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variant
Journals
5
1
BMC Bioinformatics
2
pakistan journal of pharmaceutical sciences
3
Database : the journal of biological databases and curation
4
molecular biology reports
5
human mutation
Research Groups
0
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Bibliographies
552
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-C*03:467, a novel HLA-C*03 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