Keywords: طیف جهش; HPA; hyperphenylalaninemia; PAH; phenylalanine hydroxylase; BH4; tetrahydrobiopterin; NGS; next generation sequencing; MLPA; multiplex ligation-dependent probe amplification; qRT-PCR; quantitative real-time PCR; APV; allelic phenotype values; GPV; genotyp
مقالات ISI طیف جهش (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: طیف جهش; Familial hypercholesterolemia; Mutation spectrum; LDLR; APOB; PCSK9;
Keywords: طیف جهش; Antithrombin deficiency; Mutation spectrum; Genotype-phenotype association; Antithrombin activity; Assay sensitivity;
Keywords: طیف جهش; Familial hypercholesterolemia; Mutation spectrum; Low-density lipoprotein; LDL; LDL-Cholesterol; LDL-C;
Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan
Keywords: طیف جهش; Familial hypercholesterolemia; Next generation sequencing; Mutation spectrum; LDLR; Haplotype; Structural variation;
PKD2-Related Autosomal Dominant Polycystic Kidney Disease: Prevalence, Clinical Presentation, Mutation Spectrum, and Prognosis
Keywords: طیف جهش; Autosomal dominant polycystic kidney disease (ADPKD); PKD2; end-stage renal disease (ESRD); prognosis; mutation spectrum; sequencing; genetics; disease progression; disease severity; genetic prevalence; mutation detection; renal survival; kidney function;
Review ArticleVon Willebrand disease mutation spectrum and associated mutation mechanisms
Keywords: طیف جهش; Von Willebrand disease; Von Willebrand factor; Hemostasis; Mutation spectrum; Mutation mechanism;
Identification of five novel STAR variants in ten Chinese patients with congenital lipoid adrenal hyperplasia
Keywords: طیف جهش; Congenital lipoid adrenal hyperplasia; Steroidogenic acute regulatory protein; STAR gene; Mutation spectrum
Spectrum of mutations associated with methionine adenosyltransferase I/III deficiency among individuals identified during newborn screening in Japan
Keywords: طیف جهش; Methionine adenosyltransferase; S-adenosylmethionine; MAT1A; Myelination; Mutation spectrum;
Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene × gene interactions
Keywords: طیف جهش; Holoprosencephaly; Digenic inheritance; Mutation spectrum; SHH; ZIC2; SIX3 and TGIF
Critical evaluation of random mutagenesis by error-prone polymerase chain reaction protocols, Escherichia coli mutator strain, and hydroxylamine treatment
Keywords: طیف جهش; Protein engineering; Mutation frequency; Mutation spectrum; Transition; Transversion; Amino acid substitution pattern; XL1–Red; Taq DNA polymerase; Mutazyme II DNA polymerase; 8-oxo-dGTP; dPTP; NH2OH–HCl
Cystic fibrosis transmembrane conductance regulator mutations in azoospermic and oligospermic men and their partners
Keywords: طیف جهش; assisted reproduction; cystic fibrosis transmembrane conductance regulator; mutation spectrum; polyvariant mutants; primary infertility; risk for offspring
Transcription-associated mutagenesis in yeast is directly proportional to the level of gene expression and influenced by the direction of DNA replication
Keywords: طیف جهش; Spontaneous mutagenesis; Transcription; Replication direction; Polymerase zeta; Mutation spectrum
Genetic Aspects of Neurocutaneous Disorders
Keywords: طیف جهش; incontinentia pigmenti; von Hippel-Lindau; tuberous sclerosis complex; neurofibromatosis; NEMO; vHL; hamartin; tuberin; neurofibromin; mutation spectrum; genetic testing; genetic counseling;
The mutagenicity of urban particulate matter in an enzyme free system is associated with the generation of reactive oxygen species
Keywords: طیف جهش; Urban particulate matter; supF; Mutation spectrum; Oxidative DNA damage; Metal ions;
Cellular and molecular effects for mutation induction in normal human cells irradiated with accelerated neon ions
Keywords: طیف جهش; Accelerated neon ions; Linear energy transfer (LET); HPRT locus; Mutation spectrum; Multiplex polymerase chain reaction (PCR);