You are on the new improved site. You can view the old site in view-only mode here until June 27, 2026

Filter Results

Search all journals

Enter search terms…

Advanced search

/

About

About Sage
About Sage Journals
Privacy Policy
Terms of Use
Contact Us
Help

Information for

Authors
Editors
Librarians
Researchers
Reviewers
Frequently asked questions

Copyright © 2026 by Sage Publications.京ICP备09090397号-11

Search results

Search results page

Articles (208)

Journals (0)

1-10 of 208 results for Frameshift gene

Sort by:

Relevance

Select all

Select all

Sort by:

Relevance

Select article: Frameshift Signals in Genes Associated with the Circular Code

Free access

Research article

First published 2007-2

Frameshift Signals in Genes Associated with the Circular Code

Ahmed Ahmed, Gabriel Frey, Christian J. Michel

In Silico Biology

Select article: Frameshift mutation of candidate tumor suppressor genes QK1 and TMEFF2 in gastric and colorectal cancers

Free access

Research article

First published 2019-2

Frameshift mutation of candidate tumor suppressor genes QK1 and TMEFF2 in gastric and colorectal cancers

Ha Yoon Mo, Yun Sol Jo, Nam Jin Yoo [...]

Cancer Biomarkers

Select article: Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families

Retricted access

Research article

First published 2023-09

Two Novel Frameshift Mutations in the GLI3 Gene Underlie Non-Syndromic Polydactyly in Chinese Families

Xiaoyan Guo, Tengfei Shi, Mingrui Lin [...]

Genetic Testing and Molecular Biomarkers

Select article: Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa

Retricted access

Research article

First published 2018-03

Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa

Mu Yang, Shujin Li, Wenjing Liu [...]

Genetic Testing and Molecular Biomarkers

Select article: Cochlear implantation in a Chinese patient with a novel frameshift variant in POU3F4 gene and incomplete partition type III: a case report

Open access

Case report

First published 2022-1

Cochlear implantation in a Chinese patient with a novel frameshift variant in POU3F4 gene and incomplete partition type III: a case report

Lanye Hu, Jie Chen, Ruen Yao [...]

Journal of International Medical Research

Select article: Novel somatic frameshift Mutations of Genes Related to Cell Cycle and DNA Damage Response in Gastric and Colorectal Cancers with Microsatellite Instability

Retricted access

Research article

First published 2010-11

Novel somatic frameshift Mutations of Genes Related to Cell Cycle and DNA Damage Response in Gastric and Colorectal Cancers with Microsatellite Instability

Yoo Ri Kim, Nak Gyun Chung, Mi Ran Kang [...]

Tumori Journal

Select article: Novel somatic frameshift Mutations of Genes Related to Cell Cycle and DNA Damage Response in Gastric and Colorectal Cancers with Microsatellite Instability

Retricted access

Research article

First published 2010-11

Novel somatic frameshift Mutations of Genes Related to Cell Cycle and DNA Damage Response in Gastric and Colorectal Cancers with Microsatellite Instability

Yoo Ri Kim, Nak Gyun Chung, Mi Ran Kang [...]

Tumori Journal

Select article: A Novel Homozygous Frameshift Mutation in Exon 2 of LEP Gene Associated with Severe Obesity: A Case Report

Open access

Case report

First published 2016

A Novel Homozygous Frameshift Mutation in Exon 2 of LEP Gene Associated with Severe Obesity: A Case Report

Ashwaq Shukri Altawil, Horia Ahmad Mawlawi, Khalid Ateeq Alghamdi [...]

Clinical Medicine Insights: Pediatrics

Select article: A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 ( RLBP1 ) gene causes retinitis punctata albescens

Retricted access

Case report

First published 2021-5

A novel homozygous frameshift variant in the cellular retinaldehyde-binding protein 1 ( RLBP1 ) gene causes retinitis punctata albescens

Sónia Torres-Costa, Carla Sofia Ferreira, Ana Grangeia [...]

European Journal of Ophthalmology

Select article: A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report

Free access

Case report

First published 2022

A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report

Vincenzo Montano, Michelangelo Mancuso, Costanza Simoncini [...]

Journal of Neuromuscular Diseases

1
2
3
•••
21
10 / page

Article type

Publication date

Subjects

Access