Detalhe da pesquisa
1.
Dynamics of mutations in patients with essential thrombocythemia treated with imetelstat.
Haematologica
; 106(9): 2397-2404, 2021 09 01.
Artigo
Inglês
| MEDLINE | ID: mdl-32732354
2.
Targeting Telomere Biology in Acute Lymphoblastic Leukemia.
Int J Mol Sci
; 22(13)2021 Jun 22.
Artigo
Inglês
| MEDLINE | ID: mdl-34206297
3.
Combined Lung and Liver Transplantation for Short Telomere Syndrome.
Liver Transpl
; 26(6): 840-844, 2020 06.
Artigo
Inglês
| MEDLINE | ID: mdl-32080954
4.
Higher Age (≥60 Years) Increases the Risk for Adverse Events during Autologous Hematopoietic Stem Cell Transplantation.
Cancers (Basel)
; 15(5)2023 Mar 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36900376
5.
Porcine arthrogryposis multiplex congenita (AMC): new diagnostic test and narrowed candidate region.
Mol Cell Probes
; 26(6): 248-52, 2012 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-22405934
6.
Siglec-7 represents a glyco-immune checkpoint for non-exhausted effector memory CD8+ T cells with high functional and metabolic capacities.
Front Immunol
; 13: 996746, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36211376
7.
Siglec-9 Regulates an Effector Memory CD8+ T-cell Subset That Congregates in the Melanoma Tumor Microenvironment.
Cancer Immunol Res
; 7(5): 707-718, 2019 05.
Artigo
Inglês
| MEDLINE | ID: mdl-30988027
8.
The C-Terminal Fragment of Agrin (CAF), a Novel Marker of Renal Function, Is Filtered by the Kidney and Reabsorbed by the Proximal Tubule.
PLoS One
; 11(7): e0157905, 2016.
Artigo
Inglês
| MEDLINE | ID: mdl-27380275
9.
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Nat Genet
; 48(10): 1185-92, 2016 10.
Artigo
Inglês
| MEDLINE | ID: mdl-27571260
10.
Imetelstat inhibits growth of megakaryocyte colony-forming units from patients with essential thrombocythemia.
Blood Adv
; 3(22): 3724-3728, 2019 11 26.
Artigo
Inglês
| MEDLINE | ID: mdl-31770436
11.
Injection of a soluble fragment of neural agrin (NT-1654) considerably improves the muscle pathology caused by the disassembly of the neuromuscular junction.
PLoS One
; 9(2): e88739, 2014.
Artigo
Inglês
| MEDLINE | ID: mdl-24520420
12.
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Nat Genet
; 49(2): 317, 2017 01 31.
Artigo
Inglês
| MEDLINE | ID: mdl-28138155