Varaico: Literature-Extracted Genetic Variants

Gene:STK11
Variant:p.E70*
Back to variants list

STK11

NM_000455.5:p.E70*

Associated Papers

Deciphering lung adenocarcinoma evolution and the role of LINE-1 retrotransposition.

Zhang T et al.

Biorxiv : the Preprint Server for Biology, 2025

40161734 (PubMed )
Supplement: media-2.xlsx › Supplementary_Table_4

The Utility of NGS Analysis in Homologous Recombination Deficiency Tracking.

Tsantikidi A et al.

Diagnostics (basel, Switzerland), 2023

37761329 (PubMed )
Supplement: diagnostics-13-02962-s001.zip › supplementary__Table_S2.xlsx › Table_S2_Samples_analyzed

Clinical and Genetic Analyses of 38 Chinese Patients with Peutz-Jeghers Syndrome.

Wu BD et al.

Biomed Research International, 2020

Clinical and Genetic Study of Children With Peutz-Jeghers Syndrome Identifies a High Frequency of STK11 De Novo Mutation.

Zhao HM et al.

Journal of Pediatric Gastroenterology and Nutrition, 2019

Mutational and gene fusion analyses of primary large cell and large cell neuroendocrine lung cancer.

Karlsson A et al.

Oncotarget, 2015

26124082 (PubMed )
Supplement: oncotarget-06-22028-s003.xlsx › Variants_in_Seidel

Cross-cancer profiling of molecular alterations within the human autophagy interaction network.

Lebovitz CB et al.

Autophagy, 2015

26208877 (PubMed )
Supplement: kaup-11-09-1067362-s001.zip › 1067362_supplemental_files › 2014AUTO0485R1-s03.xlsx › LUAD-mutations

Tongue carcinoma infrequently harbor common actionable genetic alterations.

Tan DS et al.

Bmc Cancer, 2014

Multiplex genomic profiling of non-small cell lung cancers from the LETS phase III trial of first-line S-1/carboplatin versus paclitaxel/carboplatin: results of a West Japan Oncology Group study.

Okamoto I et al.

Oncotarget, 2014

24810493 (PubMed )
Supplement: oncotarget-05-2293-s001.pdf

The LKB1 tumor suppressor as a biomarker in mouse and human tissues.

Nakada Y et al.

Plos One, 2013

Frequency and spectrum of cancers in the Peutz-Jeghers syndrome.

Hearle N et al.

Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2006

Exonic STK11 deletions are not a rare cause of Peutz-Jeghers syndrome.

Hearle NC et al.

Journal of Medical Genetics, 2006

STK11 genotyping and cancer risk in Peutz-Jeghers syndrome.

Schumacher V et al.

Journal of Medical Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Gene symbol: STK11. Disease: Peutz-Jeghers syndrome.

Schumacher V et al.

Human Genetics, 2005

Molecular dimensions of gastrointestinal tumors: some thoughts for digestion.

Cohen MM

American Journal of Medical Genetics. Part A, 2003

Further observations on LKB1/STK11 status and cancer risk in Peutz-Jeghers syndrome.

Lim W et al.

British Journal of Cancer, 2003

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."