanislav, Marhold Karol and 3 more
The formation of perinucleolar bodies is important for normal leaf development and requires the zinc-finger DNA-binding motif in Arabidopsis ASYMMETRIC LEAVES2.
The Plant journal : for cell and molecular biology | 2020-03-01 | PMID 31639235
Luo Lilan, Ando Sayuri, Sakamoto Yuki and 11 more
Mutations in the sonic hedgehog pathway cause macrocephaly-associated conditions due to crosstalk to the PI3K/AKT/mTOR pathway.
American journal of medical genetics. Part A | 2019-12-01 | PMID 31639285
Klein Steven D, Nguyen Dzung C, Bhakta Viraj and 4 more
Genes: PTCH1, PTEN, SHH, SUFU
Growth patterns for untreated individuals with MPS I: Report from the international MPS I registry.
American journal of medical genetics. Part A | 2019-12-01 | PMID 31639289
Viskochil David, Clarke Lorne A, Bay Luisa and 3 more
Leber congenital amaurosis: Current genetic basis, scope for genetic testing and personalized medicine.
Experimental eye research | 2019-12-01 | PMID 31639339
Kondkar Altaf A, Abu-Amero Khaled K
Long non-coding RNAs and nuclear factor-κB crosstalk in cancer and other human diseases.
Biochimica et biophysica acta. Reviews on cancer | 2020-01-01 | PMID 31639408
Gupta Subash C, Awasthee Nikee, Rai Vipin and 3 more
Functional screening of GATOR1 complex variants reveals a role for mTORC1 deregulation in FCD and focal epilepsy.
Neurobiology of disease | 2020-02-01 | PMID 31639411
Dawson Ruby E, Nieto Guil Alvaro F, Robertson Louise J and 3 more
EGFR-mediated autophagy in tumourigenesis and therapeutic resistance.
Cancer letters | 2020-01-28 | PMID 31639425
Wu Min, Zhang Pinghu
Genome-wide SNP marker discovery and phylogenetic analysis of mulberry varieties using double-digest restriction site-associated DNA sequencing.
Gene | 2020-02-05 | PMID 31639429
Muhonja Linah, Yamanouchi Hiroaki, Yang Ching-Chia and 5 more
Multiple genetic mutations implicate spectrum of phenotypes in Bardet-Biedl syndrome.
Gene | 2020-01-30 | PMID 31639430
Chakrabarty Sanjiban, Savantre Swheta B, Ramachandra Bhat C and 1 more
NLRP3 is associated with coronary artery disease in Vietnam veterans.
Gene | 2020-01-30 | PMID 31639433
Akosile Wole, Voisey Joanne, Lawford Bruce and 3 more
Reprograming of peripheral Foxp3+ regulatory T cell towards Th17-like cell in patients with active systemic lupus erythematosus.
Clinical immunology (Orlando, Fla.) | 2019-12-01 | PMID 31639448
Jiang Cen, Wang Huaizhou, Xue Minghui and 4 more
A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues.
Mitochondrion | 2020-01-01 | PMID 31639449
Panadés-de Oliveira Luísa, Montoya Julio, Emperador Sonia and 7 more
Effects of sclerostin on lipopolysaccharide-induced inflammatory phenotype in human odontoblasts and dental pulp cells.
The international journal of biochemistry & cell biology | 2019-12-01 | PMID 31639458
Liao Chufang, Wang Yining, Ou Yanjing and 3 more
Phenotypic diversity in an emerging mycoplasmal disease.
Microbial pathogenesis | 2020-01-01 | PMID 31639466
Perez Kailey, Mullen Nathan, Canter Jessica A and 2 more
Whole-genome sequencing of Staphylococcus epidermidis bloodstream isolates from a prospective clinical trial reveals that complicated bacteraemia is caused by a limited number of closely related sequence types.
Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases | 2020-05-01 | PMID 31639470
Shelburne S A, Dib R W, Endres B T and 20 more
New role for crinamine as a potent, safe and selective inhibitor of human monoamine oxidase B: In vitro and in silico pharmacology and modeling.
Journal of ethnopharmacology | 2020-02-10 | PMID 31639490
Naidoo D, Roy A, Slavětínská L Poštová and 3 more
Avian interspecific differences in VKOR activity and inhibition: Insights from amino acid sequence and mRNA expression ratio of VKORC1 and VKORC1L1.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP | 2020-02-01 | PMID 31639498
Nakayama Shouta M M, Morita Ayuko, Ikenaka Yoshinori and 10 more
Accuracy and applicability of different phenotypic methods for carbapenemase detection in Enterobacteriaceae: A systematic review and meta-analysis.
Journal of global antimicrobial resistance | 2020-06-01 | PMID 31639543
Zhong Hong, Wu Meng-Lu, Feng Wen-Juan and 2 more
Extended-spectrum β-lactamase-producing Proteus mirabilis with multidrug resistance isolated from raw chicken in Singapore: Genotypic and phenotypic analysis.
Journal of global antimicrobial resistance | 2019-12-01 | PMID 31639544
Guo Siyao, Aung Kyaw Thu, Tay Moon Y F and 3 more
Application of ultra-high performance liquid chromatography coupled to high-resolution mass spectrometry (Orbitrap™) for the determination of beta-casein phenotypes in cow milk.
Food chemistry | 2020-03-01 | PMID 31639578
Nguyen Duc Doan, Solah Vicky Ann, Busetti Francesco and 2 more
Relevance of calcification and contrast enhancement pattern for molecular diagnosis and survival prediction of gliomas based on the 2016 World Health Organization Classification.
Clinical neurology and neurosurgery | 2019-12-01 | PMID 31639630
Michiwaki Yuhei, Hata Nobuhiro, Mizoguchi Masahiro and 11 more
Dimethylarginine Dimethylaminohydrolase 1 Polymorphisms and Venous Intimal Hyperplasia in Hemodialysis Patients.
American journal of nephrology | 2019-01-01 | PMID 31639806
Wu Chih-Cheng, Hsieh Mu-Yang, Lee Chih-Kuo and 3 more
A Thrombin-Activatable Factor X Variant Corrects Hemostasis in a Mouse Model for Hemophilia A.
Thrombosis and haemostasis | 2019-12-01 | PMID 31639831
Muczynski Vincent, Verhenne Sebastien, Casari Caterina and 8 more
Neuropathy Associated with Systemic Amyloidosis.
Seminars in neurology | 2019-10-01 | PMID 31639841
Kaku Michelle, Berk John L
APOE Genotype Differentially Modulates Plasma Lipids in Healthy Older Individuals, with Relevance to Brain Health.
Journal of Alzheimer's disease : JAD | 2019-01-01 | PMID 31640095
Wong Matthew Wai Kin, Braidy Nady, Crawford John and 7 more
Calcilytic NPS 2143 Reduces Amyloid Secretion and Increases sAβPPα Release from PSEN1 Mutant iPSC-Derived Neurons.
Journal of Alzheimer's disease : JAD | 2019-01-01 | PMID 31640098
Lo Giudice Maria, Mihalik Balázs, Turi Zsófia and 2 more
Genome-Wide Methylation of Mild Cognitive Impairment in Mexican Americans Highlights Genes Involved in Synaptic Transport, Alzheimer's Disease-Precursor Phenotypes, and Metabolic Morbidities.
Journal of Alzheimer's disease : JAD | 2019-01-01 | PMID 31640099
Pathak Gita A, Silzer Talisa K, Sun Jie and 6 more
Genes: ALOX12, BCL2L2, CCNY, CPLX3, CTSG, KLHL29, OR2C3, PABPN1
A Genome-Wide Association Study Revealed Key SNPs/Genes Associated With Salinity Stress Tolerance In Upland Cotton.
Genes | 2019-10-21 | PMID 31640174
Yasir Muhammad, He Shoupu, Sun Gaofei and 5 more
Molecular Characterization of Leishmania RNA virus 2 in Leishmaniamajor from Uzbekistan.
Genes | 2019-10-21 | PMID 31640177
Kleschenko Yuliya, Grybchuk Danyil, Matveeva Nadezhda S and 4 more
Gut DNA Virome Diversity and Its Association with Host Bacteria Regulate Inflammatory Phenotype and Neuronal Immunotoxicity in Experimental Gulf War Illness.
Viruses | 2019-10-21 | PMID 31640184
Seth Ratanesh K, Maqsood Rabia, Mondal Ayan and 9 more
The Mechanisms of Mating in Pathogenic Fungi-A Plastic Trait.
Genes | 2019-10-21 | PMID 31640207
Usher Jane
Gene Influence in the Effectiveness of Plant Sterols Treatment in Children: Pilot Interventional Study.
Nutrients | 2019-10-21 | PMID 31640222
San Mauro Martín Ismael, Garicano Vilar Elena, Sanz Rojo Sara and 4 more
The Charcot-Marie Tooth Disease Mutation R94Q in MFN2 Decreases ATP Production but Increases Mitochondrial Respiration under Conditions of Mild Oxidative Stress.
Cells | 2019-10-21 | PMID 31640251
Wolf Christina, Zimmermann Rahel, Thaher Osamah and 5 more
Disclosing the Impact of Carcinogenic SF3b Mutations on Pre-mRNA Recognition Via All-Atom Simulations.
Biomolecules | 2019-10-21 | PMID 31640290
Borišek Jure, Saltalamacchia Andrea, Gallì Anna and 4 more
Mutation of ten-eleven translocation-2 is associated with increased risk of autoimmune disease in patients with myelodysplastic syndrome.
The Korean journal of internal medicine | 2020-03-01 | PMID 31640337
Oh Yoon-Jeong, Shin Dong-Yeop, Hwang Sang Mee and 9 more