LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
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
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
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 | bioRxiv
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
Rare variants in SOS2 and LZTR1 are associated with Noonan syndrome | Journal of Medical Genetics
LZTR1 is a regulator of RAS ubiquitination and signaling | Science
LZTR1: A promising adaptor of the CUL3 family (Review)
To investigate the genetic basis in RASopathy patients | TACG
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
LZTR1: A promising adaptor of the CUL3 family (Review)
Noonan Syndrome spectrum panels should include mutations in LZTR1 gene
