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ING1 and ING2: multifaceted tumor suppressor genes

Cellular and molecular life sciences : CMLS, 2013-10, Vol.70 (20), p.3753-3772

2013

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The ING tumor suppressor genes: Status in human tumors

Cancer letters, 2014-04, Vol.345 (1), p.1-16

2014

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Newly identified tumor suppressor functions of ING proteins

Current opinion in pharmacology, 2023-02, Vol.68, p.102324-102324, Article 102324

2023

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Focus-ING on DNA Integrity: Implication of ING Proteins in Cell Cycle Regulation and DNA Repair Modulation

Cancers, 2019-12, Vol.12 (1), p.58

2019

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Afatinib or Bevacizumab in combination with Osimertinib efficiently control tumor development in orthotopic murine models of non-small lung cancer

PloS one, 2024-06, Vol.19 (6), p.e0304914

2024

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ING3 is required for ATM signaling and DNA repair in response to DNA double strand breaks

Cell death and differentiation, 2019-11, Vol.26 (11), p.2344-2357

2019

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ING2 tumor suppressive protein translocates into mitochondria and is involved in cellular metabolism homeostasis

Oncogene, 2021-06, Vol.40 (24), p.4111-4123

2021

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The Identification of New c-FLIP Inhibitors for Restoring Apoptosis in TRAIL-Resistant Cancer Cells

Current issues in molecular biology, 2024-01, Vol.46 (1), p.710-728

2024

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Regulat-INGs in tumors and diseases: Focus on ncRNAs

Cancer letters, 2019-04, Vol.447, p.66-74

2019

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Orthotopic model of lung cancer: isolation of bone micro-metastases after tumor escape from Osimertinib treatment

BMC cancer, 2021-05, Vol.21 (1), p.530-530, Article 530

2021

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Noninvasive Urine-Based Tests to Diagnose or Detect Recurrence of Bladder Cancer

Cancers, 2021-04, Vol.13 (7), p.1650

2021

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Exploiting ING2 Epigenetic Modulation as a Therapeutic Opportunity for Non-Small Cell Lung Cancer

Cancers, 2019-10, Vol.11 (10), p.1601

2019

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Preclinical Models for Acquired Resistance to Third-Generation EGFR Inhibitors in NSCLC: Functional Studies and Drug Combinations Used to Overcome Resistance

Frontiers in oncology, 2022-04, Vol.12, p.853501-853501

2022

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Characterization of the Peri-Membrane Fluorescence Phenomenon Allowing the Detection of Urothelial Tumor Cells in Urine

Cancers, 2022-04, Vol.14 (9), p.2171

2022

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The new tumor suppressor genes ING: Genomic structure and status in cancer

International journal of cancer, 2008-10, Vol.123 (7), p.1483-1490

2008

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tert -Butylphenolic Derivatives from Paenibacillus odorifer -A Case of Bioconversion

Molecules (Basel, Switzerland), 2018-08, Vol.23 (8), p.1951

2018

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Reply: Standardized procedure for bone marrow MSCs preparation for clinical use

Stem cells (Dayton, Ohio), 2016-07, Vol.34 (7), p.1994-1995

2016

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Correction to: Orthotopic model of lung cancer: isolation of bone micro-metastases after tumor escape from Osimertinib treatment

BMC cancer, 2021-05, Vol.21 (1), p.574-574, Article 574

2021

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SharING out the roles in replicatING DNA

Cell cycle (Georgetown, Tex.), 2009-11, Vol.8 (22), p.3623-3624

2009

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Genotoxic stress triggers the activation of IRE1α-dependent RNA decay to modulate the DNA damage response

Nature communications, 2020-05, Vol.11 (1), p.2401-2401, Article 2401

2020

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When Endoplasmic Reticulum Proteostasis Meets the DNA Damage Response

Trends in cell biology, 2020-11, Vol.30 (11), p.881-891

2020

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ING2 controls the G1 to S-phase transition by regulating p21 expression

Cell cycle (Georgetown, Tex.), 2010-10, Vol.9 (19), p.3984-3990

2010

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SUMOylation of the ING1b tumor suppressor regulates gene transcription

Carcinogenesis (New York), 2014-10, Vol.35 (10), p.2214-2223

2014

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ING2 controls the progression of DNA replication forks to maintain genome stability

EMBO reports, 2009-10, Vol.10 (10), p.1168-1174

2009

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Simple elaboration of drug-SPION nanocapsules (hybridosomes®) by solvent shifting: Effect of the drug molecular structure and concentration

International journal of pharmaceutics, 2024-01, Vol.649, p.123645-123645, Article 123645

2024

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ING1 and ING2: multifaceted tumor suppressor genes

The ING tumor suppressor genes: Status in human tumors

Newly identified tumor suppressor functions of ING proteins

Focus-ING on DNA Integrity: Implication of ING Proteins in Cell Cycle Regulation and DNA Repair Modulation

Afatinib or Bevacizumab in combination with Osimertinib efficiently control tumor development in orthotopic murine models of non-small lung cancer

ING3 is required for ATM signaling and DNA repair in response to DNA double strand breaks

ING2 tumor suppressive protein translocates into mitochondria and is involved in cellular metabolism homeostasis

The Identification of New c-FLIP Inhibitors for Restoring Apoptosis in TRAIL-Resistant Cancer Cells

Regulat-INGs in tumors and diseases: Focus on ncRNAs

Orthotopic model of lung cancer: isolation of bone micro-metastases after tumor escape from Osimertinib treatment

Noninvasive Urine-Based Tests to Diagnose or Detect Recurrence of Bladder Cancer

Exploiting ING2 Epigenetic Modulation as a Therapeutic Opportunity for Non-Small Cell Lung Cancer

Preclinical Models for Acquired Resistance to Third-Generation EGFR Inhibitors in NSCLC: Functional Studies and Drug Combinations Used to Overcome Resistance

Characterization of the Peri-Membrane Fluorescence Phenomenon Allowing the Detection of Urothelial Tumor Cells in Urine

The new tumor suppressor genes ING: Genomic structure and status in cancer

tert -Butylphenolic Derivatives from Paenibacillus odorifer -A Case of Bioconversion

Reply: Standardized procedure for bone marrow MSCs preparation for clinical use

Correction to: Orthotopic model of lung cancer: isolation of bone micro-metastases after tumor escape from Osimertinib treatment

SharING out the roles in replicatING DNA

Genotoxic stress triggers the activation of IRE1α-dependent RNA decay to modulate the DNA damage response

When Endoplasmic Reticulum Proteostasis Meets the DNA Damage Response

ING2 controls the G1 to S-phase transition by regulating p21 expression

SUMOylation of the ING1b tumor suppressor regulates gene transcription

ING2 controls the progression of DNA replication forks to maintain genome stability

Simple elaboration of drug-SPION nanocapsules (hybridosomes®) by solvent shifting: Effect of the drug molecular structure and concentration

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