Search Results - "Straub, Devan"

A sensitive and reproducible qRT-PCR assay detects physiological relevant trace levels of FMR1 mRNA in individuals with Fragile X syndrome by Straub, Devan, Schmitt, Lauren M., Boggs, Anna E., Horn, Paul S., Dominick, Kelli C., Gross, Christina, Erickson, Craig A.

“…Fragile X syndrome (FXS) is the most common inherited intellectual disability. FXS is caused by a trinucleotide repeat expansion in the 5′ untranslated region…”
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Genetic mapping and phenotypic analysis of shotH.3.2 in Drosophila melanogaster by Talley, Elyse M, Watts, Charlie T, Aboyer, Sonia, Adamson, Madeline G, Akoto, Harriet Ab, Altemus, Haley, Avella, Philip J, Bailey, Rebecca, Bell, Elizabeth R, Bell, Katheryn L, Breneman, Kelsey, Burkhart, Jessica S, Chanley, Logan J, Cook, Savannah S, DesLaurier, Mackenzie T, Dorsey, Timothy R, Doyle, Cassandra J, Egloff, Merris E, Fasawe, Ayoola S, Garcia, Katy K, Graves, Nathaniel P, Gray, Tyler K, Gustafson, Evan M, Hall, Makayla J, Hayes, Jaden D, Holic, Lindsay J, Jarvis, Brice A, Klos, Piotr S, Kritzmire, Sidney, Kuzovko, Lera, Lainez, Edwyna, McCoy, Shamerra, Mierendorf, James C, Neri, Nicole A, Neville, Caley R, Osborn, Kelley, Parker, Kaitlyn, Parks, Megan E, Peck, Kylee, Pitt, Robyn, Platta, Matthew E, Powell, Brianna, Rodriguez, Katalina, Ruiz, Clara, Schaefer, Mariah N, Shields, Amanda B, Smiley, Jasmine B, Stauffer, Briona, Straub, Devan, Sweeney, John L, Termine, Kaitlyn M, Thomas, Brett, Toth, Sophia D, Veile, Taylor R, Walker, Kayla S, Webster, Paige N, Woodard, Brian J, Yoder, Quentin L, Young, McKenzie K, Zeedyk, McKenzie L, Ziegler, Logan N, Bieser, Kayla L, Puthoff, David P, Stamm, Joyce, Vrailas-Mortimer, Alysia D, Kagey, Jacob D, Merkle, Julie A

“…Genetic screens are used to identify genes involved in specific biological processes. An EMS mutagenesis screen in Drosophila melanogaster identified growth…”
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