↓ Direkt till sidans innehåll
↓ Direkt till sidans sekundära innehåll (sidomenyn)

Träfflista för sökning "WFRF:(Venter JC) "

Search: WFRF:(Venter JC)

Result 1-6 of 6

Sort/group result

Sort by: Hits per page:

Enumeration	Reference	Cover	Find
1.	Ridker, PM, et al. (author) Cardiovascular Efficacy and Safety of Bococizumab in High-Risk Patients 2017 In: The New England journal of medicine. - 1533-4406 .- 0028-4793. ; 376:16, s. 1527-1539 Journal article (peer-reviewed)
2.	Bonaca, MP, et al. (author) Long-term use of ticagrelor in patients with prior myocardial infarction 2015 In: The New England journal of medicine. - 1533-4406. ; 372:19, s. 1791-1800 Journal article (peer-reviewed)
3.	Lissek, T, et al. (author) Building Bridges through Science 2017 In: Neuron. - : Elsevier BV. - 1097-4199 .- 0896-6273. ; 96:4, s. 730-735 Journal article (peer-reviewed)
4.	CLARK, RF, et al. (author) The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families 1995 In: Nature genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 11:2, s. 219-222 Journal article (peer-reviewed)
5.	Jiang, QF, et al. (author) Inflammation-driven deaminase deregulation fuels human pre-leukemia stem cell evolution 2021 In: Cell reports. - : Elsevier BV. - 2211-1247. ; 34:4, s. 108670- Journal article (peer-reviewed)
6.	Scherer, SW, et al. (author) Human chromosome 7: DNA sequence and biology 2003 In: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 300:5620, s. 767-772 Journal article (peer-reviewed)abstract DNA sequence and annotation of the entire human chromosome 7, encompassing nearly 158 million nucleotides of DNA and 1917 gene structures, are presented. To generate a higher order description, additional structural features such as imprinted genes, fragile sites, and segmental duplications were integrated at the level of the DNA sequence with medical genetic data, including 440 chromosome rearrangement breakpoints associated with disease. This approach enabled the discovery of candidate genes for developmental diseases including autism.

Skapa referenser, mejla, bekava och länka

Permalink

Result 1-6 of 6

Refine your search

Type of publication: journal article (6)

Type of content: peer-reviewed (6)

Author/Editor: Li, S. (2); Li, Y. (2); Schmidt, E. (2); Johnson, M. (2); Yoon, J. (2); Weiss, R. (2); show more...; Yang, X. (2); Konstantinov, V. (2); Nagy, K (2); Thompson, P. (2); Koenig, W. (2); Connelly, T (2); Kim, C. (2); Ferrari, E. (2); Chang, KC (2); Singh, B (2); Ponikowski, P (2); Hayashi, Y (2); Stellbrink, C (2); Dion, D (2); Karpov, Y (2); Caccavo, A (2); De Wolf, L (2); Vervoort, G (2); Cools, F (2); Nicolau, JC (2); Pesant, Y (2); Vizel, S (2); Montalescot, G (2); Appel, KF (2); Dorsel, T (2); Lupkovics, G (2); Edes, I (2); Herrman, JPR (2); Ronner, E (2); Piepiorka, M (2); Minescu, B (2); Pella, D (2); Hranai, M (2); Dzupina, A (2); Kamensky, G (2); Ranjith, N (2); Van Zyl, LJ (2); Fillat, ARC (2); Fernandez, JMC (2); Cortada, JB (2); Perez, IP (2); Moriarty, A (2); Chandna, H (2); Labroo, A (2); show less...

University: Karolinska Institutet (6); Lund University (1)

Language: English (6)

Research subject (UKÄ/SCB): Medical and Health Sciences (1)

Year

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

Copyright © LIBRIS - National Library Systems
LIBRIS.kb.se

pil uppåt

Close

Copy and save the link in order to return to this view