Torthaí cuardaigh - Sachin Sah
- 1 - 8 toradh as 8 á dtaispeáint
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1
Functional DNA quantification guides accurate next-generation sequencing mutation detection in formalin-fixed, paraffin-embedded tumor biopsies de réir Sachin Sah, Liangjing Chen, Jeffrey Houghton, Jon Kemppainen, Adam C. Marko, R. Zeigler, Gary J. Latham
Foilsithe / Cruthaithe 2013Artigo -
2
High-resolution methylation polymerase chain reaction for fragile X analysis: Evidence for novel FMR1 methylation patterns undetected in Southern blot analyses de réir Liangjing Chen, Andrew G. Hadd, Sachin Sah, Jeffrey Houghton, Stela Filipovic-Sadic, Wenting Zhang, Paul J. Hagerman, Flora Tassone, Gary J. Latham
Foilsithe / Cruthaithe 2011Artigo -
3
Fragile X full mutation expansions are inhibited by one or more AGG interruptions in premutation carriers de réir Sarah L. Nolin, Anne Glicksman, Nicole Ersalesi, Carl Dobkin, W. Ted Brown, Ru Cao, Eliot B. Blatt, Sachin Sah, Gary J. Latham, Andrew G. Hadd
Foilsithe / Cruthaithe 2014Artigo -
4
A Novel FMR1 PCR Method for the Routine Detection of Low Abundance Expanded Alleles and Full Mutations in Fragile X Syndrome de réir Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Julie Krosting, Edward A. Sekinger, Wenting Zhang, Paul J. Hagerman, Timothy T. Stenzel, Andrew G. Hadd, Gary J. Latham, Flora Tassone
Foilsithe / Cruthaithe 2010Artigo -
5
An Information-Rich CGG Repeat Primed PCR That Detects the Full Range of Fragile X Expanded Alleles and Minimizes the Need for Southern Blot Analysis de réir Liangjing Chen, Andrew G. Hadd, Sachin Sah, Stela Filipovic-Sadic, Julie Krosting, Edward A. Sekinger, Ruiqin Pan, Paul J. Hagerman, Timothy T. Stenzel, Flora Tassone, Gary J. Latham
Foilsithe / Cruthaithe 2010Artigo -
6
Targeted, High-Depth, Next-Generation Sequencing of Cancer Genes in Formalin-Fixed, Paraffin-Embedded and Fine-Needle Aspiration Tumor Specimens de réir Andrew G. Hadd, Jeff Houghton, Ashish Choudhary, Sachin Sah, Liangjing Chen, Adam C. Marko, Tiffany Sanford, Kalyan Buddavarapu, Julie Krosting, Lana X. Garmire, Dennis Wylie, Rupali Shinde, Sylvie Beaudenon, Erik K. Alexander, Elizabeth Mambo, Alex Adai, Gary J. Latham
Foilsithe / Cruthaithe 2013Artigo -
7
Fragile X AGG analysis provides new risk predictions for 45–69 repeat alleles de réir Sarah L. Nolin, Sachin Sah, Anne Glicksman, Stephanie L. Sherman, Emily G. Allen, Elizabeth Berry‐Kravis, Flora Tassone, Carolyn M. Yrigollen, Amy Cronister, Marcia Jodah, Nicole Ersalesi, Carl Dobkin, W. Ted Brown, Raghav Shroff, Gary J. Latham, Andrew G. Hadd
Foilsithe / Cruthaithe 2013Artigo -
8
Profiling Cancer Gene Mutations in Clinical Formalin-Fixed, Paraffin-Embedded Colorectal Tumor Specimens Using Targeted Next-Generation Sequencing de réir Liangxuan Zhang, Liangjing Chen, Sachin Sah, Gary J. Latham, Rajesh Patel, Qinghua Song, Hartmut Koeppen, Rachel Tam, Erica Schleifman, Haider Mashhedi, Sreedevi Chalasani, Ling Fu, Teiko Sumiyoshi, Rajiv Raja, William F. Forrest, Garret M. Hampton, Mark R. Lackner, Priti S. Hegde, Shidong Jia
Foilsithe / Cruthaithe 2014Artigo
Uirlisí cuardaigh:
Ábhair a bhaineann le hábhar
Biology
Gene
Genetics
Allele
Fragile X syndrome
Polymerase chain reaction
Computational biology
DNA sequencing
FMR1
Fragile x
Southern blot
Cancer
Genome
Genomics
Ion semiconductor sequencing
Medicine
Microsatellite
Molecular biology
Mutation
Personal genomics
Amplicon
Bioinformatics
Biopsy
Blot
Colorectal cancer
Composite material
DNA
DNA methylation
Gene expression
Gene mutation