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1 . Report
Haplotypic characterization of BRCA1 c.5266dupC, the prevailing mutation in Brazilian hereditary breast/ovarian cancer
저자
by
Gomes, Renan
;
Soares, Barbara Luisa
;
Felicio, Paula Silva
;
Michelli, Rodrigo
;
Netto, Cristina B. O.
, et al.
소스
Genetics and Molecular Biology
. January 2020 43(2)
Open Access (SciELO)
Web of Science
Scopus
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7 . Academic Journal
BRCA1 and BRCA2 rearrangements in Brazilian individuals with Hereditary Breast and Ovarian Cancer Syndrome
저자
by
Ewald, Ingrid Petroni
;
Cossio, Silvia Liliana
;
Palmero, Edenir Inez
;
Pinheiro, Manuela
;
Nascimento, Ivana Lucia de Oliveira
, et al.
소스
Genetics and Molecular Biology
. June 2016 39(2)
Open Access (SciELO)
Web of Science
Scopus
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7 . Academic Journal
Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil
저자
by
Palmero, Edenir Inêz
;
Alemar, Bárbara
;
Schüler-Faccini, Lavínia
;
Hainaut, Pierre
;
Moreira-Filho, Carlos Alberto
, et al.
소스
Genetics and Molecular Biology
. June 2016 39(2)
Open Access (SciELO)
Web of Science
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7 . Academic Journal
Genomic rearrangements in BRCA1 and BRCA2: a literature review
저자
by
Ewald, Ingrid Petroni
;
Ribeiro, Patricia Lisboa Izetti
;
Palmero, Edenir Inêz
;
Cossio, Silvia Liliana
;
Giugliani, Roberto
, et al.
소스
Genetics and Molecular Biology
. January 2009 32(3)
Open Access (SciELO)
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7 .
Cancer-related worry and risk perception in Brazilian individuals seeking genetic counseling for hereditary breast cancer
저자
by
Palmero, Edenir Inêz
;
Campacci, Natalia
;
Schüler-Faccini, Lavinia
;
Giugliani, Roberto
;
Rocha, José Claudio Casali da
, et al.
소스
Genetics and Molecular Biology
. January 2020 43(2)
Open Access (SciELO)
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7 . Academic Journal
Functional pri-miR-34b/c rs4938723 and KRAS 3′UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?
저자
by
Vieira, Igor Araujo
;
Pezzi, Eduarda Heidrich
;
Bandeira, Isabel Cristina
;
Reis, Larissa Brussa
;
de Araújo Rocha, Yasminne Marinho
, et al.
소스
In
Gene
10 March 2024 898
Full Text (ScienceDirect)
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7 . Academic Journal
Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome
저자
by
de Paula, André Escremim
;
Galvão, Henrique de Campos Reis
;
Bonatelli, Murilo
;
Sabato, Cristina
;
Fernandes, Gabriela Carvalho
, et al.
소스
In
Cancer Genetics
June 2021 254-255:82-91
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7 . Academic Journal
The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?
저자
by
Campacci, Natalia
;
Silveira Grasel, Rebeca
;
de Campos Reis Galvão, Henrique
;
França Garcia, Lucas
;
Carvalho Ribeiro, Paula
, et al.
소스
Frontiers in Psychology; 2024, p01-11, 11p
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7 . Academic Journal
Unveiling the role of MGMT and DAPK hypermethylation in response to anti‐EGFR agents: Molecular insights for advancing HNSCC treatment.
저자
by
Arantes, Lidia Maria Rebolho Batista
;
Silva‐Oliveira, Renato José
;
de Carvalho, Ana Carolina
;
Melendez, Matias Eliseo
;
Sorroche, Bruna Pereira
, et al.
소스
Head & Neck; Mar2024, Vol. 46 Issue 3, p461-472, 12p
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7 . Academic Journal
Neoadjuvant carboplatin in triple-negative breast cancer: results from NACATRINE, a randomized phase II clinical trial.
저자
by
de Pádua Souza, Cristiano
;
Carneiro, Ana Suellen Barroso
;
de Oliveira Lessa, Ana Cecília
;
Lacerda, Domício Carvalho
;
Paiva, Carlos Eduardo
, et al.
소스
Breast Cancer Research & Treatment; Nov2023, Vol. 202 Issue 1, p57-65, 9p
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