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Journal of Immunology (Baltimore, Md. : 1950)|July 4, 2012
Transcription factor zinc finger and BTB domain 1 is essential for lymphocyte developmentDivya Punwani, Karen Simon, Youngnim Choi, et al.
Genes, Chromosomes & Cancer|January 18, 2012
Mitotic recombination of chromosome arm 17q as a cause of loss of heterozygosity of NF1 in neurofibromatosis type 1-associated glomus tumorsDouglas R Stewart, Alexander Pemov, Peter Van Loo, et al.
Stem Cell Research|December 24, 2014
Long term maintenance of myeloid leukemic stem cells cultured with unrelated human mesenchymal stromal cellsSawa Ito, A John Barrett, Amalia Dutra, et al.
Science Translational Medicine|June 13, 2014
Macrophage models of Gaucher disease for evaluating disease pathogenesis and candidate drugsElma Aflaki, Barbara K Stubblefield, Emerson Maniwang, et al.
Stem Cell Research|October 26, 2024
Generation and characterization of two iPSC lines derived from subjects with Free Sialic Acid Storage Disorder (FSASD)Marya S Sabir, Petcharat Leoyklang, Mary E Hackbarth, et al.
ACS Pharmacology & Translational Science|August 23, 2021
Genome-Edited Coincidence and PMP22-HiBiT Fusion Reporter Cell Lines Enable an Artifact-Suppressive Quantitative High-Throughput Screening Strategy for PMP22 Gene-Dosage Disorder Drug DiscoveryNatalia J Martinez, John C Braisted, Patricia K Dranchak, et al.
Lancet (London, England)|April 4, 2003
Differentiation of human bone marrow-derived cells into buccal epithelial cells in vivo: a molecular analytical studySimon D Tran, Stanley R Pillemer, Amalia Dutra, et al.
Molecular Genetics and Metabolism|January 14, 2011
Minimal evidence for a direct involvement of twisted gastrulation homolog 1 (TWSG1) gene in human holoprosencephalyEmily F Kauvar, Ping Hu, Daniel E Pineda-Alvarez, et al.
Haematologica|April 22, 2011
Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implicationsKatherine R Calvo, Donald C Vinh, Irina Maric, et al.
Human Genetics|May 6, 2015
Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large familyAnand Pathak, Alexander Pemov, Mary L McMaster, et al.
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