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Samuel Deutsch

Showing results (21-30 of 67) with videos related to

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American Journal of Human Genetics|April 13, 2004
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with variation in vertebral bone mass, vertebral bone size, and stature in whitesSerge L Ferrari, Samuel Deutsch, Urmila Choudhury, et al.
American Journal of Human Genetics|August 2, 2007
Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypesPraveen Sethupathy, Christelle Borel, Maryline Gagnebin, et al.
Nucleic Acids Research|November 4, 2008
Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular originKayole Kazadi, Corinne Loeuillet, Samuel Deutsch, et al.
Journal of Molecular Biology|January 28, 2019
Extent and Origins of Functional Diversity in a Subfamily of Glycoside HydrolasesEvan M Glasgow, Kirk A Vander Meulen, Taichi E Takasuka, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 19, 2020
An Integrated Computer-Aided Design and Manufacturing Workflow for Synthetic BiologyErnst Oberortner, Robert Evans, Xianwei Meng, et al.
Blood|March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeSamuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Human Molecular Genetics|October 28, 2005
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genesSamuel Deutsch, Robert Lyle, Emmanouil T Dermitzakis, et al.
ACS Central Science|May 4, 2022
A Synthetic Gene Library Yields a Previously Unknown Glycoside Phosphorylase That Degrades and Assembles Poly-β-1,3-GlcNAc, Completing the Suite of β-Linked GlcNAc PolysaccharidesSpencer S Macdonald, Jose H Pereira, Feng Liu, et al.
Nature|December 6, 2002
Numerous potentially functional but non-genic conserved sequences on human chromosome 21Emmanouil T Dermitzakis, Alexandre Reymond, Robert Lyle, et al.
European Journal of Human Genetics : EJHG|April 12, 2012
Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmusUppala Radhakrishna, Uppala Ratnamala, Samuel Deutsch, et al.
Pageof 7

Showing results (21-30 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|April 13, 2004
Polymorphisms in the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with variation in vertebral bone mass, vertebral bone size, and stature in whitesSerge L Ferrari, Samuel Deutsch, Urmila Choudhury, et al.
American Journal of Human Genetics|August 2, 2007
Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypesPraveen Sethupathy, Christelle Borel, Maryline Gagnebin, et al.
Nucleic Acids Research|November 4, 2008
Genomic determinants of the efficiency of internal ribosomal entry sites of viral and cellular originKayole Kazadi, Corinne Loeuillet, Samuel Deutsch, et al.
Journal of Molecular Biology|January 28, 2019
Extent and Origins of Functional Diversity in a Subfamily of Glycoside HydrolasesEvan M Glasgow, Kirk A Vander Meulen, Taichi E Takasuka, et al.
Methods in Molecular Biology (Clifton, N.J.)|August 19, 2020
An Integrated Computer-Aided Design and Manufacturing Workflow for Synthetic BiologyErnst Oberortner, Robert Evans, Xianwei Meng, et al.
Blood|March 22, 2003
Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndromeSamuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, et al.
Human Molecular Genetics|October 28, 2005
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genesSamuel Deutsch, Robert Lyle, Emmanouil T Dermitzakis, et al.
ACS Central Science|May 4, 2022
A Synthetic Gene Library Yields a Previously Unknown Glycoside Phosphorylase That Degrades and Assembles Poly-β-1,3-GlcNAc, Completing the Suite of β-Linked GlcNAc PolysaccharidesSpencer S Macdonald, Jose H Pereira, Feng Liu, et al.
Nature|December 6, 2002
Numerous potentially functional but non-genic conserved sequences on human chromosome 21Emmanouil T Dermitzakis, Alexandre Reymond, Robert Lyle, et al.
European Journal of Human Genetics : EJHG|April 12, 2012
Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmusUppala Radhakrishna, Uppala Ratnamala, Samuel Deutsch, et al.
Pageof 7