Keywords: کم خونی Fanconi; RIBE; radiation-induced bystander effect; TIBE; tumour-induced bystander effect; SCE; sister chromatid exchange; ROS; reactive oxygen species; NO; nitric oxide; NF-kappaB; nuclear factor-kappa B; COX-2; cyclooxygenase-2; FA; Fanconi anaemia; ATM; ataxia-t
مقالات ISI کم خونی Fanconi (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: کم خونی Fanconi; aplastic anaemia; congenital amegakaryocytic thrombocytopenia; diagnosis; Diamond–Blackfan anaemia; Dyskeratosis Congenita; Fanconi anaemia; genetics; inherited bone marrow failure syndromes; severe congenital neutropenia; Shwachman–Diamond syndrome
Keywords: کم خونی Fanconi; Fanconi anaemia; BRCA2; Glioblastoma multiforme
Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei
Keywords: کم خونی Fanconi; Fanconi Anaemia; DNA repair; Chromosomal radiosensitivity; Genomic instability; Radiosensitivity;
Manejo anestésico del trabajo de parto en embarazadas con anemia de Fanconi. Revisión bibliográfica a propósito de un caso
Keywords: کم خونی Fanconi; Anestesia epidural; Anemia de Fanconi; Embarazo; Trombocitopenia; Epidural anaesthesia; Fanconi anaemia; Pregnancy; Thrombocytopenia;
BRCA1, FANCD2 and Chk1 are potential molecular targets for the modulation of a radiation-induced DNA damage response in bystander cells
Keywords: کم خونی Fanconi; Radiation-induced bystander effect; Ionising radiation; DNA damage response; BRCA; Fanconi anaemia;
Quality control mechanisms in cellular and systemic DNA damage responses
Keywords: کم خونی Fanconi; DNA damage; Ageing; Ubiquitin proteasome system; DNA repair; Progeroid syndromes; Genome stability; ARF; adenosine diphosphate ribosylation factor; AT; ataxia telangiectasia; ATM; ataxia telangiectasia mutated; ATP; adenosine triphosphate; BER; base excis
SILAC-iPAC: A quantitative method for distinguishing genuine from non-specific components of protein complexes by parallel affinity capture
Keywords: کم خونی Fanconi; AP-MS; Affinity purification mass spectrometry; CS; Chicken serum; FA; Fanconi anaemia; FDR; False discovery rate; LTQ; Linear trap quadrupole; PI5P4K2β/α; Phosphatidyl inositol 5-phosphate 4-kinase 2 β/α subunits; PPI; Protein protein interactions; S
Structural peculiarities of the (MHF1-MHF2)4 octamer provide a long DNA binding patch to anchor the MHF-FANCM complex to chromatin: A solution SAXS study
Keywords: کم خونی Fanconi; FA; Fanconi anemia; ICLs; interstrand crosslinks; dsDNA; double strand DNA; MHF; MHF1-MHF2; MHF-FANCM-F; MHF in complex with a fragment of FANCM; SEC; size-exclusion chromatography; MM; molecular mass; Fanconi anaemia; MHF complex; FANCM; DNA binding
Fanconi’s anaemia and unilateral thumb polydactyly – Don’t miss it
Keywords: کم خونی Fanconi; Fanconi anaemia; Radial longitudinal deficiency; Thumb hypoplasia; Thumb duplication; Syndrome
Fatal course of tonsillar squamous cell carcinoma associated with Fanconi anaemia: A mini review
Keywords: کم خونی Fanconi; Fanconi anaemia; Tonsillar squamous cell carcinoma; Cancer predisposition syndromes; Secondary prevention; Radiotherapy
Evaluation of Fanconi anaemia genes FANCA, FANCC and FANCL in cervical cancer susceptibility
Keywords: کم خونی Fanconi; Cervical cancer; FANCA; FANCC; FANCL; Fanconi anaemia; Genetic variants
Several tetratricopeptide repeat (TPR) motifs of FANCG are required for assembly of the BRCA2/D1-D2-G-X3 complex, FANCD2 monoubiquitylation and phleomycin resistance
Keywords: کم خونی Fanconi; Fanconi anaemia; FANCG; Tetratricopeptide motif; Homologous recombination; Radiomimetic; SH3 domain
Understanding aplastic anaemia/bone-marrow failure syndromes
Keywords: کم خونی Fanconi; aplastic anaemia; congenital amegakaryocytic thrombocytopenia; Diamond–Blackfan anaemia; dyskeratosis congenital; Fanconi anaemia; inherited bone-marrow failure syndromes; Shwachman–Diamond syndrome; severe congenital neutropenia
Inherited aplastic anaemias/bone marrow failure syndromes
Keywords: کم خونی Fanconi; Congenital amegakaryocytic thrombocytopenia; Diamond-Blackfan anaemia; DNA repair; Dyskeratosis congenita; Fanconi anaemia; Inherited aplastic anaemia/bone marrow failure; Ribosome biogenesis; Shwachman-Diamond syndrome; Telomerase; Telomeres
Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2
Keywords: کم خونی Fanconi; Fanconi anaemia; TPR motifs; FANCG; XRCC3; BRCA2; Homologous recombination