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Keyword Connections - variant Keywords

Connection Type	Connection
Journals	BMC Bioinformatics pakistan journal of pharmaceutical sciences Database : the journal of biological databases and curation molecular biology reports human mutation
Research Groups	No Research Group Connected
Bibliographies	[1] An insight into clinical outcome of XPG polymorphisms in breast cancer. [2] Prunus domestica alters functions of frog's heart. [3] PyCellBase, an efficient python package for easy retrieval of biological data from heterogeneous sources. [4] A late-binding, distributed, NoSQL warehouse for integrating patient data from clinical trials. [5] characterization of intra-type variants of oncogenic human papillomaviruses by next-generation deep sequencing of the e6/e7 region [6] Multiple Instance Learning with Differential Evolutionary Pooling [7] Frequency of CDH1 germline variants and contribution of dietary habits in early age onset gastric cancer patients in Brazil. [8] The serotonin transporter gene variants modulate acute stress-induced hippocampus and dorsomedial prefrontal cortex activity during memory retrieval. [9] A new approach to analytic, non-perturbative, gauge-invariant QCD renormalization is described, with applications to high energy elastic pp-scattering. [10] VCF/Plotein: Visualisation and prioritisation of genomic variants from human exome sequencing projects. [11] New germline BRCA2 gene variant in the Tuvinian Mongol breast cancer patients. [12] Genetic variants of flavin-containing monooxygenase 3 (FMO3) derived from Japanese subjects with the trimethylaminuria phenotype and whole-genome sequence data from a large Japanese database. [13] Erratum: Identification of a novel variant form of aspergillus fumigatus CalC and generation of Anti-CalC monoclonal antibodies (Medical Mycology Journal, (2019), 60, 1, (11-16), 10.3314/mmj.18-00013) [14] Association of a complement receptor 1 gene variant with baseline erythrocyte sedimentation rate levels in patients starting anti-TNF therapy in a UK rheumatoid arthritis cohort: results from the Biologics in Rheumatoid Arthritis Genetics and Genomics Study Syndicate cohort. [15] Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. [16] Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus [17] Characterization of antimicrobial resistance mechanisms in carbapenem-resistant Pseudomonas aeruginosa carrying IMP variants recovered from a Mexican Hospital [18] Role of small colony variants in persistence of Pseudomonas aeruginosa infections in cystic fibrosis lungs [19] Pseudomonas aeruginosa induces pigment production and enhances virulence in a white phenotypic variant of Staphylococcus aureus [20] Clinical outcomes of rare hepatocellular carcinoma variants compared to pure hepatocellular carcinoma [21] Who will benefit from anticoagulant therapy? Use of the CHADS2 score and its variants [22] Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus [23] Evaluation of agar culture plates to efficiently identify small colony variants of methicillin-resistant Staphylococcus aureus [24] Multiobjective Simulated Annealing: Principles and Algorithm Variants [25] Characterization of antimicrobial resistance mechanisms in carbapenem-resistant Pseudomonas aeruginosa carrying IMP variants recovered from a Mexican Hospital [26] Idiopathic CRMO and MEFV Gene Variant Alleles: Is There Any Relationship? [27] A Case Study of Malrotated Kidneys with Asymmetric Multiple Renal Arteries, Variant Venous Drainage, and Unilateral Ureteral Duplication [28] Role of small colony variants in persistence of Pseudomonas aeruginosa infections in cystic fibrosis lungs [29] Pseudomonas aeruginosa induces pigment production and enhances virulence in a white phenotypic variant of Staphylococcus aureus [30] Urinary Uromodulin Levels and UMOD Variants in Black South Africans with Hypertension-Attributed Chronic Kidney Disease [31] VDR Variants rather than Early Pregnancy Vitamin D Concentrations Are Associated with the Risk of Gestational Diabetes: The Ma’anshan Birth Cohort (MABC) Study [32] Clinical outcomes of rare hepatocellular carcinoma variants compared to pure hepatocellular carcinoma [33] Genetic characterisation of African swine fever virus from 2017 outbreaks in Zambia: Identification of p72 genotype II variants in domestic pigs [34] Who will benefit from anticoagulant therapy? Use of the CHADS2 score and its variants [35] Insights into Interprotein Electron Transfer of Human Cytochrome c Variants Arranged in Multilayer Architectures by Means of an Artificial Silica Nanoparticle Matrix [36] De Novo GRIN Variants in NMDA Receptor M2 Channel Pore-Forming Loop Are Associated with Neurological Diseases. [37] Variant Call Format (VCF)-Diagnostic Annotation and Reporting Tool (VCF-DART) A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data. [38] Integrating a scale-invariant feature of fractal geometry into the Hopfield neural network for super-resolution mapping [39] The representation of semantic information across human cerebral cortex during listening versus reading is invariant to stimulus modality. [40] Association of genetic variants in IGF-1 gene with susceptibility to gestational and type 2 diabetes mellitus [41] Impact of histologic variants on the oncological outcomes of patients with upper urinary tract cancers treated with radical surgery: a multi-institutional retrospective study. [42] Receptividad y extremismo nacionalista en el País Vasco (1977-2007): una evaluación multivariante [43] Reevaluation of genetic variants previously associated with arrhythmogenic right ventricular cardiomyopathy integrating population-based cohorts and proteomics data. [44] Variants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos. [45] Scanning of Genetic Variants and Genetic Mapping of Phenotypic Traits in Gilthead Sea Bream Through ddRAD Sequencing. [46] Different effects of high-protein/low-carbohydrate versus standard hypocaloric diet on insulin resistance and lipid profile: role of rs16147 variant of neuropeptide Y. [47] The application of HPLC/MS analysis with a multi-enzyme digest strategy to characterize different interferon product variants produced from Pichia pastoris. [48] Gene Variants at Loci Related to Blood Pressure Account for Variation in Response to Antihypertensive Drugs Between Black and White Individuals. [49] Effect of non- 180 <sup>∘</sup> polarization invariants on the exchange bias of tetragonal ⟨ 001 ⟩ and rhombohedral ⟨ 111 ⟩ orientations of bismuth ferrite epitaxial thin films [50] Isomorphic semantic mapping of variant call format (VCF2RDF). [51] FunVar: A Systematic Pipeline to Unravel the Convergence Patterns of Genetic Variants in ASD, a Paradigmatic Complex Disease. [52] VARIANTS OF THE REPUBLIKA SRPSKA'S INVOLVEMENT IN THE WORLD ECONOMIC TRENDS [53] [Study of genetic variants in the BDNF, COMT, DAT1 and SERT genes in Colombian children with attention deficit disorder]. [54] Quaternion weighted spherical Bessel-Fourier moment and its invariant for color image reconstruction and object recognition [55] The TMEM106B FTLD-protective variant, rs1990621, is also associated with increased neuronal proportion. [56] Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China [57] Phenotypic severity in a family with MEND syndrome is directly associated with the accumulation of potentially functional variants of cholesterol homeostasis genes. [58] Population-specific long-range linkage disequilibrium in the human genome and its influence on identifying common disease variants. [59] Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis. [60] Response of thermoelectric generators to Bi<inf>2</inf>Te<inf>3</inf> and Zn<inf>4</inf>Sb<inf>3</inf> energy harvester materials under variant solar radiation [61] Improving the Visual Quality of Size-Invariant Visual Cryptography for Grayscale Images: An Analysis-by-Synthesis (AbS) Approach. [62] Image size invariant visual cryptography for general access structures subject to display quality constraints. [63] Improving the Visual Quality of Size-Invariant Visual Cryptography for Grayscale Images: An Analysis-by-Synthesis (AbS) Approach [64] Developmental and epileptic encephalopathy in two siblings with a novel, homozygous missense variant in SCN1B. [65] Symmetric identities for carlitz’s generalized twisted q-bernoulli numbers and polynomials associated with p-adic invariant integral on z <inf>p</inf> [66] Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. [67] Novel GABRA2 variants in epileptic encephalopathy and intellectual disability with seizures. [68] Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature. [69] A DNA electrochemical biosensor based on triplex DNA-templated Ag/Pt nanoclusters for the detection of single-nucleotide variant [70] Evolving role of cytoreductive nephrectomy in metastatic renal cell carcinoma of variant histology [71] VARIANTS, MEANING AND THE GEOGRAPHICAL SPREAD OF TEMPORAL ADVERBS TOČ AND TOLIČ [72] AVADA: toward automated pathogenic variant evidence retrieval directly from the full-text literature. [73] Clinical utility of noninvasive prenatal screening for pathogenic copy number variants. [74] HLA-C03:467, a novel HLA-C03 variant, detected in a Taiwanese individual. [75] Comparative study of nutritional mode and mycorrhizal fungi in green and albino variants of Goodyera velutina, an orchid mainly utilizing saprotrophic rhizoctonia. [76] Evaluating correlation between the ocular biometry and genetic variants of and with primary angle-closure glaucoma in a cohort from northern China. [77] A rare heterozygous TREM2 coding variant identified in familial clustering of dementia affects an intrinsically disordered protein region and function of TREM2. [78] Full and fragmented permutationally invariant polynomial potential energy surfaces for trans and cis N-methyl acetamide and isomerization saddle points. [79] Uniparental isodisomy caused autosomal recessive diseases: NGS-based analysis allows the concurrent detection of homogenous variants and copy-neutral loss of heterozygosity. [80] Mapping of IDUA gene variants in Pakistani patients with mucopolysaccharidosis type 1. [81] A variant in the MICA gene is associated with liver fibrosis progression in chronic hepatitis C through TGF-β1 dependent mechanisms [82] Exogenous Administration of Low-Dose Lipopolysaccharide Potentiates Liver Fibrosis in a Choline-Deficient <span style="font-variant: small-caps">l</span>-Amino-Acid-Defined Diet-Induced Murine Steatohepatitis Model [83] Treatment for Word Retrieval in Semantic and Logopenic Variants of Primary Progressive Aphasia: Immediate and Long-Term Outcomes. [84] Assessing the Functional Relevance of Variants in the () in a Cohort of Patients With Primary Immunodeficiency. [85] On the concept of “variant” in lexicon studies from a historic-variational perspective [86] A rotation and translation invariant method for 3D organ image classification using deep convolutional neural networks [87] Transcriptional variants of Dmrt1 and expression of four Dmrt genes in the blunt snout bream, Megalobrama amblycephala [88] Variant in Central Centrifugal Cicatricial Alopecia. [89] Variant PADI3 in central centrifugal cicatricial alopecia [90] Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration. [91] A Novel Variant of HOXA10 gene, Ser19Cys, among Patients with Endometriosis and its Relationship with the Severity of the Disease [92] Proteomic genotyping of fingermark donors with genetically variant peptides. [93] Difference inequality for attracting and quasi-invariant sets for a class of impulsive stochastic difference equations with continuous time [94] MMSplice: modular modeling improves the predictions of genetic variant effects on splicing [95] Protective Innate Immune Variants in Racial/Ethnic Disparities of Breast and Prostate Cancer. [96] A linkage and exome study implicates rare variants of KANK4 and CAP2 in bipolar disorder in a multiplex family. [97] CCR5 genetic variants and epidemiological determinants for HPV infection and cervical premalignant lesions. [98] Fast, Sensitive and Specific Detection of and its Variants Using One-Step Real-Time Reverse-Transcription Polymerase Chain Reaction Assay. [99] A Substantial Proportion of Apparently Heterozygous TP53 Pathogenic Variants Detected with a Next-Generation Sequencing Hereditary Pan-Cancer Panel Are Acquired Somatically. [100] A frequent variant in the Japanese population determines quasi-Mendelian inheritance of rare retinal ciliopathy. [101] MalDeep: A Deep Learning Classification Framework against Malware Variants Based on Texture Visualization