Association of the Asn306Ser variant of the SP4 transcription factor and an intronic variant in the β-subunit of transducin with digenic disease

por Gao, Yong-Qing, Danciger, Michael, Özgül, Riza Köksal, Gribanova, Yekaterina E., Jacobson, Samuel G., Farber, Debora B.
Publicado 2007

A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration

por Ali, Manir, Ramprasad, Vedam Lakshmi, Soumittra, Nagasamy, Mohamed, Moin D., Jafri, Hussain, Rashid, Yasmin, Danciger, Michael, McKibbin, Martin, Kumaramanickavel, Govindasamy, Inglehearn, Chris F.
Publicado 2008

Candidate genes for chromosomes 6 and 10 quantitative trait loci for age-related retinal degeneration in mice

por Ogando, Diego G., Dahlquist, Kam D., Alizadeh, Mitra, Kunchithapautham, Kannan, Li, Jun, Yu, Nicole, LaVail, Matthew M., Rohrer, Bärbel, Vollrath, Douglas, Danciger, Michael
Publicado 2010

Loss of the Metalloprotease ADAM9 Leads to Cone-Rod Dystrophy in Humans and Retinal Degeneration in Mice

por Parry, David A., Toomes, Carmel, Bida, Lina, Danciger, Michael, Towns, Katherine V., McKibbin, Martin, Jacobson, Samuel G., Logan, Clare V., Ali, Manir, Bond, Jacquelyn, Chance, Rebecca, Swendeman, Steven, Daniele, Lauren L., Springell, Kelly, Adams, Matthew, Johnson, Colin A., Booth, Adam P., Jafri, Hussain, Rashid, Yasmin, Banin, Eyal, Strom, Tim M., Farber, Debora B., Sharon, Dror, Blobel, Carl P., Pugh, Edward N., Pierce, Eric A., Inglehearn, Chris F.
Publicado 2009