Prediction models of persistent taxane-induced peripheral neuropathy among breast cancer survivors using whole-exome sequencing

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Prediction models of persistent taxane-induced peripheral neuropathy among breast cancer survivors using whole-exome sequencing ; volume:8 ; number:1 ; day:16 ; month:5 ; year:2024 ; pages:1-9 ; date:12.2024
npj precision oncology ; 8, Heft 1 (16.5.2024), 1-9, 12.2024

Creator: Engvall, Kristina
Uvdal, Hanna
Björn, Niclas
Åvall-Lundqvist, Elisabeth
Gréen, Henrik

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41698-024-00594-x

URN: urn:nbn:de:101:1-2407252107255.390976486780

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:58 AM CEST

Data provider

This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.

Show original at data provider

Associated

Engvall, Kristina
Uvdal, Hanna
Björn, Niclas
Åvall-Lundqvist, Elisabeth
Gréen, Henrik
SpringerLink (Online service)

Other Objects (12)

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

Cultural heritage institutions wishing to register will find more information here.

Fields marked * need to be filled in.

Username*

Please enter your username

Email*

Please enter your email address

Please do not fill this field

First name

Last name

Password*

Please enter your password

Confirm password*

Please enter the same password

I have read the terms of use and the privacy policy for the collection of personal data and accept them. *

This field is required.

I would like to subscribe to the newsletter of the Deutsche Digitale Bibliothek. See newsletter subscription info.

Account created

Your "My DDB" account has been successfully created. Before you can log in to your account, you must click the confirmation link in the message we just sent to the email address you provided.

Prediction models of persistent taxane-induced peripheral neuropathy among breast cancer survivors using whole-exome sequencing

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

A Prospective Study of Taxane-Induced Neuropathy with Breast Cancer: Proper Assessment Tool for Taxane-Induced Neuropathy

Whole-exome sequencing of a pedigree segregating asthma

Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

Comprehensive comparison of three commercial human whole-exome capture platforms

Genomic alterations in gastric cancers discovered via whole-exome sequencing

Human whole-exome genotype data for Alzheimer’s disease

EXCAVATOR: detecting copy number variants from whole-exome sequencing data

Azoospermia and reciprocal translocations: should whole-exome sequencing be recommended?

Whole-exome analysis of 177 pediatric patients with undiagnosed diseases

WEP: a high-performance analysis pipeline for whole-exome data

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation

Whole-exome sequencing in 168 Korean patients with inherited retinal degeneration

Related objects

Reset password