Mouse Models in the Study of Mature B-Cell Malignancies.
Cold Spring Harbor perspectives in medicine | 2021-04-01 | PMID 32398289
Pasqualucci Laura, Klein Ulf
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 8145 of 10600
Morbidity and mortality in carriers of the cystic fibrosis mutation CFTR Phe508del in the general population.
The European respiratory journal | 2020-09-01 | PMID 32398304
Çolak Yunus, Nordestgaard Børge G, Afzal Shoaib
Mutations in TAC1B: a Novel Genetic Determinant of Clinical Fluconazole Resistance in Candida auris.
mBio | 2020-05-12 | PMID 32398311
Rybak Jeffrey M, Muñoz José F, Barker Katherine S and 10 more
Core N-Glycan Structures Are Critical for the Pathogenicity of Cryptococcus neoformans by Modulating Host Cell Death.
mBio | 2020-05-12 | PMID 32398313
Thak Eun Jung, Lee Su-Bin, Xu-Vanpala Shengjie and 6 more
Endogenous CRISPR/Cas9 arrays for scalable whole-organism lineage tracing.
Development (Cambridge, England) | 2020-05-12 | PMID 32398353
Cotterell James, Vila-Cejudo Marta, Batlle-Morera Laura and 1 more
Secure large-scale genome-wide association studies using homomorphic encryption.
Proceedings of the National Academy of Sciences of the United States of America | 2020-05-26 | PMID 32398369
Blatt Marcelo, Gusev Alexander, Polyakov Yuriy and 1 more
Genetic susceptibility, inflammation and specific types of depressive symptoms: evidence from the English Longitudinal Study of Ageing.
Translational psychiatry | 2020-05-12 | PMID 32398645
Frank Philipp, Ajnakina Olesya, Steptoe Andrew and 1 more
Do AKT1, COMT and FAAH influence reports of acute cannabis intoxication experiences in patients with first episode psychosis, controls and young adult cannabis users?
Translational psychiatry | 2020-05-12 | PMID 32398646
Hindocha Chandni, Quattrone Diego, Freeman Tom P and 7 more
Pairwise common variant meta-analyses of schizophrenia with other psychiatric disorders reveals shared and distinct gene and gene-set associations.
Translational psychiatry | 2020-05-12 | PMID 32398653
Reay William R, Cairns Murray J
A brief report: de novo copy number variants in children with attention deficit hyperactivity disorder.
Translational psychiatry | 2020-05-12 | PMID 32398668
Martin Joanna, Hosking Grace, Wadon Megan and 7 more
Causal association of circulating cholesterol levels with dementia: a mendelian randomization meta-analysis.
Translational psychiatry | 2020-05-12 | PMID 32398686
Zhang Xiaoyu, Tian Qiuyue, Liu Di and 9 more
Metallothioneins regulate ATP7A trafficking and control cell viability during copper deficiency and excess.
Scientific reports | 2020-05-12 | PMID 32398691
Gudekar Nikita, Shanbhag Vinit, Wang Yanfang and 3 more
Association analysis in a Latin American population revealed ethnic differences in rheumatoid arthritis-associated SNPs in Caucasian and Asian populations.
Scientific reports | 2020-05-12 | PMID 32398702
Castro-Santos P, Verdugo R A, Alonso-Arias R and 8 more
Association of early-onset Alzheimer's disease with germline-generated high affinity self-antigen load.
Translational psychiatry | 2020-05-12 | PMID 32398703
Huang Poyin, Yang Yuan-Han, Chang Ya-Hsuan and 5 more
Quantitative Genetic Assessment of Female Reproductive Traits in a Domesticated Pacific White Shrimp (Penaeus vannamei) Line in China.
Scientific reports | 2020-05-12 | PMID 32398707
Ren Shengjie, Mather Peter B, Prentis Peter and 3 more
Interaction Between Apolipoprotein M Gene Single-Nucleotide Polymorphisms and Obesity and its Effect on Type 2 Diabetes Mellitus Susceptibility.
Scientific reports | 2020-05-12 | PMID 32398715
Liu Dan, Pan Jian-Min, Pei Xiang and 1 more
Conditional GWAS analysis to identify disorder-specific SNPs for psychiatric disorders.
Molecular psychiatry | 2021-06-01 | PMID 32398722
Byrne Enda M, Zhu Zhihong, Qi Ting and 16 more
Genetic Polymorphisms, Mediterranean Diet and Microbiota-Associated Urolithin Metabotypes can Predict Obesity in Childhood-Adolescence.
Scientific reports | 2020-05-12 | PMID 32398726
Cortés-Martín Adrián, Colmenarejo Gonzalo, Selma María Victoria and 1 more
Detection of low-frequency resistance-mediating SNPs in next-generation sequencing data of Mycobacterium tuberculosis complex strains with binoSNP.
Scientific reports | 2020-05-12 | PMID 32398743
Dreyer Viola, Utpatel Christian, Kohl Thomas A and 4 more
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.
Journal of human genetics | 2020-09-01 | PMID 32398759
Li Yuanzhe, Ikeda Aya, Yoshino Hiroyo and 20 more
Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes.
Genetics in medicine : official journal of the American College of Medical Genetics | 2020-08-01 | PMID 32398770
Schönauer Ria, Baatz Sebastian, Nemitz-Kliemchen Melanie and 8 more
Contribution of CTCF binding to transcriptional activity at the HOXA locus in NPM1-mutant AML cells.
Leukemia | 2021-02-01 | PMID 32398790
Ghasemi Reza, Struthers Heidi, Wilson Elisabeth R and 1 more
Genes: CTCF, NPM1, SKAP2, SNX10
Arid1b haploinsufficiency in parvalbumin- or somatostatin-expressing interneurons leads to distinct ASD-like and ID-like behavior.
Scientific reports | 2020-05-12 | PMID 32398858
Smith Amanda L, Jung Eui-Man, Jeon Byeong Tak and 1 more
Whole-genome sequencing of 508 patients identifies key molecular features associated with poor prognosis in esophageal squamous cell carcinoma.
Cell research | 2020-10-01 | PMID 32398863
Cui Yongping, Chen Hongyan, Xi Ruibin and 35 more
Phylogeography of the iconic Australian red-tailed black-cockatoo (Calyptorhynchus banksii) and implications for its conservation.
Heredity | 2020-09-01 | PMID 32398870
Ewart Kyle M, Lo Nathan, Ogden Rob and 6 more
Assessing established BMI variants for a role in nighttime eating behavior in robustly phenotyped Southwestern American Indians.
European journal of clinical nutrition | 2020-12-01 | PMID 32398872
Köroğlu Çiğdem, Gluck Marci E, Traurig Michael and 7 more
The effects of microchipping C57BL/6N mice on standard phenotyping tests.
F1000Research | 2020-01-01 | PMID 32399198
Bains R S, Cater H L, Stewart M and 2 more
Phosphoregulation provides specificity to biomolecular condensates in the cell cycle and cell polarity.
The Journal of cell biology | 2020-07-06 | PMID 32399546
Gerbich Therese M, McLaughlin Grace A, Cassidy Katelyn and 3 more
Protein exchange is reduced in calcium-independent epithelial junctions.
The Journal of cell biology | 2020-06-01 | PMID 32399559
Bartle Emily I, Rao Tejeshwar C, Beggs Reena R and 4 more
Prp5-Spt8/Spt3 interaction mediates a reciprocal coupling between splicing and transcription.
Nucleic acids research | 2020-06-19 | PMID 32399566
Shao Wei, Ding Zhan, Zheng Zeng-Zhang and 6 more
Exposure of a cryptic Hsp70 binding site determines the cytotoxicity of the ALS-associated SOD1-mutant A4V.
Protein engineering, design & selection : PEDS | 2019-12-31 | PMID 32399571
Claes Filip, Rudyak Stanislav, Laird Angela S and 19 more
New Approach to Paediatric Mastocytosis: Implications of KIT D816V Mutation Detection in Peripheral Blood.
Acta dermato-venereologica | 2020-05-28 | PMID 32399575
Czarny Justyna, Żuk Monika, Zawrocki Anton and 8 more
Genomic sequencing highlights the diverse molecular causes of Perrault syndrome: a peroxisomal disorder (PEX6), metabolic disorders (CLPP, GGPS1), and mtDNA maintenance/translation disorders (LARS2, TFAM).
Human genetics | 2020-10-01 | PMID 32399598
Tucker Elena J, Rius Rocio, Jaillard Sylvie and 20 more
Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders.
Human genetics | 2020-11-01 | PMID 32399599
Tran Mau-Them Frederic, Moutton Sebastien, Racine Caroline and 26 more
Speed breeding short-day crops by LED-controlled light schemes.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik | 2020-08-01 | PMID 32399653
Jähne Felix, Hahn Volker, Würschum Tobias and 1 more
Association between LGR4 polymorphisms and peak bone mineral density and body composition.
Journal of bone and mineral metabolism | 2020-09-01 | PMID 32399675
Yu Wei-Jia, Zhang Zeng, Fu Wen-Zhen and 3 more
Screening for genetic mutations in patients with neuropathy without definite etiology is useful.
Journal of neurology | 2020-09-01 | PMID 32399692
Vogt Braden, Chahin Nizar, Wiszniewski Wojciech and 2 more
IL-6, IL-8 and IL-10 polymorphisms may impact predisposition of Alzheimer's disease: a meta-analysis.
Acta neurologica Belgica | 2021-12-01 | PMID 32399737
Yang Rongmei, Duan Jinfeng, Luo Fugang and 2 more
Genomic Strategies Toward Identification of Novel Therapeutic Targets.
Handbook of experimental pharmacology | 2022-01-01 | PMID 32399778
Kessler Thorsten, Schunkert Heribert
Studies on the clinical symptoms, virus distribution, and mRNA expression of several antiviral immunity-related genes in grass carp after infection with genotype II grass carp reovirus.
Archives of virology | 2020-07-01 | PMID 32399788
Wu Minglin, Li Haiyang, Chen Xiaowu and 2 more
Interaction of thrombophilic SNPs in patients with unexplained infertility-multifactor dimensionality reduction (MDR) model analysis.
Journal of assisted reproduction and genetics | 2020-06-01 | PMID 32399796
Milenkovic Jelena, Milojkovic Maja, Mitic Dejan and 5 more
Application of Next-Generation Sequencing in Neurodegenerative Diseases: Opportunities and Challenges.
Neuromolecular medicine | 2021-06-01 | PMID 32399804
Shademan Behrouz, Biray Avci Cigir, Nikanfar Masoud and 1 more
Association of autoimmune regulator gene polymorphism with susceptibility to rheumatoid arthritis in Egyptian population.
Immunologic research | 2020-04-01 | PMID 32399858
A Moneim Nermeen Hassan, Mansour Mona Farouk, Omar Hanan Hassan and 4 more
mRNA and microRNA Profiles in the Amygdala Are Relevant to Susceptibility and Resilience to Psychological Stress Induced in Mice.
Journal of molecular neuroscience : MN | 2020-11-01 | PMID 32399861
Sun Jinyan, Lu Yanjun, Yang Jiuyong and 3 more
Anoctamin 5 (ANO5) muscular dystrophy-three different phenotypes and a new histological pattern.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology | 2020-10-01 | PMID 32399949
Seguí Ferran, Gonzalez-Quereda Lidia, Sanchez Aurora and 6 more
Molecular profiling of Chinese R-CHOP treated DLBCL patients: Identifying a high-risk subgroup.
International journal of cancer | 2020-11-01 | PMID 32399964
Jiang Shiyu, Qin Yan, Jiang Hongxin and 13 more
Bayesian interval mapping of count trait loci based on zero-inflated generalized Poisson regression model.
Biometrical journal. Biometrische Zeitschrift | 2020-10-01 | PMID 32399977
Chi Jinling, Zhou Ying, Chen Lili and 1 more
Influence of ABCB-1, ERCC-1 and ERCC-2 gene polymorphisms on response to capecitabine and oxaliplatin (CAPOX) treatment in colorectal cancer (CRC) patients of South India.
Journal of clinical pharmacy and therapeutics | 2020-08-01 | PMID 32399998
Varma Ashok, Mathaiyan Jayanthi, Shewade Deepak and 2 more
Assessment of associations between clinical and immune microenvironmental factors and tumor mutation burden in resected nonsmall cell lung cancer by applying machine learning to whole-slide images.
Cancer medicine | 2020-07-01 | PMID 32400056
Ono Akira, Terada Yukihiro, Kawata Takuya and 17 more
Identification of two novel mutations in three Chinese families with Kallmann syndrome using whole exome sequencing.
Andrologia | 2020-08-01 | PMID 32400067
Zhang Qin, He Hong-Hui, Janjua Muhammad Usman and 5 more
The point mutation analysis of Cyp2C9*2 (Arg144Cys C>T), Cyp2C9*3 (Ile359Leu A>C) and VKORC1 (1639G>A) in women with cervical cancer related to HPV: A case-control study.
Journal of cellular physiology | 2020-12-01 | PMID 32400078
Golshekan Elham, Sohrabi Amir
Novel mutations in the PITX2 gene in Pakistani and Mexican families with Axenfeld-Rieger syndrome.
Molecular genetics & genomic medicine | 2020-07-01 | PMID 32400113
Lo Faro Valeria, Siddiqui Sorath N, Khan Muhammad I and 5 more
Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing.
Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology | 2020-08-01 | PMID 32400230
Lee Hae Sang, Jeong Hwal Rim, Rho Jung Gi and 6 more
The Rs12569232 SNP Association with Vogt-Koyanagi-Harada Disease and Behcet's Disease is Probably Mediated by Regulation of Linc00467 Expression.
Ocular immunology and inflammation | 2021-11-17 | PMID 32400232
Wang Qingfeng, Yi Shenglan, Du Ziyu and 6 more
Sham surgical embryo transfer affects offspring neurodevelopment and manifestation of hypertensive phenotype in ISIAH rats.
Hypertension in pregnancy | 2020-08-01 | PMID 32400240
Rozkova Irina, Brusentsev Eugeny, Igonina Tatyana and 7 more
Toxic epidermal necrolysis syndrome induced by tigecycline: a case report.
The Journal of international medical research | 2020-05-01 | PMID 32400243
Yang Jiahui, Wu Fangli, Luo Dan and 4 more
Combining Supervised and Unsupervised Machine Learning Methods for Phenotypic Functional Genomics Screening.
SLAS discovery : advancing life sciences R & D | 2020-07-01 | PMID 32400262
Omta Wienand A, van Heesbeen Roy G, Shen Ian and 11 more
Effects of Maternal Obesity On Placental Phenotype.
Current vascular pharmacology | 2021-01-01 | PMID 32400334
Fowden A L, Camm E J, Sferruzzi-Perri A N
Dissecting the phenotypic and functional heterogeneity of mouse inflammatory osteoclasts by the expression of Cx3cr1.
eLife | 2020-05-13 | PMID 32400390
Madel Maria-Bernadette, Ibáñez Lidia, Ciucci Thomas and 9 more
Tritan color vision deficiency may be associated with an OPN1SW splicing defect and haploinsufficiency.
Journal of the Optical Society of America. A, Optics, image science, and vision | 2020-04-01 | PMID 32400513
Neitz Maureen, Krekling Elise D, Hagen Lene A and 6 more
Novel GNE mutations in three Chinese patients with typical GNE myo-pathy.
JPMA. The Journal of the Pakistan Medical Association | 2020-05-01 | PMID 32400752
Ban Rui, Lu Xianghui, Pu Chuanqiang and 4 more
Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.
Bioscience reports | 2020-05-29 | PMID 32400865
Ding Yu, Lang Jianyong, Zhang Junkun and 5 more
Endangered Pinzgauer cattle subtype Jochberger Hummel are genetically distinct.
Animal genetics | 2020-08-01 | PMID 32400895
Brenig B
Discovery of selection-driven genetic differences of Duroc, Landrace, and Yorkshire pig breeds by EigenGWAS and Fst analyses.
Animal genetics | 2020-08-01 | PMID 32400898
Tang Z, Fu Y, Xu J and 5 more
The 5-HTTLPR long allele predicts two-year longitudinal increases in cortisol and declines in verbal memory in older adults.
International journal of geriatric psychiatry | 2020-09-01 | PMID 32400901
Hirst Rayna B, Jordan Joshua T, Schüssler-Fiorenza Rose Sophia Miryam and 8 more
Mutation of MEDIATOR 18 and chromate trigger twinning of the primary root meristem in Arabidopsis.
Plant, cell & environment | 2020-08-01 | PMID 32400913
Ruiz-Aguilar Bricia, Raya-González Javier, López-Bucio Jesús Salvador and 5 more
Systemic involvement in adult-onset leukoencephalopathy with intracranial calcifications and cysts (Labrune syndrome) with a novel mutation of the SNORD118 gene.
European journal of neurology | 2020-11-01 | PMID 32400930
Bonomo G, Monfrini E, Borellini L and 5 more
Sodium hydrogen exchanger 9 NHE9 (SLC9A9) and its emerging roles in neuropsychiatric comorbidity.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics | 2020-07-01 | PMID 32400953
Patak Jameson, Faraone Stephen V, Zhang-James Yanli
Electrophysiological features: The next precise step for SCN2A developmental epileptic encephalopathy.
Molecular genetics & genomic medicine | 2020-07-01 | PMID 32400968
Miao Pu, Tang Siyang, Ye Jia and 7 more
MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2020-07-01 | PMID 32400971
Strickland Samantha L, Reddy Joseph S, Allen Mariet and 13 more
Genes: MAPT, GABRG2, NECTIN2
Measurement and characterization of distinctive clinical phenotypes using the Frontotemporal Lobar Degeneration Module (FTLD-MOD).
Alzheimer's & dementia : the journal of the Alzheimer's Association | 2020-06-01 | PMID 32400973
Gefen Tamar, Teylan Merilee A, Besser Lilah and 3 more
Angiotensin-converting enzyme gene insertion/deletion polymorphism and hypertension disease.
Archives of physiology and biochemistry | 2022-10-01 | PMID 32401071
Hadian Babak, Zafarmohtashami Azita, Chaghervand Zeinab and 1 more
The role of two common FOXP3 gene promoter polymorphisms in preeclampsia in a Turkish population: a case-control study.
Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology | 2020-05-01 | PMID 32401107
Cekin Nilgun, Pinarbasi Ergun, Esra Bildirici Aslihan and 3 more
BRAFV600E expression in neural progenitors results in a hyperexcitable phenotype in neocortical pyramidal neurons.
Journal of neurophysiology | 2020-06-01 | PMID 32401131
Goz Roman U, Akgül Gülcan, LoTurco Joseph J
RAD52 variants influence NSCLC risk in the Chinese population in a high altitude area.
Therapeutic advances in respiratory disease | 2000-01-01 | PMID 32401173
Li Miao, Chen Rong, Ji Baoyan and 4 more
Synergistic roles of Synaptotagmin-1 and complexin in calcium-regulated neuronal exocytosis.
eLife | 2020-05-13 | PMID 32401194
Ramakrishnan Sathish, Bera Manindra, Coleman Jeff and 2 more
Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing.
eLife | 2020-05-13 | PMID 32401198
Baslan Timour, Kendall Jude, Volyanskyy Konstantin and 22 more
Weighted gene correlation network analysis reveals novel regulatory modules associated with recurrent early pregnancy loss.
Bioscience reports | 2020-06-26 | PMID 32401299
Li Xiaoxiao, He Yuanqi, Hao Cuifang and 2 more
Genetic susceptibility, plant-based dietary patterns, and risk of cardiovascular disease.
The American journal of clinical nutrition | 2020-07-01 | PMID 32401300
Heianza Yoriko, Zhou Tao, Sun Dianjianyi and 3 more
Genetic variants and source of introduction of SARS-CoV-2 in South America.
Journal of medical virology | 2020-10-01 | PMID 32401345
Poterico Julio A, Mestanza Orson
A-kinase-interacting protein 1 promotes EMT and metastasis via PI3K/Akt/IKKβ pathway in cervical cancer.
Cell biochemistry and function | 2020-08-01 | PMID 32401379
Zhang Xiujuan, Liu Shuxian, Zhu Yongqing
Histological phenotypic subtypes predict recurrence risk and response to adjuvant chemotherapy in patients with stage III colorectal cancer.
The journal of pathology. Clinical research | 2020-10-01 | PMID 32401426
Roseweir Antonia K, Park James H, Hoorn Sanne Ten and 17 more
CRISPR-Based Screen Links an Inhibitor of Nonsense-Mediated Decay to eIF4A3 Target Engagement.
ACS chemical biology | 2020-06-19 | PMID 32401488
Cencic Regina, Naineni Sai Kiran, Pugsley Lauren and 3 more
Estimating the Effect of Single-Point Mutations on Protein Thermodynamic Stability and Analyzing the Mutation Landscape of the p53 Protein.
Journal of chemical information and modeling | 2020-06-22 | PMID 32401507
Banerjee Anupam, Mitra Pralay
PD-L1 and PD-L2 Mutations in Pediatric Hodgkin Lymphoma: Do They Have Any Prognostic Significance?
Fetal and pediatric pathology | 2022-02-01 | PMID 32401663
Gül Gülen, Ince Dilek, Olgun Nur and 1 more
Influences of UGT2B7 rs7439366 and rs12233719 Polymorphisms on Fentanyl Sensitivity in Chinese Gynecologic Patients.
Medical science monitor : international medical journal of experimental and clinical research | 2020-05-13 | PMID 32401749
Yang Zhenling, Yin Qingfeng, Li Xiaodong
Genetic diversity of Echinococcus multilocularis and Echinococcus granulosus sensu lato in Kyrgyzstan: The A2 haplotype of E. multilocularis is the predominant variant infecting humans.
PLoS neglected tropical diseases | 2020-05-01 | PMID 32401754
Alvarez Rojas Cristian A, Kronenberg Philipp A, Aitbaev Sezdbek and 6 more
Use of multiple traits genomic prediction, genotype by environment interactions and spatial effect to improve prediction accuracy in yield data.
PloS one | 2020-01-01 | PMID 32401769
Tsai Hsin-Yuan, Cericola Fabio, Edriss Vahid and 6 more
Evidence of recombination of vaccine strains of lumpy skin disease virus with field strains, causing disease.
PloS one | 2020-01-01 | PMID 32401805
Sprygin Alexander, Pestova Yana, Bjadovskaya Olga and 7 more
Newly sequenced genomes of four Bacillus Calmette Guerin vaccines.
Memorias do Instituto Oswaldo Cruz | 2020-01-01 | PMID 32401897
Sisco Maria Carolina, Silva Marlei Gomés, Lopez Beatriz and 5 more
High levels of chemerin associated with variants in the NOS3 and APOB genes in rural populations of Ouro Preto, Minas Gerais, Brazil.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas | 2020-01-01 | PMID 32401924
Batista A P, Barbosa K F, Masioli C Z and 4 more
Frequency of first and second-line drug resistance-associated mutations among resistant Mycobacterium tuberculosis clinical isolates from São Paulo, Brazil.
Memorias do Instituto Oswaldo Cruz | 2020-01-01 | PMID 32401997
Matsui Tania, Pinhata Juliana Maíra Watanabe, Rabello Michelle Christiane da Silva and 5 more
Nontuberculous mycobacteria in patients with suspected tuberculosis and the genetic diversity of Mycobacterium avium in the extreme south of Brazil.
Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia | 2000-01-01 | PMID 32402014
Busatto Caroline, Vianna Júlia Silveira, Silva Ana Barbara Scholante and 5 more
Structural disruption of exonic stem-loops immediately upstream of the intron regulates mammalian splicing.
Nucleic acids research | 2020-06-19 | PMID 32402057
Saha Kaushik, England Whitney, Fernandez Mike Minh and 3 more
Familial primary ovarian insufficiency associated with an SYCE1 point mutation: defective meiosis elucidated in humanized mice.
Molecular human reproduction | 2020-07-01 | PMID 32402064
Hernández-López Diego, Geisinger Adriana, Trovero María Fernanda and 5 more
Loss of SIRT1 in diabetes accelerates DNA damage-induced vascular calcification.
Cardiovascular research | 2021-02-22 | PMID 32402066
Bartoli-Leonard Francesca, Wilkinson Fiona L, Schiro Andrew and 3 more
SNP Markers as a Successful Molecular Tool for Assessing Species Identity and Geographic Origin of Trees in the Economically Important South American Legume Genus Dipteryx.
The Journal of heredity | 2020-08-12 | PMID 32402074
Honorio Coronado Eurídice N, Blanc-Jolivet Céline, Mader Malte and 15 more
Neuronal Function and Dopamine Signaling Evolve at High Temperature in Drosophila.
Molecular biology and evolution | 2020-09-01 | PMID 32402077
Jakšić Ana Marija, Karner Julia, Nolte Viola and 7 more
Effects of STAT3 polymorphisms and pharmacokinetics on the clinical outcomes of gefitinib treatment in patients with EGFR-mutation positive non-small cell lung cancer.
Journal of clinical pharmacy and therapeutics | 2020-08-01 | PMID 32402096
Yokota Hayato, Sato Kazuhiro, Sakamoto Sho and 5 more
Frailty Phenotype and Healthcare Costs and Utilization in Older Men.
Journal of the American Geriatrics Society | 2020-09-01 | PMID 32402097
Ensrud Kristine E, Kats Allyson M, Schousboe John T and 5 more