Search details
1.
The history and conceptual framework of assays and screens.
Bioessays
; 45(4): e2200191, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36789580
2.
Most synonymous allelic variants in HIV tat are not silent.
Genomics
; 115(3): 110603, 2023 05.
Article
in English
| MEDLINE | ID: mdl-36893872
3.
GigaAssay - An adaptable high-throughput saturation mutagenesis assay platform.
Genomics
; 114(4): 110439, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35905834
4.
Synonymous Variants of Uncertain Silence.
Int J Mol Sci
; 24(13)2023 Jun 23.
Article
in English
| MEDLINE | ID: mdl-37445732
5.
Accurate Prediction of Transcriptional Activity of Single Missense Variants in HIV Tat with Deep Learning.
Int J Mol Sci
; 24(7)2023 Mar 24.
Article
in English
| MEDLINE | ID: mdl-37047108
6.
XRCC4 and MRE11 Roles and Transcriptional Response to Repair of TALEN-Induced Double-Strand DNA Breaks.
Int J Mol Sci
; 23(2)2022 Jan 06.
Article
in English
| MEDLINE | ID: mdl-35054780
7.
The carboxy-terminus, a key regulator of protein function.
Crit Rev Biochem Mol Biol
; 54(2): 85-102, 2019 04.
Article
in English
| MEDLINE | ID: mdl-31106589
8.
Can Designer Indels Be Tailored by Gene Editing?: Can Indels Be Customized?
Bioessays
; 41(12): e1900126, 2019 12.
Article
in English
| MEDLINE | ID: mdl-31693213
9.
Minimotif Miner 4: a million peptide minimotifs and counting.
Nucleic Acids Res
; 46(D1): D465-D470, 2018 01 04.
Article
in English
| MEDLINE | ID: mdl-29140456
10.
Prioritization of Variants for Investigation of Genotype-Directed Nutrition in Human Superpopulations.
Int J Mol Sci
; 20(14)2019 Jul 18.
Article
in English
| MEDLINE | ID: mdl-31323740
11.
Natural variability of minimotifs in 1092 people indicates that minimotifs are targets of evolution.
Nucleic Acids Res
; 43(13): 6399-412, 2015 Jul 27.
Article
in English
| MEDLINE | ID: mdl-26068475
12.
TALEN gene editing takes aim on HIV.
Hum Genet
; 135(9): 1059-70, 2016 09.
Article
in English
| MEDLINE | ID: mdl-27170155
13.
The human phosphotyrosine signaling network: evolution and hotspots of hijacking in cancer.
Genome Res
; 22(7): 1222-30, 2012 Jul.
Article
in English
| MEDLINE | ID: mdl-22194470
14.
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Am J Hum Genet
; 88(2): 127-37, 2011 Feb 11.
Article
in English
| MEDLINE | ID: mdl-21255762
15.
Minimotif Miner 3.0: database expansion and significantly improved reduction of false-positive predictions from consensus sequences.
Nucleic Acids Res
; 40(Database issue): D252-60, 2012 Jan.
Article
in English
| MEDLINE | ID: mdl-22146221
16.
Systematic Assessment of Protein C-Termini Mutated in Human Disorders.
Biomolecules
; 13(2)2023 02 12.
Article
in English
| MEDLINE | ID: mdl-36830724
17.
Single-cell RNA sequencing reveals in vivo osteoimmunology interactions between the immune and skeletal systems.
Front Endocrinol (Lausanne)
; 14: 1107511, 2023.
Article
in English
| MEDLINE | ID: mdl-37051201
18.
Data supporting a saturation mutagenesis assay for Tat-driven transcription with the GigaAssay.
Data Brief
; 45: 108641, 2022 Dec.
Article
in English
| MEDLINE | ID: mdl-36426049
19.
A computational tool for identifying minimotifs in protein-protein interactions and improving the accuracy of minimotif predictions.
Proteins
; 79(1): 153-64, 2011 Jan.
Article
in English
| MEDLINE | ID: mdl-20938975
20.
VENN, a tool for titrating sequence conservation onto protein structures.
Nucleic Acids Res
; 37(18): e124, 2009 Oct.
Article
in English
| MEDLINE | ID: mdl-19656955