Zobrazeno 1 - 10 of 59 pro vyhledávání: '"G. Nozari"'
1
Akademický článek
Scanning by DOVAM-S Detects All Unique Sequence Changes in Blinded Analyses: Evidence that the Scanning Conditions Are Generic
Autor: C.H. Buzin, C.Y. Wen, V.Q. Nguyen, G. Nozari, A. Mengos, X. Li, J.S. Chen, Q. Liu, R.A. Gatti, F.K. Fujimura, S.S. Sommer
Publikováno v: BioTechniques, Vol 28, Iss 4, Pp 746-753 (2000)
The [detection of virtually all mutations]-SSCP (DOVAM-S) is a highly sensitive variant of single strand conformation polymorphism (SSCP). Mutations in the factor IX gene were used to find a set of five SSCP conditions that detects virtually all muta
Externí odkaz: https://doaj.org/article/a6e02840d8804bc0b0984cd0611b3ca9
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2
Akademický článek
Detection of Virtually All Mutations-SSCP (DOVAM-S): A Rapid Method for Mutation Scanning with Virtually 100% Sensitivity
Autor: Q. Liu, J. Feng, C. Buzin, C. Wen, G. Nozari, A. Mengos, V. Nguyen, J. Liu, L. Crawford, F.K. Fujimura, S.S. Sommer
Publikováno v: BioTechniques, Vol 26, Iss 5, Pp 932-942 (1999)
Dideoxy fingerprinting (ddF) was used as a tool to search for a generic set of conditions with sufficient power to detect virtually all mutations. For each condition tested, a very large sample of mutation-containing, single-stranded segments (about
Externí odkaz: https://doaj.org/article/7a386106e3b24392b5d0b8195d619879
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3
HB Watts [α74(EF3) OR α75(EF4)ASP→0]: A Shortened α Chain Variant Due to the Deletion of Three Nucleotides in Exon 2 of the α2-Globin Gene
Autor: Virgil F. Fairbanks, C. Lee, Kathleen S. Kubik, Daniel J. McCormick, B. J. Madden, Samuel Rahbar, G. Nozari
Publikováno v: Hemoglobin. 21:321-330
We have identified a new, slightly unstable α chain hemoglobin variant, present in a Mexican-American family. Amino acid sequencing and mass spectral analysis of the aberrant peptide (αT-9) of the variant revealed that the aspartic acid is deleted
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::63e70b5d987a74373da2baf6b0f5cc1c
https://doi.org/10.3109/03630269709000665
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5
A Novel Intrachromosomal Rearrangement in the β-Globin Gene Fd in An African-American Family
Autor: G. Nozari, G. Forrest, Stephen J. Forman, T. Gelbart, Samuel Rahbar, Ernest Beutler
Publikováno v: Hemoglobin. 19:375-388
We describe here a deletion of 34 nucleotides from the 3' end of the first intervening sequence of the beta-globin gene covering the AGGC splice junction, and the insertion of 32 nucleotides of the delta-globin gene at the same location. This gene re
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b308a8e11af24e1fa7ec3c67d1ae849d
https://doi.org/10.3109/03630269509005829
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8
Hb Watts [alpha 74(EF3) or alpha 75(EF4)Asp--0]: a shortened alpha chain variant due to the deletion of three nucleotides in exon 2 of the alpha 2-globin gene
Autor: S, Rahbar, C, Lee, V F, Fáirbanks, D J, McCormick, K, Kubik, B J, Madden, G, Nozari
Publikováno v: Hemoglobin. 21(4)
We have identified a new, slightly unstable alpha chain hemoglobin variant, present in a Mexican-American family. Amino acid sequencing and mass spectral analysis of the aberrant peptide (alpha T-9) of the variant revealed that the aspartic acid is d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::8911b65da42f676886b4a1864585b3e7
https://pubmed.ncbi.nlm.nih.gov/9255611
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