LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome | Semantic Scholar
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
22q11.2 duplication malformation of the bladder and urethra LZTR1 gene
LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
LZTR1: A promising adaptor of the CUL3 family (Review)
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
The four hits-three steps model of tumourigenesis in schwannomatosis... | Download Scientific Diagram
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
What is LZTR1 Gene Noonan syndrome type 10 NGS Genetic DNA Test ?
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
Partial ideogram of chromosome 22 indicating the location of the LZTR1,... | Download Scientific Diagram
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
