Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs | eLife
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination – Science Mission
LZTR1: A promising adaptor of the CUL3 family (Review)
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
To investigate the genetic basis in RASopathy patients | TACG
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
