Search Results - Streb, Luan M

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  1. 1
    Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa

    Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa by Tucker, Budd A, Mullins, Robert F, Streb, Luan M, Anfinson, Kristin, Eyestone, Mari E, Kaalberg, Emily, Riker, Megan J, Drack, Arlene V, Braun, Terry A, Stone, Edwin M

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  2. 2
    Elevated membrane attack complex in human choroid with high risk complement factor H genotypes

    Elevated membrane attack complex in human choroid with high risk complement factor H genotypes by Mullins, Robert F., Dewald, Aaron D., Streb, Luan M., Wang, Kai, Kuehn, Markus H., Stone, Edwin M.

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  3. 3
    Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confirm eligibility for enrollment into a clinical gene augmentation trial

    Using patient-specific induced pluripotent stem cells to interrogate the pathogenicity of a novel retinal pigment epithelium-specific 65 kDa cryptic splice site mutation and confir... by Tucker, Budd A, Cranston, Cathryn M, Anfinson, Kristin A, Shrestha, Suruchi, Streb, Luan M, Leon, Alejandro, Mullins, Robert F, Stone, Edwin M

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  4. 4
    LOXL1 Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States

    LOXL1 Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States by Fingert, John H, Alward, Wallace L.M, Kwon, Young H, Wang, Kai, Streb, Luan M, Sheffield, Val C, Stone, Edwin M

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  5. 5
    Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)

    Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25) by Héon, Elise, Sheth, Bhavna P., Kalenak, Jeffrey W., Sunden, Sara L.F., Streb, Luan M., Taylor, Chris M., Alward, Wallace L.M., C.Sheffield, Val, Stone, Edwin M.

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  6. 6
    LOXL1Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States

    LOXL1Mutations Are Associated with Exfoliation Syndrome in Patients from the Midwestern United States by Fingert, John H, Alward, Wallace LM, Kwon, Young H, Wang, Kai, Streb, Luan M, Sheffield, Val C, Stone, Edwin M

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  7. 7
    Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13

    Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13 by Stone, Edwin M., Kimura, Alan E., Folk, James C., Bennett, Steven R., Nichols, Brian E., Streb, Luan M., Sheffield, Val C.

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