关注
John N  Milligan
John N Milligan
Asuragen
在 utexas.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
Real-time detection of isothermal amplification reactions with thermostable catalytic hairpin assembly
Y Jiang, B Li, JN Milligan, S Bhadra, AD Ellington
Journal of the American Chemical Society 135 (20), 7430-7433, 2013
2732013
Robust strand exchange reactions for the sequence-specific, real-time detection of nucleic acid amplicons
YS Jiang, S Bhadra, B Li, YR Wu, JN Milligan, AD Ellington
Analytical chemistry 87 (6), 3314-3320, 2015
1542015
Cercarial transformation and in vitro cultivation of Schistosoma mansoni schistosomules
JN Milligan, ER Jolly
JoVE (Journal of Visualized Experiments), e3191, 2011
712011
Evolution of a thermophilic strand-displacing polymerase using high-temperature isothermal compartmentalized self-replication
JN Milligan, R Shroff, DJ Garry, AD Ellington
Biochemistry 57 (31), 4607-4619, 2018
472018
In Vitro Selection for Small-Molecule-Triggered Strand Displacement and Riboswitch Activity
L Martini, AJ Meyer, JW Ellefson, JN Milligan, M Forlin, AD Ellington, ...
ACS Synthetic Biology 4 (10), 1144-1150, 2015
232015
Recommendations for interpreting and reporting silent carrier and disease-modifying variants in SMA testing workflows
JN Milligan, L Blasco-Pérez, M Costa-Roger, M Codina-Solà, EF Tizzano
Genes 13 (9), 1657, 2022
132022
Using RecA protein to enhance kinetic rates of DNA circuits
JN Milligan, AD Ellington
Chemical Communications 51 (46), 9503-9506, 2015
112015
Identification and characterization of a Mef2 transcriptional activator in schistosome parasites
JN Milligan, ER Jolly
PLoS neglected tropical diseases 6 (1), e1443, 2012
102012
Shuffle optimizer: a program to optimize DNA shuffling for protein engineering
JN Milligan, DJ Garry
Synthetic DNA: Methods and Protocols, 35-45, 2017
62017
Multisite evaluation and validation of a sensitive diagnostic and screening system for spinal muscular atrophy that reports SMN1 and SMN2 copy number, along with disease …
JN Milligan, JL Larson, S Filipovic-Sadic, W Laosinchai-Wolf, YW Huang, ...
The Journal of Molecular Diagnostics 23 (6), 753-764, 2021
42021
Streamlined, Single-tube PCR Assay that Quantifies SMN1 and SMN2 Copy Numbers using Capillary Electrophoresis
W Laosinchai-Wolf, S Filipovic-Sadic, L Chen, S Gokul, J Janovsky, V Le, ...
J Mol Diagn 20, 895-1039, 2018
12018
Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic …
B Hall, JN Milligan, K Kelnar, E Hallmark, JD Ashton, CA Parker, ...
Archives of Pathology & Laboratory Medicine, 2024
2024
Accessible fragment analysis instrumentation allows resolution of challenging genotypes associated with pathogenic repeats, structural variants, SNVs and INDELs
S Edelmon, S Partin, A Lara, J Peda, J Hedges, J Milligan
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 624-624, 2024
2024
Impact of Variants of Varying Clinical Consequence in Underrepresented Populations and Implications for a Minimum Variant Set for Pan-Ancestry Cystic Fibrosis Carrier Screening
G Latham, BC Haynes, B Hall, JN Milligan
JOURNAL OF MOLECULAR DIAGNOSTICS 25 (11), S6-S6, 2023
2023
P514: High-resolution analysis of pathogenic trinucleotide and hexanucleotide repeats, copy number changes, SNVs and INDELs using flexible, easy-to-use fragment sizing …
A Lara, S Partin, C Parker, J Hedges, J Milligan
Genetics in Medicine Open 1 (1), 2023
2023
Methods and devices related to amplifying nucleic acid at a variety of temperatures
A Ellington, C Jung, S Cai, S Bhadra, JN Milligan, D Garry, R Shroff
US Patent App. 17/579,085, 2022
2022
Methods and devices related to amplifying nucleic acid at a variety of temperatures
A Ellington, C Jung, S Cai, S Bhadra, JN Milligan, D Garry, R Shroff
US Patent 11,299,776, 2022
2022
Automated Deep Learning Software for PCR/Capillary Electrophoresis Fragment Analysis Enables Efficient Pan-Ethnic CFTR Testing at Scale
E Hallmark, J Ashton, R Routsong, BC Haynes, B Hall, J Milligan, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 30 (SUPPL 1), 484-484, 2022
2022
Buccal swab testing with the AmplideX PCR/CE SMN1/2 Plus Kit that assesses copy number and critical mutations for SMA
J Janovsky, S Edelmon, I Wolf, G Latham, JN Milligan
Molecular Genetics and Metabolism 132, S270-S271, 2021
2021
Analytical validation of a multiplex PCR/CE assay for simultaneous determination of SMN1/SMN2 exon 7 copy number and variant status
W Laosinchai-Wolf, JL Larson, J Janovsky, K Jefferson, D Patel, M Church, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 445-446, 2020
2020
系统目前无法执行此操作,请稍后再试。
文章 1–20