Výsledky vyhledávání - "H. Lightstone"

Elektronická kniha

Nonarchimedean Fields and Asymptotic Expansions

Autor: A. H. Lightstone, Abraham Robinson

North-Holland Mathematical Library, Volume 13: Nonarchimedean Fields and Asymptotic Expansions focuses on the connection between nonarchimedean systems and the orders of infinity and smallness that are related with the asymptotic behavior of a functi

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Characterization of an unstable variant (BChE115D) of human butyrylcholinesterase

Autor: H Lightstone, S. L. Primo-Parmo, B N La Du

Publikováno v: Pharmacogenetics. 7:27-34

An unstable variant of human butyrylcholinesterase (BChE) is described in four apparently unrelated individuals sensitive to succinylcholine. Sequencing of genomic DNA revealed a single nucleotide substitution which results in the replacement of amin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b86ca54e0504e7ea49f92e3da7f18b60
https://doi.org/10.1097/00008571-199702000-00004

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Phenotypic and molecular biological analysis of human butyrylcholinesterase variants

Autor: Amitav Hajra, Cynthia F. Bartels, A. F. L. Van Der Spek, Oksana Lockridge, B. N. La Du, H. Lightstone, C. P. Nogueira

Publikováno v: Clinical Biochemistry. 23:423-431

Our laboratory has recently shown that several variant forms of human butyrylcholinesterase, associated with unusual sensitivity to succinylcholine, are caused by specific mutations within the structural DNA coding for this enzyme. Atypical (dibucain

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab4392de15bb1f355f0c2de2690e55d5
https://doi.org/10.1016/0009-9120(90)90187-y

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Akademický článek

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Identification of a frameshift mutation responsible for the silent phenotype of human serum cholinesterase, Gly 117 (GGT----GGAG)

Autor: C P, Nogueira, M C, McGuire, C, Graeser, C F, Bartels, M, Arpagaus, A F, Van der Spek, H, Lightstone, O, Lockridge, B N, La Du

Publikováno v: American journal of human genetics. 46(5)

A frameshift mutation that causes a silent phenotype for human serum cholinesterase was identified in the DNA of seven individuals of two unrelated families. The mutation, identified using the polymerase chain reaction, causes a shift in the reading

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::cee5d009c1b5a1dd8eb35bb35df008f5
https://pubmed.ncbi.nlm.nih.gov/2339692

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Akademický článek

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Dirac Delta Functions Via Nonstandard Analysis

Autor: A. H. Lightstone, Kam Wong

Publikováno v: Canadian Mathematical Bulletin. 18:759-762

We recall that a Dirac delta function δ(x) in the real number system is the idealization of a function that vanishes outside a "short" interval and satisfies It is conceived as a function δ for which δ(0)=+ ∞, δ(t)=0 if t≠0, and This function

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::397934b5e989e6edae8508df9526cab8
https://doi.org/10.4153/cmb-1975-132-3

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