Fabı́ola Traina - Concepedia

Author

Fabı́ola Traina

Universidade Estadual de Campinas (UNICAMP)ORCID

Also Known As

Elvira Deolinda Rodrigues Pereira Velloso, F Traina, F. TRAINA, F. Traina, F. Tráina, Fabiola Traina, Fabíola Traina, Fabíola Traina, Fabíola Traina (5657200), Fabı́ola Traina

351

Publications

4.3K

Citations

H-Index

Concepts

All Affiliations

Universidade Estadual de Campinas (UNICAMP)Universidade de São Paulo Universidade Federal de São Paulo Cleveland Clinic Universidade Federal de Pernambuco

About

Fabı́ola Traina is an author at Universidade Estadual de Campinas (UNICAMP) specializing in medicine, cell biology, and hematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	37	1.6K
2	Cell Biology	21	30	1.3K
3	Health Sciences	7	7	187
4	Allergy	2	2	153
5	Blood Transplantation	2	2	77

Fabı́ola Traina

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
Mutational spectrum analysis of chronic myelomonocytic leukemia includes genes associated with epigenetic regulation: UTX, EZH2, and DNMT3A A. Jankowska, Hideki Makishima, Ramón V. Tiu, Blood	2011	320
Impact of molecular mutations on treatment response to DNMT inhibitors in myelodysplasia and related neoplasms Fabı́ola Traina, Valeria Visconte, Paul Elson, Leukemia Hematological MalignancyMolecular MutationsMedicineTreatment ResponseDnmt Inhibitors	2013	283
SF3B1 haploinsufficiency leads to formation of ring sideroblasts in myelodysplastic syndromes Valeria Visconte, Heesun J. Rogers, Jarnail Singh, Blood	2012	180
Single Nucleotide Polymorphism Array Lesions, TET2, DNMT3A, ASXL1 and CBL Mutations Are Present in Systemic Mastocytosis Fabı́ola Traina, Valeria Visconte, A. Jankowska, PLoS ONE Mast Cell DisorderGeneticsSystemic MastocytosisPathologyMolecular Genetics	2012	116
Rho Kinase Regulates the Survival and Transformation of Cells Bearing Oncogenic Forms of KIT, FLT3, and BCR-ABL Raghuveer Singh Mali, Baskar Ramdas, Peilin Ma, Cancer Cell Signal TransductionSignaling PathwayRho KinaseOncogenic AgentCell Regulation	2011	96
Spliceosomal gene mutations are frequent events in the diverse mutational spectrum of chronic myelomonocytic leukemia but largely absent in juvenile myelomonocytic leukemia Sarah Abu Kar, Ania Jankowska, Hirokazu Makishima, Haematologica Chronic Myelomonocytic LeukemiaSpliceosomal Gene MutationsMixed-phenotype Acute LeukemiaGeneticsPathology	2012	79
ARHGAP21 is a RhoGAP for RhoA and RhoC with a role in proliferation and migration of prostate adenocarcinoma cells Mariana Lazarini, Fabı́ola Traina, João Agostinho Machado‐Neto, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease UrologyMedicineProstate Adenocarcinoma CellsTumor SuppressorProstatic Disease	2012	64
Expansion strategies for human mesenchymal stromal cells culture under xeno‐free conditions Patrícia A. Tozetti, Sâmia Rigotto Caruso, Amanda Mizukami, Biotechnology Progress	2017	62
Therapy with hydroxyurea is associated with reduced adhesion molecule gene and protein expression in sickle red cells with a concomitant reduction in adhesive properties Sheley Gambero, Andréia A. Canalli, Fabı́ola Traina, European Journal Of Haematology	2006	60
CXCR7 Is Highly Expressed in Acute Lymphoblastic Leukemia and Potentiates CXCR4 Response to CXCL12 Rita de Cássia Carvalho Melo, Ana Leda F. Longhini, Carolina L. Bigarella, PLoS ONE Cxcl12-binding ReceptorMixed-phenotype Acute LeukemiaT-regulatory CellImmunologyImmunologic Mechanism	2014	58

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