Lista de obras - Cornel Popovici - Dominio Público Uruguay

A pair as a minimum: the two fibroblast growth factors of the nematode Caenorhabditis elegans

artículo científico publicado en 2005

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene

artículo científico publicado en 2003

An evolutionary history of the FGF superfamily.

artículo científico publicado en 2005

CDKN2A/B Deletion and Double-hit Mutations of the MAPK Pathway Underlie the Aggressive Behavior of Langerhans Cell Tumors.

artículo científico publicado en 2017

Caenorhabditis elegans receptors related to mammalian vascular endothelial growth factor receptors are expressed in neural cells

artículo científico publicado en 2002

Characterization of the novel Sezary lymphoma cell line BKP1.

artículo científico publicado en 2014

Chromosome arm 8p and cancer: a fragile hypothesis.

artículo científico publicado en 2003

Chromosome region 8p11-p21: Refined mapping and molecular alterations in breast cancer

artículo científico publicado en 1998

Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.

artículo científico publicado en 2010

Coparalogy: physical and functional clusterings in the human genome.

artículo científico publicado en 2001

Direct and heterologous approaches to identify the LET-756/FGF interactome

artículo científico publicado en 2006

E6a2 BCR-ABL fusion with BCR exon 5-deleted transcript in a Philadelphia positive CML responsive to Imatinib.

artículo científico publicado en 2005

Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3).

artículo científico publicado en 2002

Fluorescent in situ hybridization (FISH) on corneal impression cytology specimens (CICS): study of epithelial cell survival after keratoplasty

scientific article published on 22 February 2011

Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history.

artículo científico publicado en 2014

Intracellular trafficking of LET-756, a fibroblast growth factor of C. elegans, is controlled by a balance of export and nuclear signals

artículo científico publicado en 2006

Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes

article

Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer.

artículo científico publicado en 2003

Neural tissue in ascidian embryos is induced by FGF9/16/20, acting via a combination of maternal GATA and Ets transcription factors

artículo científico publicado en 2003

Phylogenetic analysis of Ciona intestinalis gene superfamilies supports the hypothesis of successive gene expansions.

artículo científico publicado en 2004

Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene

artículo científico publicado en 2002

Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients.

artículo científico publicado en 2010

Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study

scientific article published on 18 October 2016

The power of high-resolution non-targeted array-CGH in identifying intragenic rearrangements responsible for Cohen syndrome

scientific article published on 17 February 2011

Variant MYST4-CBP gene fusion in a t(10;16) acute myeloid leukaemia.

artículo científico publicado en 2004

Whole ARX gene duplication is compatible with normal intellectual development

artículo científico publicado en 2014

Y253H mutation appearing in a micro-BCR-ABL (e19a2) CML

scientific article published on 06 April 2007

let-756, a C. elegans fgf essential for worm development.

artículo científico publicado en 1999

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12

scientific article published on 01 February 1998

Lista de obras de Cornel Popovici

A pair as a minimum: the two fibroblast growth factors of the nematode Caenorhabditis elegans

A recurrent chromosome translocation breakpoint in breast and pancreatic cancer cell lines targets the neuregulin/NRG1 gene

An evolutionary history of the FGF superfamily.

CDKN2A/B Deletion and Double-hit Mutations of the MAPK Pathway Underlie the Aggressive Behavior of Langerhans Cell Tumors.

Caenorhabditis elegans receptors related to mammalian vascular endothelial growth factor receptors are expressed in neural cells

Characterization of the novel Sezary lymphoma cell line BKP1.

Chromosome arm 8p and cancer: a fragile hypothesis.

Chromosome region 8p11-p21: Refined mapping and molecular alterations in breast cancer

Coffin-Siris syndrome with multiple congenital malformations and intrauterine death: towards a better delineation of the severe end of the spectrum.

Coparalogy: physical and functional clusterings in the human genome.

Direct and heterologous approaches to identify the LET-756/FGF interactome

E6a2 BCR-ABL fusion with BCR exon 5-deleted transcript in a Philadelphia positive CML responsive to Imatinib.

Endogenous retroviral sequence is fused to FGFR1 kinase in the 8p12 stem-cell myeloproliferative disorder with t(8;19)(p12;q13.3).

Fluorescent in situ hybridization (FISH) on corneal impression cytology specimens (CICS): study of epithelial cell survival after keratoplasty

Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history.

Intracellular trafficking of LET-756, a fibroblast growth factor of C. elegans, is controlled by a balance of export and nuclear signals

Intragenic rearrangements in X-linked intellectual deficiency: results of a-CGH in a series of 54 patients and identification of TRPC5 and KLHL15 as potential XLID genes

Loss of FHIT protein expression is a marker of adverse evolution in good prognosis localized breast cancer.

Neural tissue in ascidian embryos is induced by FGF9/16/20, acting via a combination of maternal GATA and Ets transcription factors

Phylogenetic analysis of Ciona intestinalis gene superfamilies supports the hypothesis of successive gene expansions.

Reciprocal translocations in breast tumor cell lines: cloning of a t(3;20) that targets the FHIT gene

Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patients.

Targeted NGS, array-CGH, and patient-derived tumor xenografts for precision medicine in advanced breast cancer: a single-center prospective study

The power of high-resolution non-targeted array-CGH in identifying intragenic rearrangements responsible for Cohen syndrome

Variant MYST4-CBP gene fusion in a t(10;16) acute myeloid leukaemia.

Whole ARX gene duplication is compatible with normal intellectual development

Y253H mutation appearing in a micro-BCR-ABL (e19a2) CML

let-756, a C. elegans fgf essential for worm development.

t(6;8), t(8;9) and t(8;13) translocations associated with stem cell myeloproliferative disorders have close or identical breakpoints in chromosome region 8p11-12