397 results on '"Hahn, Christopher N"'
Search Results
2. Germline genetic variants that predispose to myeloproliferative neoplasms and hereditary myeloproliferative phenotypes
3. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
4. TP53 mutation variant allele frequency of ≥10% is associated with poor prognosis in therapy-related myeloid neoplasms
5. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41
6. Role of Germline Predisposition to Therapy-Related Myeloid Neoplasms
7. Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma
8. Allogeneic hematopoietic stem cell transplant outcomes in adults with inherited myeloid malignancies
9. Novel modes of MPL activation in triple-negative myeloproliferative neoplasms
10. Genomic subtyping and therapeutic targeting of acute erythroleukemia
11. IDH-mutant myeloid neoplasms are associated with seronegative rheumatoid arthritis and innate immune activation
12. Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer
13. Germ line ERG haploinsufficiency defines a new syndrome with cytopenia and hematological malignancy predisposition
14. IDH-mutant myeloid neoplasms are associated with seronegative rheumatoid arthritis and innate immune activation
15. The mutational burden of therapy-related myeloid neoplasms is similar to primary myelodysplastic syndrome but has a distinctive distribution
16. ERG Is a New Predisposition Gene for Bone Marrow Failure and Hematological Malignancy
17. Unraveling facets of MECOM-associated syndrome: somatic genetic rescue, clonal hematopoiesis, and phenotype expansion
18. A Vascular Cell-Restricted RhoGAP, p73RhoGAP, Is a Key Regulator of Angiogenesis
19. Transcription factor genetics and biology in predisposition to bone marrow failure and hematological malignancy
20. Two monogenic disorders masquerading as one: severe congenital neutropenia with monocytosis and non-syndromic sensorineural hearing loss
21. Correction of Murine Galactosialidosis by Bone Marrow-Derived Macrophages Overexpressing Human Protective Protein/Cathepsin A under Control of the Colony-Stimulating Factor-1 Receptor Promoter
22. The 10th Barossa meeting: Cell Signalling to Cancer Medicine.
23. Identification and targeted management of a neurodegenerative disorder caused by biallelic mutations in SLC5A6
24. Seronegative Rheumatoid Arthritis and Innate Immune Activation is Frequent in Myeloid Neoplasms with Isocitrate Dehydrogenase 1/2 Mutations
25. TP53 mutation in therapy-related myeloid neoplasm defines a distinct molecular subtype
26. Myeloid neoplasms with germline DDX41 mutation
27. TP53 Mutation Status Defines a Distinct Clinicopathological Entity of Therapy-Related Myeloid Neoplasm, Characterized By Genomic Instability and Extremely Poor Outcome
28. Integrated Personalized Prediction Model Identifies a Subgroup of Wild-Type TP53therapy-Related Myeloid Neoplasm Patients with Poor Outcome
29. Somatic Mutational Landscape of Hereditary Hematopoietic Malignancies Associated with Germline Variants in RUNX1, GATA2 and DDX41
30. Allogeneic Hematopoietic Stem Cell Transplant Outcomes in Adults with Inherited Myeloid Malignancies
31. Regulation of vascular leak and recovery from ischemic injury by general and VE-cadherin–restricted miRNA antagonists of miR-27
32. Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations
33. Clinical implications of transient myeloproliferative disorder in a neonate without Down syndrome features
34. GATA2 is required for lymphatic vessel valve development and maintenance
35. Loss-of-function germline GATA2 mutations in patients with MDS/AML or MonoMAC syndrome and primary lymphedema reveal a key role for GATA2 in the lymphatic vasculature
36. A practical guide to interpreting germline variants that drive hematopoietic malignancies, bone marrow failure, and chronic cytopenias
37. Pathogenic variants in MDFIC cause recessive central conducting lymphatic anomaly with lymphedema
38. Childhood acute myeloid leukemia shows a high level of germline predisposition
39. Stress-induced premature senescence mediated by a novel gene, SENEX, results in an anti-inflammatory phenotype in endothelial cells
40. Unexpected High Frequency of Pathogenic Germline Variants in Older Adults with Primary Myelodysplastic Syndrome
41. Cover, Volume 42, Issue 11
42. Allan–Herndon–Dudley Syndrome with Unusual Profound Sensorineural Hearing Loss
43. GATA2 deficiency syndrome: A decade of discovery
44. The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy
45. Childhood acute myeloid leukemia shows a high level of germline predisposition
46. Basal and angiopoietin-1–mediated endothelial permeability is regulated by sphingosine kinase-1
47. ARMC5 Mutations Are Common in Familial Bilateral Macronodular Adrenal Hyperplasia
48. Additional file 20 of Deep sequencing analysis of the developing mouse brain reveals a novel microRNA
49. Additional file 16 of Deep sequencing analysis of the developing mouse brain reveals a novel microRNA
50. Additional file of Deep sequencing analysis of the developing mouse brain reveals a novel microRNA
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.