Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Cooper, David Neil"'
Publikováno v:
eLS
Besides the canonical right‐handed double helix, biologically important noncanonical deoxyribonucleic acid (DNA) secondary structures have been characterised, including quadruplexes, triplexes, slipped/hairpins, Z‐DNA and cruciforms, collectively
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b72c96134c0109a7ea11f1ece1a08bc
https://doi.org/10.1002/9780470015902.a0022657.pub2
https://doi.org/10.1002/9780470015902.a0022657.pub2
Autor:
Zou, Wen-Bin, Wu, Hao, Boulling, Arnaud, Cooper, David Neil, Li, Zhao-Shen, Liao, Zhuan, Chen, Jian-Min, Férec, Claude
Publikováno v:
Human Genomics
Human Genomics, BioMed Central, 2017, 11 (1), ⟨10.1186/s40246-017-0103-9⟩
Human Genomics, Vol 11, Iss 1, Pp 1-7 (2017)
Human Genomics, BioMed Central, 2017, 11 (1), ⟨10.1186/s40246-017-0103-9⟩
Human Genomics, Vol 11, Iss 1, Pp 1-7 (2017)
Background SPINK1 (serine protease inhibitor, kazal-type, 1), which encodes human pancreatic secretory trypsin inhibitor, is one of the most extensively studied genes underlying chronic pancreatitis. Recently, based upon data from qualitative reverse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::47bd938143c612cc86f4ba2686fa8a67
https://hal.inrae.fr/hal-02946980
https://hal.inrae.fr/hal-02946980
Autor:
Zou, Wen-Bin, Masson, Emmanuelle, Boulling, Arnaud, Cooper, David Neil, Li, Zhao-Shen, Liao, Zhuan, Férec, Claude, Chen, Jian-Min
We read with great interest the recent paper by Beer and Sahin-Tóth1 addressing the ‘missing heritability’ observed in approximately 60% of German cases of chronic pancreatitis.2 These authors opined that ‘discovery studies tend to focus on ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::28a9b705665dad75a6a63f315faf9dd5
Autor:
Shihab, H. A., Rogers, M. F., Gough, J., Mort, Matthew, Cooper, David Neil, Day, I. N. M., Gaunt, T. R., Campbell, C.
Motivation: Technological advances have enabled the identification of an increasingly large spectrum of single nucleotide variants within the human genome, many of which may be associated with monogenic disease or complex traits. Here, we propose an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::f5e6f855a00a1786446f5924485356c4
https://orca.cardiff.ac.uk/id/eprint/84066/1/Bioinformatics-2015-Shihab-1536-43.pdf
https://orca.cardiff.ac.uk/id/eprint/84066/1/Bioinformatics-2015-Shihab-1536-43.pdf