Browsing HMS Scholarly Articles by Author "6c9d254584a794cf3278a1f63032dbf0"

DSpace/Manakin Repository

DASH Home
Harvard Medical School
HMS Scholarly Articles
Browsing HMS Scholarly Articles by Author

Browsing HMS Scholarly Articles by Author "6c9d254584a794cf3278a1f63032dbf0"

Now showing items 1-11 of 11

Analysis of Human Sarcospan as a Candidate Gene for CFEOM1

O'Brien, Kristine F; Engle, Elizabeth Carson; Kunkel, Louis Martens (BMC Genetics, 2001) Link to Published Version
Automated DNA Mutation Detection Using Universal Conditions Direct Sequencing: Application to Ten Muscular Dystrophy Genes

Bennett, Richard R; Schneider, Hal E; Estrella, Elicia; Burgess, Stephanie; Cheng, Andrew S; Barrett, Caitlin; Lip, Va et al. (BMC Genetics, 2009) Link to Published Version
Beta-Synemin Expression in Cardiotoxin-Injected Rat Skeletal Muscle

Mizuno, Yuji; Guyon, Jeffrey R; Ishii, Akiko; Hoshino, Sachiko; Ohkoshi, Norio; Tamaoka, Akira; Okamoto, Koichi et al. (BMC Musculoskeletal Disorders, 2007) Link to Published Version
Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders

Kong, Sek Won; Collins, Christin D.; Shimizu-Motohashi, Yuko; Holm, Ingrid A.; Campbell, Malcolm G.; Lee, In-Hee; Brewster, Stephanie J. et al. (PLoS ONE, 2012) Link to Published Version
The Co-Morbidity Burden of Children and Young Adults with Autism Spectrum Disorders

Wattanasin, Nich; Churchill, Susanne; Kohane, Isaac Samuel; McMurry, Andrew; MacFadden, Douglas; Rappaport, Leonard Allan; Kunkel, Louis Martens et al. (PLoS ONE, 2012) Link to Published Version
Detection of Mutations in the Dystrophin Gene via Automated DHPLC Screening and Direct Sequencing

Bennett, Richard R; den Dunnen, Johan; O'Brien, Kristine F; Darras, Basil T.; Kunkel, Louis Martens (BMC Genetics, 2001) Link to Published Version
Genomic Organization and Single-Nucleotide Polymorphism Map of Desmuslin, a Novel Intermediate Filament Protein on Chromosome 15q26.3

Mizuno, Yuji; Puca, Annibale A; O'Brien, Kristine F; Beggs, Alan Hendrie; Kunkel, Louis Martens (BMC Genetics, 2001) Link to Published Version
High-Density Genomewide Linkage Analysis of Exceptional Human Longevity Identifies Multiple Novel Loci

Boyden, Steven Edward; Kunkel, Louis Martens (PLoS ONE, 2010) Link to Published Version
Mutations in the Satellite Cell Gene MEGF10 Cause a Recessive Congenital Myopathy with Minicores

Mahoney, Lane J.; Myers, Jennifer A.; Estrella, Elicia A.; Duncan, Anna R.; Dey, Friederike; DeChene, Elizabeth T.; Blasko-Goehringer, Jessica M. et al. (Neurogenetics, 2012) Link to Published Version
Reproducibility of Gene Expression Across Generations of Affymetrix Microarrays

Nimgaonkar, Ashish; Sanoudou, Despina; Butte, Atul J; Haslett, Judith N; Kunkel, Louis Martens; Beggs, Alan Hendrie; Kohane, Isaac Samuel (BMC Bioinformatics, 2003) Link to Published Version
A Splice Site Mutation in Laminin-α2 Results in a Severe Muscular Dystrophy and Growth Abnormalities in Zebrafish

Myers, Jennifer A.; Chen, Aye T.; Hall, Thomas E.; Currie, Peter D.; Gupta, Vandana; Kawahara, Genri; Manzini, Maria Chiara et al. (PLoS ONE, 2012) Link to Published Version

Now showing items 1-11 of 11

Advanced Search

All of DASH
This Collection