Zobrazeno 1 - 10
of 52
pro vyhledávání: '"S A Stass"'
Publikováno v:
Gene Therapy. 7:1698-1705
Development of nonviral delivery systems is progressing toward a transfection efficiency sufficient to affect metabolic and neoplastic diseases in humans. Nevertheless, inadequate transfection efficiency of target cells with current nonviral systems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d14f412ad299a471533f0cee0810b2a
https://doi.org/10.1038/sj.gt.3301294
https://doi.org/10.1038/sj.gt.3301294
Autor:
Sherry Pierce, Madeleine Duvic, L. E. Robertson, Elihu H. Estey, Michael J. Keating, Susan O'Brien, S. A. Stass, Razelle Kurzrock, Hagop M. Kantarjian
Publikováno v:
Blood. 84:733-738
Mature T-cell lymphoproliferative disorders comprise a heterogenous group of diseases for which there is no standard therapy. These disorders are uncommon, and are usually treated similarly to their B- cell counterparts, but with less success. Nucleo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e3a68534a600d42d2dcfeeb26025846
https://doi.org/10.1182/blood.v84.3.733.bloodjournal843733
https://doi.org/10.1182/blood.v84.3.733.bloodjournal843733
Publikováno v:
Blood. 84:279-286
Annexin VIII is a calcium-dependent phospholipid-binding protein previously identified as a blood anticoagulant based on in vitro studies. However, the physiologic function of annexin VIII remains unknown. In acute promyelocytic leukemia (APL) the an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a24f92bd23ccbffc344da6b54c5423
https://doi.org/10.1182/blood.v84.1.279.bloodjournal841279
https://doi.org/10.1182/blood.v84.1.279.bloodjournal841279
Autor:
J Q, Guo, J Y, Lian, Y M, Xian, M S, Lee, A B, Deisseroth, S A, Stass, R E, Champlin, M, Talpaz, J Y, Wang, R B, Arlinghaus
Publikováno v:
Blood. 83:3629-3637
Chronic myelogenous leukemia (CML) is a myeloproliferative disorder associated with the Philadelphia chromosome (Ph1) in more than 95% of these patients. The Ph1 and the resulting BCR-ABL fused genes are markers for this type of leukemia. In CML, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ed61cabd070af4d29babb7218a882af
https://doi.org/10.1182/blood.v83.12.3629.bloodjournal83123629
https://doi.org/10.1182/blood.v83.12.3629.bloodjournal83123629
Autor:
Hagop M. Kantarjian, Jennifer M. Trujillo, Emil J. Freireich, S. A. Stass, Issa F. Khouri, Albert B. Deisseroth, M. S. Lee, Richard E. Champlin, Moshe Talpaz
Publikováno v:
British Journal of Haematology. 82:708-714
The prognostic significance of detecting minimal residual disease by polymerase chain reaction (PCR) amplification of bcr/abl mRNA transcripts was investigated in 27 bone marrow samples from 20 patients with Philadelphia chromosome (Ph1) positive chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6fac4df77111a9d92ba148c7b244389
https://doi.org/10.1111/j.1365-2141.1992.tb06948.x
https://doi.org/10.1111/j.1365-2141.1992.tb06948.x
Publikováno v:
Blood. 79:1802-1810
Since the translocation breakpoint t(15;17) (q22;q21) in acute promyelocytic leukemia (APL) occurs within the retinoic acid receptor- alpha (RARA) gene, the expression of many genes normally regulated by RARA may be affected by this translocation. To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::658a6fe7fb4e13e24f1607f795d82305
https://doi.org/10.1182/blood.v79.7.1802.bloodjournal7971802
https://doi.org/10.1182/blood.v79.7.1802.bloodjournal7971802
Publikováno v:
Cancer research. 59(14)
Gene therapy transfer of angiostatin and endostatin represents an alternative method of delivering angiogenic polypeptide inhibitors. We examined whether liposomes complexed to plasmids encoding angiostatin or endostatin inhibited angiogenesis and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c395b9289ae8c6fe03f1810b4c7f8280
https://pubmed.ncbi.nlm.nih.gov/10728714
https://pubmed.ncbi.nlm.nih.gov/10728714
Autor:
W, Grizzle, W W, Grody, W W, Noll, M E, Sobel, S A, Stass, T, Trainer, H, Travers, V, Weedn, K, Woodruff
Publikováno v:
Archives of pathologylaboratory medicine. 123(4)
As recipients of tissue and medical specimens, pathologists and other medical specialists regard themselves as stewards of patient tissues and consider it their duty to protect the best interests of both the individual patient and the public. The ste
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf058ba6fe926d299271343d2ac73e2d
https://pubmed.ncbi.nlm.nih.gov/10320140
https://pubmed.ncbi.nlm.nih.gov/10320140
Autor:
S A, Stass, J, Mixson
Publikováno v:
Clinical cancer research : an official journal of the American Association for Cancer Research. 3(12 Pt 2)
Genetic instability is a hallmark of cancer. Alterations in DNA through mutations, deletions, and translocations affect genes that are fundamental to normal cell growth differentiation and programmed cell death. Here, we discuss these alterations as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5d851f2fdce57dae875dbf44f6e005a
https://pubmed.ncbi.nlm.nih.gov/10068275
https://pubmed.ncbi.nlm.nih.gov/10068275
Publikováno v:
Cancer. 76(6)
There have been published reports on cytogenetic, immunophenotypic, and molecular changes at relapse in childhood acute lymphoblastic leukemia (ALL) including lineage switch and secondary leukemia. There are limited data, however, on the cytogenetic,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a554c1df0d3b78feb7249fcb844c1e1
https://pubmed.ncbi.nlm.nih.gov/8625224
https://pubmed.ncbi.nlm.nih.gov/8625224