Genomic and Functional Variation of Human Centromeres

द्वारा Sullivan, Lori L., Sullivan, Beth A.
में प्रकाशित Exp Cell Res (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

द्वारा Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
प्रकाशित 2007

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

द्वारा Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
में प्रकाशित Cold Spring Harb Perspect Med (2015)

α satellite DNA variation and function of the human centromere

द्वारा Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
में प्रकाशित Nucleus (2017)

Identifying and mapping novel retinal-expressed ESTs from humans

द्वारा Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
प्रकाशित 1999

Human centromeres produce chromosome-specific and array-specific alpha satellite transcripts that are complexed with CENP-A and CENP-C

द्वारा McNulty, Shannon M., Sullivan, Lori L., Sullivan, Beth A.
में प्रकाशित Dev Cell (2017)

Comparative analysis of aryl-hydrocarbon receptor interacting protein-like 1 (Aipl1), a gene associated with inherited retinal disease in humans

द्वारा Sohocki, Melanie M., Sullivan, Lori S., Tirpak, Dayna L., Daiger, Stephen P.
प्रकाशित 2001

Nucleolar Organization, Ribosomal DNA Array Stability, and Acrocentric Chromosome Integrity Are Linked to Telomere Function

द्वारा Stimpson, Kaitlin M., Sullivan, Lori L., Kuo, Molly E., Sullivan, Beth A.
प्रकाशित 2014

Genomic size of CENP-A domain is proportional to total alpha satellite array size at human centromeres and expands in cancer cells

द्वारा Sullivan, Lori L., Boivin, Christopher D., Mravinac, Brankica, Song, Ihn Young, Sullivan, Beth A.
प्रकाशित 2011

Characterization of Zinc Uptake, Binding, and Translocation in Intact Seedlings of Bread and Durum Wheat Cultivars

द्वारा Hart, Jonathan J., Norvell, Wendell A., Welch, Ross M., Sullivan, Lori A., Kochian, Leon V.
प्रकाशित 1998

Characterization of Cadmium Binding, Uptake, and Translocation in Intact Seedlings of Bread and Durum Wheat Cultivars

द्वारा Hart, Jonathan J., Welch, Ross M., Norvell, Wendell A., Sullivan, Lori A., Kochian, Leon V.
प्रकाशित 1998

Human centromere repositioning within euchromatin after partial chromosome deletion

द्वारा Sullivan, Lori L., Maloney, Kristin A., Towers, Aaron J., Gregory, Simon G., Sullivan, Beth A.
में प्रकाशित Chromosome Res (2016)

Genomic variation within alpha satellite DNA influences centromere location on human chromosomes with metastable epialleles

द्वारा Aldrup-MacDonald, Megan E., Kuo, Molly E., Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
में प्रकाशित Genome Res (2016)

MUTATIONS IN KNOWN GENES ACCOUNT FOR 58% OF AUTOSOMAL DOMINANT RETINITIS PIGMENTOSA (adRP)

द्वारा Daiger, Stephen P., Sullivan, Lori S., Gire, Anisa I., Birch, David G., Heckenlively, John R., Bowne, Sara J.
प्रकाशित 2008

Investigating the Mechanism of Disease in the RP10 Form of Retinitis Pigmentosa

द्वारा Spellicy, Catherine J., Xu, Dong, Cobb, Garrett, Hedstrom, Lizbeth, Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P.
प्रकाशित 2010

Molecular Defects of the Disease-Causing Human Arrestin-1 C147F Mutant

द्वारा Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.
में प्रकाशित Invest Ophthalmol Vis Sci (2018)

Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa

द्वारा Kiser, Kelly, Webb-Jones, Kaylie D., Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Birch, David G.
में प्रकाशित Am J Ophthalmol (2018)

IDENTIFICATION OF THE RP1 AND RP10 (IMPDH1) GENES CAUSING AUTOSOMAL DOMINANT RP

द्वारा Daiger, Stephen P., Sullivan, Lori S., Bowne, Sara J., Kennan, Avril, Humphries, Peter, Birch, David G., Heckenlively, John R.
प्रकाशित 2003

PITPNM3 is an uncommon cause of cone and cone-rod dystrophies

द्वारा Köhn, Linda, Kohl, Susanne, Bowne, Sara J, Sullivan, Lori S, Kellner, Ulrich, Daiger, Stephen P, Sandgren, Ola, Golovleva, Irina
प्रकाशित 2010

Breakpoint characterization of a novel ∼59 kb genomic deletion on 19q13.42 in autosomal-dominant retinitis pigmentosa with incomplete penetrance

द्वारा Köhn, Linda, Bowne, Sara J, S Sullivan, Lori, Daiger, Stephen P, Burstedt, Marie SI, Kadzhaev, Konstantin, Sandgren, Ola, Golovleva, Irina
प्रकाशित 2009