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Nicholas J Marini

Showing results (1-10 of 12) with videos related to

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Plos Genetics|June 5, 2010
The use of orthologous sequences to predict the impact of amino acid substitutions on protein functionNicholas J Marini, Paul D Thomas, Jasper Rine
Plos One|November 13, 2010
Comprehensive approach to analyzing rare genetic variantsThomas 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 BloodspotKripa 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 palateNicholas 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 vitroDago Dimster-Denk, Katherine W Tripp, Nicholas J Marini, et al.
Chemistry & Biology|August 2, 2003
DNA binding hairpin polyamides with antifungal activityNicholas 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 humansNicholas 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 palateNicholas 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 riskSemira 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 analysisNicholas J Marini, Thomas J Hoffmann, Edward J Lammer, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Plos Genetics|June 5, 2010
The use of orthologous sequences to predict the impact of amino acid substitutions on protein functionNicholas J Marini, Paul D Thomas, Jasper Rine
Plos One|November 13, 2010
Comprehensive approach to analyzing rare genetic variantsThomas 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 BloodspotKripa 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 palateNicholas 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 vitroDago Dimster-Denk, Katherine W Tripp, Nicholas J Marini, et al.
Chemistry & Biology|August 2, 2003
DNA binding hairpin polyamides with antifungal activityNicholas 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 humansNicholas 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 palateNicholas 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 riskSemira 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 analysisNicholas J Marini, Thomas J Hoffmann, Edward J Lammer, et al.
Pageof 2