Rare mutations inapoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-4889
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Rare mutations inapoptosis related genes APAF1, CASP9, and CASP3 contribute to human neural tube defects ; volume:9 ; number:2 ; day:19 ; month:1 ; year:2018 ; pages:1-3 ; date:2.2018
Cell death & disease ; 9, Heft 2 (19.1.2018), 1-3, 2.2018
- Creator
-
Zhou, Xiangyu
- Contributor
-
Zeng, Weijia
Li, Huili
Chen, Haitao
Wei, Gang
Yang, Xueyan
Zhang, Ting
Wang, Hongyan
SpringerLink (Online service)
- DOI
-
10.1038/s41419-017-0096-2
- URN
-
urn:nbn:de:1111-201804119304
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:00 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Zhou, Xiangyu
- Zeng, Weijia
- Li, Huili
- Chen, Haitao
- Wei, Gang
- Yang, Xueyan
- Zhang, Ting
- Wang, Hongyan
- SpringerLink (Online service)
Other Objects (12)
Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes
Genetic analysis of Wnt/PCP genes in neural tube defects
Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects
A Cognitive Method for Musicology Based Melody Transcription
A New Pathology in the Simulation of Chaotic Dynamical Systems on Digital Computers
How cybercrime challenges the theory of joint commission : in German and Chinese perspectives
Recombinant DENV 2 NS5: An Effective Antigen for Diagnosis of Dengue Infection
Epigenetic regulation of muscle stem cell expansion
Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects
Characterization of NiCas12b for In Vivo Genome Editing
Msps governs acentrosomal microtubule assembly and reactivation of quiescent neural stem cells
Elevated H3K79 homocysteinylation causes abnormal gene expression during neural development and subsequent neural tube defects
Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes
Genetic analysis of Wnt/PCP genes in neural tube defects
Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects
A Cognitive Method for Musicology Based Melody Transcription
A New Pathology in the Simulation of Chaotic Dynamical Systems on Digital Computers
How cybercrime challenges the theory of joint commission : in German and Chinese perspectives
Recombinant DENV 2 NS5: An Effective Antigen for Diagnosis of Dengue Infection
Epigenetic regulation of muscle stem cell expansion
Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects
Characterization of NiCas12b for In Vivo Genome Editing
Msps governs acentrosomal microtubule assembly and reactivation of quiescent neural stem cells
Elevated H3K79 homocysteinylation causes abnormal gene expression during neural development and subsequent neural tube defects
Association between rare variants in specific functional pathways and human neural tube defects multiple subphenotypes
Genetic analysis of Wnt/PCP genes in neural tube defects
Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects
A Cognitive Method for Musicology Based Melody Transcription
A New Pathology in the Simulation of Chaotic Dynamical Systems on Digital Computers
How cybercrime challenges the theory of joint commission : in German and Chinese perspectives
Recombinant DENV 2 NS5: An Effective Antigen for Diagnosis of Dengue Infection
Epigenetic regulation of muscle stem cell expansion
Inhibiting MARSs reduces hyperhomocysteinemia‐associated neural tube and congenital heart defects
Characterization of NiCas12b for In Vivo Genome Editing
Msps governs acentrosomal microtubule assembly and reactivation of quiescent neural stem cells