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1.
Enhancer release and retargeting activates disease-susceptibility genes.
Nature
; 595(7869): 735-740, 2021 07.
Article
in English
| MEDLINE | ID: mdl-34040254
2.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
; 28(5): 2071-2080, 2023 May.
Article
in English
| MEDLINE | ID: mdl-36869225
3.
HEDD: Human Enhancer Disease Database.
Nucleic Acids Res
; 46(D1): D113-D120, 2018 01 04.
Article
in English
| MEDLINE | ID: mdl-29077884
4.
Analysis of Escherichia coli RNase E and RNase III activity in vivo using tiling microarrays.
Nucleic Acids Res
; 39(8): 3188-203, 2011 Apr.
Article
in English
| MEDLINE | ID: mdl-21149258
5.
Polygenic prediction of human longevity on the supposition of pervasive pleiotropy.
medRxiv
; 2023 Dec 11.
Article
in English
| MEDLINE | ID: mdl-38168353
6.
Deep post-GWAS analysis identifies potential risk genes and risk variants for Alzheimer's disease, providing new insights into its disease mechanisms.
Sci Rep
; 11(1): 20511, 2021 10 15.
Article
in English
| MEDLINE | ID: mdl-34654853
7.
Genomic expansion of Aldh1a1 protects beavers against high metabolic aldehydes from lipid oxidation.
Cell Rep
; 37(6): 109965, 2021 11 09.
Article
in English
| MEDLINE | ID: mdl-34758328
8.
Rare genetic coding variants associated with human longevity and protection against age-related diseases.
Nat Aging
; 1(9): 783-794, 2021 09.
Article
in English
| MEDLINE | ID: mdl-37117627
9.
BAL1 and BBAP are regulated by a gamma interferon-responsive bidirectional promoter and are overexpressed in diffuse large B-cell lymphomas with a prominent inflammatory infiltrate.
Mol Cell Biol
; 26(14): 5348-59, 2006 Jul.
Article
in English
| MEDLINE | ID: mdl-16809771
10.
Using recurrence quantification analysis descriptors for protein sequence classification with support vector machines.
J Biomol Struct Dyn
; 25(3): 289-98, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-17937490
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