Lucia Nacci

Milan, Italy

Last Updated: 09/26/2026

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Found 10 publications

High-Resolution Laser Microdissection to Investigate Transcriptional States in Formalin-Fixed Paraffin-Embedded Samples.

High-Resolution Laser Microdissection to Investigate Transcriptional States in Formalin-Fixed Paraffin-Embedded Samples.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: February 02, 2026

Native extracellular matrix probes to target patient- and tissue-specific cell-microenvironment interactions by force spectroscopy.

Native extracellular matrix probes to target patient- and tissue-specific cell-microenvironment interactions by force spectroscopy.

Journal: Nanoscale

Published: September 13, 2023

Mapping functional to morphological variation reveals the basis of regional extracellular matrix subversion and nerve invasion in pancreatic cancer.

Mapping functional to morphological variation reveals the basis of regional extracellular matrix subversion and nerve invasion in pancreatic cancer.

Journal: Cancer cell

Published: December 21, 2022

Genetics for understanding the clinical features of Shwachman-Diamond Syndrome.

Genetics for understanding the clinical features of Shwachman-Diamond Syndrome.

Journal: British journal of haematology

Published: December 22, 2018

Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations.

Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations.

Journal: British journal of haematology

Published: September 11, 2018

Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.

Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.

Journal: Pediatric blood & cancer

Published: October 10, 2016

Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients.

Structural variation in SBDS gene, with loss of exon 3, in two Shwachman-Diamond patients.

Journal: Blood cells, molecules & diseases

Published: May 26, 2016

Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.

Parental origin of the deletion del(20q) in Shwachman-Diamond patients and loss of the paternally derived allele of the imprinted L3MBTL1 gene.

Journal: Genes, chromosomes & cancer

Published: May 11, 2016

Radiosensitivity in lymphoblastoid cell lines derived from Shwachman-Diamond syndrome patients.

Radiosensitivity in lymphoblastoid cell lines derived from Shwachman-Diamond syndrome patients.

Journal: Radiation protection dosimetry

Published: April 15, 2015

Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome.

Absence of acquired copy number neutral loss of heterozygosity (CN-LOH) of chromosome 7 in a series of 10 patients with Shwachman-Diamond syndrome.

Journal: British journal of haematology

Published: February 04, 2014

Showing 1-10 of 10

Last Updated: 09/26/2026