Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
To investigate the genetic basis in RASopathy patients | TACG
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
LZTR1 Antibodies & ELISA Kits, LZTR1 Proteins
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
