Diversity and evolution of oligopeptide permease systems in staphylococcal species
Keywords: تکثیر; Oligopeptide permease; Staphylococci; Duplication; Gene cluster
مقالات ISI تکثیر (ترجمه نشده)
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Does rare matter? Copy number variants at 16p11.2 and the risk of psychosis: A systematic review of literature and meta-analysis
Keywords: تکثیر; CNV; Copy number variation; 16p11.2; Duplication; Psychosis; Schizophrenia; Bipolar disorders; Schizoaffective disorder;
Novel homozygous mutations in the WNT10B gene underlying autosomal recessive split hand/foot malformation in three consanguineous families
Keywords: تکثیر; WNT10B; wingless-type MMTV integration site family, member 10B; SHFM; Split hand foot malformation; TP63; tumor protein p63; DLX5; distal-less homeobox 5; bp; base pair; EDTA; Ethylene diamine tetra acetic acid; PCR; Polymerase Chain Reaction; cDNA; compl
New insights into the evolution of vertebrate CRH (corticotropin-releasing hormone) and invertebrate DH44 (diuretic hormone 44) receptors in metazoans
Keywords: تکثیر; Evolution; Duplication; CRH and DH44 receptors
Rapid replacement of human respiratory syncytial virus A with the ON1 genotype having 72 nucleotide duplication in G gene
Keywords: تکثیر; Human respiratory syncytial virus (HRSV); Attachment G gene; Duplication; Diversity; Evolution;
On the spectrum of the normalized Laplacian for signed graphs: Interlacing, contraction, and replication
Keywords: تکثیر; 05C50; 05C22; 15A18; 05C76Signed graph; Interlacing; Normalized Laplacian; Contraction; Replication; Duplication
Duplication of exon 7-12 in the low-density lipoprotein receptor gene in three Danish patients with familial hypercholesterolemia
Keywords: تکثیر; Cholesterol; Duplication; Familial hypercholesterolemia; Genomic rearrangements; LDL receptor;
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21 â qter) and partial monosomy 6q (6q27 â qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold
Keywords: تکثیر; MoM; multiples of the median; AFP; α-fetoprotein; dup; duplication; del; deletion; aCGH; array comparative genomic hybridization; FISH; fluorescence in situ hybridization; BAC; bacterial artificial chromosome; t; translocation; der; derivative; QF-PCR; q
A small de novo 16q24.1 duplication in a woman with severe clinical features
Keywords: تکثیر; 16q24.1; Duplication; Mental retardation; Array-CGH; QFM-PCR;
A de novo 1.38 Mb duplication of 1q31.1 in a boy with hemifacial microsomia, anophthalmia, anotia, macrostomia, and cleft lip and palate
Keywords: تکثیر; Craniofacial malformation; Anophthalmia; Anotia; 1q31.1; Duplication; Oculoauriculovertebral; Goldenhar;
Development of a comprehensive real-time PCR assay for dystrophin gene analysis and prenatal diagnosis of Chinese families
Keywords: تکثیر; Carrier detection; Duchenne muscular dystrophy; Deletion; Duplication; Prenatal diagnosis; Real-time PCR;
Short CommunicationPrenatal diagnosis of partial trisomy 3q (3q27.3âqter) and partial monosomy 14q (14q31.3âqter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
Keywords: تکثیر; Dup; duplication; del; deletion; pat; paternal; mat; maternal; UPD; uniparental disomy; ACGH; array comparative genomic hybridization; FISH; fluorescence in situ hybridization; QF-PCR; quantitative fluorescent polymerase chain reaction; t; translocation;
Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development
Keywords: تکثیر; DSD; Disorders of sexual development; GTG banding; G-banding using Trypsin and Giemsa; NOR; Nuclear organizing regions; FISH; Fluorescence in situ hybridization; WCP; Whole chromosome paint; STR; Short tandem repeats; BAC; Bacterial artificial chromosome;
3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: Prenatal diagnosis and aCGH characterization
Keywords: تکثیر; aCGH; array comparative genomic hybridization; NT; nuchal translucency; del; deletion; MoM; multiples of the median; β-hCG; β-human chorionic gonadotropin; dn; de novo; PAPP-A; pregnancy-associated plasma protein-A; der; derivative chromosome; dup; dupl
Evolution of the tissue factor pathway inhibitor-like Kunitz domain-containing protein family in Rhipicephalus microplus
Keywords: تکثیر; Rhipicephalus microplus; Kunitz domain; Tissue factor pathway inhibitor (TFPI); Phylogenetic; Bayesian Markov Chain Monte Carlo; Duplication;
Double Meckel’s Diverticulum Presenting as Acute Appendicitis: A Case Report and Literature Review
Keywords: تکثیر; double Meckel’s diverticulum; duplication; congenital anomaly; unusual presentation
Autosomal insertional translocation mimicking an X-linked mode of inheritance
Keywords: تکثیر; Mental retardation; X-linked intellectual disability; Insertion; Deletion; Duplication; ZFPM2
Comparison of polyurethane and epoxy resist master mold for nanoscale soft lithography
Keywords: تکثیر; Nanostructured silicon master mold; Polyurethane; Epoxy resist; Nanoimprint; Soft lithography; Duplication
A Portuguese case of Fukuyama congenital muscular dystrophy caused by a multi-exonic duplication in the fukutin gene
Keywords: تکثیر; Duplication; Fukutin; FKTN; Fukuyama congenital muscular; Dystrophy; α-Dystroglycanopathies
Clinical and cytogenetic features of a Potocki–Lupski syndrome with the shortest 0.25 Mb microduplication in 17p11.2 including RAI1
Keywords: تکثیر; Array-CGH; 17p11.2; Duplication; Potocki–Lupski syndrome (PTLS); RAI1
Combined Dup(7)(q22.1q32.2), Inv(7)(q31.31q31.33), and Ins(7;19)(q22.1;p13.2p13.2) in a 12-year-old boy with developmental delay and various dysmorphism
Keywords: تکثیر; Duplication; Inversion; Complex rearrangement; SNP array
Duplication forgery detection using improved DAISY descriptor
Keywords: تکثیر; Digital image forensics; Image matching; Copy-move attack; Authenticity verification; Duplication
Duplication of Optic Canal in Human Skulls
Keywords: تکثیر; Duplication; optic canal;
Duplication of 7q36.3 encompassing the Sonic Hedgehog (SHH) gene is associated with congenital muscular hypertrophy
Keywords: تکثیر; Duplication; 7q36.3; Muscular hypertrophy; Sonic Hedgehog; SHH; Array-CGH
Biliary duplication cyst with heterotopic gastric mucosa resulting in obstruction of the biliary system: a case report
Keywords: تکثیر; Duplication; Common bile duct; Gastric mucosa; Mirizzi syndrome
X-linked myotubular myopathy due to a complex rearrangement involving a duplication of MTM1 exon 10
Keywords: تکثیر; X-linked myotubular myopathy (XLMTM); Myotubularin (MTM1) gene; Rearrangement; mRNA; Duplication;
Perinatally discovered complete tubular colonic duplication associated with anal atresia
Keywords: تکثیر; Duplication; Colon; Anal atresia; Children; Malformation
Clinical and pathological analysis of malignancies arising from alimentary tract duplications
Keywords: تکثیر; Duplication; Malignant; Tumour; Alimentary tract; Analysis;
Identification and characterization of three inherited genomic copy number variations associated with familial schizophrenia
Keywords: تکثیر; Schizophrenia; Copy number variation; Genetics; Deletion; Duplication; Rearrangement;
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series
Keywords: تکثیر; APP; Duplication; PRNP; Prion; Chromosome 21; Dementia;
Do children think that duplicating the body also duplicates the mind?
Keywords: تکثیر; Identity; Haecceity; Duplication; Dualism;
Duodenal duplication cyst: A rare cause of geriatric gastrointestinal bleeding
Keywords: تکثیر; Duodenum; Duplication; Gastrointestinal hemorrhage
A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis
Keywords: تکثیر; CFTR; mRNA; Duplication; Array-CGH
Original articleBiparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
Keywords: تکثیر; Mental retardation; Translocation; Inversion; Deletion; Duplication; Biparental inheritance;
Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)
Keywords: تکثیر; dup(15q); Duplication; 15q Overgrowth syndrome; Prenatal diagnosis
Palaeogenomics in cereals: Modeling of ancestors for modern species improvement
Keywords: تکثیر; Synteny; Duplication; Genome; Chromosome; Evolution; Speciation; MarkersSynténie; Duplication; Génome; Chromosome; Évolution; Spéciation; Marqueurs
Genome-Wide Analysis Shows Increased Frequency of Copy Number Variation Deletions in Dutch Schizophrenia Patients
Keywords: تکثیر; Candidate gene; copy number variation; cytogenetic abnormality; deletion; duplication; schizophrenia
Congenital hand anomalies
Keywords: تکثیر; birth defect; congenital hand anomalies; duplication; finger abnormalities; forearm abnormalities; hand deformity; newborn; syndactyly; thumb abnormalities; toe transfer
Interpretation of Copy Number Alterations Identified Through Clinical Microarray-Comparative Genomic Hybridization
Keywords: تکثیر; Oligonucleotide microarray; Copy number alteration; Variant of unknown significance; Deletion; Duplication;
Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting
Keywords: تکثیر; ASDs, autism spectrum disorders; CNV, copy number variation; ID, intellectual disability; PDD-NOS, pervasive developmental disorder not otherwise specifiedAutism; Intellectual disability; Mutation; Copy number variation; Deletion; Duplication
Copy Number Variation in Schizophrenia in the Japanese Population
Keywords: تکثیر; Deletion; duplication; NRXN1; 16p13.1; 1q21.1; schizophrenia
Duplication du pouce de type IV-D : une nouvelle méthode de reconstruction
Keywords: تکثیر; Duplication; Pouce; Bilhaut-Cloquet; Wassel
A de novo 11p12-p15.4 duplication in a patient with pharmacoresistant epilepsy, mental retardation, and dysmorphisms
Keywords: تکثیر; Epilepsy; Chromosome abnormalities; Duplication; Array-CGH; Mental retardation
Investigation of gene dosage imbalances in patients with Noonan syndrome using multiplex ligation-dependent probe amplification analysis
Keywords: تکثیر; MLPA; Noonan syndrome; Mutation; RAS-MAPK; Duplication; Deletion
Multiplex ligation-dependent probe amplification (MLPA) analysis is an effective tool for the detection of novel intragenic PLA2G6 mutations: Implications for molecular diagnosis
Keywords: تکثیر; PLA2G6; PLAN; Duplication; Deletion; MLPA; ARMD;
Allelic diversity at MHC class II DQ loci in buffalo (Bubalus bubalis): Evidence for duplication
Keywords: تکثیر; DQA; DQB; Duplication; PBS; Phylogeny; Water buffalo
List scheduling with duplication for heterogeneous computing systems
Keywords: تکثیر; List scheduling; Heterogeneous computing systems; DAG; Duplication
A trichotomy of attitudes for decision-making under complete ignorance
Keywords: تکثیر; D81; Complete ignorance; Quasi-transitivity; Independence; Duplication; Protective criterion;
Reliability-aware scheduling strategy for heterogeneous distributed computing systems
Keywords: تکثیر; Heterogeneous distributed systems; Scheduling algorithm; Reliability; Duplication; Precedence constrained tasks
Elucidation of the sex-pheromone biosynthesis producing 5,7-dodecadienes in Dendrolimus punctatus (Lepidoptera: Lasiocampidae) reveals Δ11- and Δ9-desaturases with unusual catalytic properties
Keywords: تکثیر; Chemical communication; Sex pheromone; Conjugated diene; Heterologous expression; Gene family evolution; Duplication; Subfunctionalization