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List of works by Lygia Veiga Pereira

A Report from a Workshop of the International Stem Cell Banking Initiative, Held in Collaboration of Global Alliance for iPSC Therapies and the Harvard Stem Cell Institute, Boston, 2017

scientific article published on 06 August 2019

A new mouse model for marfan syndrome presents phenotypic variability associated with the genetic background and overall levels of Fbn1 expression

scientific article

A survey of parameters involved in the establishment of new lines of human embryonic stem cells.

scientific article

Aberrant patterns of X chromosome inactivation in bovine clones

scientific article

Allele-specific X-linked gene activity in normal human cells assayed by expressed single nucleotide polymorphisms (cSNPs).

scientific article

Association of thoracic spine deformity and cardiovascular disease in a mouse model for Marfan syndrome

scientific article published on 14 November 2019

Candidate gene linkage analysis indicates genetic heterogeneity in Marfan syndrome ⬇️

scientific article published on July 29, 2011

Establishment of a Brazilian line of human embryonic stem cells in defined medium: implications for cell therapy in an ethnically diverse population.

scientific article published on 18 August 2010

Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndrome.

scientific article published on July 1993

Human dental pulp cells: a new source of cell therapy in a mouse model of compressive spinal cord injury

scientific article published on 8 August 2011

Is HSPG2 a modifier gene for Marfan syndrome?

scientific article published on 08 June 2020

Isolation and characterization of a population of immature dental pulp stem cells expressing OCT-4 and other embryonic stem cell markers

scientific article

Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.

scientific article

Mutations of extracellular matrix components in vascular disease.

scientific article published in June 1999

Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1

scientific article

Pluripotent Reprogramming of Fibroblasts by Lentiviralmediated Insertion of SOX2, C-MYC, and TCL-1A

article

Random X inactivation and extensive mosaicism in human placenta revealed by analysis of allele-specific gene expression along the X chromosome

scientific article

Retroviral-mediated transfer of the human acid sphingomyelinase cDNA: correction of the metabolic defect in cultured Niemann-Pick disease cells ⬇️

scientific article published on April 15, 1992

Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage

scientific article

Structural organization and complete nucleotide sequence of the gene encoding human acid sphingomyelinase (SMPD1) ⬇️

scientific article published on February 1, 1992

Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome

scientific article published in October 1997

Tay-Sachs disease in Brazilian patients: prevalence of the IVS7+1g>c mutation.

scientific article published in January 2004

The fibrillins

scientific article

X chromosome inactivation: how human are mice?

scientific article

XIST repression in the absence of DNMT1 and DNMT3B.

scientific article

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