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LZTR1: A promising adaptor of the CUL3 family (Review)
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
Typical 22q11.2 deletion syndrome appears to confer a reduced risk of schwannoma | Genetics in Medicine
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis | BMC Medical Genomics | Full Text
IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1, 2, and Schwannomatosis
Schematic structure of LZTR1 mutations or variants identified to date.... | Download Scientific Diagram
LZTR1 inactivation promotes MAPK/ ERK pathway activation in glioblastoma by stabilizing oncoprotein RIT1 | bioRxiv
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination | Science
Delineation of dominant and recessive forms of LZTR1‐associated Noonan syndrome - Pagnamenta - 2019 - Clinical Genetics - Wiley Online Library
Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas | Nature Genetics
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 is a regulator of RAS ubiquitination and signaling | Science
The Noonan Syndrome Gene Lztr1 Controls Cardiovascular Function by Regulating Vesicular Trafficking | Circulation Research
LZTR1: A promising adaptor of the CUL3 family (Review)
Lztr1expression in the developing telencephalon. Lztr1 gene... | Download Scientific Diagram
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation
Comprehensive mutation analysis of all three genes, LZTR1, SMARCB1, and... | Download Scientific Diagram
Expanding the mutational spectrum of LZTR1 in schwannomatosis | European Journal of Human Genetics
Delineation of LZTR1 mutation-positive patients with Noonan syndrome and identification of LZTR1 binding to RAF1–PPP1CB complexes | SpringerLink
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
LZTR1-Related Hypertrophic Cardiomyopathy Without Typical Noonan Syndrome Features | Circulation: Genomic and Precision Medicine
LZTR1 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody
Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination – Science Mission