Patricia Ashton-Prolla
Patricia Ashton-Prolla
Universidade Federal do Rio Grande do Sul, Hospital de Clinicas de Porto Alegre
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Cited by
The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families
MIW Achatz, M Olivier, F Le Calvez, G Martel-Planche, A Lopes, BM Rossi, ...
Cancer letters 245 (1-2), 96-102, 2007
Fabry disease: twenty-two novel mutations in the alpha-galactosidase A gene and genotype/phenotype correlations in severely and mildly affected hemizygotes and heterozygotes.
P Ashton-Prolla, B Tong, J Shabbeer, KH Astrin, CM Eng, RJ Desnick
Journal of investigative medicine: the official publication of the American …, 2000
Thalidomide, a current teratogen in South America
EE Castilla, P Ashton‐Prolla, E Barreda‐Mejia, D Brunoni, DP Cavalcanti, ...
Teratology 54 (6), 273-277, 1996
Detailed haplotype analysis at the TP53 locus in p.R337H mutation carriers in the population of Southern Brazil: evidence for a founder effect
S Garritano, F Gemignani, EI Palmero, M Olivier, G Martel‐Planche, ...
Human mutation 31 (2), 143-150, 2010
An alternative protocol for DNA extraction from formalin fixed and paraffin wax embedded tissue
R Coura, JC Prolla, L Meurer, P Ashton-Prolla
Journal of clinical pathology 58 (8), 894-895, 2005
Tumor protein 53 mutations and inherited cancer: beyond Li-Fraumeni syndrome
EI Palmero, MIW Achatz, P Ashton-Prolla, M Olivier, P Hainaut
Current opinion in oncology 22 (1), 64-69, 2010
Detection of R337H, a germline TP53 mutation predisposing to multiple cancers, in asymptomatic women participating in a breast cancer screening program in Southern Brazil
EI Palmero, L Schüler-Faccini, M Caleffi, MIW Achatz, M Olivier, ...
Cancer letters 261 (1), 21-25, 2008
Pregnancy outcome after exposure to misoprostol in Brazil: a prospective, controlled study
L Schüler, A Pastuszak, MTV Sanseverino, IM Orioliz, D Brunoni, ...
Reproductive Toxicology 13 (2), 147-151, 1999
Genomic rearrangements in BRCA1 and BRCA2: a literature review
IP Ewald, PLI Ribeiro, EI Palmero, SL Cossio, R Giugliani, ...
Genetics and molecular biology 32 (3), 437-446, 2009
Impact of β1-adrenergic receptor polymorphisms on susceptibility to heart failure, arrhythmogenesis, prognosis, and response to beta-blocker therapy
A Biolo, N Clausell, KG Santos, R Salvaro, P Ashton-Prolla, A Borges, ...
The American journal of cardiology 102 (6), 726-732, 2008
TP53 PIN3 and MDM2 SNP309 polymorphisms as genetic modifiers in the Li–Fraumeni syndrome: impact on age at first diagnosis
V Marcel, EI Palmero, P Falagan-Lotsch, G Martel-Planche, ...
Journal of medical genetics 46 (11), 766-772, 2009
Development and validation of a simple questionnaire for the identification of hereditary breast cancer in primary care
P Ashton-Prolla, J Giacomazzi, AV Schmidt, FL Roth, EI Palmero, ...
BMC cancer 9 (1), 283, 2009
Highly prevalent TP53 mutation predisposing to many cancers in the Brazilian population: a case for newborn screening?
MIW Achatz, P Hainaut, P Ashton-Prolla
The lancet oncology 10 (9), 920-925, 2009
BDNF/TrkB content and interaction with gastrin-releasing peptide receptor blockade in colorectal cancer
CB De Farias, DB Rosemberg, TE Heinen, P Koehler-Santos, ...
Oncology 79 (5-6), 430-439, 2010
Reviewing the history of HIV-1: spread of subtype B in the Americas
DM Junqueira, RM De Medeiros, MCC Matte, LAL Araújo, JAB Chies, ...
PloS one 6 (11), 2011
PRIMA-1, a mutant p53 reactivator, induces apoptosis and enhances chemotherapeutic cytotoxicity in pancreatic cancer cell lines
P Izetti, A Hautefeuille, AL Abujamra, CB de Farias, J Giacomazzi, ...
Investigational new drugs 32 (5), 783-794, 2014
A model to optimize public health care and downstage breast cancer in limited-resource populations in southern Brazil.(Porto Alegre Breast Health Intervention Cohort)
M Caleffi, RA Ribeiro, DL Duarte Filho, P Ashton-Prolla, AJ Bedin, ...
BMC public health 9 (1), 83, 2009
Non–pseudogene-derived complex acid β-glucosidase mutations causing mild type 1 and severe type 2 Gaucher disease
ME Grace, P Ashton-Prolla, GM Pastores, A Soni, RJ Desnick
The Journal of clinical investigation 103 (6), 817-823, 1999
TP53 PIN3 and PEX4 polymorphisms and infertility associated with endometriosis or with post-in vitro fertilization implantation failure
DD Paskulin, JSL Cunha-Filho, CAB Souza, MC Bortolini, P Hainaut, ...
Cell death & disease 3 (9), e392-e392, 2012
Fabry disease: comparison of enzymatic, linkage, and mutation analysis for carrier detection in a family with a novel mutation (30delG)
P Ashton‐Prolla, GA Ashley, R Giugliani, RF Pires, RJ Desnick, CM Eng
American journal of medical genetics 84 (5), 420-424, 1999
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