Cargando…

Prognostic significance of the genetic variant of lymphotoxin alpha (p.Thr60Asn) in egyptian patients with advanced hepatocellular carcinoma

BACKGROUND: Hepatocellular carcinoma (HCC) is one of the most common malignancies worldwide in terms of mortality, and susceptibility is attributed to genetic, lifestyle, and environmental factors. Lymphotoxin alpha (LTA) has a crucial role in communicating the lymphocytes with stromal cells and pro...

Descripción completa

Detalles Bibliográficos
Autores principales:	Alhelf, Maha, Shoaib, Rasha M. S., Elsaid, Afaf, Bastawy, Nermeen, Elbeltagy, Nanis S., Salem, Eman T., Refaat, Sherif, Abuelnadar, Eman H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Netherlands 2023
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147750/ https://www.ncbi.nlm.nih.gov/pubmed/36929286 http://dx.doi.org/10.1007/s11033-023-08281-z

Ejemplares similares

Association between the p.Thr1406Asn polymorphism of the carbamoyl-phosphate synthetase 1 gene and necrotizing enterocolitis: A prospective multicenter study
por: Moonen, Rob M., et al.
Publicado: (2016)

Association of A1AT genetic polymorphism and NSCLC: a case- control study in Egyptian population
por: El-Dawa, Aliaa N., et al.
Publicado: (2023)

MUC7 VNTR polymorphism and association with bronchial asthma in Egyptian children
por: Saad, Entsar A., et al.
Publicado: (2022)

Variable phenotypic expression of nonsense mutation p.Thr5* in the APOE gene
por: Leren, Trond P., et al.
Publicado: (2016)

Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia
por: Zhou, Zhifan, et al.
Publicado: (2016)

Detection of EGFR gene polymorphisms in non-small cell lung cancer Egyptian patients: a case–control study
por: El-khawaga, Omali Y., et al.
Publicado: (2023)

Kir2.2 p.Thr140Met: a genetic susceptibility to sporadic periodic paralysis
por: FAN, CHUNXIANG, et al.
Publicado: (2018)

Multimodal Imaging Characteristics of ADRP in a Family with p.Thr58Arg Substituted RHO Mutation
por: Ruppert, Misty, et al.
Publicado: (2020)

Myocardial Infarction and AGT p.Thr174Met Polymorphism: A Meta-Analysis of 7657 Subjects
por: Li, Yan-yan, et al.
Publicado: (2021)

PSEN1 p.Thr116Ile Variant in Two Korean Families with Young Onset Alzheimer’s Disease
por: Bagyinszky, Eva, et al.
Publicado: (2018)

Silent variant in F8:c.222G>T (p.Thr74Thr) causes a partial exon skipping in a patient with mild hemophilia A
por: Letelier, Anna, et al.
Publicado: (2021)

Attention-deficit hyperactivity disorder in Egyptian medical students and how it relates to their academic performance
por: Shebl, Eman M., et al.
Publicado: (2023)

Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopenia
por: Schönfeld, Mascha, et al.
Publicado: (2020)

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
por: Romozzi, Marina, et al.
Publicado: (2021)

CHCHD2 p.Thr61Ile knock‐in mice exhibit motor defects and neuropathological features of Parkinson's disease
por: Fan, Liyuan, et al.
Publicado: (2022)

First Observation of Hemoglobin Kansas [β102(G4)Asn→Thr, AAC>ACC] in the Turkish Population
por: Keser, İbrahim, et al.
Publicado: (2015)

Association of NOS3 (rs 2070744) and SOD2Val16Ala (rs4880) gene polymorphisms with increased risk of ESRD among Egyptian patients
por: Elsaid, Afaf, et al.
Publicado: (2021)

Structural insights into the pSer/pThr dependent regulation of the SHP2 tyrosine phosphatase in insulin and CD28 signaling
por: Zeke, András, et al.
Publicado: (2022)

Association between XRCC3 p.Thr241Met polymorphism and risk of glioma: A systematic review and meta-analysis
por: Tan, Shing Cheng, et al.
Publicado: (2022)

Type 2 deiodinase p.Thr92Ala polymorphism does not affect the severity of obesity and weight loss after bariatric surgery
por: Benenati, Nicoletta, et al.
Publicado: (2022)

Plasma urotensin-2 level and Thr21Met but not Ser89Asn polymorphisms of the urotensin-2 gene are associated with migraines
por: Geyik, Sırma, et al.
Publicado: (2016)

Genetic and biochemical studies of hepatic carcinoma in the Egyptian population
por: Elkhoudary, Amany F, et al.
Publicado: (2021)

The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant
por: Corvillo, Fernando, et al.
Publicado: (2020)

AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant
por: Szczałuba, Krzysztof, et al.
Publicado: (2020)

Low FODMAP diet in Egyptian patients with Crohn's disease in remission phase with functional gastrointestinal symptoms
por: Elhusseiny, Maha H, et al.
Publicado: (2018)

p.(Asp47Asn) and p.(Thr62Met): non deleterious LDL receptor missense variants functionally characterized in vitro
por: Benito-Vicente, A., et al.
Publicado: (2018)

Cytogenetic screening of chromosomal abnormalities and genetic analysis of FSH receptor Ala307Thr and Ser680Asn genes in amenorrheic patients
por: Kanaan, Bushra A., et al.
Publicado: (2023)

Formula Feeding and Associated Factors among a Group of Egyptian Mothers
por: Tawfik, Safaa, et al.
Publicado: (2019)

Genomic organization and phylogenetic utility of deer mouse (Peromyscus maniculatus) lymphotoxin-alpha and lymphotoxin-beta
por: Richens, Tiffany, et al.
Publicado: (2008)

A method for measurement of human asparagine synthetase (ASNS) activity and application to ASNS protein variants associated with ASNS deficiency
por: Chang, Mario C, et al.
Publicado: (2023)

Pharmacokinetic Evaluation of Empagliflozin in Healthy Egyptian Volunteers Using LC-MS/MS and Comparison with Other Ethnic Populations
por: Ayoub, Bassam M., et al.
Publicado: (2017)

Genome sequencing identifies somatic BRAF duplication c.1794_1796dupTAC;p.Thr599dup in pediatric patient with low-grade ganglioglioma
por: Miller, Katherine E., et al.
Publicado: (2018)

Non-Small-Cell Lung Cancer-Sensitive Detection of the p.Thr790Met EGFR Alteration by Preamplification before PNA-Mediated PCR Clamping and Pyrosequencing
por: Billaud, Amandine, et al.
Publicado: (2020)

Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family
por: Li, Mengmeng, et al.
Publicado: (2019)

The dominant p.Thr274Pro mutation in the von Willebrand factor propeptide causes the von Willebrand disease type 1 phenotype in two unrelated patients
por: Pagliari, Maria Teresa, et al.
Publicado: (2022)

Coping Strategies in Egyptian Ladies with Breast Cancer
por: Elsheshtawy, Eman A., et al.
Publicado: (2014)

PTHrP and the PTH/PTHrP receptor are co-expressed in human breast and colon tumours.
por: Carron, J. A., et al.
Publicado: (1997)

The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration
por: Rossi, Giacomina, et al.
Publicado: (2022)

The Clinical Value of VDR and CTLA 4 in Evaluating the Prognosis of Invasive Duct Carcinoma of Egyptian Patients and their Benefit as a Target Therapy
por: Holah, Nanis Shawky
Publicado: (2021)

Parathyroid hormone receptor 1 (PTHR1) is a prognostic indicator in canine osteosarcoma
por: Al-Khan, Awf A., et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_vm6b6fp3cmnnosei3ucur4hprs