Cargando…

Correction: CAPN1 is a novel binding partner and regulator of the tumor suppressor NF1 in melanoma

Detalles Bibliográficos
Autores principales:	Alon, Michal, Arafeh, Rand, Lee, Joo Sang, Madan, Sanna, Kalaora, Shelly, Nagler, Adi, Abgarian, Tereza, Greenberg, Polina, Ruppin, Eytan, Samuels, Yardena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Impact Journals LLC 2019
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407687/ https://www.ncbi.nlm.nih.gov/pubmed/30863494 http://dx.doi.org/10.18632/oncotarget.26685

Ejemplares similares

CAPN1 is a novel binding partner and regulator of the tumor suppressor NF1 in melanoma
por: Alon, Michal, et al.
Publicado: (2018)

A genome‐wide CRISPR screen identifies FBXO42 involvement in resistance toward MEK inhibition in NRAS‐mutant melanoma
por: Nagler, Adi, et al.
Publicado: (2019)

NRas activity is regulated by dynamic interactions with nanoscale signaling clusters at the plasma membrane
por: Yakovian, Oren, et al.
Publicado: (2022)

Immunoproteasome expression is associated with better prognosis and response to checkpoint therapies in melanoma
por: Kalaora, Shelly, et al.
Publicado: (2020)

Identification of presented SARS-CoV-2 HLA class I and HLA class II peptides using HLA peptidomics
por: Nagler, Adi, et al.
Publicado: (2021)

Combined inhibition of MEK and nuclear ERK translocation has synergistic antitumor activity in melanoma cells
por: Arafeh, Rand, et al.
Publicado: (2017)

Author Correction: Combined inhibition of MEK and nuclear ERK translocation has synergistic antitumor activity in melanoma cells
por: Arafeh, Rand, et al.
Publicado: (2019)

An anti-CAPN5 intracellular antibody acts as an inhibitor of CAPN5-mediated neuronal degeneration
por: Wang, Yan, et al.
Publicado: (2017)

Use of HLA peptidomics and whole exome sequencing to identify human immunogenic neo-antigens
por: Kalaora, Shelly, et al.
Publicado: (2016)

CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76
por: Garcia-Berlanga, Jesus Eduardo, et al.
Publicado: (2019)

Synthetic lethality across normal tissues is strongly associated with cancer risk, onset, and tumor suppressor specificity
por: Cheng, Kuoyuan, et al.
Publicado: (2021)

Proteomic insight into the pathogenesis of CAPN5-vitreoretinopathy
por: Velez, Gabriel, et al.
Publicado: (2019)

Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations
por: Méreaux, Jean-Loup, et al.
Publicado: (2021)

Quantitative Analysis of Genetic and Neuronal Multi-Perturbation Experiments
por: Kaufman, Alon, et al.
Publicado: (2005)

Gene Expression of Caenorhabditis elegans Neurons Carries Information on Their Synaptic Connectivity
por: Kaufman, Alon, et al.
Publicado: (2006)

A single nucleotide polymorphism in CAPN1 associated with marbling score in Korean cattle
por: Cheong, Hyun Sub, et al.
Publicado: (2008)

Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families
por: Kocoglu, Cemile, et al.
Publicado: (2018)

Novel CAPN1 mutations extend the phenotypic heterogeneity in combined spastic paraplegia and ataxia
por: Lai, Lu‐Lu, et al.
Publicado: (2020)

Effects of polymorphisms in CAPN1 and CAST genes on meat tenderness of Chinese Simmental cattle
por: Sun, Xiaomei, et al.
Publicado: (2018)

A Novel Mutation of CAPN1 Gene Causing Hereditary Spastic Paraplegia-76
por: Chinta, Vijayendra R., et al.
Publicado: (2022)

Prognostic Significance of Capn4 Overexpression in Intrahepatic Cholangiocarcinoma
por: Zhang, Chi, et al.
Publicado: (2013)

Capn5 Expression in the Healthy and Regenerating Zebrafish Retina
por: Coomer, Cagney E., et al.
Publicado: (2018)

CAPN6 in disease: An emerging therapeutic target (Review)
por: Chen, Lin, et al.
Publicado: (2020)

Selection for Translation Efficiency on Synonymous Polymorphisms in Recent Human Evolution
por: Waldman, Yedael Y., et al.
Publicado: (2011)

Missense Mutation in CAPN1 Is Associated with Spinocerebellar Ataxia in the Parson Russell Terrier Dog Breed
por: Forman, Oliver P., et al.
Publicado: (2013)

CAPN3, DCT, MLANA and TYRP1 are overexpressed in skin of vitiligo vulgaris Mexican patients
por: Salinas-Santander, Mauricio, et al.
Publicado: (2018)

Experimental Verification of CAPN1 and CAST Gene Polymorphisms in Different Generations of Da-Heng Broilers
por: Zhou, Yu-Guang, et al.
Publicado: (2017)

Novel CAPN1 missense variants in complex hereditary spastic paraplegia with early‐onset psychosis
por: Alecu, Julian E., et al.
Publicado: (2022)

Harnessing synthetic lethality to predict the response to cancer treatment
por: Lee, Joo Sang, et al.
Publicado: (2018)

Pan-Cancer Analysis of Patient Tumor Single-Cell Transcriptomes Identifies Promising Selective and Safe Chimeric Antigen Receptor Targets in Head and Neck Cancer
por: Madan, Sanna, et al.
Publicado: (2023)

Transcriptional and Translational Effects of Intronic CAPN3 Gene Mutations
por: Nascimbeni, Anna Chiara, et al.
Publicado: (2010)

CAPN5 gene silencing by short hairpin RNA interference
por: Nelson, Nnamdi G, et al.
Publicado: (2014)

Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations
por: Park, Hyung Jun, et al.
Publicado: (2016)

Secondary glaucoma in CAPN5-associated neovascular inflammatory vitreoretinopathy
por: Cham, Abdourahman, et al.
Publicado: (2016)

CAPN: a Combine Attention Partial Network for glove detection
por: Yu, Feng, et al.
Publicado: (2023)

The association of CAPN1 316 marker genotypes with growth and meat quality traits of steers finished on pasture
por: Miquel, María C., et al.
Publicado: (2009)

A Novel CAPN1 Mutation Causes a Pure Hereditary Spastic Paraplegia in an Italian Family
por: Cotti Piccinelli, Stefano, et al.
Publicado: (2019)

Two novel homozygous mutations of CAPN1 in Chinese patients with hereditary spastic paraplegia and literatures review
por: Peng, Fang, et al.
Publicado: (2019)

ADCY5, CAPN10 and JAZF1 Gene Polymorphisms and Placental Expression in Women with Gestational Diabetes
por: Ustianowski, Przemysław, et al.
Publicado: (2021)

Parkinson disease (PARK) genes are somatically mutated in cutaneous melanoma
por: Inzelberg, Rivka, et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_6512f70nrui4sljndmbnns4k5o