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The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1: A promising adaptor of the CUL3 family (Review)
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
LZTR1 Antibodies & ELISA Kits, LZTR1 Proteins
Providing more evidence on LZTR1 variants in Noonan syndrome patients - Chinton - 2020 - American Journal of Medical Genetics Part A - Wiley Online Library
Biomolecules | Free Full-Text | Exome Survey and Candidate Gene Re-Sequencing Identifies Novel Exstrophy Candidate Genes and Implicates LZTR1 in Disease Formation
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1 siRNA (m), shRNA and Lentiviral Particle Gene Silencers | SCBT - Santa Cruz Biotechnology
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
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 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
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-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination – Science Mission
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation