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LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1: A promising adaptor of the CUL3 family (Review)

Cross-species analysis of LZTR1 loss-of-function mutants demonstrates  dependency to RIT1 orthologs | eLife
Cross-species analysis of LZTR1 loss-of-function mutants demonstrates dependency to RIT1 orthologs | eLife

Germline loss-of-function mutations in LZTR1 predispose to an inherited  disorder of multiple schwannomas | Nature Genetics
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
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
Frontiers | Generation of a Mouse Model to Study the Noonan Syndrome Gene Lztr1 in the Telencephalon

LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome  Features | Circulation: Genomic and Precision Medicine
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine

LZTR1 is a regulator of RAS ubiquitination and signaling | Science
LZTR1 is a regulator of RAS ubiquitination and signaling | Science

Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination  | Science
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science

LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody

Lztr1expression in the developing telencephalon. Lztr1 gene... | Download  Scientific Diagram
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram

LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody

LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody

LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by  stabilizing oncoprotein RIT1 | bioRxiv
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv

Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination  – Science Mission
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination – Science Mission

Typical 22q11.2 deletion syndrome appears to confer a reduced risk of  schwannoma | Genetics in Medicine
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine

Delineation of LZTR1 mutation-positive patients with Noonan syndrome and  identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink

The role of germline heterozygous LZTR1 variants in pediatric cancer  predisposition
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition

The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by  Regulating Vesicular Trafficking | Circulation Research
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research

Schematic structure of LZTR1 mutations or variants identified to date.... |  Download Scientific Diagram
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram

LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody

A Chinese family with Noonan syndrome caused by a heterozygous variant in  LZTR1: a case report and literature review | BMC Endocrine Disorders | Full  Text
A Chinese family with Noonan syndrome caused by a heterozygous variant in LZTR1: a case report and literature review | BMC Endocrine Disorders | Full Text

LZTR1 molecular genetic overlap with clinical implications for Noonan  syndrome and schwannomatosis | BMC Medical Genomics | Full Text
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text

The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by  Regulating Vesicular Trafficking | Circulation Research
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
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram

Germline loss-of-function mutations in LZTR1 predispose to an inherited  disorder of multiple schwannomas | Nature Genetics
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics