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Journal of the American Society of Nephrology : JASN
|
October 30, 2021
Impaired Humoral but Substantial Cellular Immune Response to Variants of Concern B1.1.7 and B.1.351 in Hemodialysis Patients after Vaccination with BNT162b2
Constantin J Thieme, Arturo Blazquez-Navarro, Lema Safi, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2008
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome
Thomas E Neumann, Judith Allanson, Ines Kavamura, et al.
Acta Neuropathologica
|
January 20, 2024
Temporal change of DNA methylation subclasses between matched newly diagnosed and recurrent glioblastoma
Richard Drexler, Robin Khatri, Ulrich Schüller, et al.
Neuropathology and Applied Neurobiology
|
February 13, 2022
Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC
Martin Hasselblatt, Christian Thomas, Aniello Federico, et al.
Nature Medicine
|
September 12, 2017
A mouse model for embryonal tumors with multilayered rosettes uncovers the therapeutic potential of Sonic-hedgehog inhibitors
Julia E Neumann, Annika K Wefers, Sander Lambo, et al.
Nature Communications
|
July 23, 2024
Multiomic profiling of medulloblastoma reveals subtype-specific targetable alterations at the proteome and N-glycan level
Shweta Godbole, Hannah Voß, Antonia Gocke, et al.
Nature Communications
|
July 29, 2022
Mouse fetal growth restriction through parental and fetal immune gene variation and intercellular communications cascade
Gurman Kaur, Caroline B M Porter, Orr Ashenberg, et al.
Neuro-Oncology
|
April 5, 2022
Comprehensive profiling of myxopapillary ependymomas identifies a distinct molecular subtype with relapsing disease
Michael Bockmayr, Kim Harnisch, Lara C Pohl, et al.
Nature Communications
|
November 24, 2023
Mouse models of pediatric high-grade gliomas with MYCN amplification reveal intratumoral heterogeneity and lineage signatures
Melanie Schoof, Shweta Godbole, Thomas K Albert, et al.
Neurology
|
August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
G Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
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of 77
Search research articles
Search
Showing results (751-760 of 769) with videos related to
Sort By:
Page
of 77
Journal of the American Society of Nephrology : JASN
|
October 30, 2021
Impaired Humoral but Substantial Cellular Immune Response to Variants of Concern B1.1.7 and B.1.351 in Hemodialysis Patients after Vaccination with BNT162b2
Constantin J Thieme, Arturo Blazquez-Navarro, Lema Safi, et al.
European Journal of Human Genetics : EJHG
|
October 16, 2008
Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome
Thomas E Neumann, Judith Allanson, Ines Kavamura, et al.
Acta Neuropathologica
|
January 20, 2024
Temporal change of DNA methylation subclasses between matched newly diagnosed and recurrent glioblastoma
Richard Drexler, Robin Khatri, Ulrich Schüller, et al.
Neuropathology and Applied Neurobiology
|
February 13, 2022
Low-grade diffusely infiltrative tumour (LGDIT), SMARCB1-mutant: A clinical and histopathological distinct entity showing epigenetic similarity with ATRT-MYC
Martin Hasselblatt, Christian Thomas, Aniello Federico, et al.
Nature Medicine
|
September 12, 2017
A mouse model for embryonal tumors with multilayered rosettes uncovers the therapeutic potential of Sonic-hedgehog inhibitors
Julia E Neumann, Annika K Wefers, Sander Lambo, et al.
Nature Communications
|
July 23, 2024
Multiomic profiling of medulloblastoma reveals subtype-specific targetable alterations at the proteome and N-glycan level
Shweta Godbole, Hannah Voß, Antonia Gocke, et al.
Nature Communications
|
July 29, 2022
Mouse fetal growth restriction through parental and fetal immune gene variation and intercellular communications cascade
Gurman Kaur, Caroline B M Porter, Orr Ashenberg, et al.
Neuro-Oncology
|
April 5, 2022
Comprehensive profiling of myxopapillary ependymomas identifies a distinct molecular subtype with relapsing disease
Michael Bockmayr, Kim Harnisch, Lara C Pohl, et al.
Nature Communications
|
November 24, 2023
Mouse models of pediatric high-grade gliomas with MYCN amplification reveal intratumoral heterogeneity and lineage signatures
Melanie Schoof, Shweta Godbole, Thomas K Albert, et al.
Neurology
|
August 1, 2007
Location and type of mutation in the LIS1 gene do not predict phenotypic severity
G Uyanik, D J Morris-Rosendahl, J Stiegler, et al.
Page
of 77