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

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

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

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

IJMS | Free Full-Text | Current Understanding of Neurofibromatosis Type 1,  2, and Schwannomatosis
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
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
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
The role of germline heterozygous LZTR1 variants in pediatric cancer predisposition

Mutations in LZTR1 drive human disease by dysregulating RAS ubiquitination  | Science
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
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
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
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
LZTR1 is a regulator of RAS ubiquitination and signaling | Science

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

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

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

LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell  Death & Differentiation
LZTR1 facilitates polyubiquitination and degradation of RAS-GTPases | Cell Death & Differentiation

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

Expanding the mutational spectrum of LZTR1 in schwannomatosis | European  Journal of Human Genetics
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
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 Gene - GeneCards | LZTR1 Protein | LZTR1 Antibody

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

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