Pages that link to "Q79843707"

The following pages link to Dyskeratosis congenita (Q79843707):

Displaying 38 items.

• Mitotic spindle destabilization and genomic instability in Shwachman-Diamond syndrome (Q24321611) (← links)
• Mutations in the SBDS gene in acquired aplastic anemia (Q24682080) (← links)
• Translation matters: protein synthesis defects in inherited disease (Q28239576) (← links)
• Frequency and natural history of inherited bone marrow failure syndromes: the Israeli Inherited Bone Marrow Failure Registry. (Q33389382) (← links)
• Genomic characterization of the inherited bone marrow failure syndromes (Q33411559) (← links)
• Inherited bone marrow failure syndromes in adolescents and young adults (Q33415672) (← links)
• Neonatal manifestations of inherited bone marrow failure syndromes (Q33428864) (← links)
• Dyskerin ablation in mouse liver inhibits rRNA processing and cell division (Q33558833) (← links)
• Defective proliferative capacity and accelerated telomeric loss of hematopoietic progenitor cells in rheumatoid arthritis (Q33646411) (← links)
• Genetic Variations in Telomere Maintenance, with Implications on Tissue Renewal Capacity and Chronic Disease Pathologies (Q34506827) (← links)
• Cancer in dyskeratosis congenita (Q34605382) (← links)
• Genetics in Pulmonary Fibrosis—Familial Cases Provide Clues to the Pathogenesis of Idiopathic Pulmonary Fibrosis (Q35010171) (← links)
• Oral and dental phenotype of dyskeratosis congenita (Q35126202) (← links)
• Cellular senescence and organismal aging (Q35815320) (← links)
• Telomeres, stem cells, and hematology (Q36445787) (← links)
• Telomere maintenance and human bone marrow failure (Q36591289) (← links)
• Characterization of primitive hematopoietic cells from patients with dyskeratosis congenita (Q36591308) (← links)
• Anemia of Central Origin (Q36784115) (← links)
• A pathogenic dyskerin mutation impairs proliferation and activates a DNA damage response independent of telomere length in mice (Q36786840) (← links)
• Telomerase reverse transcriptase haploinsufficiency and telomere length in individuals with 5p- syndrome (Q36973951) (← links)
• Genetic instability syndromes with progeroid features (Q36974281) (← links)
• Diamond Blackfan anemia: a disorder of red blood cell development (Q37087644) (← links)
• Telomerase insufficiency in rheumatoid arthritis (Q37132884) (← links)
• Genetic and environmental factors influencing human diseases with telomere dysfunction. (Q37285981) (← links)
• Concise Review: Getting to the Core of Inherited Bone Marrow Failures. (Q37633372) (← links)
• Telomerase deficiency and cancer susceptibility syndromes (Q37633757) (← links)
• Response to androgen therapy in patients with dyskeratosis congenita (Q37699500) (← links)
• Telomere, DNA damage, and oxidative stress in stem cell aging (Q37823488) (← links)
• Genetic determinants of pulmonary fibrosis: evolving concepts (Q38210815) (← links)
• Telomeres in molecular epidemiology studies. (Q38226127) (← links)
• Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders. (Q38750036) (← links)
• Dyskeratosis congenita with malignant transformation (Q42583730) (← links)
• Clinical heterogeneity in a family with DKC1 mutation, dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome in first cousins (Q42692218) (← links)
• Progressive reticulate skin pigmentation and anonychia in a patient with bone marrow failure. (Q50071641) (← links)
• Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenita (Q58388012) (← links)
• Dyskeratosis congenita (Q58388056) (← links)
• Translational research in pulmonary fibrosis (Q91622811) (← links)
• CNS manifestations in patients with telomere biology disorders (Q92223357) (← links)