Detalhe da pesquisa
1.
Functional Enhancers Shape Extrachromosomal Oncogene Amplifications.
Cell
; 179(6): 1330-1341.e13, 2019 11 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-31761532
2.
IGJ and SPATS2L immunohistochemistry sensitively and specifically identify BCR::ABL1+ and BCR::ABL1-like B-acute lymphoblastic leukaemia.
Br J Haematol
; 204(1): 229-239, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37871900
3.
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
Acta Neuropathol
; 146(1): 121-143, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37156880
4.
ZBTB16::RARA variant acute promyelocytic leukemia (vAPL) treated with gemtuzumab ozogamicin (GO) with unique pathology and genetic findings.
Br J Haematol
; 202(6): 1077-1078, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37495505
5.
Correction: A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques.
Acta Neuropathol
; 146(1): 167-170, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37253983
6.
Impact of an alternative chromosome 17 probe and the 2013 American Society of Clinical Oncology and College of American Pathologists guidelines on fluorescence in situ hybridization for the determination of HER2 gene amplification in breast cancer.
Cancer
; 123(12): 2230-2239, 2017 Jun 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-28192599
7.
Lifting the Limit: Updated ISSCR Guidance for Lab-Grown Human Embryos.
Clin Chem
; 68(5): 738, 2022 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35584794
8.
Transient abnormal myelopoiesis of a newborn not associated with chromosome 21 abnormalities or GATA1 mutations.
Pediatr Blood Cancer
; 62(2): 353-355, 2015 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-25175265
9.
Subjectivity in chromosome band-level estimation: a multicenter study.
Genet Med
; 16(2): 170-5, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23887773
10.
Aggressive Lymphoplasmacytic Neoplasm With an Unusual In-frame Deletion of MYD88 Associated With TRAF3 and TP53 Mutations and Complex Karyotype.
Int J Surg Pathol
; 32(1): 5-10, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37093763
11.
Philadelphia chromosome-positive T-cell acute lymphoblastic leukemia: a case report.
J Int Med Res
; 52(2): 3000605231156757, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38422030
12.
Mucin 4 protein is expressed in B-acute lymphoblastic leukemia and is restricted to BCR::ABL1-positive and BCR::ABL-like subtypes.
Hum Pathol
; 136: 75-83, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-37023866
13.
CCMCL1: a new model of aggressive mantle cell lymphoma.
Blood
; 125(17): 2730-2, 2015 Apr 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-25907904
14.
Genetic aspects of human prion diseases.
Front Neurol
; 13: 1003056, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36277922
15.
Identification of a Cancer-Predisposing Germline POT1 p.Ile49Metfs*7 Variant by Targeted Sequencing of a Splenic Marginal Zone Lymphoma.
Genes (Basel)
; 13(4)2022 03 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-35456397
16.
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Genet Med
; 13(9): 777-84, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21844811
17.
Acute myeloid leukemia with inv(16)(p13.1q22), abnormal eosinophils, and absence of peripheral blood and bone marrow blasts.
Am J Hematol
; 91(4): E273-4, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26719044
18.
An unusual case of cutaneous blastic plasmacytoid dendritic cell neoplasm with concomitant B-cell lymphoproliferative disorder.
Am J Dermatopathol
; 33(3): e31-6, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20861710
19.
PDGFRB-rearranged T-lymphoblastic leukemia/lymphoma occurring with myeloid neoplasms: the missing link supporting a stem cell origin.
Haematologica
; 99(9): e148-51, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24951465
20.
Clinicopathologic and molecular characterization of myeloid neoplasms harboring isochromosome 17(q10).
Am J Hematol
; 89(8): 862, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24796269