Why is "Frameshift mutation" trending?

Search Interest Perspective

• A Frameshift Mutation in the Methyltransferase rlmN Is Associated with Increased Linezolid Resistance in Mycobacterium tuberculosis - Science Partner Journals
• A Novel Neurofibromatosis Type 1 (NF1) Frameshift Mutation Associated With Atypical Hypotensive Pheochromocytoma: A Case Report - Cureus
• PTEN frameshift mutation in two atypical meningiomas: case reports and review of the literature - Wiley Online Library
• Uneventful pregnancies with homozygous KISS1 frameshift mutation - The Lancet
• A rare autoinflammatory syndrome associated with a C2orf69 frameshift mutation: a case report - Springer Nature Link
• The shared frameshift mutation landscape of microsatellite-unstable cancers suggests immunoediting during tumor evolution - Nature
• A novel ANK1 frameshift mutation associated with neonatal hereditary spherocytosis: a case report - Frontiers
• Antibiotic resistance by high-level intrinsic suppression of a frameshift mutation in an essential gene - PNAS
• Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation - The New England Journal of Medicine
• Lissencephaly: LIS1 Gene Frameshift Mutation - Physician's Weekly
• The patient-specific mouse model with Foxg1 frameshift mutation provides insights into the pathophysiology of FOXG1 syndrome - Nature
• Case report: A frameshift mutation in CLCN2-related leukoencephalopathy and retinopathy - Frontiers
• Genetic influence of a STAU2 frameshift mutation and RELN regulatory elements on performance in Icelandic horses - Nature
• Identification of a homozygous frameshift mutation in the FGF3 gene in a consanguineous Iranian family: First report of labyrinthine aplasia, microtia, and microdontia syndrome in Iran and literature review - Wiley Online Library
• frameshift mutation are associated with the activation of autophagy - Nature
• ASTE1 frameshift mutation triggers the immune response in Epstein-Barr virus-associated gastric cancer - Nature
• The CFTR frameshift mutation 3905insT and its effect at transcript and protein level - Nature
• A novel frameshift mutation of SYNE1 in a Japanese family with autosomal recessive cerebellar ataxia type 8 - Nature
• A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease - Nature
• Metabolic remodeling and calcium handling abnormality in induced pluripotent stem cell-derived cardiomyocytes in dilated phase of hypertrophic cardiomyopathy with MYBPC3 frameshift mutation - Nature
• Frameshift-mutation-derived peptides as tumor-specific antigens in inherited and spontaneous colorectal cancer - PNAS
• Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome - EurekAlert!
• A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndrome - Nature
• A Novel Homozygous Frameshift Mutation in CCN6 Causing Progressive Pseudorheumatoid Dysplasia (PPRD) in a Consanguineous Yemeni Family - Frontiers
• Case report: genetic analysis of a novel frameshift mutation in FMR1 gene in a Chinese family - Frontiers
• Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A - Frontiers
• Outer retinal structural anomaly due to frameshift mutation in CACNA1F gene - Nature
• A de novo frameshift mutation in ZEB2 causes polledness, abnormal skull shape, small body stature and subfertility in Fleckvieh cattle - Nature
• Novel pathogenic frameshift mutation in the POLH gene contributes to xeroderma pigmentosum variant type in a 16-year-old girl - Wiley Online Library
• CCDC82 frameshift mutation associated with intellectual disability, spastic paraparesis, and dysmorphic features - Wiley Online Library
• A Chromosomal Deletion and New Frameshift Mutation Cause ARSACS in an African-American - Frontiers
• Case Report: A Frameshift Mutation in MSH2 Exon 2 in a Kidney Recipient With Muir–Torre Syndrome - Frontiers
• Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation - The New England Journal of Medicine
• Case report: A novel frameshift mutation in BRSK2 causes autism in a 16-year old Chinese boy - Frontiers
• Whole exome sequencing identifies a novel SPTB frameshift mutation causing hereditary spherocytosis in the Chinese population - Springer Nature Link
• A novel frameshift mutation of malonyl-CoA decarboxylase deficiency: clinical signs and therapy response of a late-diagnosed case - Wiley Online Library
• Severe neurodegeneration, progressive cerebral volume loss and diffuse hypomyelination associated with a homozygous frameshift mutation in CSTB - Nature
• An AP4B1 frameshift mutation in siblings with intellectual disability and spastic tetraplegia further delineates the AP-4 deficiency syndrome - Nature
• Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population - Nature
• A novel DSPP frameshift mutation causing dentin dysplasia type 2 and disease management strategies - Wiley Online Library
• A homozygous frameshift mutation in the mouse Flg gene facilitates enhanced percutaneous allergen priming - Nature
• A novel frameshift mutation in TRPV6 is associated with hereditary pancreatitis - Frontiers
• A frameshift mutation in Disrupted in Schizophrenia 1 in an American family with schizophrenia and schizoaffective disorder - Nature
• Functional analysis of a promoter variant identified in the CFTR gene in cis of a frameshift mutation - Nature
• Frame shift defines molecular diagnosis in rare disease - Baylor College of Medicine Blog Network -
• Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27 | Journal of Human Genetics - Nature
• A frameshift mutation in MC4R associated with dominantly inherited human obesity - Nature
• A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis-2 with impaired intellectual development - Wiley Online Library
• A frameshift mutation in human MC4R is associated with a dominant form of obesity - Nature
• Homozygous frameshift mutation in TMCO1 causes a syndrome with craniofacial dysmorphism, skeletal anomalies, and mental retardation - PNAS
• A tale of (disordered) tail - Nature
• A Heterozygous Frameshift Mutation in the Endothelin-3 EDN-3 ) Gene in Isolated Hirschsprung's Disease - Nature
• Missense, Nonsense and Frameshift Mutations: A Genetic Guide - Technology Networks
• Marfan syndrome with neonatal progeroid syndrome‐like lipodystrophy associated with a novel frameshift mutation at the 3′ terminus of the FBN1‐gene - Wiley Online Library
• Novel frameshift mutations of ANKUB1, GLI3, and TAS2R3 associated with polysyndactyly in a Chinese family - Wiley Online Library
• Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 - Nature
• Frameshift mutation in the collagen VI gene causes Ullrich's disease - Higuchi - 2001 - Annals of Neurology - Wiley Online Library
• Frameshift Mutation - YouTube
• Frameshift mutation 3-D - YouTube