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Cancer Research|October 20, 2004
Combined total genome loss of heterozygosity scan of breast cancer stroma and epithelium reveals multiplicity of stromal targetsKoichi Fukino, Lei Shen, Satoshi Matsumoto, et al.
European Journal of Human Genetics : EJHG|February 12, 2015
KLLN epigenotype-phenotype associations in Cowden syndromeEmily A Nizialek, Jessica L Mester, Vineet K Dhiman, et al.
Protein Science : a Publication of the Protein Society|April 28, 2022
Shape shifting: The multiple conformational substates of the PTEN N-terminal PIP2 -binding domainJennifer E Dawson, Iris Nira Smith, William Martin, et al.
Plos Computational Biology|October 2, 2024
Quantitative evaluation of DNA damage repair dynamics to elucidate predictors of autism vs. cancer in individuals with germline PTEN variantsRuipeng Wei, Masahiro Hitomi, Tammy Sadler, et al.
European Journal of Human Genetics : EJHG|February 24, 2011
Analysis of prevalence and degree of macrocephaly in patients with germline PTEN mutations and of brain weight in Pten knock-in murine modelJessica L Mester, Amanda K Tilot, Lisa A Rybicki, et al.
Urology|March 13, 2016
The Urinary Microbiome Differs Significantly Between Patients With Chronic Prostatitis/Chronic Pelvic Pain Syndrome and Controls as Well as Between Patients With Different Clinical PhenotypesDaniel A Shoskes, Jessica Altemus, Alan S Polackwich, et al.
The Journal of Molecular Diagnostics : JMD|May 3, 2002
A 39-bp deletion polymorphism in PTEN in African American individuals: implications for molecular diagnostic testingXiao-Ping Zhou, Heather Hampel, Jennifer Roggenbuck, et al.
Nature Genetics|October 16, 2002
Frequent somatic mutations in PTEN and TP53 are mutually exclusive in the stroma of breast carcinomasKeisuke Kurose, Kristie Gilley, Satoshi Matsumoto, et al.
American Journal of Human Genetics|June 15, 2006
Distinct expression profiles for PTEN transcript and its splice variants in Cowden syndrome and Bannayan-Riley-Ruvalcaba syndromeMarta S Sarquis, Shipra Agrawal, Lei Shen, et al.
American Journal of Human Genetics|September 12, 2007
Cowden syndrome-affected patients with PTEN promoter mutations demonstrate abnormal protein translationRosemary E Teresi, Kevin M Zbuk, Marcus G Pezzolesi, et al.
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