Genomic and Functional Variation of Human Centromeres

по Sullivan, Lori L., Sullivan, Beth A.
Опубликовано в: Exp Cell Res (2020)

Perspective on Genes and Mutations Causing Retinitis Pigmentosa

по Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Опубликовано 2007

Genes and Mutations Causing Autosomal Dominant Retinitis Pigmentosa

по Daiger, Stephen P., Bowne, Sara J., Sullivan, Lori S.
Опубликовано в: Cold Spring Harb Perspect Med (2015)

α satellite DNA variation and function of the human centromere

по Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Опубликовано в: Nucleus (2017)

Identifying and mapping novel retinal-expressed ESTs from humans

по Malone, Kimberly, Sohocki, Melanie M., Sullivan, Lori S., Daiger, Stephen P.
Опубликовано 1999

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

по McNulty, Shannon M., Sullivan, Lori L., Sullivan, Beth A.
Опубликовано в: Dev Cell (2017)

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

по Sohocki, Melanie M., Sullivan, Lori S., Tirpak, Dayna L., Daiger, Stephen P.
Опубликовано 2001

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

по Stimpson, Kaitlin M., Sullivan, Lori L., Kuo, Molly E., Sullivan, Beth A.
Опубликовано 2014

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

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

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

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

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

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

Human centromere repositioning within euchromatin after partial chromosome deletion

по Sullivan, Lori L., Maloney, Kristin A., Towers, Aaron J., Gregory, Simon G., Sullivan, Beth A.
Опубликовано в: Chromosome Res (2016)

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

по Aldrup-MacDonald, Megan E., Kuo, Molly E., Sullivan, Lori L., Chew, Kimberline, Sullivan, Beth A.
Опубликовано в: Genome Res (2016)

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

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

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

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

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

по Vishnivetskiy, Sergey A., Sullivan, Lori S., Bowne, Sara J., Daiger, Stephen P., Gurevich, Eugenia V., Gurevich, Vsevolod V.
Опубликовано в: Invest Ophthalmol Vis Sci (2018)

Time Course of Disease Progression of PRPF31-mediated Retinitis Pigmentosa

по Kiser, Kelly, Webb-Jones, Kaylie D., Bowne, Sara J., Sullivan, Lori S., Daiger, Stephen P., Birch, David G.
Опубликовано в: Am J Ophthalmol (2018)

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

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

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

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

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

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