Genomic and Functional Variation of Human Centromeres

di Sullivan, Lori L., Sullivan, Beth A.
Pubblicato in Exp Cell Res (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

di Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Pubblicazione 2007

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

di Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Pubblicato in Cold Spring Harb Perspect Med (2015)

α satellite DNA variation and function of the human centromere

di Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Pubblicato in Nucleus (2017)

Identifying and mapping novel retinal-expressed ESTs from humans

di Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
Pubblicazione 1999

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

di McNulty, Shannon M., Sullivan, Lori L., Sullivan, Beth A.
Pubblicato in Dev Cell (2017)

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

di Sohocki, Melanie M., Sullivan, Lori S., Tirpak, Dayna L., Daiger, Stephen P.
Pubblicazione 2001

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

di Stimpson, Kaitlin M., Sullivan, Lori L., Kuo, Molly E., Sullivan, Beth A.
Pubblicazione 2014

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

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

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

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

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

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

Human centromere repositioning within euchromatin after partial chromosome deletion

di Sullivan, Lori L., Maloney, Kristin A., Towers, Aaron J., Gregory, Simon G., Sullivan, Beth A.
Pubblicato in Chromosome Res (2016)

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

di Aldrup-MacDonald, Megan E., Kuo, Molly E., Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Pubblicato in Genome Res (2016)

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

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

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

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

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

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

Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa

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

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

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

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

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

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

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