Found: 24
Select item for more details and to access through your institution.
Induced Pluripotent Stem Cells with a Mitochondrial DNA Deletion.
- Published in:
- Stem Cells, 2013, v. 31, n. 7, p. 1287, doi. 10.1002/stem.1354
- By:
- Publication type:
- Article
Large intergenic non-coding RNA-RoR modulates reprogramming of human induced pluripotent stem cells.
- Published in:
- Nature Genetics, 2010, v. 42, n. 12, p. 1113, doi. 10.1038/ng.710
- By:
- Publication type:
- Article
Successful cord blood transplantation for del7q myelodysplastic syndrome in Pearson marrow pancreas syndrome.
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 12, p. E376, doi. 10.1002/ajh.27107
- By:
- Publication type:
- Article
Congenital X‐linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6.
- Published in:
- American Journal of Hematology, 2022, v. 97, n. 1, p. 18, doi. 10.1002/ajh.26382
- By:
- Publication type:
- Article
TID1, a mammalian homologue of the drosophila tumor suppressor lethal(2) tumorous imaginal discs, regulates activation-induced cell death in Th2 cells.
- Published in:
- Oncogene, 2003, v. 22, n. 30, p. 4636, doi. 10.1038/sj.onc.1206569
- By:
- Publication type:
- Article
Telomerase RNA processing: Implications for human health and disease.
- Published in:
- Stem Cells, 2020, v. 38, n. 12, p. 1532, doi. 10.1002/stem.3270
- By:
- Publication type:
- Article
Genome-wide mapping of 5-hydroxymethylcytosine in embryonic stem cells.
- Published in:
- Nature, 2011, v. 473, n. 7347, p. 394, doi. 10.1038/nature10102
- By:
- Publication type:
- Article
Somatic coding mutations in human induced pluripotent stem cells.
- Published in:
- Nature, 2011, v. 471, n. 7336, p. 63, doi. 10.1038/nature09805
- By:
- Publication type:
- Article
Impaired hydroxylation of 5-methylcytosine in myeloid cancers with mutant TET2.
- Published in:
- Nature, 2010, v. 468, n. 7325, p. 839, doi. 10.1038/nature09586
- By:
- Publication type:
- Article
Telomere elongation in induced pluripotent stem cells from dyskeratosis congenita patients.
- Published in:
- Nature, 2010, v. 464, n. 7286, p. 292, doi. 10.1038/nature08792
- By:
- Publication type:
- Article
Dynamic instability of genomic methylation patterns in pluripotent stem cells.
- Published in:
- Epigenetics & Chromatin, 2010, v. 3, p. 17, doi. 10.1186/1756-8935-3-17
- By:
- Publication type:
- Article
Telomere dynamics in dyskeratosis congenita: the long and the short of iPS.
- Published in:
- Cell Research, 2011, v. 21, n. 8, p. 1157, doi. 10.1038/cr.2011.120
- By:
- Publication type:
- Article
AID for reprogramming.
- Published in:
- Cell Research, 2010, v. 20, n. 3, p. 253, doi. 10.1038/cr.2010.30
- By:
- Publication type:
- Article
A Young Adult with Aplastic Anemia and Gray Hair.
- Published in:
- Clinical Chemistry, 2013, v. 59, n. 1, p. 47, doi. 10.1373/clinchem.2012.187237
- By:
- Publication type:
- Article
Posttranscriptional manipulation of TERC reverses molecular hallmarks of telomere disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Deletion of a conserved Il4 silencer impairs T helper type 1-mediated immunity.
- Published in:
- Nature Immunology, 2004, v. 5, n. 12, p. 1251, doi. 10.1038/ni1135
- By:
- Publication type:
- Article
Hepatic vascular remodelling in a patient with dyskeratosis congenita.
- Published in:
- Histopathology, 2022, v. 80, n. 2, p. 450, doi. 10.1111/his.14530
- By:
- Publication type:
- Article
Hepatic vascular remodelling in a patient with dyskeratosis congenita.
- Published in:
- Histopathology, 2022, v. 80, n. 1, p. 450, doi. 10.1111/his.14530
- By:
- Publication type:
- Article
Drug discovery for Diamond-Blackfan anemia using reprogrammed hematopoietic progenitors.
- Published in:
- Science Translational Medicine, 2017, v. 9, n. 376, p. 1, doi. 10.1126/scitranslmed.aah5645
- By:
- Publication type:
- Article
Association of Donor and Recipient Telomere Length with Clinical Outcomes following Lung Transplantation.
- Published in:
- PLoS ONE, 2016, v. 11, n. 9, p. 1, doi. 10.1371/journal.pone.0162409
- By:
- Publication type:
- Article
Impaired reproductive function and fertility preservation in a woman with a dyskeratosis congenita.
- Published in:
- Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 5, p. 1221, doi. 10.1007/s10815-020-01758-x
- By:
- Publication type:
- Article
Domain specific mutations in dyskerin disrupt 3′ end processing of scaRNA13.
- Published in:
- Nucleic Acids Research, 2022, v. 50, n. 16, p. 9413, doi. 10.1093/nar/gkac706
- By:
- Publication type:
- Article
CTC1 Mutations in a patient with dyskeratosis congenita.
- Published in:
- Pediatric Blood & Cancer, 2012, v. 59, n. 2, p. 311, doi. 10.1002/pbc.24193
- By:
- Publication type:
- Article
Systematic molecular genetic analysis of congenital sideroblastic anemia: Evidence for genetic heterogeneity and identification of novel mutations.
- Published in:
- Pediatric Blood & Cancer, 2010, v. 54, n. 2, p. 273, doi. 10.1002/pbc.22244
- By:
- Publication type:
- Article