Ectopic Mineralization and Conductive Hearing Loss in Enpp1(asj) Mutant Mice, a New Model for Otitis Media and Tympanosclerosis

por Tian, Cong, Harris, Belinda S., Johnson, Kenneth R.
Publicado no PLoS One (2016)

A novel null allele of mouse Dscam survives to adulthood on an inbred C3H background with reduced phenotypic variability

por Fuerst, Peter G., Harris, Belinda S., Johnson, Kenneth R., Burgess, Robert W.
Publicado em 2010

Notch signalling in the paraxial mesoderm is most sensitive to reduced Pofut1 levels during early mouse development

por Schuster-Gossler, Karin, Harris, Belinda, Johnson, Kenneth R, Serth, Jürgen, Gossler, Achim
Publicado em 2009

Hearing Impairment in Hypothyroid Dwarf Mice Caused by Mutations of the Thyroid Peroxidase Gene

por Johnson, Kenneth R., Gagnon, Leona H., Longo-Guess, Chantal M., Harris, Belinda S., Chang, Bo
Publicado em 2013

The Netrin 1 Receptors Unc5h3 and Dcc Are Necessary at Multiple Choice Points for the Guidance of Corticospinal Tract Axons

por Finger, Jacqueline H., Bronson, Rod T., Harris, Belinda, Johnson, Kenneth, Przyborski, Stefan A., Ackerman, Susan L.
Publicado no J Neurosci (2002)

Contrasting alterations to synaptic and intrinsic properties in upper-cervical superficial dorsal horn neurons following acute neck muscle inflammation

por Harris, Belinda M, Hughes, David I, Bolton, Philip S, Tadros, Melissa A, Callister, Robert J, Graham, Brett A
Publicado em 2014

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10

por Zheng, Qing Yin, Harris, Belinda S, Ward-Bailey, Patricia F, Yu, Heping, Bronson, Roderick T, Davisson, Muriel T, Johnson, Kenneth R
Publicado em 2004

A Novel Mouse Dscam Mutation Inhibits Localization and Shedding of DSCAM

por Schramm, R. Dee, Li, Shuai, Harris, Belinda S., Rounds, Ryan P., Burgess, Robert W., Ytreberg, F. Marty, Fuerst, Peter G.
Publicado em 2012

The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development

por Mao, Mao, Thedens, Daniel R., Chang, Bo, Harris, Belinda S., Zheng, Qing Yin, Johnson, Kenneth R., Donahue, Leah Rae, Anderson, Michael G.
Publicado em 2009

Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass

por Munroe, Robert J, Prabhu, Vinay, Acland, Greg M, Johnson, Kenneth R, Harris, Belinda S, O'Brien, Tim P, Welsh, Ian C, Noden, Drew M, Schimenti, John C
Publicado em 2009

Dsp(rul): A spontaneous mouse mutation in Desmoplakin as a model of Carvajal-Huerta Syndrome

por Pratt, C. Herbert, Potter, Christopher S., Fairfield, Heather, Reinholdt, Laura G., Bergstrom, David E., Harris, Belinda S., Greenstein, Ian, Dadras, Soheil S., Liang, Bruce T., Schofield, Paul N., Sundberg, John P.
Publicado no Exp Mol Pathol (2015)

Integrated analysis of the molecular pathogenesis of FDXR-associated disease

por Slone, Jesse D., Yang, Li, Peng, Yanyan, Queme, Luis F., Harris, Belinda, Rizzo, Stacey J. Sukoff, Green, Torrian, Ryan, Jennifer L., Jankowski, Michael P., Reinholdt, Laura G., Huang, Taosheng
Publicado no Cell Death Dis (2020)

Biallelic mutations in FDXR cause neurodegeneration associated with inflammation

por Slone, Jesse, Peng, Yanyan, Chamberlin, Adam, Harris, Belinda, Kaylor, Julie, McDonald, Marie T., Lemmon, Monica, El-Dairi, Mays Antonine, Tchapyjnikov, Dmitry, Gonzalez-Krellwitz, Laura A, Sellars, Elizabeth A., McConkie-Rosell, Allyn, Reinholdt, Laura G., Huang, Taosheng
Publicado no J Hum Genet (2018)

The mouse mutation “thrombocytopenia and cardiomyopathy” (trac) disrupts Abcg5: a spontaneous single gene model for human hereditary phytosterolemia/sitosterolemia

por Chase, Thomas H., Lyons, Bonnie L., Bronson, Roderick T., Foreman, Oded, Donahue, Leah Rae, Burzenski, Lisa M., Gott, Bruce, Lane, Priscilla, Harris, Belinda, Ceglarek, Uta, Thiery, Joachim, Wittenburg, Henning, Thon, Jonathan N., Italiano, Joseph E., Johnson, Kenneth R., Shultz, Leonard D.
Publicado em 2010

Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders

por Fairfield, Heather, Srivastava, Anuj, Ananda, Guruprasad, Liu, Rangjiao, Kircher, Martin, Lakshminarayana, Anuradha, Harris, Belinda S., Karst, Son Yong, Dionne, Louise A., Kane, Coleen C., Curtain, Michelle, Berry, Melissa L., Ward-Bailey, Patricia F., Greenstein, Ian, Byers, Candice, Czechanski, Anne, Sharp, Jocelyn, Palmer, Kristina, Gudis, Polyxeni, Martin, Whitney, Tadenev, Abby, Bogdanik, Laurent, Pratt, C. Herbert, Chang, Bo, Schroeder, David G., Cox, Gregory A., Cliften, Paul, Milbrandt, Jeffrey, Murray, Stephen, Burgess, Robert, Bergstrom, David E., Donahue, Leah Rae, Hamamy, Hanan, Masri, Amira, Santoni, Federico A., Makrythanasis, Periklis, Antonarakis, Stylianos E., Shendure, Jay, Reinholdt, Laura G.
Publicado no Genome Res (2015)

Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophy

por Peng, Yanyan, Shinde, Deepali N, Valencia, C Alexander, Mo, Jun-Song, Rosenfeld, Jill, Truitt Cho, Megan, Chamberlin, Adam, Li, Zhuo, Liu, Jie, Gui, Baoheng, Brockhage, Rachel, Basinger, Alice, Alvarez-Leon, Brenda, Heydemann, Peter, Magoulas, Pilar L, Lewis, Andrea M, Scaglia, Fernando, Gril, Solange, Chong, Shuk Ching, Bower, Matthew, Monaghan, Kristin G, Willaert, Rebecca, Plona, Maria-Renee, Dineen, Rich, Milan, Francisca, Hoganson, George, Powis, Zoe, Helbig, Katherine L, Keller-Ramey, Jennifer, Harris, Belinda, Anderson, Laura C, Green, Torrian, Sukoff Rizzo, Stacey J, Kaylor, Julie, Chen, Jiani, Guan, Min-Xin, Sellars, Elizabeth, Sparagana, Steven P, Gibson, James B, Reinholdt, Laura G, Tang, Sha, Huang, Taosheng
Publicado no Hum Mol Genet (2017)