LEDESMA, MARTÍN; POODTS, DANIELA; AMOIA, SOFÍA; HAJOS, SILVIA; FUNDIA, ARIELA; VAY, CARLOS; PIBUEL, MATÍAS; LOMPARDÍA, SILVINA

Discrimination of the chemotherapy resistance status of human leukemia and glioblastoma cell lines by MALDI-TOF-MS profiling

Scientific Reports; Lugar: Londres; Año: 2023 vol. 13 p. 5596 - 5606

FONTECHA MB; ANADÓN MR; MAZZEI JA; FUNDIA AF

AVANCES EN LA GENÉTICA DE LA HIPERTENSIÓN ARTERIAL PULMONAR

INSUFICIENCIA CARDÍACA; Lugar: Ciudad de Buenos Aires; Año: 2020 vol. 15 p. 10 - 18

FERRI C; WEICH N; GUTIERREZ L; DE BRASI CD; BENGIÓ R; ZAPATA P; FUNDIA AF; LARRIPA IB

Single nucleotide polymorphism in PTEN-Long gene: a risk factor in chronic myeloid leukemia

GENE; Lugar: Amsterdam; Año: 2019 vol. 694 p. 71 - 74

WEICH N; ROISMAN A; CERLIANI B; ARÁOZ HV; CHERTKOFF L; RICHARD SM; SLAVUTSKY IR; LARRIPA IB; FUNDIA AF

Gene polymorphism profiles of drug-metabolizing enzymes GSTM1, GSTT1 and GSTP1 in an Argentinean population

ANNALS OF HUMAN BIOLOGY; Lugar: Londres; Año: 2017 vol. 44 p. 379 - 383

WEICH N; FERRI C; MOIRAGHI B; BENGIÓ R; GIERE I; PAVLOVSKY C; LARRIPA IB; FUNDIA AF

TP53 codon 72 polymorphism predicts chronic myeloid leukemia susceptibility and treatment outcome

BLOOD CELLS MOLECULES AND DISEASES; Lugar: Amsterdam; Año: 2016 vol. 59 p. 129 - 133

WEICH N; FERRI C; MOIRAGHI B; BENGIÓ R; GIERE I; PAVLOVSKY C; LARRIPA IB; FUNDIA AF

GSTM1 and GSTP1, but not GSTT1 genetic polymorphisms are associated with chronic myeloid leukemia risk and treatment response

CANCER EPIDEMIOLOGY; Lugar: Amsterdam; Año: 2016 vol. 44 p. 16 - 21

WEICH N; NUÑEZ M; GALIMBERTI G; ELENA G; ACEVEDO S; LARRIPA IB; FUNDIA AF

Polymorphic variants of GSTM1, GSTT1, and GSTP1 genes in childhood acute leukemias: A preliminary study in Argentina.

HEMATOLOGY; Lugar: London; Año: 2015 vol. 20 p. 511 - 516

ABELLEYRO MM; RADIC CP; TETZLAFF T; MARCHIONE V; FUNDIA AF; LARRIPA IB; ROSSETTI LC; DE BRASI CD

Reliable and cost-effective approach for diagnosis of heterozygous F8/F9 large deletions by quantitative real-time PCR.

HAEMOPHILIA; Lugar: Londres; Año: 2015 p. 1 - 5

ARIELA F FUNDIA; NATALIA WEICH; CRIVELLI, ADRIANA; GRACIELA LA MOTTA; IRENE B. LARRIPA; IRMA SLAVUTSKY

Glutathione S-transferase gene polymorphisms in celiac disease and their correlation with genomic instability phenotype

Clin Res Hepatol Gastroenterol; Lugar: Paris; Año: 2014 vol. 38 p. 379 - 384

STELLA, FLAVIA; WEICH, NATALIA; PANERO, JULIETA; FANTL, DOROTEA B.; SCHUTZ, NATALIA; FUNDIA, ARIELA F; SLAVUTSKY, IRMA

Gluthatione S-transferase P1 mRNA expression in plasma cell disorders and its correlation with polymorphic variants and clinical outcome

CANCER EPIDEMIOLOGY; Lugar: Amsterdam; Año: 2013 vol. 37 p. 671 - 674

ARIELA FUNDIA; IRENE LARRIPA; IRMA SLAVUTSKY

Alteraciones genéticas, inestabilidad genómica y cáncer en enfermedad celíaca

ACTA GASTROENTEROLOGICA LATINOAMERICANA.; Lugar: Buenos Aires, Argentina; Año: 2009 vol. 39 p. 55 - 62

FUNDIA AF; COTTLIAR AS; LA MOTTA G; CRIVELLI A; GÓMEZ JC; SLAVUTSKY IR; LARRIPA IB

Analysis of genomic instability in adult-onset celiac disease patients by microsatellite instability and loss of heterozygosis

EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY; Lugar: London; Año: 2008 vol. 20 p. 1159 - 1166

ARIELA F FUNDIA; CARLOS DE BRASI; LARRIPA IRENE

Feasibility of a cost-effective approach to evaluate short tandem repeats markers suitable for chimerism follow -up

MOLECULAR DIAGNOSIS; Lugar: Minneapolis; Año: 2004 vol. 8 p. 87 - 91

GONZÁLEZ-CID M; FUNDIA AF; CUELLO MT; LARRIPA IB

Correlation between chromosome damage and apoptosis induced by fludarabine and idarubicin in normal human lymphocytes

TOXICOLOGY; Año: 2002 vol. 171 p. 215 - 222

COTTLIAR AS; FUNDIA AF; SLAVUTSKY IR

RE: Cottliar et al.: High frequencies of telomeric associations, chromosome aberrations and sister chromatid exchanges in ulcerative colitis.

AMERICAN JOURNAL OF GASTROENTEROLOGY; Lugar: Londres; Año: 2001 vol. 96 p. 1641 - 1643

COTTLIAR AS; FUNDIA AF; MORÁN C; SOSA E; GELDERN P; GÓMEZ JC; CHOPITA N; SLAVUTSKY IR

Evidence of chromosome instability in chronic pancreatitis

JOURNAL OF EXPERIMENTAL AND CLINICAL CANCER RESEARCH; Año: 2000 vol. 19 p. 513 - 517

COTTLIAR A; FUNDIA AF; BOERR L; SAMBUELLI A; NEGREIRA S; GIL A; GÓMEZ JC; CHOPITA N; BERNEDO A; SLAVUTSKY IR

High frequencies of telomeric associations, chromosome aberrations, and sister chromatid exchanges in ulcerative colitis

AMERICAN JOURNAL OF GASTROENTEROLOGY; Año: 2000 vol. 95 p. 2301 - 2307

ARIELA FUNDIA; MARÍA GOROSTIAGA; MARTA MUDRY

Expression of common fragile sites in two Ceboidea species: Saimiri boliviensis and Alouatta caraya (Primates: Platyrrhini)

GENETICS SELECTION EVOLUTION; Lugar: París; Año: 2000 vol. 32 p. 87 - 97

ARIELA F. FUNDIA; SUSANA H. ACEVEDO; IRENE B. LARRIPA

Chromosomal instability in chronic myeloid leukemia: Philadelphia breakpoints are independent of spontaneous breakage and fragile sites

HAEMATOLOGICA; Año: 2000 vol. 85 p. 1104 - 1106

FUNDIA AF; GIERE I; LARRIPA IB; SLAVUTSKY IR

Spontaneous breakage and fragile site expression in chronic lymphocytic leukemia

CANCER GENETICS AND CYTOGENETICS; Lugar: Nueva York; Año: 1998 vol. 103 p. 144 - 148

FUNDIA AF; LARRIPA IB

Participación de los sitios frágiles en cáncer

MEDICINA (BUENOS AIRES); Lugar: Buenos Aires; Año: 1996 vol. 56 p. 727 - 732

FUNDIA AF; GÓMEZ JC; MAURIÑO E; BOERR L; BAI JC; LARRIPA IB; SLAVUTSKY IR

Chromosome instability in untreated adult celiac patients

Acta Paediatr Suppl; Lugar: Oslo; Año: 1996 vol. 412 p. 82 - 84

FUNDIA AF; GORLA N; LARRIPA IB

Non-random distribution of spontaneous chromosome aberrations in two Bloom syndrome patients

HEREDITAS; Lugar: Londres; Año: 1995 vol. 122 p. 239 - 243

FUNDIA AF; GORLA N; LARRIPA IB

Spontaneous chromosome aberrations in Fanconi anemia patients are located at fragile sites and acute myeloid leukemia breakpoints

HEREDITAS; Lugar: Londres; Año: 1994 vol. 120 p. 47 - 50

FUNDIA AF; GONZALEZ CID M; BAI J; GÓMEZ JC; MAZURE R; VAZQUEZ H; LARRIPA IB; SLAVUTSKY IR

Chromosome instability in lymphocytes from patients with celiac disease.

CLINICAL GENETICS; Lugar: Londres; Año: 1994 vol. 45 p. 57 - 61

FUNDIA, AF; GORLA N; BONDUEL M M; AZPILLICUETA O; LEJARRAGA H; SACKMAN MURIEL F; LARRIPA IB

Increased expression of 5q31 fragile site in a Bloom syndrome family

HUMAN GENETICS.; Lugar: Berlin; Año: 1992 vol. 89 p. 569 - 572

ARIELA F FUNDIA; IRENE B. LARRIPA

Induction of fragile sites by chemical and physical agents

ACTA PHISIOLOGICA, PHARMACOLOGICA ET THERAPEUTICA LATIONOAMERICANA; Año: 1991 vol. 41 p. 359 - 367

GORLA N; BONDUEL M M; ARIELA F FUNDIA; LEJARRAGA H; SACKMAN MURIEL F; IRENE B. LARRIPA

Bloom syndrome. Report of 2 cases

MEDICINA (BUENOS AIRES); Lugar: Buenos Aires; Año: 1990 vol. 50 p. 89 - 90

ARIELA F FUNDIA; IRMA SLAVUTSKY; IRENE B. LARRIPA

Expression of new fragile sites detected in lymphoproliferative processes

SANGRE (Barc); Lugar: Barcelona; Año: 1990 vol. 35 p. 4 - 9

FUNDIA AF; LARRIPA IB

Coincidence in fragile site expression with fluorodeoxyuridine and bromodeoxyuridine

CANCER GENETICS AND CYTOGENETICS; Lugar: Nueva York; Año: 1989 vol. 41 p. 41 - 48