Lista de obras - Francesca D Ciccarelli - Dominio Público Uruguay

A SIMPLI (Single-cell Identification from MultiPLexed Images) approach for spatially-resolved tissue phenotyping at single-cell resolution

artículo científico publicado en 2022

A complex prediction: three-dimensional model of the yeast exosome.

artículo científico publicado en 2002

A protocol for the update of references to scientific literature in biological databases.

artículo científico publicado en 2003

AMOP, a protein module alternatively spliced in cancer cells

scientific article published on 01 March 2002

An analysis of IL-36 signature genes and individuals with IL1RL2 knockout mutations validates IL-36 as a psoriasis therapeutic target. ⬇️

artículo científico publicado en 2017

CASH--a beta-helix domain widespread among carbohydrate-binding proteins

artículo científico publicado en 2002

Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource

artículo científico publicado en 2022

Complex genomic rearrangements lead to novel primate gene function

artículo científico publicado en 2005

Corrigendum: Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

artículo científico publicado en 2015

Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas

artículo científico publicado en 2014

Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma

artículo científico publicado en 2013

Family expansion and gene rearrangements contributed to the functional specialization of PRDM genes in vertebrates.

artículo científico publicado en 2007

FancyGene: dynamic visualization of gene structures and protein domain architectures on genomic loci.

artículo científico publicado en 2009

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

artículo científico publicado en 2005

Genetic Redundancy, Functional Compensation, and Cancer Vulnerability

artículo científico publicado en 2016

Genome evolution reveals biochemical networks and functional modules

artículo científico publicado en 2003

Genome-wide analysis of mRNAs regulated by the THO complex in Drosophila melanogaster

artículo científico publicado en 2004

Global repression of cancer gene expression in a zebrafish model of melanoma is linked to epigenetic regulation

artículo científico publicado en 2009

MEGA-V: detection of variant gene sets in patient cohorts

artículo científico publicado en 2016

Mapping the Human Kinome in Response to DNA Damage

artículo científico publicado en 2019

Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

artículo científico publicado en 2014

Modification of Gene Duplicability during the Evolution of Protein Interaction Network ⬇️

artículo científico publicado el 7 de abril de 2011

Mutations differ in normal and cancer cells of the oesophagus

scientific article published on 01 January 2019

NCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomes

artículo científico publicado en 2014

NCG 5.0: updates of a manually curated repository of cancer genes and associated properties from cancer mutational screenings.

artículo científico publicado en 2015

NEAT: a domain duplicated in genes near the components of a putative Fe3+ siderophore transporter from Gram-positive pathogenic bacteria

artículo científico publicado en 2002

Network of Cancer Genes (NCG 3.0): integration and analysis of genetic and network properties of cancer genes

artículo científico publicado en 2012

Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes

artículo científico publicado en 2010

Non-random retention of protein-coding overlapping genes in Metazoa

artículo científico publicado en 2008

Nonsense-mediated mRNA decay in Drosophila: at the intersection of the yeast and mammalian pathways

artículo científico publicado en 2003

Patient-specific cancer genes contribute to recurrently perturbed pathways and establish therapeutic vulnerabilities in esophageal adenocarcinoma

scientific article published on 15 July 2019

Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.

artículo científico publicado en 2016

Preface. The seventh RECOMB-CG Workshop, September 27–29, 2009, Alfréd Rényi Institute of Mathematics, Budapest, Hungary

artículo científico publicado en 2010

RanBP2/Nup358 provides a major binding site for NXF1-p15 dimers at the nuclear pore complex and functions in nuclear mRNA export.

artículo científico publicado en 2004

Recessive cancer genes engage in negative genetic interactions with their functional paralogs.

artículo científico publicado en 2013

SMART 4.0: towards genomic data integration

artículo científico publicado en 2004

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

artículo científico publicado en 2002

Spatiotemporal segregation of human marginal zone and memory B cell populations in lymphoid tissue

artículo científico publicado en 2018

Structural analysis of the RZZ complex reveals common ancestry with multisubunit vesicle tethering machinery

artículo científico publicado en 2010

Synthetic lethal interaction between the tumour suppressor STAG2 and its paralog STAG1.

artículo científico publicado en 2017

Tandem repeats modify the structure of human genes hosted in segmental duplications

artículo científico publicado en 2009

The (r)evolution of cancer genetics

artículo científico publicado en 2010

The KIND module: a putative signalling domain evolved from the C lobe of the protein kinase fold

artículo científico publicado en 2003

The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens

artículo científico publicado en 2019

The PAM domain, a multi-protein complex-associated module with an all-alpha-helix fold

artículo científico publicado en 2003

The WHy domain mediates the response to desiccation in plants and bacteria

artículo científico publicado en 2004

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

artículo científico publicado en 2003

Toward Automatic Reconstruction of a Highly Resolved Tree of Life

artículo científico publicado en 2006

Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability

artículo científico publicado en 2010

Very-KIND is a novel nervous system specific guanine nucleotide exchange factor for Ras GTPases

artículo científico publicado en 2005

Lista de obras de Francesca D Ciccarelli

A SIMPLI (Single-cell Identification from MultiPLexed Images) approach for spatially-resolved tissue phenotyping at single-cell resolution

A complex prediction: three-dimensional model of the yeast exosome.

A protocol for the update of references to scientific literature in biological databases.

AMOP, a protein module alternatively spliced in cancer cells

An analysis of IL-36 signature genes and individuals with IL1RL2 knockout mutations validates IL-36 as a psoriasis therapeutic target. ⬇️

CASH--a beta-helix domain widespread among carbohydrate-binding proteins

Comparative assessment of genes driving cancer and somatic evolution in non-cancer tissues: an update of the Network of Cancer Genes (NCG) resource

Complex genomic rearrangements lead to novel primate gene function

Corrigendum: Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Deep sequencing of the X chromosome reveals the proliferation history of colorectal adenomas

Endogenous retrotransposition activates oncogenic pathways in hepatocellular carcinoma

Family expansion and gene rearrangements contributed to the functional specialization of PRDM genes in vertebrates.

FancyGene: dynamic visualization of gene structures and protein domain architectures on genomic loci.

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

Genetic Redundancy, Functional Compensation, and Cancer Vulnerability

Genome evolution reveals biochemical networks and functional modules

Genome-wide analysis of mRNAs regulated by the THO complex in Drosophila melanogaster

Global repression of cancer gene expression in a zebrafish model of melanoma is linked to epigenetic regulation

MEGA-V: detection of variant gene sets in patient cohorts

Mapping the Human Kinome in Response to DNA Damage

Massive gene amplification drives paediatric hepatocellular carcinoma caused by bile salt export pump deficiency

Modification of Gene Duplicability during the Evolution of Protein Interaction Network ⬇️

Mutations differ in normal and cancer cells of the oesophagus

NCG 4.0: the network of cancer genes in the era of massive mutational screenings of cancer genomes

NCG 5.0: updates of a manually curated repository of cancer genes and associated properties from cancer mutational screenings.

NEAT: a domain duplicated in genes near the components of a putative Fe3+ siderophore transporter from Gram-positive pathogenic bacteria

Network of Cancer Genes (NCG 3.0): integration and analysis of genetic and network properties of cancer genes

Network of Cancer Genes: a web resource to analyze duplicability, orthology and network properties of cancer genes

Non-random retention of protein-coding overlapping genes in Metazoa

Nonsense-mediated mRNA decay in Drosophila: at the intersection of the yeast and mammalian pathways

Patient-specific cancer genes contribute to recurrently perturbed pathways and establish therapeutic vulnerabilities in esophageal adenocarcinoma

Patients with genetically heterogeneous synchronous colorectal cancer carry rare damaging germline mutations in immune-related genes.

Preface. The seventh RECOMB-CG Workshop, September 27–29, 2009, Alfréd Rényi Institute of Mathematics, Budapest, Hungary

RanBP2/Nup358 provides a major binding site for NXF1-p15 dimers at the nuclear pore complex and functions in nuclear mRNA export.

Recessive cancer genes engage in negative genetic interactions with their functional paralogs.

SMART 4.0: towards genomic data integration

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

Spatiotemporal segregation of human marginal zone and memory B cell populations in lymphoid tissue

Structural analysis of the RZZ complex reveals common ancestry with multisubunit vesicle tethering machinery

Synthetic lethal interaction between the tumour suppressor STAG2 and its paralog STAG1.

Tandem repeats modify the structure of human genes hosted in segmental duplications

The (r)evolution of cancer genetics

The KIND module: a putative signalling domain evolved from the C lobe of the protein kinase fold

The Network of Cancer Genes (NCG): a comprehensive catalogue of known and candidate cancer genes from cancer sequencing screens

The PAM domain, a multi-protein complex-associated module with an all-alpha-helix fold

The WHy domain mediates the response to desiccation in plants and bacteria

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

Toward Automatic Reconstruction of a Highly Resolved Tree of Life

Ultradeep sequencing of a human ultraconserved region reveals somatic and constitutional genomic instability

Very-KIND is a novel nervous system specific guanine nucleotide exchange factor for Ras GTPases