Steps solidifying a role for SEPT9 in breast cancer suggest that greater strides are needed

Por Stanbery, Laura, Petty, Elizabeth M
Publicado em 2012

CHFR: A Novel Mitotic Checkpoint Protein and Regulator of Tumorigenesis

Por Privette, Lisa M, Petty, Elizabeth M
Publicado em 2008

CHFR binds to and regulates MAD2 in the spindle checkpoint through its cysteine-rich domain

Por Keller, Jennifer A., Petty, Elizabeth M.
Publicado em 2011

Conquering the complex world of human septins: Implications for health and disease

Por Peterson, Esther A., Petty, Elizabeth M.
Publicado no Clin Genet (2010)

Genetic Counseling Graduate Student Debt: Impact on Program, Career and Life Choices

Por Kuhl, Ashley, Reiser, Catherine, Eickhoff, Jens, Petty, Elizabeth M
Publicado no J Genet Couns (2014)

An AXIN2 Mutant Allele Associated With Predisposition to Colorectal Neoplasia Has Context-Dependent Effects on AXIN2 Protein Function()

Por Mazzoni, Serina M., Petty, Elizabeth M., Stoffel, Elena M., Fearon, Eric R.
Publicado no Neoplasia (2015)

The impact of insurance on equitable access to non-invasive prenatal screening (NIPT): private insurance may not pay

Por Benoy, Megan E., Iruretagoyena, J. Igor, Birkeland, Laura E., Petty, Elizabeth M.
Publicado no J Community Genet (2021)

Loss of CHFR in Human Mammary Epithelial Cells Causes Genomic Instability by Disrupting the Mitotic Spindle Assembly Checkpoint

Por Privette, Lisa M, Weier, Jingly Fung, Nguyen, Ha Nam, Yu, Xiaochun, Petty, Elizabeth M
Publicado em 2008

Up-regulation of SEPT9_v1 stabilizes c-Jun-N-Terminal Kinase and contributes to its pro-proliferative activity in mammary epithelial cells

Por Gonzalez, Maria E., Makarova, Olga, Peterson, Esther A., Privette, Lisa M., Petty, Elizabeth M.
Publicado em 2008

SEPT9_i1 and genomic instability: Mechanistic insights and relevance to tumorigenesis

Por Peterson, Esther A., Stanbery, Laura, Li, Christina, Kocak, Hande, Makarova, Olga, Petty, Elizabeth M.
Publicado em 2011

Beliefs about the Etiology of Homosexuality and about the Ramifications of Discovering Its Possible Genetic Origin

Por Sheldon, Jane P., Pfeffer, Carla A., Jayaratne, Toby Epstein, Feldbaum, Merle, Petty, Elizabeth M.
Publicado no J Homosex (2007)

AXIN2-Associated Autosomal Dominant Ectodermal Dysplasia and Neoplastic Syndrome

Por Marvin, Monica L., Mazzoni, Serina, Herron, Casey M., Edwards, Sean, Gruber, Stephen B., Petty, Elizabeth M.
Publicado em 2011

The Perennial Debate: Nature, Nurture, or Choice? Black and White Americans' Explanations for Individual Differences

Por Jayaratne, Toby Epstein, Gelman, Susan A., Feldbaum, Merle, Sheldon, Jane P., Petty, Elizabeth M., Kardia, Sharon L.R.
Publicado em 2009

White Americans’ Genetic Lay Theories of Race Differences and Sexual Orientation: Their Relationship with Prejudice toward Blacks, and Gay Men and Lesbians

Por Jayaratne, Toby Epstein, Ybarra, Oscar, Sheldon, Jane P., Brown, Tony N., Feldbaum, Merle, Pfeffer, Carla, Petty, Elizabeth M.
Publicado em 2006

Overexpressed Genes/ESTs and Characterization of Distinct Amplicons on 17q23 in Breast Cancer Cells

Por Erson, Ayse E, Niell, Bethany L, DeMers, Scott K, Rouillard, Jean-Marie, Hanash, Samir M, Petty, Elizabeth M
Publicado em 2001

Virtual Genome Scan: A Tool for Restriction Landmark-Based Scanning of the Human Genome

Por Rouillard, Jean-Marie, Erson, Ayse E., Kuick, Rork, Asakawa, Jun-ichi, Wimmer, Katharina, Muleris, Martine, Petty, Elizabeth M., Hanash, Samir
Publicado em 2001

Exploring the Public Understanding of Basic Genetic Concepts

Por Lanie, Angela D., Jayaratne, Toby Epstein, Sheldon, Jane P., Kardia, Sharon L. R., Anderson, Elizabeth S., Feldbaum, Merle, Petty, Elizabeth M.
Publicado em 2004

Autosomal Dominant Stapes Ankylosis with Broad Thumbs and Toes, Hyperopia, and Skeletal Anomalies Is Caused by Heterozygous Nonsense and Frameshift Mutations in NOG, the Gene Encod...

Por Brown, David J., Kim, Theresa B., Petty, Elizabeth M., Downs, Catherine A., Martin, Donna M., Strouse, Peter J., Moroi, Sayoko E., Milunsky, Jeff M., Lesperance, Marci M.
Publicado em 2002

High SEPT9_v1 Expression Is Associated with Poor Clinical Outcomes in Head and Neck Squamous Cell Carcinoma

Por Stanbery, Laura, D'Silva, Nisha J, Lee, Julia S, Bradford, Carol R, Carey, Thomas E, Prince, Mark E, Wolf, Gregory T, Worden, Francis P, Cordell, Kitrina G, Petty, Elizabeth M
Publicado em 2010

Mutations in the Slow Skeletal Muscle Fiber Myosin Heavy Chain Gene (MYH7) Cause Laing Early-Onset Distal Myopathy (MPD1)

Por Meredith, Christopher, Herrmann, Ralf, Parry, Cheryl, Liyanage, Khema, Dye, Danielle E., Durling, Hayley J., Duff, Rachael M., Beckman, Kaye, de Visser, Marianne, van der Graaff, Maaike M., Hedera, Peter, Fink, John K., Petty, Elizabeth M., Lamont, Phillipa, Fabian, Vicki, Bridges, Leslie, Voit, Thomas, Mastaglia, Frank L., Laing, Nigel G.
Publicado em 2004