Prevalence of germline variants in Brazilian pancreatic carcinoma patients

to related objects

Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: 1 Online-Ressource.

Language: Englisch

Bibliographic citation: Prevalence of germline variants in Brazilian pancreatic carcinoma patients ; volume:14 ; number:1 ; day:10 ; month:9 ; year:2024 ; pages:1-14 ; date:12.2024
Scientific reports ; 14, Heft 1 (10.9.2024), 1-14, 12.2024

Creator: Rodrigues, Lívia Munhoz
Maistro, Simone
Katayama, Maria Lucia Hirata
Rocha, Vinícius Marques
Lopez, Rossana Veronica Mendoza
Lopes, Edia Filomena di Tullio
Gonçalves, Fernanda Toledo
Fridman, Cintia
Serio, Pedro Adolpho de Menezes Pacheco
Barros, Luciana Rodrigues Carvalho
Leite, Luiz Antonio Senna
Segatelli, Vanderlei
Estevez-Diz, Maria del Pilar
Guindalini, Rodrigo Santa Cruz
Ribeiro Junior, Ulysses
Folgueira, Maria Aparecida Azevedo Koike

Contributor: SpringerLink (Online service)

DOI: 10.1038/s41598-024-71884-4

URN: urn:nbn:de:101:1-2411242115470.558803623306

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

Last update: 15.08.2025, 7:24 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

Rodrigues, Lívia Munhoz
Maistro, Simone
Katayama, Maria Lucia Hirata
Rocha, Vinícius Marques
Lopez, Rossana Veronica Mendoza
Lopes, Edia Filomena di Tullio
Gonçalves, Fernanda Toledo
Fridman, Cintia
Serio, Pedro Adolpho de Menezes Pacheco
Barros, Luciana Rodrigues Carvalho
Leite, Luiz Antonio Senna
Segatelli, Vanderlei
Estevez-Diz, Maria del Pilar
Guindalini, Rodrigo Santa Cruz
Ribeiro Junior, Ulysses
Folgueira, Maria Aparecida Azevedo Koike
SpringerLink (Online service)

Other Objects (12)

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

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.

Prevalence of germline variants in Brazilian pancreatic carcinoma patients

Object Details

References and Relationships

Contributors, Places and Time

Further information

Data provider

Associated

Other Objects (12)

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

Prevalence of BRCA1 and BRCA2 germline variants in an unselected pancreatic cancer patient cohort in Pakistan

Prevalence of pathogenic germline variants in the circulating tumor DNA testing

Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Functional evaluation of germline TP53 variants identified in Brazilian families at-risk for Li–Fraumeni syndrome

Prevalence of RECQL germline variants in Pakistani early-onset and familial breast cancer patients

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

Ancestry-specific predisposing germline variants in cancer

Functional germline variants as potential co-oncogenes

Correction to: Significant detection of new germline pathogenic variants in Australian Pancreatic Cancer Screening Program participants

Prevalence of Pathogenic Germline Variants in Women with Non-Familial Unilateral Triple-Negative Breast Cancer

Germline copy number variants and endometrial cancer risk

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

Related objects

Reset password