Communications biology

Materials (Basel, Switzerland)

oncology reports

acta anaesthesiologica scandinavica

Science advances

Pesticide biochemistry and physiology

Microorganisms

Journal of theoretical biology

Bioinformatics

Briefings in bioinformatics

methods in molecular biology (clifton, nj)

clinical and experimental allergy : journal of the british society for allergy and clinical immunology

Plants (Basel, Switzerland)

microbiome

the british journal of dermatology

Resuscitation

zhonghua yi xue za zhi

Indian journal of pediatrics

Frontiers in immunology

Clinical rheumatology

Frontiers in endocrinology

human mutation

[rinsho ketsueki] the japanese journal of clinical hematology

clinical cancer research : an official journal of the american association for cancer research

current opinion in endocrinology, diabetes, and obesity

Postgraduate Medical Journal

european journal of cancer care

mutation research

advances in experimental medicine and biology

the journal of asthma : official journal of the association for the care of asthma

Journal of medical case reports

Journal of translational medicine

experimental and therapeutic medicine

Nature structural & molecular biology

respiratory physiology & neurobiology

revue des maladies respiratoires

neonatal network : nn

environmental and molecular mutagenesis

Italian journal of pediatrics

new microbes and new infections

biochimica et biophysica acta general subjects

Computer methods in biomechanics and biomedical engineering

frontiers in bioscience : a journal and virtual library

Virus evolution

[1] Detection of In Vivo Mutation in the Hprt and Pig-a Genes of Rat Lymphocytes.

[2] Clinico-genetic model to predict methotrexate intolerance in rheumatoid arthritis.

[3] Dimerization defective MODY mutations of hepatocyte nuclear factor 4α.

[4] Stressing State Analysis of an Integral Abutment Curved Box-Girder Bridge Model.

[5] Clinical, radiological and genetic analysis of a male infant with neonatal respiratory distress syndrome.

[6] Increased asymptomatic airway hyper-responsiveness in obese individuals.

[7] Delayed recovery of spontaneous circulation following cessation of cardiopulmonary resuscitation in an older patient: a case report.

[8] Quantifying parenchymal tethering in a finite element simulation of a human lung slice under bronchoconstriction.

[9] Effects of dispersion of fiber orientation on the mechanical property of the arterial wall.

[10] Unilateral pulmonary hypoplasia with abdominal situs inversus.

[11] [Bronchoscopic treatment of emphysema].

[12] Effects of stomach inflation on haemodynamic and pulmonary function during spontaneous circulation in pigs.

[13] Maximal hysteresis: a new method to set positive end-expiratory pressure in acute lung injury?

[14] Influence of long-term cigarette smoking on immunoglobulin E-mediated allergy, pulmonary function, and high-resolution computed tomography lung densitometry in elderly patients with asthma.

[15] Responses of bronchial C-fiber afferents of the rabbit to changes in lung compliance.

[16] Effects of diltiazem on platelet activation and cytosolic calcium during percutaneous transluminal coronary angioplasty.

[17] Pathogenesis, pathology and pathophysiology of pulmonary sequelae of bronchopulmonary dysplasia in premature infants.

[18] Dynamic finite element implementation of nonlinear, anisotropic hyperelastic biological membranes.

[19] Flow Cytometry Contributions for the Diagnosis and Immunopathological Characterization of Primary Immunodeficiency Diseases With Immune Dysregulation.

[20] SANTA-SIM: simulating viral sequence evolution dynamics under selection and recombination.

[21] Impacts of florfenicol on the microbiota landscape and resistome as revealed by metagenomic analysis.

[22] Ciprofloxacin-Resistant Serovar Kentucky ST198 in Broiler Chicken Supply Chain and Patients, China, 2010-2016.

[23] HSPA1A conformational mutants reveal a conserved structural unit in Hsp70 proteins.

[24] Identification of TPD52 and DNAJB1 as two novel bile biomarkers for cholangiocarcinoma by iTRAQ‑based quantitative proteomics analysis.

[25] [The impact of KIT and other concomitant gene mutations on the prognoses of patients with core-binding factor acute myeloid leukemia].

[26] Clinical Relevance of Genetic Analysis in Patients With Pituitary Adenomas: A Systematic Review.

[27] British Association of Dermatologists centenary year: standing on the shoulders of giants.

[28] FANCL gene mutations in premature ovarian insufficiency.

[29] BRCA1 and S phase DNA repair pathways restrict LINE-1 retrotransposition in human cells.

[30] Combined deletions of and cause chondrodystrophy and embryonic lethality in the Creeper chicken.

[31] Surface-state Coulomb repulsion accelerates a metal-insulator transition in topological semimetal nanofilms.

[32] Protecting quantum entanglement from leakage and qubit errors via repetitive parity measurements.

[33] Emerging SARS-CoV-2 mutation hot spots include a novel RNA-dependent-RNA polymerase variant.

[34] Frequency, Spectrum, and Stability of Leaf Mutants Induced by Diverse γ-Ray Treatments in Two Hybrids.

[35] Glyphosate resistance in Eleusine indica: EPSPS overexpression and P106A mutation evolved in the same individuals.

[36] ras mutations and oncogenesis: not all ras mutations are created equally

[37] in vitro sensivity of fig plantlets to gamma rays sensitividade in vitro de brotações de figueira à radiação gama

[38] analysis of the t354p mutation of the sodium/iodide cotransporter gene in children with congenital hypothyroidism due to dyshormonogenesis

[39] molecular genetics of mycobacterium tuberculosis resistant to aminoglycosides and cyclic peptide testing by mtbdrsl in armenia

[40] helicobacter pylori genetic diversification in the mongolian gerbil model

[41] comparison of immunohistochemistry and direct sanger sequencing for detection of the mutation in thyroid neoplasm

[42] aspectos genéticos da obesidade genetics of obesity

[43] polygenic case of long qt syndrome confirmed through functional characterization informs the interpretation of genetic screening results

[44] analysis of relationship between tumor necrosis factor alpha gene (g308a polymorphism) with preterm labor

[45] the application of nuclear medicine imaging in bronchioloalveolar carcinoma

[46] optimasi dan pemekatan lipase bacillus halodurans cm1

[47] variabilidade para caracteres morfológicos em mutantes de arroz variability for morphological traits in mutated rice

[48] the mitochondrial dna mutations associated with cardiac arrhythmia investigated in an lqts family

[49] the non-coding oncogene: a case of missing dna evidence?

[50] mutations, associated with early-onset alzheimer’s disease, discovered in asian countries

[51] fractionation of sulfur isotopes by desulfovibrio vulgaris mutants lacking hydrogenases or type i tetraheme cytochrome c3

[52] identification and functional analysis of the first aquaporin from striped stem borer, chilo suppressalis

[53] transformation analysis of oral epithelial dysplasia to carcinoma in-situ and squamous cell carcinoma by p53 expression and gene mutations

[54] mutation-prone positions within the estrogen receptor

[55] a developmental approach to machine learning?

[56] analysis of prolactin gene exon 4 diversity in peking, white mojosari, and peking white mojosari crossbreed

[57] mutaciones puntuales en los genes dhfr y dhps de plasmodium falciparum de tres regiones endémicas

[58] assessment of natural variation in the first pore domain of the tomato hkt1;2 transporter and characterization of mutated versions of slhkt1;2 expressed in xenopus laevis oocytes and via complementation of the salt sensitive athkt1;1 mutant

[59] first microdeletion involving only the biotinidase gene that can cause biotinidase deficiency: a lesson for clinical practice

[60] the p-type atpase pa1429 regulates quorum-sensing systems and bacterial virulence

[61] evidence that grin2a mutations in melanoma correlate with decreased survival

[62] mutation analysis of gjb2 gene and prenatal diagnosis in a non-syndromic deafness family

[63] untagged mutation in rice gal4/vp16 transcriptional activator facilitated-enhancer trap lines

[64] a novel norrie disease pseudoglioma gene mutation, c.-1_2delaat, responsible for norrie disease in a chinese family

[65] functions and regulation of the pten gene in colorectal cancer

[66] el estado heterocigótico para mutaciones del gen fenilalanina hidroxilasa como factor de riesgo fetal the heterocygotic state for mutations of the phenylalanine hydroxylase gene as a fetal risk factor

[67] transcriptome-wide investigation of mrna/circrna in mir-184 and its r.57c > u mutant type treatment of human lens epithelial cells

[68] a novel deletion and two recurrent substitutions on type vii collagen gene in seven iranian patients with epidermolysis bullosa

[69] contribution of flagella and motility to gut colonisation and pathogenicity of salmonella enteritidis in the chicken

[70] identification of weak points prone for mutation in ferredoxin of <i> trichomonas vaginalis</i>

[71] role of diffuse low-level heteroplasmy of mitochondrial dna in alzheimer’s disease neurodegeneration

[72] amino acid substitution k470r in the nucleoprotein increases the virulence of h5n1 influenza a virus in mammals

[73] lactic acidosis in prostate cancer: consider the warburg effect

[74] increase in complexity and information through molecular evolution

[75] fitness cost of daptomycin-resistant staphylococcus aureus obtained from in vitro daptomycin selection pressure

[76] retroviral vectors for analysis of viral mutagenesis and recombination

[77] phenotype of usher syndrome type ii assosiated with compound missense mutations of c.721 c&gt;t and c.1969 c&gt;t in myo7a in a chinese usher syndrome family

[78] first report of inherited thyroxine-binding globulin deficiency in iran caused by a known de novo mutation in serpina7

[79] resistencia a los medicamentos antirretrovirales en pacientes que reciben tratamiento para vih-sida en colombia resistance to antiretrovirals in patients receiving hiv-aids therapy in colombia

[80] Wnt/β-catenin signalling in prostate cancer - Nature Reviews Urology

[81] Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients

[82] Wnt/β-catenin signalling in prostate cancer - Nature Reviews Urology

[83] Wnt/β-catenin signalling in prostate cancer

[84] Novel mutations associated with inherited human calcium-sensing receptor disorders: a clinical genetic study.

[85] Quantile-based permutation thresholds for quantitative trait loci hotspots.

[86] Robustness of coalescent estimators to between-lineage mutation rate variation.

[87] PRISMOID: a comprehensive 3D structure database for post-translational modifications and mutations with functional impact.

[88] Security mutation testing of the FileZilla FTP server

[89] Improving test adequacy assessment by novel JavaScript mutation operators

[90] Varying inocula permutations (Aspergillus oryzae and bacillus amyloliquefaciens) affect enzyme activities and metabolite levels in koji

[91] The creation and selection of mutations resistant to a gene drive over multiple generations in the malaria mosquito.

[92] High BRAFV600E mutation frequency in Chinese patients with papillary thyroid carcinoma increases diagnostic efficacy in cytologically indeterminate thyroid nodules.

[93] Acute pulmonary thromboembolism caused by factor V Leiden mutation in South Korea: A case report.

[94] In search for genetic explanation for LDLc variabily in an FH family: Common SNPs and a rare mutation in microsomal triglyceride transfer protein explain only part of LDL variability in an FH family.

[95] Frequent mutations in EGFR, KRAS and TP53 genes in human lung cancer tumors detected by ion torrent DNA sequencing.

[96] Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer.

[97] Autosomal dominant familial calcium pyrophosphate dihydrate deposition disease is caused by mutation in the transmembrane protein ANKH.

[98] Antiretroviral drug resistance mutations among patients failing first-line treatment in Hanoi, Vietnam

[99] Characterization of the most common embCAB gene mutations associated with ethambutol resistance in Mycobacterium tuberculosis isolates from Iran

[100] Mutations in gyrB play an important role in ciprofloxacin-resistant Pseudomonas aeruginosa

[101] Evaluation of the accuracy of molecular assays targeting the mutation A2059G for detecting high-level azithromycin resistance in Neisseria gonorrhoeae: a systematic review and meta-analysis