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32199 publications found in the database

*2013 (2117)

*Starting in 2010, coverage has been refocused on core journals.

2013 Publications

De Novo Mutations in the Genome Organizer CTCF Cause Intellectual Disability
Gregor, A. et al. American Journal of Human Genetics 93(1), 124-31, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Genome-wide analysis shows that Ldb1 controls essential hematopoietic genes/pathways in mouse early development and reveals novel players in hematopoiesis
Mylona, A. et al. Blood 121(15), 2902-13, 2013, Mouse Genome 430 2.0 Array  PubMed

SHORT Syndrome with Partial Lipodystrophy Due to Impaired Phosphatidylinositol 3 Kinase Signaling
Chudasama, K. K. et al. American Journal of Human Genetics 93(1), 150-7, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Foxp31 T-regulatory cells require DNA methyltransferase 1 expression to prevent development of lethal autoimmunity
Wang, L. Q. et al. Blood 121(18), 3631-9, 2013, Mouse Expression Set 430  PubMed

SOX4 is a direct target gene of FRA-2 and induces expression of HDAC8 in adult T-cell leukemia/lymphoma
Higuchi, T. et al. Blood 121(18), 3640-9, 2013, Human Genome U133 Plus 2.0 Array  PubMed

Inactivation of TP53 correlates with disease progression and low miR-34a expression in previously treated chronic lymphocytic leukemia patients
Dufour, A. et al. Blood 121(18), 3650-7, 2013  PubMed

Genetic mapping and exome sequencing identify 2 mutations associated with stroke protection in pediatric patients with sickle cell anemia
Flanagan, J. M. et al. Blood 121(16), 3237-45, 2013, Genome-Wide Human SNP Array 6.0  PubMed

Genomic instability may originate from imatinib-refractory chronic myeloid leukemia stem cells
Bolton-Gillespie, E. et al. Blood 121(20), 4175-83, 2013  PubMed

MYD88 L265P mutation in Waldenstrom macroglobulinemia
Poulain, S. et al. Blood 121(22), 4504-11, 2013, Genome-Wide Human SNP Array 6.0  PubMed

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