Characterization of a Trypanosoma brucei RNA cap (guanine N-7) methyltransferase

Por HALL, MEGAN P., HO, C. KIONG
Publicado em 2006

Functional characterization of a 48 kDa Trypanosoma brucei cap 2 RNA methyltransferase

Por Hall, Megan P., Ho, C. Kiong
Publicado em 2006

Differentiation-induced Colocalization of the KH-type Splicing Regulatory Protein with Polypyrimidine Tract Binding Protein and the c-src Pre-mRNA

Por Hall, Megan P., Huang, Sui, Black, Douglas L.
Publicado em 2004

Non-Invasive Prenatal Detection of Trisomy 13 Using a Single Nucleotide Polymorphism- and Informatics-Based Approach

Por Hall, Megan P., Hill, Matthew, Zimmermann, Bernhard, Sigurjonsson, Styrmir, Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Publicado em 2014

Quaking and PTB control overlapping splicing regulatory networks during muscle cell differentiation

Por Hall, Megan P., Nagel, Roland J., Fagg, W. Samuel, Shiue, Lily, Cline, Melissa S., Perriman, Rhonda J., Donohue, John Paul, Ares, Manuel
Publicado em 2013

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population

Por Samango-Sprouse, Carole, Kırkızlar, Eser, Hall, Megan P., Lawson, Patrick, Demko, Zachary, Zneimer, Susan M., Curnow, Kirsten J., Gross, Susan, Gropman, Andrea
Publicado no PLoS One (2016)

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy

Por Samango-Sprouse, Carole, Banjevic, Milena, Ryan, Allison, Sigurjonsson, Styrmir, Zimmermann, Bernhard, Hill, Matthew, Hall, Megan P., Westemeyer, Margaret, Saucier, Jennifer, Demko, Zachary, Rabinowitz, Matthew
Publicado em 2013

Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy

Por Du, Hongqing, Cline, Melissa S., Osborne, Robert J., Tuttle, Daniel L., Clark, Tyson A., Donohue, John Paul, Hall, Megan P., Shiue, Lily, Swanson, Maurice S., Thornton, Charles A., Ares, Manuel
Publicado em 2010

Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort

Por Pergament, Eugene, Cuckle, Howard, Zimmermann, Bernhard, Banjevic, Milena, Sigurjonsson, Styrmir, Ryan, Allison, Hall, Megan P., Dodd, Michael, Lacroute, Phil, Stosic, Melissa, Chopra, Nikhil, Hunkapiller, Nathan, Prosen, Dennis E., McAdoo, Sallie, Demko, Zachary, Siddiqui, Asim, Hill, Matthew, Rabinowitz, Matthew
Publicado em 2014

High-intensity sequencing reveals the sources of plasma circulating cell-free DNA variants

Por Razavi, Pedram, Li, Bob T., Brown, David N., Jung, Byoungsok, Hubbell, Earl, Shen, Ronglai, Abida, Wassim, Juluru, Krishna, De Bruijn, Ino, Hou, Chenlu, Venn, Oliver, Lim, Raymond, Anand, Aseem, Maddala, Tara, Gnerre, Sante, Satya, Ravi Vijaya, Liu, Qinwen, Shen, Ling, Eattock, Nicholas, Yue, Jeanne, Blocker, Alexander W., Lee, Mark, Sehnert, Amy, Xu, Hui, Hall, Megan P., Santiago-Zayas, Angie, Novotny, William F., Isbell, James M., Rusch, Valerie W., Plitas, George, Heerdt, Alexandra S., Ladanyi, Marc, Hyman, David M., Jones, David R., Morrow, Monica, Riely, Gregory J., Scher, Howard I., Rudin, Charles M., Robson, Mark E., Diaz, Luis A., Solit, David B., Aravanis, Alexander M., Reis-Filho, Jorge S.
Publicado no Nat Med (2019)