Keywords: کولونوسکوپی; Dyskeratosis congenita; Telomeres; Bone marrow failure; Bone marrow transplantation; Aplastic anemia;
مقالات ISI کولونوسکوپی (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: کولونوسکوپی; AAA; acquired aplastic anemia; IBMF; inherited bone marrow failure; IST; immunosuppressive therapy; CSA; cyclosporine A; ATG; antithymocyte globulin; CR; complete response; PR; partial response; TA; telomerase activity; TRAP; Telomeric Repeat Amplificatio
Keywords: کولونوسکوپی; dyskeratosis congenita; reticulate pigmentation; telomere; BMF; bone marrow failure; DC; dyskeratosis congenita; HCT; hematopoietic cell transplantation; HH; Hoyeraal-Hreidarsson; IUGR; intrauterine growth restriction; NIH; National Institutes of Health;
Keywords: کولونوسکوپی; Bone marrow failure syndromes; Dyskeratosis congenita; Fanconi Anemia; Stem cell Transplantation;
Keywords: کولونوسکوپی; Inherited bone marrow failure; Fanconi anemia; Severe congenital neutropenia; Dyskeratosis congenita; Shwachman Diamond syndrome; Diamond Blackfan anemia;
Keywords: کولونوسکوپی; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; AT; ataxia telangiectasia; BER; base excision repair; BFB; breakage-fusion-bridge; BMDCs; bone marrow-derived cells; BS; Bloom syndrome; CIN; chromosome instability; CNS; central nervous syste
Keywords: کولونوسکوپی; Neonate; Cytopenia; Cancer; Bone marrow failure; Fanconi anemia; Dyskeratosis congenita
Keywords: کولونوسکوپی; Bloom syndrome; dyskeratosis congenita; genetic testing; Gorlin syndrome; Muir-Torre syndrome; nonmelanoma skin cancer; oculocutaneous albinism; Rothmund-Thomson syndrome; Werner syndrome; 5-FU; 5-fluorouracil; ADA1; adenosine deaminase 1; ADA-SCID; a
Keywords: کولونوسکوپی; Dyskeratosis congenita; Hematopoietic stem cell transplantation; Telomere; Pulmonary fibrosis; Transplant-related mortality; Review;
Keywords: کولونوسکوپی; Dyskeratosis congenita; Gastric cancer; Perioperative management; Thrombocytopenia
Keywords: کولونوسکوپی; 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: کولونوسکوپی; Human papillomavirus; Vaccine; Fanconi anemia; dyskeratosis congenita; Inherited bone marrow failure syndromes;
Keywords: کولونوسکوپی; DC; dyskeratosis congenita; DOXO; doxorubicin; HDACi; histone deacetylase inhibitor; TSA; trichostatin A; CQ; chloroquine; SAH; senescence-associated heterochromatinization; Senescence-associated heterochromatinization; Dyskeratosis congenita; DNA damage;
Keywords: کولونوسکوپی; Dyskeratosis congenita; Allogeneic transplantation; Long-term survival; Pulmonary toxicity;
Telomere Length as Cardiovascular Aging Biomarker
Keywords: کولونوسکوپی; atherosclerosis; biological aging; epidemiology; telomerase; aCVD; atherosclerotic cardiovascular disease; DKC; dyskeratosis congenita; GWAS; genome-wide association study; qPCR; quantitative polymerase chain reaction; SNP; single nucleotide polymorphism;
High-throughput gene expression analysis identifies p53-dependent and -independent pathways contributing to the adrenocortical dysplasia (acd) phenotype
Keywords: کولونوسکوپی; TPP1; protein encoded by adrenocortical dysplasia gene; Acd; adrenocortical dysplasia gene; acd; adrenocortical dysplasia mutation; p53; transformation related protein 53; DNA; Deoxyribonucleic acid; DC; Dyskeratosis congenita; HHS; Hoyeraal-Hreidarsson s
ReportLate Effects Screening Guidelines after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement From the Second Pediatric Blood and Marrow Transplant Consortium International Conference on Late Effects Aft
Keywords: کولونوسکوپی; Late effects; Pediatric allogeneic hematopoietic cell transplant; Inherited bone marrow failure syndromes; Fanconi anemia; Dyskeratosis congenita; Diamond Blackfan anemia;
Current Knowledge and Priorities for Future Research in Late Effects after Hematopoietic Cell Transplantation for Inherited Bone Marrow Failure Syndromes: Consensus Statement from the Second Pediatric Blood and Marrow Transplant Consortium International C
Keywords: کولونوسکوپی; Late effects; Pediatric allogeneic hematopoietic cell transplantation; Inherited bone marrow failure syndromes; Fanconi anemia; Dyskeratosis congenita; Diamond Blackfan anemia;
A Reduced-Intensity Conditioning Regimen for Patients with Dyskeratosis Congenita Undergoing Hematopoietic Stem Cell Transplantation
Keywords: کولونوسکوپی; Dyskeratosis congenita; Hematopoietic stem cell transplantation; Reduced-intensity conditioning
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up
Keywords: کولونوسکوپی; dyskeratosis congenita; Hoyeraal-Hreidarsson syndrome; telomere; PARN; microcephaly; CNS calcification;
Hypo- and Hyper-Assembly Diseases of RNA–Protein Complexes
Keywords: کولونوسکوپی; RNP assembly; stress granules; spinal muscular atrophy; dyskeratosis congenita; RNA quality control; therapy
Pulmonary fibrosis in dyskeratosis congenita: report of 2 cases
Keywords: کولونوسکوپی; Dyskeratosis congenita; Hoyeraal-Hreidarsson syndrome; DKC1 mutation; Pulmonary fibrosis; Usual interstitial pneumonia;
Development of surface modified biodegradable polymeric nanoparticles to deliver GSE24.2 peptide to cells: A promising approach for the treatment of defective telomerase disorders
Keywords: کولونوسکوپی; Biodegradable nanoparticles; Cell-penetrating peptides; GSE24.2 peptide; Telomerase reactivation; Dyskeratosis congenita; Polycations;
Genetic predisposition syndromes: When should they be considered in the work-up of MDS?
Keywords: کولونوسکوپی; myelodysplastic syndromes; MDS; bone marrow failure syndromes; genetic predisposition; familial MDS; familial leukemia; Fanconi Anemia; Dyskeratosis Congenita; GATA2; MonoMac; Emberger Syndrome; RUNX1; FPD/AML; CEBPA; SRP72; Diamond-Blackfan Anemia; Shwac
Hoyeraal-Hreidarsson syndrome with a DKC1 mutation identified by whole-exome sequencing
Keywords: کولونوسکوپی; SNV; single nucleotide variant; Hoyeraal-Hreidarsson syndrome; Dyskeratosis congenita; Telomere dysfunction; DKC1; Whole-exome sequencing;
A Novel Dyskerin (DKC1) Mutation Is Associated With Familial Interstitial Pneumonia
Keywords: کولونوسکوپی; AEC; alveolar epithelial cell; DC; dyskeratosis congenita; FIP; familial interstitial pneumonia; HRCT; high-resolution CT; ILD; interstitial lung disease; IPF; idiopathic pulmonary fibrosis; PBMC; peripheral blood mononuclear cell; PCR; polymerase chain r
Oxidative stress, DNA damage, and the telomeric complex as therapeutic targets in acute neurodegeneration
Keywords: کولونوسکوپی; MDA; malondialdehyde; 4-HNE; 4-hydroxynonenal; EAE; experimental allergic encephalomyelitis; MS; mutiple sclerosis; SSB; single strand break; DSB; double strand break; 8-OxoG; 8-hydroxyguanosine; 8-NO(2)-G; 8-nitroguanine; AP; apurinic/apyrmidinic; OGG1;
Telomere dysfunction and tumor suppression responses in dyskeratosis congenita: Balancing cancer and tissue renewal impairment
Keywords: کولونوسکوپی; Dyskeratosis congenita; Telomeres; Tumor suppression; Clinical variability; ASCs impairment; Cancer;
Telomerase and idiopathic pulmonary fibrosis
Keywords: کولونوسکوپی; Dyskeratosis congenita; Interstitial lung disease; Aplastic anemia; Liver cirrhosis; Emphysema; Diabetes;
High resolution melting analysis for the identification of novel mutations in DKC1 and TERT genes in patients with dyskeratosis congenita
Keywords: کولونوسکوپی; Telomerase; Dyskeratosis congenita; HRM; DKC1; hTERT
Pulmonary Complications of Dermatological Disorders
Keywords: کولونوسکوپی; yellow nail syndrome; neurofibromatosis; tuberous sclerosis complex; hereditary haemorrhagic telangiectasia; klippel-trénaunay-weber syndrome; cutis laxa; ehlers-danlos syndrome; hermansky-pudlak syndrome; erythema multiforme; mastocytosis; dyskeratosis
Dyskeratosis congenita as a disorder of telomere maintenance
Keywords: کولونوسکوپی; Dyskeratosis congenita; Telomerase; Telomere;
It all comes together at the ends: Telomerase structure, function, and biogenesis
Keywords: کولونوسکوپی; TERT; TR; Dyskerin; Dyskeratosis congenita; Pulmonary fibrosis; Aplastic anemia;
Heterogeneous telomere defects in patients with severe forms of dyskeratosis congenita
Keywords: کولونوسکوپی; Telomere; dyskeratosis congenita; Hoyeraal-Hreidarsson syndrome; senescence; immune deficiencies; bone marrow failure; CO-FISH; Chromosome orientation-fluorescence in situ hybridization; DC; Dyskeratosis congenita; DSB; Double-strand break; HH; Hoyeraal
Prenatal and postnatal growth retardation, microcephaly, developmental delay, and pigmentation abnormalities: Naegeli syndrome, dyskeratosis congenita, poikiloderma Clericuzio type, or separate entity?
Keywords: کولونوسکوپی; Naegeli syndrome; Naegeli-Franceschetti-Jadassohn syndrome; Dermatopathia pigmentosa reticularis; Dyskeratosis congenita; Reticulate hyperpigmentation; Poikiloderma Clericuzio type;
A new human dyskerin isoform with cytoplasmic localization
Keywords: کولونوسکوپی; DC; Dyskeratosis Congenita; X-DC; X-linked Dyskeratosis Congenita; snoRNA; small nucleolar RNA; snoRNPs; small nucleolar RNA ribonucleoproteins; hTERT; human telomerase reverse transcriptase; hTR; human telomerase RNA component; IRES; Internal Ribosome En
Telomere biology in hematopoiesis and stem cell transplantation
Keywords: کولونوسکوپی; HSCT, hematopoietic stem cell transplantation; GvHD, graft versus host diseaseTelomeres; Bone marrow failure disorders; Hematopoietic stem cell transplant; Dyskeratosis congenita; Myelodysplastic syndrome; Pluripotent stem cells
Dyskeratosis congenita
Keywords: کولونوسکوپی; AML; acute myeloid leukemia; BMF; bone marrow failure; DC; dyskeratosis congenita; HHS; Hoyeraal Hreidarrson syndrome; MDS; myelodysplastic syndrome; OP; osteoporosis; PF; pulmonary fibrosis; POT1; protection of telomeres 1; TIN2; TRF1-interacting nuclear
Driving ribosome assembly
Keywords: کولونوسکوپی; Ribosome assembly; Nuclear export of ribosomes; Diamond-Blackfan anemia; Shwachman-Diamond syndrome; Dyskeratosis congenita; Cartilage–hair hypoplasia; Bowen-Conradi syndrome; Cancer; Quality control of ribosomes
Pathophysiology and management of inherited bone marrow failure syndromes
Keywords: کولونوسکوپی; Aplastic anemia; Fanconi; Dyskeratosis congenita; Diamond–Blackfan anemia; Shwachman–Diamond syndrome; Inherited bone marrow failure syndromes
Hereditary Genodermatoses with Cancer Predisposition
Keywords: کولونوسکوپی; Genodermatoses; Nevoid basal cell carcinoma syndrome; Neurofibromatosis type 1; Neurofibromatosis type 2; Tuberous sclerosis; Melanoma; Xeroderma pigmentosum; Dyskeratosis congenita;
Dyskeratosis congenita, stem cells and telomeres
Keywords: کولونوسکوپی; Dyskeratosis congenita; Stem cell; Telomerase; Telomere;
Dyskeratosis Congenita
Keywords: کولونوسکوپی; Dyskeratosis congenita; Telomere; DKC1; TERC; TERT; TINF2; Bone marrow failure;
Physiological assembly and activity of human telomerase complexes
Keywords: کولونوسکوپی; Human telomerase; Telomerase RNA; Telomerase reverse transcriptase; Ribonucleoprotein; Biogenesis; Dyskeratosis congenita
Dyskeratosis congenita: The diverse clinical presentation of mutations in the telomerase complex
Keywords: کولونوسکوپی; Aplastic anaemia; Dyskeratosis congenita; Ribosome biogenesis; Telomerase; TelomeresDC, dyskeratosis congenita; AA, aplastic anaemia; TERC, telomerase RNA component; TERT, telomerase reverse transcriptase component; snoRNA, small nucleolar RNA; HH, Hoyera
Dyskeratosis Congenita: A historical perspective
Keywords: کولونوسکوپی; Aplastic anaemia; Dyskeratosis Congenita; Dyskerin; TERC; TERT; Telomerase
Inherited aplastic anaemias/bone marrow failure syndromes
Keywords: کولونوسکوپی; 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
The role of telomere biology in bone marrow failure and other disorders
Keywords: کولونوسکوپی; Telomere; Bone marrow failure; Dyskeratosis congenita; Pulmonary fibrosis; Aplastic anemia
Discussion nosologique entre dyskératose congénitale et maladie de Fanconi : à  propos de 1 cas d'aplasie médullaire constitutionnelle
Keywords: کولونوسکوپی; Aplasie médullaire; Maladie de Fanconi; Dyskératose congénitale; Aplastic anemia; Fanconi anemia; Dyskeratosis congenita;
Dyskeratosis congenita
Keywords: کولونوسکوپی; Oral mucosa; Oral cancer; Dyskeratosis congenita; Dyskerin; DKC1 gene; Review