Genetic modifiers of Velo- cardio- facial syndrome/DiGeorge syndrome

بواسطة Aggarwal, Vimla S., Morrow, Bernice E.
منشور في 2008

Canonical Wnt signaling modulates Tbx1, Eya1 and Six1 expression, restricting neurogenesis in the otic vesicle

بواسطة Freyer, Laina, Morrow, Bernice E.
منشور في 2010

Tbx1 and Jag1 act in concert to modulate the fate of neurosensory cells of the mouse otic vesicle

بواسطة Macchiarulo, Stephania, Morrow, Bernice E.
الحاوية / القاعدة Biol Open (2017)

Tbx1 and Foxi3 genetically interact in the pharyngeal pouch endoderm in a mouse model for 22q11.2 deletion syndrome

بواسطة Hasten, Erica, Morrow, Bernice E.
الحاوية / القاعدة PLoS Genet (2019)

Identification of putative retinoic acid target genes downstream of mesenchymal Tbx1 during inner ear development

بواسطة Monks, Dennis C., Morrow, Bernice E.
منشور في 2012

Genomic Disorders on 22q11

بواسطة McDermid, Heather E., Morrow, Bernice E.
منشور في 2002

Dual embryonic origin of the mammalian otic vesicle forming the inner ear

بواسطة Freyer, Laina, Aggarwal, Vimla, Morrow, Bernice E.
منشور في 2011

Interstitial duplication of 22q13.2 in a girl with short stature, impaired speech and language, and dysmorphism

بواسطة Samanich, Joy, Montagna, Cristina, Morrow, Bernice E., Babcock, Melanie
الحاوية / القاعدة J Pediatr Genet (2012)

Mammalian TBX1 Preferentially Binds and Regulates Downstream Targets Via a Tandem T-site Repeat

بواسطة Castellanos, Raquel, Xie, Qing, Zheng, Deyou, Cvekl, Ales, Morrow, Bernice E.
منشور في 2014

Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome

بواسطة Pavlicek, Adam, House, Reniqua, Gentles, Andrew J., Jurka, Jerzy, Morrow, Bernice E.
منشور في 2005

AT-rich repeats associated with chromosome 22q11.2 rearrangement disorders shape human genome architecture on Yq12

بواسطة Babcock, Melanie, Yatsenko, Svetlana, Stankiewicz, Pawel, Lupski, James R., Morrow, Bernice E.
منشور في 2007

Conditional and constitutive expression of a Tbx1-GFP fusion protein in mice

بواسطة Freyer, Laina, Nowotschin, Sonja, Pirity, Melinda K, Baldini, Antonio, Morrow, Bernice E
منشور في 2013

Identification of downstream genetic pathways of Tbx1 in the second heart field

بواسطة Liao, Jun, Aggarwal, Vimla S., Nowotschin, Sonja, Bondarev, Alexei, Lipner, Shari, Morrow, Bernice E.
منشور في 2008

Cooperative Function of Tbx1 and Brn4 in the Periotic Mesenchyme is Necessary for Cochlea Formation

بواسطة Braunstein, Evan M., Crenshaw III, E. Bryan, Morrow, Bernice E., Adams, Joe C.
منشور في 2008

Tbx1 and Brn4 regulate retinoic acid metabolic genes during cochlear morphogenesis

بواسطة Braunstein, Evan M, Monks, Dennis C, Aggarwal, Vimla S, Arnold, Jelena S, Morrow, Bernice E
منشور في 2009

Mesodermal Tbx1 is required for patterning the proximal mandible in mice

بواسطة Aggarwal, Vimla S., Carpenter, Courtney, Freyer, Laina, Liao, Jun, Petti, Marilena, Morrow, Bernice E.
منشور في 2010

A Pedigree-Based Map of Recombination in the Domestic Dog Genome

بواسطة Campbell, Christopher L., Bhérer, Claude, Morrow, Bernice E., Boyko, Adam R., Auton, Adam
الحاوية / القاعدة G3 (Bethesda) (2016)

Integrated rare variant-based risk gene prioritization in disease case-control sequencing studies

بواسطة Lin, Jhih-Rong, Zhang, Quanwei, Cai, Ying, Morrow, Bernice E., Zhang, Zhengdong D.
الحاوية / القاعدة PLoS Genet (2017)

Spatiotemporal Gene Coexpression and Regulation in Mouse Cardiomyocytes of Early Cardiac Morphogenesis

بواسطة Liu, Yang, Lu, Pengfei, Wang, Yidong, Morrow, Bernice E., Zhou, Bin, Zheng, Deyou
الحاوية / القاعدة J Am Heart Assoc (2019)

Whole genome sequencing and integrative genomic analysis approach on two 22q11.2 deletion syndrome family trios for genotype to phenotype correlations

بواسطة Chung, Jonathan H., Cai, Jinlu, Suskin, Barrie G., Zhang, Zhengdong, Coleman, Karlene, Morrow, Bernice E.
الحاوية / القاعدة Hum Mutat (2015)