13
results
for author:"Quade B.J."
in Literature Citations
| Disruption of chromodomain helicase DNA binding protein 2 (CHD2) causes scoliosis. Kulkarni S., Nagarajan P., Wall J., Donovan D.J., Donell R.L., Ligon A.H., Venkatachalam S., Quade B.J. Am. J. Med. Genet. A 146A:1117-1127(2008) · Mapped (3) |
| Disruption of neurexin 1 associated with autism spectrum disorder. Kim H.G., Kishikawa S., Higgins A.W., Seong I.S., Donovan D.J., Shen Y., Lally E., Weiss L.A., Najm J., Kutsche K. et al. Am. J. Hum. Genet. 82:199-207(2008) · UniProtKB (1) · Mapped (8) |
| Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann-Laband syndrome. Abo-Dalo B., Kim H.G., Roes M., Stefanova M., Higgins A., Shen Y., Mundlos S., Quade B.J., Gusella J.F., Kutsche K. Am. J. Med. Genet. A 143A:2668-2674(2007) · Mapped (6) |
| A spatially and temporally restricted mouse model of soft tissue sarcoma. Kirsch D.G., Dinulescu D.M., Miller J.B., Grimm J., Santiago P.M., Young N.P., Nielsen G.P., Quade B.J., Chaber C.J., Schultz C.P. et al. Nat. Med. 13:992-997(2007) · Mapped (15) |
| NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. Lu W., Quintero-Rivera F., Fan Y., Alkuraya F.S., Donovan D.J., Xi Q., Turbe-Doan A., Li Q.G., Campbell C.G., Shanske A.L. et al. PLoS Genet. 3:e80-e80(2007) · Mapped (22) |
| Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice. Leach N.T., Sun Y., Michaud S., Zheng Y., Ligon K.L., Ligon A.H., Sander T., Korf B.R., Lu W., Harris D.J. et al. Am. J. Hum. Genet. 80:792-799(2007) · Mapped (4) |
| Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux. Lu W., van Eerde A.M., Fan X., Quintero-Rivera F., Kulkarni S., Ferguson H., Kim H.-G., Fan Y., Xi Q., Li Q.-G. et al. Am. J. Hum. Genet. 80:616-632(2007) · UniProtKB (2) · Mapped (9) |
| Role of K-ras and Pten in the development of mouse models of endometriosis and endometrioid ovarian cancer. Dinulescu D.M., Ince T.A., Quade B.J., Shafer S.A., Crowley D., Jacks T. Nat. Med. 11:63-70(2005) · Mapped (8) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
| Fusion transcripts involving HMGA2 are not a common molecular mechanism in uterine leiomyomata with rearrangements in 12q15. Quade B.J., Weremowicz S., Neskey D.M., Vanni R., Ladd C., Dal Cin P., Morton C.C. |
| p63 Coordinates anogenital modeling and epithelial cell differentiation in the developing female urogenital tract. Ince T.A., Cviko A.P., Quade B.J., Yang A., McKeon F.D., Mutter G.L., Crum C.P. Am. J. Pathol. 161:1111-1117(2002) · Mapped (4) |
| Granulocyte macrophage colony-stimulating factor in adenomyosis and autologous endometrium. Propst A.M., Quade B.J., Nowak R.A., Stewart E.A. J. Soc. Gynecol. Investig. 9:93-97(2002) · Mapped (2) |
| The human VASA gene is specifically expressed in the germ cell lineage. Castrillon D.H., Quade B.J., Wang T.Y., Quigley C., Crum C.P. Proc. Natl. Acad. Sci. U.S.A. 97:9585-9590(2000) · UniProtKB (1) · Mapped (2) |
