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Birth Defects Research. Part A, Clinical and Molecular Teratology
|
April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region
Markus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Current Biology : CB
|
May 21, 2019
Mitigating Anticipated Effects of Systematic Errors Supports Sister-Group Relationship between Xenacoelomorpha and Ambulacraria
Hervé Philippe, Albert J Poustka, Marta Chiodin, et al.
Human Mutation
|
July 26, 2019
Iranome: A catalog of genomic variations in the Iranian population
Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, et al.
Science (New York, N.Y.)
|
October 9, 2020
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
Francisca M Real, Stefan A Haas, Paolo Franchini, et al.
Blood Cancer Discovery
|
February 19, 2021
Preneoplastic Alterations Define CLL DNA Methylome and Persist through Disease Progression and Therapy
Helene Kretzmer, Anat Biran, Noelia Purroy, et al.
The Journal of Pathology
|
July 21, 2017
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome
Hans Binder, Lydia Hopp, Michal R Schweiger, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
Nature Biotechnology
|
June 28, 2020
COVID-19 severity correlates with airway epithelium-immune cell interactions identified by single-cell analysis
Robert Lorenz Chua, Soeren Lukassen, Saskia Trump, et al.
Nature
|
February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
Lila Allou, Sara Balzano, Andreas Magg, et al.
Communications Biology
|
October 16, 2020
Network integration and modelling of dynamic drug responses at multi-omics levels
Nathalie Selevsek, Florian Caiment, Ramona Nudischer, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 122) with videos related to
Sort By:
Page
of 13
Birth Defects Research. Part A, Clinical and Molecular Teratology
|
April 26, 2014
Classic bladder exstrophy: Frequent 22q11.21 duplications and definition of a 414 kb phenocritical region
Markus Draaken, Friederike Baudisch, Bernd Timmermann, et al.
Current Biology : CB
|
May 21, 2019
Mitigating Anticipated Effects of Systematic Errors Supports Sister-Group Relationship between Xenacoelomorpha and Ambulacraria
Hervé Philippe, Albert J Poustka, Marta Chiodin, et al.
Human Mutation
|
July 26, 2019
Iranome: A catalog of genomic variations in the Iranian population
Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, et al.
Science (New York, N.Y.)
|
October 9, 2020
The mole genome reveals regulatory rearrangements associated with adaptive intersexuality
Francisca M Real, Stefan A Haas, Paolo Franchini, et al.
Blood Cancer Discovery
|
February 19, 2021
Preneoplastic Alterations Define CLL DNA Methylome and Persist through Disease Progression and Therapy
Helene Kretzmer, Anat Biran, Noelia Purroy, et al.
The Journal of Pathology
|
July 21, 2017
Genomic and transcriptomic heterogeneity of colorectal tumours arising in Lynch syndrome
Hans Binder, Lydia Hopp, Michal R Schweiger, et al.
Journal of Inherited Metabolic Disease
|
May 22, 2019
Low catalytic activity is insufficient to induce disease pathology in triosephosphate isomerase deficiency
Joanna Segal, Michael Mülleder, Antje Krüger, et al.
Nature Biotechnology
|
June 28, 2020
COVID-19 severity correlates with airway epithelium-immune cell interactions identified by single-cell analysis
Robert Lorenz Chua, Soeren Lukassen, Saskia Trump, et al.
Nature
|
February 11, 2021
Non-coding deletions identify Maenli lncRNA as a limb-specific En1 regulator
Lila Allou, Sara Balzano, Andreas Magg, et al.
Communications Biology
|
October 16, 2020
Network integration and modelling of dynamic drug responses at multi-omics levels
Nathalie Selevsek, Florian Caiment, Ramona Nudischer, et al.
Page
of 13