Genomic and Functional Variation of Human Centromeres

Por Sullivan, Lori L., Sullivan, Beth A.
Publicado no Exp Cell Res (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

Por Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Publicado em 2007

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

Por Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Publicado no Cold Spring Harb Perspect Med (2015)

α satellite DNA variation and function of the human centromere

Por Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Publicado no Nucleus (2017)

Identifying and mapping novel retinal-expressed ESTs from humans

Por Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
Publicado em 1999

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

Por McNulty, Shannon M., Sullivan, Lori L., Sullivan, Beth A.
Publicado no Dev Cell (2017)

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

Por Sohocki, Melanie M., Sullivan, Lori S., Tirpak, Dayna L., Daiger, Stephen P.
Publicado em 2001

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

Por Stimpson, Kaitlin M., Sullivan, Lori L., Kuo, Molly E., Sullivan, Beth A.
Publicado em 2014

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

Por Sullivan, Lori L., Boivin, Christopher D., Mravinac, Brankica, Song, Ihn Young, Sullivan, Beth A.
Publicado em 2011

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

Por Hart, Jonathan J., Norvell, Wendell A., Welch, Ross M., Sullivan, Lori A., Kochian, Leon V.
Publicado em 1998

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

Por Hart, Jonathan J., Welch, Ross M., Norvell, Wendell A., Sullivan, Lori A., Kochian, Leon V.
Publicado em 1998

Human centromere repositioning within euchromatin after partial chromosome deletion

Por Sullivan, Lori L., Maloney, Kristin A., Towers, Aaron J., Gregory, Simon G., Sullivan, Beth A.
Publicado no Chromosome Res (2016)

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

Por Aldrup-MacDonald, Megan E., Kuo, Molly E., Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Publicado no Genome Res (2016)

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

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

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

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

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

Por Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.
Publicado no Invest Ophthalmol Vis Sci (2018)

Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa

Por Kiser, Kelly, Webb-Jones, Kaylie D., Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Birch, David G.
Publicado no Am J Ophthalmol (2018)

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

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

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

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

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

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