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Plos Genetics
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June 5, 2010
The use of orthologous sequences to predict the impact of amino acid substitutions on protein function
Nicholas J Marini, Paul D Thomas, Jasper Rine
Plos One
|
November 13, 2010
Comprehensive approach to analyzing rare genetic variants
Thomas J Hoffmann, Nicholas J Marini, John S Witte
Genetic Testing and Molecular Biomarkers
|
June 14, 2017
DNA Methylome Profiling on the Infinium HumanMethylation450 Array from Limiting Quantities of Genomic DNA from a Single, Small Archived Bloodspot
Kripa Asrani, Gary M Shaw, Jasper Rine, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2019
Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate
Nicholas J Marini, Kripa Asrani, Wei Yang, et al.
G3 (Bethesda, Md.)
|
August 13, 2013
Mono and dual cofactor dependence of human cystathionine β-synthase enzyme variants in vivo and in vitro
Dago Dimster-Denk, Katherine W Tripp, Nicholas J Marini, et al.
Chemistry & Biology
|
August 2, 2003
DNA binding hairpin polyamides with antifungal activity
Nicholas J Marini, Ramesh Baliga, Matthew J Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 5, 2008
The prevalence of folate-remedial MTHFR enzyme variants in humans
Nicholas J Marini, Jennifer Gin, Janet Ziegle, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate
Nicholas J Marini, Wei Yang, Kripa Asrani, et al.
Epigenetics
|
March 15, 2019
Epigenomic profiling of newborns with isolated orofacial clefts reveals widespread DNA methylation changes and implicates metastable epiallele regions in disease risk
Semira Gonseth, Gary M Shaw, Ritu Roy, et al.
Plos One
|
December 6, 2011
A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis
Nicholas J Marini, Thomas J Hoffmann, Edward J Lammer, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Plos Genetics
|
June 5, 2010
The use of orthologous sequences to predict the impact of amino acid substitutions on protein function
Nicholas J Marini, Paul D Thomas, Jasper Rine
Plos One
|
November 13, 2010
Comprehensive approach to analyzing rare genetic variants
Thomas J Hoffmann, Nicholas J Marini, John S Witte
Genetic Testing and Molecular Biomarkers
|
June 14, 2017
DNA Methylome Profiling on the Infinium HumanMethylation450 Array from Limiting Quantities of Genomic DNA from a Single, Small Archived Bloodspot
Kripa Asrani, Gary M Shaw, Jasper Rine, et al.
American Journal of Medical Genetics. Part A
|
May 8, 2019
Accumulation of rare coding variants in genes implicated in risk of human cleft lip with or without cleft palate
Nicholas J Marini, Kripa Asrani, Wei Yang, et al.
G3 (Bethesda, Md.)
|
August 13, 2013
Mono and dual cofactor dependence of human cystathionine β-synthase enzyme variants in vivo and in vitro
Dago Dimster-Denk, Katherine W Tripp, Nicholas J Marini, et al.
Chemistry & Biology
|
August 2, 2003
DNA binding hairpin polyamides with antifungal activity
Nicholas J Marini, Ramesh Baliga, Matthew J Taylor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 5, 2008
The prevalence of folate-remedial MTHFR enzyme variants in humans
Nicholas J Marini, Jennifer Gin, Janet Ziegle, et al.
American Journal of Medical Genetics. Part A
|
September 9, 2016
Sequence variation in folate pathway genes and risks of human cleft lip with or without cleft palate
Nicholas J Marini, Wei Yang, Kripa Asrani, et al.
Epigenetics
|
March 15, 2019
Epigenomic profiling of newborns with isolated orofacial clefts reveals widespread DNA methylation changes and implicates metastable epiallele regions in disease risk
Semira Gonseth, Gary M Shaw, Ritu Roy, et al.
Plos One
|
December 6, 2011
A genetic signature of spina bifida risk from pathway-informed comprehensive gene-variant analysis
Nicholas J Marini, Thomas J Hoffmann, Edward J Lammer, et al.
Page
of 2