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List of works by Liliana Dain

CYP21A2 mutation update: Comprehensive analysis of databases and published genetic variants

scientific article published on 16 October 2017

Classical and nonclassical 21-hydroxylase deficiency: a molecular study of Argentine patients.

scientific article published in February 2002

Controversial role of inhibin alpha-subunit gene in the aetiology of premature ovarian failure

scientific article published on 05 January 2006

Distribution of FMR1 and FMR2 Repeats in Argentinean Patients with Primary Ovarian Insufficiency.

scientific article

Expression of fragile X mental retardation protein and Fmr1 mRNA during folliculogenesis in the rat

scientific journal article

Functional studies of p.R132C, p.R149C, p.M283V, p.E431K, and a novel c.652-2A>G mutations of the CYP21A2 gene

scientific article

Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects

article

Genetic characterization of a large cohort of Argentine 21-hydroxylase deficiency

scientific article published on 14 April 2020

Genetics and genomic medicine in Argentina

scientific article published on 05 February 2019

Gonadotropin-releasing hormone agonist affects rat ovarian follicle development by interfering with FSH and growth factors on the prevention of apoptosis.

scientific article

Human granulosa cells express HLA-DR antigen and are capable of synthesizing interleukin-1

scientific article published on 01 November 1995

Implementation of chromosomal microarrays in a cohort of patients with intellectual disability at the Argentinean public health system

scientific article published on 13 September 2020

In vitro analysis of the cellular proliferative response to 17-beta-estradiol of human breast cancer

scientific article published on 01 May 1988

Misregulation effect of a novel allelic variant in the Z promoter region found in cis with the CYP21A2 p.P482S mutation: implications for 21-hydroxylase deficiency

scientific article published on 17 July 2015

Mosaic trisomy 9 syndrome with unusual phenotype

scientific article published on 01 October 1985

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.

scientific article published on 24 January 2018

Putative association of a mutant ROM1 allele with retinitis pigmentosa

scientific article published on 01 June 1997

Screening of FSH receptor gene in Argentine women with premature ovarian failure (POF).

scientific article

Structure-based activity prediction of CYP21A2 stability variants: A survey of available gene variations.

scientific article published on 14 December 2016

Update of genetic variants in the NKX2-5 gene

scientific article published on 05 May 2020

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