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	1.	A mutation in the mouse ttc26 gene leads to impaired hedgehog signaling. [electronic resource] by Swiderski, Ruth E Nakano, Yoko Mullins, Robert F Seo, Seongjin Bánfi, Botond Producer: 20150702 In: PLoS genetics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Structural defects in cilia of the choroid plexus, subfornical organ and ventricular ependyma are associated with ventriculomegaly. [electronic resource] by Swiderski, Ruth E Agassandian, Khristofor Ross, Jean L Bugge, Kevin Cassell, Martin D Yeaman, Charles Producer: 20121224 In: Fluids and barriers of the CNS vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Gene expression analysis of photoreceptor cell loss in bbs4-knockout mice reveals an early stress gene response and photoreceptor cell damage. [electronic resource] by Swiderski, Ruth E Nishimura, Darryl Y Mullins, Robert F Olvera, Marissa A Ross, Jean L Huang, Jian Stone, Edwin M Sheffield, Val C Producer: 20070823 In: Investigative ophthalmology & visual science vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Bardet-Biedl syndrome type 4 (BBS4)-null mice implicate Bbs4 in flagella formation but not global cilia assembly. [electronic resource] by Mykytyn, Kirk Mullins, Robert F Andrews, Michael Chiang, Annie P Swiderski, Ruth E Yang, Baoli Braun, Terry Casavant, Thomas Stone, Edwin M Sheffield, Val C Producer: 20040817 In: Proceedings of the National Academy of Sciences of the United States of America vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene. [electronic resource] by Honkanen, Robert A Nishimura, Darryl Y Swiderski, Ruth E Bennett, Steven R Hong, Sungpyo Kwon, Young H Stone, Edwin M Sheffield, Val C Alward, Wallace L M Producer: 20030317 In: American journal of ophthalmology vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene. [electronic resource] by Nishimura, Darryl Y Swiderski, Ruth E Searby, Charles C Berg, Erik M Ferguson, Amanda L Hennekam, Raoul Merin, Saul Weleber, Richard G Biesecker, Leslie G Stone, Edwin M Sheffield, Val C Producer: 20060130 In: American journal of human genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin. [electronic resource] by Nishimura, Darryl Y Fath, Melissa Mullins, Robert F Searby, Charles Andrews, Michael Davis, Roger Andorf, Jeaneen L Mykytyn, Kirk Swiderski, Ruth E Yang, Baoli Carmi, Rivka Stone, Edwin M Sheffield, Val C Producer: 20041227 In: Proceedings of the National Academy of Sciences of the United States of America vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Regulation of gene expression in the mammalian eye and its relevance to eye disease. [electronic resource] by Scheetz, Todd E Kim, Kwang-Youn A Swiderski, Ruth E Philp, Alisdair R Braun, Terry A Knudtson, Kevin L Dorrance, Anne M DiBona, Gerald F Huang, Jian Casavant, Thomas L Sheffield, Val C Stone, Edwin M Producer: 20061030 In: Proceedings of the National Academy of Sciences of the United States of America vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Abnormal development of NG2+PDGFR-α+ neural progenitor cells leads to neonatal hydrocephalus in a ciliopathy mouse model. [electronic resource] by Carter, Calvin S Vogel, Timothy W Zhang, Qihong Seo, Seongjin Swiderski, Ruth E Moninger, Thomas O Cassell, Martin D Thedens, Daniel R Keppler-Noreuil, Kim M Nopoulos, Peggy Nishimura, Darryl Y Searby, Charles C Bugge, Kevin Sheffield, Val C Producer: 20130211 In: Nature medicine vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11). [electronic resource] by Chiang, Annie P Beck, John S Yen, Hsan-Jan Tayeh, Marwan K Scheetz, Todd E Swiderski, Ruth E Nishimura, Darryl Y Braun, Terry A Kim, Kwang-Youn A Huang, Jian Elbedour, Khalil Carmi, Rivka Slusarski, Diane C Casavant, Thomas L Stone, Edwin M Sheffield, Val C Producer: 20060623 In: Proceedings of the National Academy of Sciences of the United States of America vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesity. [electronic resource] by Davis, Roger E Swiderski, Ruth E Rahmouni, Kamal Nishimura, Darryl Y Mullins, Robert F Agassandian, Khristofor Philp, Alisdair R Searby, Charles C Andrews, Michael P Thompson, Stewart Berry, Christopher J Thedens, Daniel R Yang, Baoli Weiss, Robert M Cassell, Martin D Stone, Edwin M Sheffield, Val C Producer: 20080118 In: Proceedings of the National Academy of Sciences of the United States of America vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)