Found: 22
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Efficient Introduction and Transient Expression of Exogenous Genes in Human Hemopoietic Cellsa.
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- Annals of the New York Academy of Sciences, 1987, v. 511, n. 1, p. 418, doi. 10.1111/j.1749-6632.1987.tb36271.x
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- Article
Effect of capsid confinement on the chromatin organization of the SV40 minichromosome.
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- Nucleic Acids Research, 2013, v. 41, n. 3, p. 1569, doi. 10.1093/nar/gks1270
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- Article
Integrin-Mediated Signaling Induced by Simian Virus 40 Leads to Transient Uncoupling of Cortical Actin and the Plasma Membrane.
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- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0055799
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- Article
DNA-Free Recombinant SV40 Capsids Protect Mice from Acute Renal Failure by Inducing Stress Response, Survival Pathway and Apoptotic Arrest.
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- PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002998
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- Article
Simian virus 40 vectors for pulmonary gene therapy.
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- Respiratory Research, 2007, v. 8, p. 74, doi. 10.1186/1465-9921-8-74
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- Article
High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews.
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- Human Genetics, 2000, v. 107, n. 6, p. 630, doi. 10.1007/s004390000426
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- Article
Y chromosome evidence for a founder effect in Ashkenazi Jews.
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- European Journal of Human Genetics, 2005, v. 13, n. 3, p. 388, doi. 10.1038/sj.ejhg.5201319
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- Article
Haplogroup-specific deviation from the stepwise mutation model at the microsatellite loci DYS388 and DYS392.
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- European Journal of Human Genetics, 2001, v. 9, n. 1, p. 22, doi. 10.1038/sj.ejhg.5200577
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- Article
GM1 structure determines SV40-induced membrane invagination and infection.
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- Nature Cell Biology, 2010, v. 12, n. 1, p. 11, doi. 10.1038/ncb1999
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- Article
Receptor Concentration and Diffusivity Control Multivalent Binding of Sv40 to Membrane Bilayers.
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- PLoS Computational Biology, 2013, v. 9, n. 11, p. 1, doi. 10.1371/journal.pcbi.1003310
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- Article
Sickle cell trait in a white Jewish family presenting as splenic infarction at high altitude.
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- American Journal of Hematology, 1988, v. 27, n. 1, p. 46, doi. 10.1002/ajh.2830270111
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- Article
Diversity of α-globin mutations and clinical presentation of α-thalassemia in Israel.
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- American Journal of Hematology, 2000, v. 65, n. 3, p. 196, doi. 10.1002/1096-8652(200011)65:3<196::AID-AJH4>3.0.CO;2-8
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- Article
Rapid detection of the common mediterranean α-globin deletions/rearrangements using PCR.
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- American Journal of Hematology, 1998, v. 58, n. 4, p. 306, doi. 10.1002/(SICI)1096-8652(199808)58:4<306::AID-AJH10>3.0.CO;2-5
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- Article
Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype.
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- American Journal of Hematology, 1997, v. 54, n. 1, p. 16, doi. 10.1002/(SICI)1096-8652(199701)54:1<16::AID-AJH3>3.0.CO;2-7
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- Article
Prenatal diagnosis based on simultaneous DNA analysis for α and B-globin genes.
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- American Journal of Hematology, 1996, v. 53, n. 3, p. 203, doi. 10.1002/(SICI)1096-8652(199611)53:3<203::AID-AJH12>3.0.CO;2-E
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- Article
Probable identity by descent and discovery of familial relationships by means of a rare β-thalassemia haplotype.
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- Human Mutation, 1997, v. 9, n. 1, p. 86, doi. 10.1002/(SICI)1098-1004(1997)9:1<86::AID-HUMU20>3.0.CO;2-K
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- Article
A frameshift mutation in codon 10 of the β-globin gene.
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- Human Mutation, 1995, v. 6, n. 3, p. 278, doi. 10.1002/humu.1380060320
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- Article
Spectrum of β-thalassemia mutations in the Gaza area.
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- Human Mutation, 1995, v. 5, n. 4, p. 351, doi. 10.1002/humu.1380050416
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- Article
Sporadic alleles, including a novel mutation, characterize β-thalassemia in ashkenazi jews.
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- Human Mutation, 1993, v. 2, n. 2, p. 155, doi. 10.1002/humu.1380020219
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- Article
A Novel Mechanism Generating Short Deletion/Insertions Following Slippage is Suggested by a Mutation in the Human α2-Globin Gene.
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- Human Molecular Genetics, 1997, v. 6, n. 6, p. 881, doi. 10.1093/hmg/6.6.881
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- Article
SV40 assembly in vivo and in vitro.
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- Computational & Mathematical Methods in Medicine, 2008, v. 9, n. 3/4, p. 265, doi. 10.1080/17486700802168312
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- Article
Severe thalassaemia intermedia caused by interaction of homozygosity for α-globin gene triplication with heterozygosity for β thalassaemia.
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- British Journal of Haematology, 1994, v. 86, n. 2, p. 377, doi. 10.1111/j.1365-2141.1994.tb04743.x
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- Article