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Janatova

Showing results (71-80 of 101) with videos related to

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Clinical Genetics|January 30, 2016
Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patientsF Lhota, P Zemankova, P Kleiblova, et al.
Cellular Signalling|January 17, 2012
The BRCA1 alternative splicing variant Δ14-15 with an in-frame deletion of part of the regulatory serine-containing domain (SCD) impairs the DNA repair capacity in MCF-7 cellsJan Sevcik, Martin Falk, Petra Kleiblova, et al.
Clinical Immunology (Orlando, Fla.)|October 15, 2022
Metal hypersensitivity and pro-inflammatory cytokine production in patients with failed orthopedic implants: A case-control studyStepan Podzimek, Lucie Himmlova, Tatjana Janatova, et al.
Breast Cancer Research : BCR|September 20, 2005
High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague areaPetr Pohlreich, Michal Zikan, Jana Stribrna, et al.
Frontiers in Cellular and Infection Microbiology|March 29, 2021
R/G Value-A Numeric Index of Individual Periodontal Health and Oral Microbiome DynamicsLucie Najmanova, Lenka Sabova, Magdalena Lenartova, et al.
Gene|September 19, 2017
Multiplex PCR and NGS-based identification of mRNA splicing variants: Analysis of BRCA1 splicing pattern as a modelJan Hojny, Petra Zemankova, Filip Lhota, et al.
Cellular Signalling|February 19, 2013
Expression of human BRCA1Δ17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage responseJan Sevcik, Martin Falk, Libor Macurek, et al.
Plos One|April 13, 2018
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromesJana Soukupova, Petra Zemankova, Klara Lhotova, et al.
Biomedicines|October 14, 2020
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 GenesLenka Stolarova, Sandra Jelinkova, Radka Storchova, et al.
Cancer Management and Research|January 23, 2019
Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterationsMartin Lovecek, Marketa Janatova, Pavel Skalicky, et al.
Pageof 11

Showing results (71-80 of 101) with videos related to

Sort By:
Pageof 11
Clinical Genetics|January 30, 2016
Hereditary truncating mutations of DNA repair and other genes in BRCA1/BRCA2/PALB2-negatively tested breast cancer patientsF Lhota, P Zemankova, P Kleiblova, et al.
Cellular Signalling|January 17, 2012
The BRCA1 alternative splicing variant Δ14-15 with an in-frame deletion of part of the regulatory serine-containing domain (SCD) impairs the DNA repair capacity in MCF-7 cellsJan Sevcik, Martin Falk, Petra Kleiblova, et al.
Clinical Immunology (Orlando, Fla.)|October 15, 2022
Metal hypersensitivity and pro-inflammatory cytokine production in patients with failed orthopedic implants: A case-control studyStepan Podzimek, Lucie Himmlova, Tatjana Janatova, et al.
Breast Cancer Research : BCR|September 20, 2005
High proportion of recurrent germline mutations in the BRCA1 gene in breast and ovarian cancer patients from the Prague areaPetr Pohlreich, Michal Zikan, Jana Stribrna, et al.
Frontiers in Cellular and Infection Microbiology|March 29, 2021
R/G Value-A Numeric Index of Individual Periodontal Health and Oral Microbiome DynamicsLucie Najmanova, Lenka Sabova, Magdalena Lenartova, et al.
Gene|September 19, 2017
Multiplex PCR and NGS-based identification of mRNA splicing variants: Analysis of BRCA1 splicing pattern as a modelJan Hojny, Petra Zemankova, Filip Lhota, et al.
Cellular Signalling|February 19, 2013
Expression of human BRCA1Δ17-19 alternative splicing variant with a truncated BRCT domain in MCF-7 cells results in impaired assembly of DNA repair complexes and aberrant DNA damage responseJan Sevcik, Martin Falk, Libor Macurek, et al.
Plos One|April 13, 2018
Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromesJana Soukupova, Petra Zemankova, Klara Lhotova, et al.
Biomedicines|October 14, 2020
Identification of Germline Mutations in Melanoma Patients with Early Onset, Double Primary Tumors, or Family Cancer History by NGS Analysis of 217 GenesLenka Stolarova, Sandra Jelinkova, Radka Storchova, et al.
Cancer Management and Research|January 23, 2019
Genetic analysis of subsequent second primary malignant neoplasms in long-term pancreatic cancer survivors suggests new potential hereditary genetic alterationsMartin Lovecek, Marketa Janatova, Pavel Skalicky, et al.
Pageof 11