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List of works by Sara Frías

7p15 deletion as the cause of hand-foot-genital syndrome: a case report, literature review and proposal of a minimum region for this phenotype

scientific article

A Boolean network model of human gonadal sex determination

scientific article

A Boolean network model of the FA/BRCA pathway.

scientific article published on 20 January 2012

A Strategy to Detect Chromosomal Abnormalities in Children With Acute Lymphoblastic Leukemia

scientific article published on 01 May 2004

A clinical syndrome associated with dup(5p)

scientific article published on 01 November 1982

Acrocentric cryptic translocation associated with nondisjunction of chromosome 21

scientific article published on 01 January 2008

An assessment of immediate DNA damage to occupationally exposed workers to low dose ionizing radiation by using the comet assay

scientific article published on 01 January 2010

Analysis of gene rearrangements using a fluorescence in situ hybridization method in Mexican patients with acute lymphoblastic leukemia: experience at a single institution

scientific article published on 01 July 2008

Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits.

scientific article

Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndrome.

scientific article published on May 1997

Cytogenetics in acute lymphoblastic leukemia in Mexican children: an institutional experience

scientific article published on 01 May 2001

DEB test for Fanconi anemia detection in patients with atypical phenotypes

scientific article published on 01 January 2004

DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation.

scientific article published on 12 November 2017

Delayed repair of DNA damage by ionizing radiation in cells from patients with juvenile systemic lupus erythematosus and rheumatoid arthritis.

scientific article published in January 1997

Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics.

scientific article

Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: experience at a single institution

scientific article published on 01 October 2005

Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring

scientific article published on 01 September 2002

Detection of short-term chromosomal damage due to therapeutic 131I exposure in patients with thyroid cancer.

scientific article published in January 2010

Differential expression of TP53 associated genes in Fanconi anemia cells after mitomycin C and hydroxyurea treatment.

scientific article

Effect of hydroxyurea and normal plasma on DNA synthesis in lymphocytes from Fanconi anemia patients

scientific article published on 01 October 1996

Effect of mitomycin C and bromodeoxyuridine on Fanconi anemia lymphocytes

scientific article published on 01 January 1991

External ear microRNA expression profiles during mouse development.

scientific article

FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México.

scientific article published in May 2019

Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG

scientific article published on 21 February 2022

Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process

scientific article

Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease.

scientific article published on January 2011

Genetic heterogenicity study in Fanconi's anemia by the addition of plasma

scientific article published on July 1986

Genotypes B and C hepatocellular carcinoma–associated hepatitis B virus pre‐S mutants: their detection among F1b and A2 – but not F4 – isolates from Argentina ⬇️

scientific article published on May 21, 2012

Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in <i>TP53-</i> and <i>BRCA1</i>-Deficient Cells

scientific article published on 29 January 2021

Heterogeneous Diagnoses Underlying Radial Ray Anomalies.

scientific article published on 17 December 2016

Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells

scientific article published on 6 February 2015

Identification of chromosome anomalies by G banding in patients with apparently normal karyotype (author's transl)

scientific article published on April 1, 1978

In Reference to Fanconi Anemia and Laron Syndrome

scientific article published on 07 February 2018

Interstitial deletion of 2q24.2: further delineation of an emerging syndrome associated with intellectual disability, severe hypotonia and moderate intrauterine growth restriction

scientific article published on 19 December 2013

Interstitial deletion of long arm of chromosome 13.

scientific article published in January 1984

Local and circulating microchimerism is associated with hypersensitivity pneumonitis.

scientific article published on 12 April 2007

Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma

scientific article published on 28 December 2020

Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues.

scientific article published on 24 June 2016

Mitomycin C effect on Robertsonian translocations

scientific article published on 01 January 1988

Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature.

scientific article published on January 2008

NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model.

scientific article published on January 2015

NOVP chemotherapy for Hodgkin's disease transiently induces sperm aneuploidies associated with the major clinical aneuploidy syndromes involving chromosomes X, Y, 18, and 21.

scientific article

Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review

scientific article published on 07 September 2020

Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma

article

Partial trisomy 16q resulting from maternal translocation 11p/16q

scientific article published on 01 January 1984

Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14)(p11;p11)

scientific article published on 01 October 1978

Persistent genomic instability in peripheral blood lymphocytes from Hodgkin lymphoma survivors.

scientific article published on 21 March 2012

Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples

scientific article published on 23 October 2019

RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy

scientific article

The clastogenic response of the 1q12 heterochromatic region to DNA cross-linking agents is independent of the Fanconi anaemia pathway

scientific article published in August 2002

Unusual mixed gonadal dysgenesis associated with Müllerian duct persistence, polygonadia, and a 45,X/46,X,idic(Y)(p) karyotype.

scientific article published in August 2005

[C band polymorphisms of chromosomes 1, 9 and 16 in families with children with Down's syndrome (author's transl)]

scientific article published on 01 January 1982

[Cytogenetics in pediatric practice. Experience of 10 years (author's transl)]

scientific article published on 01 April 1981

[Detection of aneuploidies using in situ hybridization in cells of the oral mucosa]

scientific article published on 01 September 1996

[Effects of the addition of conditioned media on the response of Fanconi anemia lymphocytes to mitomycin C]

scientific article published on 01 October 1992

[Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes]

scientific article published on 01 January 1996

[Use of a test exposing lymphocytes to mitomycin C in the diagnosis of Fanconi's anemia]

scientific article published on 01 July 1984

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