Search Results - "Stansberry, Leah"

Hyperoxia Inhibits Oxidant-induced Apoptosis in Lung Epithelial Cells by Franek, William R., Horowitz, Stuart, Stansberry, Leah, Kazzaz, Jeffrey A., Koo, Hshi-Chi, Li, Yuchi, Arita, Yuko, Davis, Jonathan M., Mantell, Abraham S., Scott, William, Mantell, Lin L.

“…It has previously been shown that hyperoxia induces nonapoptotic cell death in cultured lung epithelial cells, whereas hydrogen peroxide (H2O2) and paraquat…”
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Towards implementation whole genome sequencing as a first tier test in genomic testing by Liu, Ruby, Collins, Christin, Duraisamy, Arul, Behlmann, Andrea, Stansberry, Leah, Mathur, Abhinav, Ma, Zeqiang, Hegde, Madhuri

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eP394 - Genome and exome analysis for detection of coding and non-coding sequencing and copy number variants in disorders of sexual development by Behlmann, Andrea, Reddy Nallamilli, Babi Ramesh, Collins, Christin D., Stansberry, Leah, Hegde, Madhuri

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eP368 - Towards implementation whole genome sequencing as a first tier test in genomic testing by Liu, Ruby, Collins, Christin, Duraisamy, Arul, Behlmann, Andrea, Stansberry, Leah, Mathur, Abhinav, Ma, Zeqiang, Hegde, Madhuri

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Genome and exome analysis for detection of coding and non-coding sequencing and copy number variants in disorders of sexual development by Behlmann, Andrea, Reddy Nallamilli, Babi Ramesh, Collins, Christin D., Stansberry, Leah, Hegde, Madhuri

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A single NGS‐based assay covering the entire genomic sequence of the DMD gene facilitates diagnostic and newborn screening confirmatory testing by Nallamilli, Babi R. R., Chaubey, Alka, Valencia, C. A., Stansberry, Leah, Behlmann, Andrea M., Ma, Zeqiang, Mathur, Abhinav, Shenoy, Suresh, Ganapathy, Vidya, Jagannathan, Lakshmanan, Ramachander, Vinish, Ferlini, Alessandra, Bean, Lora, Hegde, Madhuri

“…Molecular diagnosis for Duchenne and Becker muscular dystrophies (DMD/BMD) involves a two‐tiered approach for detection of deletions/duplications using MLPA or…”
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Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional Microarray by Chaubey, Alka, Shenoy, Suresh, Mathur, Abhinav, Ma, Zeqiang, Valencia, C Alexander, Reddy Nallamilli, Babi R, Szekeres, Jr, Edward, Stansberry, Leah, Liu, Ruby, Hegde, Madhuri R

“…DNA copy number variants (CNVs) account for approximately 300 Mb of sequence variation in the normal human genome. Significant numbers of pathogenic CNVs…”
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Low-Pass Genome Sequencing by Chaubey, Alka, Shenoy, Suresh, Mathur, Abhinav, Ma, Zeqiang, Valencia, C. Alexander, Reddy Nallamilli, Babi R., Szekeres, Edward, Stansberry, Leah, Liu, Ruby, Hegde, Madhuri R.

“…DNA copy number variants (CNVs) account for approximately 300 Mb of sequence variation in the normal human genome. Significant numbers of pathogenic CNVs…”
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Pulmonary apoptosis in aged and oxygen-tolerant rats exposed to hyperoxia by Otterbein, L E, Chin, B Y, Mantell, L L, Stansberry, L, Horowitz, S, Choi, A M

“…Accumulating evidence demonstrates that genotoxic and oxidant stress can induce programmed cell death or apoptosis in cultured cells. However, little is known…”
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