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Journal of the American Academy of Dermatology
|
July 24, 2023
EGFR expression is associated with relapse in a melanoma cohort receiving adjuvant PD-1-based immunotherapy
Teresa Amaral, Oltin Tiberiu Pop, Eftychia Chatziioannou, et al.
BMC Cancer
|
June 27, 2022
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers
Julika Borde, Yael Laitman, Britta Blümcke, et al.
Journal of Hepatology
|
December 3, 2014
Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias
Xiaoye Schneider-Yin, Anne-Moon van Tuyll van Serooskerken, Marko Siegesmund, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 10, 2022
Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approaches
Cristiana Roggia, Sorin Armeanu-Ebinger, Axel Gschwind, et al.
Breast Care (Basel, Switzerland)
|
June 15, 2022
Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian Cancer
Kerstin Rhiem, Bernd Auber, Susanne Briest, et al.
Frontiers in Immunology
|
December 6, 2019
A Non-interventional Clinical Trial Assessing Immune Responses After Radiofrequency Ablation of Liver Metastases From Colorectal Cancer
Markus W Löffler, Bianca Nussbaum, Günter Jäger, et al.
Journal of Medical Genetics
|
September 17, 2025
Heterozygous alterations of <i>GTF2I</i> at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder
Jeanne Jury, Thomas Besnard, Wallid Deb, et al.
Neuro-Oncology Advances
|
March 24, 2026
Clinical outcome of biomarker-guided therapies in adult neuro-oncology patients: An update from the Tübingen molecular tumor board cohort
David Rieger, Hannes Becker, Bianca Walter, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1
Lars R Jensen, Wei Chen, Bettina Moser, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2015
Next-generation sequencing in X-linked intellectual disability
Andreas Tzschach, Ute Grasshoff, Stefanie Beck-Woedl, et al.
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Search research articles
Search
Showing results (51-60 of 78) with videos related to
Sort By:
Page
of 8
Journal of the American Academy of Dermatology
|
July 24, 2023
EGFR expression is associated with relapse in a melanoma cohort receiving adjuvant PD-1-based immunotherapy
Teresa Amaral, Oltin Tiberiu Pop, Eftychia Chatziioannou, et al.
BMC Cancer
|
June 27, 2022
Polygenic risk scores indicate extreme ages at onset of breast cancer in female BRCA1/2 pathogenic variant carriers
Julika Borde, Yael Laitman, Britta Blümcke, et al.
Journal of Hepatology
|
December 3, 2014
Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias
Xiaoye Schneider-Yin, Anne-Moon van Tuyll van Serooskerken, Marko Siegesmund, et al.
European Journal of Cancer (Oxford, England : 1990)
|
December 10, 2022
Germline findings in patients with advanced malignancies screened with paired blood-tumour testing for personalised treatment approaches
Cristiana Roggia, Sorin Armeanu-Ebinger, Axel Gschwind, et al.
Breast Care (Basel, Switzerland)
|
June 15, 2022
Consensus Recommendations of the German Consortium for Hereditary Breast and Ovarian Cancer
Kerstin Rhiem, Bernd Auber, Susanne Briest, et al.
Frontiers in Immunology
|
December 6, 2019
A Non-interventional Clinical Trial Assessing Immune Responses After Radiofrequency Ablation of Liver Metastases From Colorectal Cancer
Markus W Löffler, Bianca Nussbaum, Günter Jäger, et al.
Journal of Medical Genetics
|
September 17, 2025
Heterozygous alterations of <i>GTF2I</i> at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder
Jeanne Jury, Thomas Besnard, Wallid Deb, et al.
Neuro-Oncology Advances
|
March 24, 2026
Clinical outcome of biomarker-guided therapies in adult neuro-oncology patients: An update from the Tübingen molecular tumor board cohort
David Rieger, Hannes Becker, Bianca Walter, et al.
European Journal of Human Genetics : EJHG
|
January 27, 2011
Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1
Lars R Jensen, Wei Chen, Bettina Moser, et al.
European Journal of Human Genetics : EJHG
|
February 5, 2015
Next-generation sequencing in X-linked intellectual disability
Andreas Tzschach, Ute Grasshoff, Stefanie Beck-Woedl, et al.
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of 8