The power of comparative and developmental studies for mouse models of Down syndrome

Por Moore, Clara S., Roper, Randall J.
Publicado em 2007

Understanding the Basis for Down Syndrome Phenotypes

Por Roper, Randall J, Reeves, Roger H
Publicado em 2006

Trisomic and Allelic Differences Influence Phenotypic Variability During Development of Down Syndrome Mice

Por Deitz, Samantha L., Roper, Randall J.
Publicado em 2011

Targeting trisomic treatments: optimizing Dyrk1a inhibition to improve Down syndrome deficits

Por Stringer, Megan, Goodlett, Charles R., Roper, Randall J.
Publicado no Mol Genet Genomic Med (2017)

Commonality in Down and Fetal Alcohol Syndromes

Por Solzak, Jeffrey P., Liang, Yun, Zhou, Feng C., Roper, Randall J.
Publicado em 2013

Disruption of bone development and homeostasis by trisomy in Ts65Dn Down syndrome mice

Por Blazek, Joshua D., Gaddy, Anna, Meyer, Rachel, Roper, Randall J., Li, Jiliang
Publicado em 2010

A neural crest deficit in Down syndrome mice is associated with deficient mitotic response to Sonic hedgehog

Por Roper, Randall J., VanHorn, Justin F., Cain, Colyn C., Reeves, Roger H.
Publicado em 2008

PCR prescreen for genotyping the Ts65Dn mouse model of Down syndrome

Por Lorenzi, Hernan, Duvall, Nichole, Cherry, Sheila M., Reeves, Roger H., Roper, Randall J.
Publicado em 2010

Perinatal Loss of Ts65Dn Down Syndrome Mice

Por Roper, Randall J., St. John, Heidi K., Philip, Jessica, Lawler, Ann, Reeves, Roger H.
Publicado em 2006

Inferring gene regulatory networks from asynchronous microarray data with AIRnet

Por Oviatt, David, Clement, Mark, Snell, Quinn, Sundberg, Kenneth, Lai, Chun Wan J, Allen, Jared, Roper, Randall
Publicado em 2010

Identification of Genetic Loci Controlling the Characteristics and Severity of Brain and Spinal Cord Lesions in Experimental Allergic Encephalomyelitis

Por Butterfield, Russell J., Blankenhorn, Elizabeth P., Roper, Randall J., Zachary, James F., Doerge, R. W., Teuscher, Cory
Publicado em 2000

Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice

Por Roper, Randall J., Baxter, Laura L., Saran, Nidhi G., Klinedinst, Donna K., Beachy, Philip A., Reeves, Roger H.
Publicado em 2006

Role of Osteopontin in Murine Lyme Arthritis and Host Defense against Borrelia burgdorferi

Por Potter, Melissa R., Rittling, Susan R., Denhardt, David T., Roper, Randall J., Weis, John H., Teuscher, Cory, Weis, Janis J.
Publicado em 2002

Obstructive Sleep Apnea in Young Infants with Down Syndrome Evaluated in a Down Syndrome Specialty Clinic

Por Goffinski, Alida, Stanley, Maria A., Shepherd, Nicole, Duvall, Nichole, Jenkinson, Sandra B., Davis, Charlene, Bull, Marilyn J., Roper, Randall J.
Publicado no Am J Med Genet A (2015)

Sex-specific quantitative trait loci govern susceptibility to Theiler's murine encephalomyelitis virus-induced demyelination.

Por Butterfield, Russell J, Roper, Randall J, Rhein, Dominic M, Melvold, Roger W, Haynes, Lia, Ma, Runlin Z, Doerge, R W, Teuscher, Cory
Publicado em 2003

Differential effects of Epigallocatechin-3-gallate containing supplements on correcting skeletal defects in a Down syndrome mouse model

Por Abeysekera, Irushi, Thomas, Jared, Georgiadis, Taxiarchis M., Berman, Alycia G., Hammond, Max A., Dria, Karl J., Wallace, Joseph M., Roper, Randall J.
Publicado no Mol Nutr Food Res (2016)

Influence of prenatal EGCG treatment and Dyrk1a dosage reduction on craniofacial features associated with Down syndrome

Por McElyea, Samantha D, Starbuck, John M, Tumbleson-Brink, Danika M, Harrington, Emily, Blazek, Joshua D, Ghoneima, Ahmed, Kula, Katherine, Roper, Randall J
Publicado no Hum Mol Genet (2016)

Molecular Characterization of the Translocation Breakpoints in the Down Syndrome Mouse Model, Ts65Dn

Por Reinholdt, Laura G., Ding, Yueming, Gilbert, Griffith J., Czechanski, Anne, Solzak, Jeffrey P., Roper, Randall J., Johnson, Mark T., Donahue, Leah Rae, Lutz, Cathleen, Davisson, Muriel T.
Publicado em 2011

Epigallocatechin-3-gallate (EGCG) consumption in the Ts65Dn model of Down syndrome fails to improve behavioral deficits and is detrimental to skeletal phenotypes

Por Stringer, Megan, Abeysekera, Irushi, Thomas, Jared, LaCombe, Jonathan, Stancombe, Kailey, Stewart, Robert J., Dria, Karl J., Wallace, Joseph M., Goodlett, Charles R., Roper, Randall J.
Publicado no Physiol Behav (2017)

Non-trisomic Homeobox Gene Expression during Craniofacial Development in the Ts65Dn Mouse Model of Down Syndrome

Por Billingsley, Cherie N., Allen, Jared R., Baumann, Douglas D., Deitz, Samantha L., Blazek, Joshua D., Newbauer, Abby, Darrah, Andrew, Long, Brad C., Young, Brandon, Clement, Mark, Doerge, R.W., Roper, Randall J.
Publicado em 2013