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N Dear

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Articles 7
Citations 127
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Recent Articles
1.
Dismer A, Charles M, Dear N, Louis-Jean J, Barthelemy N, Richard M, et al.
Public Health Action . 2021 Jun; 11(2):101-107. PMID: 34159071
Background: Haiti has the highest incidence rate of TB in the Western Hemisphere, with an estimated 170 cases per 100,000 in 2019. Since 2010, control efforts have focused on targeted...
2.
Smith A, Polley S, Wells S, Stewart M, Vizor L, Humphreys J, et al.
Lab Anim . 2008 Nov; 43(1):1-10. PMID: 18987059
N'-ethyl-N'-nitrosourea (ENU) is a powerful germline mutagen used in conjunction with phenotype-driven screens to generate novel mouse mutants. ENU also induces genetic lesions in somatic cells and dosage requires optimization...
3.
Matena K, Boehm T, Dear N
Genomics . 1998 Mar; 48(1):117-20. PMID: 9503024
CAPN5 and CAPN6 are recently identified human and mouse genes lacking a calmodulin-like domain with homology to the calpain family of proteases. To clarify their relationship to the known calpains,...
4.
Dear N, Matena K, Vingron M, Boehm T
Genomics . 1997 Oct; 45(1):175-84. PMID: 9339374
Calpains are calcium-dependent intracellular nonlysosomal proteases that are believed to participate in signal transduction. In vertebrates, five different calpains have so far been identified, of which three, mu-, m-, and...
5.
Kreissig S, Schuddekopf K, Dear N, Boehm T
Nucleic Acids Res . 1996 Nov; 24(21):4358-9. PMID: 8932395
New synthetic approaches, such as combinatorial chemistry, provide a rich source of potential drug candidates. At the same time, the human genome initiative and other large-scale sequencing projects provide a...
6.
Wu L, Mak C, Dear N, Boehm T, Foroni L, Rabbitts T
Nucleic Acids Res . 1993 Nov; 21(22):5067-73. PMID: 8255760
The somatic V(D)J recombination for the assembly of the Ig and TCR genes is mediated by the recombination signal sequences (Rss) and the V(D)J recombinase. A cDNA clone was isolated...
7.
Kennedy M, Gonzalez-Sarmiento R, Kees U, Lampert F, Dear N, Boehm T, et al.
Proc Natl Acad Sci U S A . 1991 Oct; 88(20):8900-4. PMID: 1681546
A common chromosomal abnormality in childhood T-cell acute leukemia is a translocation, t(10;14) (q24;q11), that together with the variant t(7;10)(q35;q24) is present in up to 7% of this tumor type....