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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 2
Patrick 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 sequencing
Anna 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 karyotype
Magdalena 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 cells
Alina 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 Patients
Anna 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 Targets
Damir 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 variants
Maria 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 applications
Patrick 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 syndromes
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
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of 5
Search research articles
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Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 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 2
Patrick 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 sequencing
Anna 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 karyotype
Magdalena 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 cells
Alina 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 Patients
Anna 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 Targets
Damir 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 variants
Maria 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 applications
Patrick 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 syndromes
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, et al.
Page
of 5