Genomic and Functional Variation of Human Centromeres

por Sullivan, Lori L., Sullivan, Beth A.
Publicado en Exp Cell Res (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

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

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

por Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Publicado en 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 en Nucleus (2017)

Identifying and mapping novel retinal-expressed ESTs from humans

por Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
Publicado 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 en 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 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 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 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 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 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 en 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 en 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 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 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 en 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 en 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 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 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 2009