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Patrick G Buckley

Showing results (41-50 of 49) with videos related to

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Human Mutation|November 16, 2005
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2Patrick G Buckley, Kiran K Mantripragada, Teresita Díaz de Ståhl, et al.
NPJ Breast Cancer|June 29, 2022
High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencingAnna Kostecka, Tomasz Nowikiewicz, Paweł Olszewski, et al.
Scientific Reports|December 2, 2022
Personalized health risk assessment based on single-cell RNA sequencing analysis of a male with 45, X/48, XYYY karyotypeMagdalena Koczkowska, Marcin Jąkalski, Dorota Birkholz-Walerzak, et al.
Scientific Reports|July 29, 2018
Immunophenotyping and transcriptional profiling of in vitro cultured human adipose tissue derived stem cellsAlina Mieczkowska, Adriana Schumacher, Natalia Filipowicz, et al.
Human Mutation|July 30, 2015
Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer PatientsAnna Ronowicz, Anna Janaszak-Jasiecka, Jarosław Skokowski, et al.
Journal of the National Cancer Institute|July 3, 2018
Transcriptome Characterization of Matched Primary Breast and Brain Metastatic Tumors to Detect Novel Actionable TargetsDamir Varešlija, Nolan Priedigkeit, Ailís Fagan, et al.
BMC Cancer|May 1, 2026
Beyond tumors: uninvolved breast tissue of breast cancer patients with adverse prognoses is enriched for pathogenic PIK3CA and TP53 post-zygotic variantsMaria Andreou, Katarzyna Chojnowska, Natalia Filipowicz, et al.
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Human Mutation|November 16, 2005
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2Patrick G Buckley, Kiran K Mantripragada, Teresita Díaz de Ståhl, et al.
NPJ Breast Cancer|June 29, 2022
High prevalence of somatic PIK3CA and TP53 pathogenic variants in the normal mammary gland tissue of sporadic breast cancer patients revealed by duplex sequencingAnna Kostecka, Tomasz Nowikiewicz, Paweł Olszewski, et al.
Scientific Reports|December 2, 2022
Personalized health risk assessment based on single-cell RNA sequencing analysis of a male with 45, X/48, XYYY karyotypeMagdalena Koczkowska, Marcin Jąkalski, Dorota Birkholz-Walerzak, et al.
Scientific Reports|July 29, 2018
Immunophenotyping and transcriptional profiling of in vitro cultured human adipose tissue derived stem cellsAlina Mieczkowska, Adriana Schumacher, Natalia Filipowicz, et al.
Human Mutation|July 30, 2015
Concurrent DNA Copy-Number Alterations and Mutations in Genes Related to Maintenance of Genome Stability in Uninvolved Mammary Glandular Tissue from Breast Cancer PatientsAnna Ronowicz, Anna Janaszak-Jasiecka, Jarosław Skokowski, et al.
Journal of the National Cancer Institute|July 3, 2018
Transcriptome Characterization of Matched Primary Breast and Brain Metastatic Tumors to Detect Novel Actionable TargetsDamir Varešlija, Nolan Priedigkeit, Ailís Fagan, et al.
BMC Cancer|May 1, 2026
Beyond tumors: uninvolved breast tissue of breast cancer patients with adverse prognoses is enriched for pathogenic PIK3CA and TP53 post-zygotic variantsMaria Andreou, Katarzyna Chojnowska, Natalia Filipowicz, et al.
Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.
American Journal of Human Genetics|April 20, 2010
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromesErin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Pageof 5