Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
To investigate the genetic basis in RASopathy patients | TACG
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
Further Evidence for the Implication of LZTR1, a Gene not Associated with the Ras-Mapk Pathway, in the Pathogenesis of Noonan Syndrome | Semantic Scholar
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs | eLife
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Mutation of the LZTR1 gene in sporadic schwannomatosis. a From top to... | Download Scientific Diagram
LZTR1: A promising adaptor of the CUL3 family (Review)
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
