D
David Leibowitz
Researcher at Columbia University
Publications - 58
Citations - 1220
David Leibowitz is an academic researcher from Columbia University. The author has contributed to research in topics: Internal medicine & Medicine. The author has an hindex of 17, co-authored 46 publications receiving 1152 citations. Previous affiliations of David Leibowitz include Indiana University & Icahn School of Medicine at Mount Sinai.
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Journal ArticleDOI
Organization of human δ- and β-globin genes in cellular DNA and the presence of intragenic inserts
TL;DR: The results indicate that unique restriction fragments are presented in normal DNA and absent in Lepore DNA, and allow preliminary ordering of these fragments on a restriction enzyme map.
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CML patients in blast crisis have breakpoints localized to a specific region of the BCR
TL;DR: Restriction mapping of the chromosome 22 translocation breakpoints performed for 26 patients showed that the breakpoints of eight of the nine patients in blast crisis were in the 3′ portion of the bcr, whereas the break points in the 17 patients in the chronic phase were clustered in the 5′ portionof the bCr, suggesting a strong correlation between a 3′ bcr breakpoint and blast crisis in CML.
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Four-year prospective study of pulmonary venous thrombosis after lung transplantation.
Larry L. Schulman,Thiruvengadam Anandarangam,David Leibowitz,Marco R. DiTullio,Carlton C. McGregor,Mark Galantowicz,Shunichi Homma +6 more
TL;DR: Larger thrombus size and flow velocity at the anastomotic site may guide prognosis and clinical management and greater acceleration of flow through a narrowed pulmonary vein correlated with poor clinical outcome.
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Frequent and extensive deletion during the 9,22 translocation in CML
TL;DR: The location of the deletions suggests that some mechanism maintains the chromosomal breakpoint on the Philadelphia chromosome within a limited region, and complicate the interpretation of Southern blots as a means of detecting the translocation.
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Changes in restricted human cellular DNA fragments containing globin gene sequences in thalassemias and related disorders
J. Gregory Mears,Francesco Ramirez,David Leibowitz,Frank T. Nakamura,Arthur D. Bloom,Felix Konotey-Ahulu,Arthur Bank +6 more
TL;DR: Human cellular DNA fragments from cells of normal subjects and patients with thalassemia obtained by restriction enzyme digestion were analyzed for their globin gene content and results are consistent with deletion of specific restriction human DNA fragments in subjects with these disorders and a greater deletion of beta-like gene sequences in Subjects with hereditary persistence of fetal hemoglobin.