J. Feunteun

发表

High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors.

A. Vincent-Salomon, O. Delattre, M. Stern, 2009, Cancer research.

Dynamic Changes of BRCA1 Subnuclear Location and Phosphorylation State Are Initiated by DNA Damage

Ralph Scully, D. Livingston, Junjie Chen, 1997, Cell.

Association of BRCA1 with Rad51 in Mitotic and Meiotic Cells

Yonghong Xiao, Ralph Scully, Yonghong Xiao, 1997, Cell.

The protein phosphatase 2A regulatory subunit PR70 is a gonosomal melanoma tumor suppressor gene

D. Schadendorf, C. Greenwood, F. Pontén, 2016, Science Translational Medicine.

Sequence homology between polyoma virus, simian virus 40, and a papilloma-producing virus from a Syrian hamster: evidences for highly conserved sequences.

F. Vogel, S. Scherneck, J. Feunteun, 1984, Virology.

Genetic evidence of a precisely tuned dysregulation in the hypoxia signaling pathway during oncogenesis.

S. Richard, W. Kaelin, William Y. Kim, 2014, Cancer research.

Tumor cell malignancy: A complex trait built through reciprocal interactions between tumors and tissue-body system

S. Delaloge, J. Feunteun, Paul Ostyn, 2022, iScience.

PML induces a novel caspase-independent death process

M. Koken, J. Ameisen, J. Feunteun, 1998, Nature Genetics.

Loss of FADD protein expression results in a biased Fas-signaling pathway and correlates with the development of tumoral status in thyroid follicular cells

L. Rénia, V. Devauchelle, J. Feunteun, 2003, Oncogene.

Development of medullary thyroid carcinoma in transgenic mice expressing the RET protooncogene altered by a multiple endocrine neoplasia type 2A mutation.

G. Lenoir, B. Caillou, J. Feunteun, 1997, Proceedings of the National Academy of Sciences of the United States of America.

A 1-kb Alu-mediated germ-line deletion removing BRCA1 exon 17.

G. Lenoir, S. Mazoyer, H. Lynch, 1997, Cancer research.

Genetic epidemiology of neuroblastoma: A study of 426 cases at the Institut Gustave‐Roussy in France

C. Bonaïti‐pellié, A. Chompret, L. Brugières, 2004, Pediatric blood & cancer.

A single mutated BRCA1 allele leads to impaired fidelity of double strand break end-joining

D. Papadopoulo, D. Stoppa-Lyonnet, J. Smith, 2002, Oncogene.

The Human Nuclear SRcyp Is a Cell Cycle-regulated Cyclophilin*

G. Fischer, M. Weiwad, J. Feunteun, 2004, Journal of Biological Chemistry.

Adipose Tissue Properties in Tumor-Bearing Breasts

B. Le Bizec, J. Antignac, H. Perdry, 2020, Frontiers in Oncology.

Familial breast-ovarian cancer locus on chromosome 17q12-q23

G. Lenoir, S. Narod, H. Lynch, 1991, The Lancet.

Distinct deregulation of the hypoxia inducible factor by PHD2 mutants identified in germline DNA of patients with polycythemia

S. Richard, A. Baruchel, R. Wenger, 2012, Haematologica.

amplification Megakaryocyte polyploidization is associated with a functional gene

G. Kroemer, W. Vainchenker, N. Debili, 2013 .

Proliferation and ovarian hormone signaling are impaired in normal breast tissues from women with BRCA1 mutations: benefit of a progesterone receptor modulator treatment as a breast cancer preventive strategy in women with inherited BRCA1 mutations

P. Pujol, S. Delaloge, P. Forgez, 2016, Oncotarget.

Childhood leukaemia, polymorphisms of metabolism enzyme genes, and interactions with maternal tobacco, coffee and alcohol consumption during pregnancy

M. Loriot, P. Beaune, D. Hémon, 2005, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Metastatic phenotype of murine tumor cells expressing different cooperating oncogenes

J. Feunteun, R. Monier, A. Zerial, 1992, International journal of cancer.

Episomal amplification or chromosomal integration of the viral genome: alternative pathways in hamster polyomavirus-induced lymphomas

J. Feunteun, C. de la Roche Saint André, S. Mazur, 1995, Journal of virology.

BRCA1 and BRCA2 are necessary for the transcription-coupled repair of the oxidative 8-oxoguanine lesion in human cells.

M. Perricaudet, A. Sarasin, J. Feunteun, 2000, Cancer research.

Breast cancer and genetic instability: the molecules behind the scenes.

J. Feunteun, 1998, Molecular medicine today.

Nucleotide sequence deletions within the coding region for small-t antigen of simian virus 40

W. Fiers, G. Volckaert, L. Crawford, 1979, Journal of Virology.

The tumor suppressor activity induced by adenovirus-mediated BRCA1 overexpression is not restricted to breast cancers

P. Opolon, E. Connault, M. Perricaudet, 2006, Gene Therapy.

BRCA1 carries tumor suppressor activity distinct from that of p53 and p21

P. Opolon, E. Connault, M. Perricaudet, 2001, Cancer Gene Therapy.

A breast-ovarian cancer susceptibility gene maps to chromosome 17q21.

P. O'Connell, R. White, G. Lenoir, 1993, American journal of human genetics.

Prereplicative events involving simian virus 40 DNA in permissive cells

B. H. Rosenberg, J. Feunteun, A. Rinaldy, 1982, Journal of virology.

Epidermolytic palmoplantar keratoderma cosegregates with a keratin 9 mutation in a pedigree with breast and ovarian cancer

G. Lenoir, A. Bernheim, S. Narod, 1994, Nature Genetics.

Stable cell line of TSV 4 O immortalized human glomerular visceral epithelial cells F 1

C. Adida, E. Rondeau, J. Hagège, 2015 .

A 100-kb physical and transcriptional map around the EDH17B2 gene: identification of three novel genes and a pseudogene of a human homologue of the rat PRL-1 tyrosine phosphatase

G. Lenoir, B. Sylla, M. Montagna, 1995, Human Genetics.

BRCA1, a gene involved in inherited predisposition to breast and ovarian cancer.

G. Lenoir, J. Feunteun, 1996, Biochimica et biophysica acta.

SV40‐immortalization of rabbit articular chondrocytes: Alteration of differentiated functions

P. Benya, M. Adolphe, S. Demignot, 1992, Journal of cellular physiology.

Immortalization of rodent embryo fibroblasts by SV40 is maintained by the A gene.

C. Petit, J. Feunteun, M. Gardes, 1983, Virology.

Oncogenic potential of a mutant human thyrotropin receptor expressed in FRTL-5 cells

E. Milgrom, J. Feunteun, M. Misrahi, 1998, Oncogene.

cis activation of the c-myc gene in bovine papilloma virus type 1/human c-myc hybrid plasmids.

J. Feunteun, O. Brison, N. Modjtahedi, 1988, Experimental cell research.

ARCAD: A method for estimating age‐dependent disease risk associated with mutation carrier status from family data

C. Bonaïti‐pellié, C. Moutou, L. Brugières, 1995, Genetic epidemiology.

The human insulin-like growth factor-binding protein 4 gene maps to chromosome region 17q12-q21.1 and is close to the gene for hereditary breast-ovarian cancer.

H. Huynh, P. Tonin, G. Lenoir, 1993, Genomics.

[Li-Fraumeni syndrome: update, new data and guidelines for clinical management].

O. Delattre, D. Frappaz, C. Bonaiti-Pellié, 2001, Bulletin du cancer.

Studies on the DNA of an oncogenic papovavirus of the Syrian hamster.

S. Scherneck, M. Böttger, J. Feunteun, 1979, Virology.

DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study.

G. Lenoir, S. Narod, H. Lynch, 1993, Archives of internal medicine.

Novel FH mutations in families with hereditary leiomyomatosis and renal cell cancer (HLRCC) and patients with isolated type 2 papillary renal cell carcinoma

L. Thomas, S. Richard, B. Teh, 2011, Journal of Medical Genetics.

Genetic transmission of susceptibility to cancer in families of children with soft tissue sarcomas

C. Bonaïti‐pellié, N. Poisson, A. Chompret, 1996, Cancer.

Induced mutagenesis of Simian virus 40 in carcinogen-treated monkey cells.

A. Sarasin, J. Feunteun, C. Gaillard, 1983, Basic life sciences.

p53 compound heterozygosity in a severely affected child with Li-Fraumeni Syndrome

C. Portwine, J. Garber, D. Malkin, 1999, Oncogene.

Oncolytic Activity of the E 1 B-55 kDa-deleted Adenovirus ONYX-015 Is Independent of Cellular p 53 Status in Human Malignant Glioma Xenografts 1

P. Opolon, B. Geoerger, G. Vassal, 2002 .

Increasing incidence of breast cancer in family with BRCA1 mutation

G. Lenoir, H. Lynch, S. Narod, 1993, The Lancet.

Histology of BRCA1-associated ovarian tumours

P. Tonin, G. Lenoir, H. Lynch, 1994, The Lancet.

Oncogenic potential of guanine nucleotide stimulatory factor alpha subunit in thyroid glands of transgenic mice.

B. Caillou, M. Schlumberger, J. Feunteun, 1994, Proceedings of the National Academy of Sciences of the United States of America.

[53] Isolation and characterization of 5 S RNA from Escherichia coli

J. Feunteun, R. Monier, 1971 .

The Hamster Polyomavirus

S. Scherneck, J. Feunteun, 1995 .

Localization of gene functions in polyoma virus DNA.

T. Benjamin, J. Feunteun, L. Sompayrac, 1976, Proceedings of the National Academy of Sciences of the United States of America.

Viral genomes maintained extrachromosomally in hamster polyomavirus-induced lymphomas display a cell-specific replication in vitro

J. Feunteun, C. de la Roche Saint André, S. Mazur, 1993, Journal of virology.

Stable cell lines of T-SV40 immortalized human glomerular mesangial cells.

F. Pinet, E. Rondeau, J. Hagège, 1996, Kidney international.

Stable cell line of T-SV40 immortalized human glomerular visceral epithelial cells.

C. Adida, E. Rondeau, J. Hagège, 1991, Kidney international.

The gene for hereditary breast-ovarian cancer, BRCA1, maps distal to EDH17B2 in chromosome region 17q12-q21.

P. Tonin, J. Simard, G. Lenoir, 1994, Human molecular genetics.

Properties of a simian virus 40 mutant deleted in the carboxyl-terminus domain of large T antigen and defective for small T-antigen production

J. Feunteun, F. Pecceu, M. Gardes, 1987 .

Influence of amino acids encoded in the 3' open reading frame of the SV40 early region on transformation and antigenicity of large T antigen.

R. Anderson, C. Cole, M. J. Tevethia, 1986, Virology.

A new member of the polyomavirus family: the hamster papovavirus. Complete nucleotide sequence and transformation properties.

S. Scherneck, V. Delmas, J. Feunteun, 1985, The EMBO journal.

Transformation by hamster polyomavirus: identification and functional analysis of the early genes

L. Goutebroze, J. Feunteun, 1992, Journal of virology.

Viable deletion mutants in the simian virus 40 early region.

M. Kress, J. Feunteun, R. Monier, 1978, Proceedings of the National Academy of Sciences of the United States of America.

Identification and characterization of the hamster polyomavirus middle T antigen

S. Scherneck, L. Goutebroze, S. Courtneidge, 1991, Journal of virology.

Induction of lymphomas by the hamster papovavirus correlates with massive replication of nonrandomly deleted extrachromosomal viral genomes

F. Vogel, S. Scherneck, V. Delmas, 1987, Journal of virology.

Human BAHD1 promotes heterochromatic gene silencing

P. Cossart, J. Seeler, C. Muchardt, 2009, Proceedings of the National Academy of Sciences.

A simple method for screening for Farber disease on cultured skin fibroblasts.

R. Salvayre, T. Levade, J. Feunteun, 1996, Clinica chimica acta; international journal of clinical chemistry.

Model SV40-transformed fibroblast lines for metabolic studies of human prosaposin and acid ceramidase deficiencies.

Y. Kishimoto, R. Salvayre, T. Levade, 1997, Clinica chimica acta; international journal of clinical chemistry.

Transfer of immortality by transfection of genomic DNA from SV40 established cell lines into rat embryo fibroblasts

J. Feunteun, H. Jacquemin-Sablon, Leonard Ganz, 1990, Biology of the cell.

X-Chromosome Genetics and Human Cancer

C. Borg, A. Spatz, J. Feunteun, 2004, Nature Reviews Cancer.

Mutant carrying deletions in the two simian virus 40 early genes

G. Carmichael, J. Nicolas, M. Kress, 1981, Journal of virology.

Isolation of renin-producing human cells by transfection with three simian virus 40 mutants.

J. Ménard, F. Pinet, P. Corvol, 1985, Proceedings of the National Academy of Sciences of the United States of America.

Role of the BAHD1 Chromatin-Repressive Complex in Placental Development and Regulation of Steroid Metabolism

T. Sorg, J. Coppee, P. Cossart, 2016, PLoS genetics.

Oncolytic activity of the E1B-55 kDa-deleted adenovirus ONYX-015 is independent of cellular p53 status in human malignant glioma xenografts.

P. Opolon, B. Geoerger, G. Vassal, 2002, Cancer research.

Combining Homologous Recombination and Phosphopeptide-binding Data to Predict the Impact of BRCA1 BRCT Variants on Cancer Risk

Jean-Christophe Aude, Etienne Rouleau, Sandrine M. Caputo, 2018, Molecular Cancer Research.

PHD2 mutation and congenital erythrocytosis with paraganglioma.

F. Galateau-Sallé, S. Richard, J. Pouysségur, 2008, The New England journal of medicine.

BRCA1 haploinsufficiency for replication stress suppression in primary cells

A. Richardson, K. Polyak, D. Livingston, 2014, Nature Communications.

Association of BRCA1 with the inactive X chromosome and XIST RNA.

R. Greenberg, D. Livingston, S. Ganesan, 2004, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Down-regulation of BRCA1 in BCR-ABL-expressing hematopoietic cells.

Eric Deutsch, Jean Bourhis, J. Bourhis, 2003, Blood.

BRCA1 Supports XIST RNA Concentration on the Inactive X Chromosome

C. Deng, R. Greenberg, D. Livingston, 2002, Cell.

BRCA1/FANCD2/BRG1-Driven DNA Repair Stabilizes the Differentiation State of Human Mammary Epithelial Cells.

A. Giobbie-Hurder, K. Polyak, R. Gelman, 2016, Molecular cell.

BRCA1 is required for postreplication repair after UV-induced DNA damage.

D. Livingston, G. Adelmant, J. Marto, 2011, Molecular cell.

PML nuclear bodies are highly organised DNA-protein structures with a function in heterochromatin remodelling at the G2 phase

M. Mitchell, M. Mattéi, A. Mégarbané, 2006, Journal of Cell Science.

Sensitivity and predictive value of criteria for p53germline mutation screening

C. Bonaïti‐pellié, D. Stoppa-Lyonnet, A. Chompret, 2001, Journal of medical genetics.

Megakaryocyte polyploidization is associated with a functional gene amplification.

Guido Kroemer, William Vainchenker, G. Kroemer, 2003, Blood.

P53 germline mutations in childhood cancers and cancer risk for carrier individuals

C. Bonaïti‐pellié, T. Frebourg, A. Chompret, 2000, British Journal of Cancer.

Location of BRCA1 in Human Breast and Ovarian Cancer Cells

C. Osborne, S. Schnitt, D. Livingston, 1996, Science.

FLI1 monoallelic expression combined with its hemizygous loss underlies Paris-Trousseau/Jacobsen thrombopenia.

W. Vainchenker, N. Debili, R. Favier, 2004, The Journal of clinical investigation.

Consensus on precision medicine for metastatic cancers: a report from the MAP conference.

C Caldas, C Sotiriou, C. Sotiriou, 2016, Annals of oncology : official journal of the European Society for Medical Oncology.

Gamma-rays-induced death of human cells carrying mutations of BRCA1 or BRCA2

M. Perricaudet, G. Lenoir, N. Foray, 1999, Oncogene.

Radiation and genetic factors in the risk of second malignant neoplasms after a first cancer in childhood

C. Bonaïti‐pellié, F. Eschwège, A. Chompret, 1997, The Lancet.

Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma

J. Barrett, G. Mann, P. Terrier, 2017, Journal of Medical Genetics.

Mitotic catastrophe constitutes a special case of apoptosis whose suppression entails aneuploidy

G. Kroemer, R. Medema, W. Vainchenker, 2004, Oncogene.

Apoptosis is antagonized by large T antigens in the pathway to immortalization by polyomaviruses.

P. Petit, B. Mignotte, J. Vayssière, 1994, Oncogene.

Abnormal maturation of precursor 16S RNA in a ribosomal assembly defective mutant of E. coli.

R Rosset, P. Stiegler, C. Ehresmann, 1974, Nucleic acids research.

Further Evidence for BRCA1 Communication with the Inactive X Chromosome

R. Gelman, D. Livingston, J. Mar, 2007, Cell.

Abnormalities of the inactive X chromosome are a common feature of BRCA1 mutant and sporadic basal-like breast cancer.

A. Richardson, D. Livingston, S. Ganesan, 2005, Cold Spring Harbor symposia on quantitative biology.

A high incidence of BRCA1 mutations in 20 breast-ovarian cancer families.

P. Tonin, G. Lenoir, S. Narod, 1996, American Journal of Human Genetics.

Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12-21: exclusion of candidate genes EDH17B2 and RARA.

P. Tonin, J. Simard, G. Rouleau, 1993, Human molecular genetics.

Screening for TP53 rearrangements in families with the Li–Fraumeni syndrome reveals a complete deletion of the TP53 gene

T. Frebourg, A. Chompret, G. Bougeard, 2003, Oncogene.

Accessibility of 5S RNA to ribonucleases in Escherichia coli ribosomes.

J. Feunteun, R. Monier, 1971, Biochimie.

Heterozygote BRCA1 status and skewed chromosome X inactivation

G. Lenoir, A. Helbling-Leclerc, J. Feunteun, 2006, Familial Cancer.

cer who have female offspring have a greater motivation to un- dergo genetic testing. Our results indicate that sex-ratio ob- servations must be carefully interpreted in diseases that selectively affect one sex vs the other.

D. Stoppa-Lyonnet, A. Helbling-Leclerc, M. Belotti, 2017 .

Sex ratio among the offspring of BRCA mutation carriers.

C. Bonaïti‐pellié, D. Stoppa-Lyonnet, A. Chompret, 2004, JAMA.

Study of the maturation of 5 s RNA precursors in Escherichia coli.

B. Jordan, J. Feunteun, R. Monier, 1972, Journal of molecular biology.

In vivo replication of the hamster polyomavirus genome and generation of specific deletions in the process of lymphomagenesis

J. Feunteun, C. de la Roche Saint André, M. Goodhardt, 1994, Journal of virology.

The hamster papovavirus: evolutionary relationships with other polyomaviruses.

F. Vogel, S. Scherneck, V. Delmas, 1986, Virology.

Steroid hormone profiling in human breast adipose tissue using semi-automated purification and highly sensitive determination of estrogens by GC-APCI-MS/MS

J. Antignac, E. Bichon, S. Delaloge, 2017, Analytical and Bioanalytical Chemistry.

Resistance of MCF7 human breast carcinoma cells to TNF-induced cell death is associated with loss of p53 function

C. Moyret-Lalle, S. Chouaib, A. Larsen, 1997, Oncogene.

A Thermosensitive mutant defective in ribosomal 30 S subunit assembly

J. Feunteun, R. Monier, C. Vola, 1971, FEBS letters.

Ribosomal assembly defective mutants of Escherichia coli.

J. Feunteun, R. Monier, C. Vola, 1974, Nucleic acids research.

Reversibility of the transformed and neoplastic phenotype. IV. Effects of long‐term interferon treatment of C3H/10T1/2 cells transformed by methylcholanthrene and SV40 virus

I. Gresser, J. Feunteun, D. Brouty‐boye, 1984, International journal of cancer.

Targeted oncogenesis in the thyroid of transgenic mice.

B. Caillou, M. Schlumberger, J. Feunteun, 1997, Hormone research.

Thyroid pathologies in transgenic mice expressing a human activated Ras gene driven by a thyroglobulin promoter.

C. Ledent, B. Caillou, M. Schlumberger, 1996, Oncogene.

Identification and Characterization of Moca-cyp

L. Cavarec, F. Lemeunier, G. Fischer, 2002, The Journal of Biological Chemistry.

The Hamster Polyomavirus—a Brief Review of Recent Knowledge*

S. Scherneck, J. Feunteun, R. Ulrich, 2004, Virus Genes.

Overexpression of MDM2, due to enhanced translation, results in inactivation of wild-type p53 in Burkitt's lymphoma cells

T. Tursz, B. Paillerets, J. Feunteun, 1998, Oncogene.

Distinct segments of the hamster polyomavirus regulatory region have differential effects on DNA replication.

J. Feunteun, C. de la Roche Saint André, 1993, The Journal of general virology.

SV40 induced cellular immortalization: phenotypic changes associated with the loss of proliferative capacity in a conditionally immortalized cell line.

D. Coulaud, J. Feunteun, J. Larcher, 1990, Oncogene.

Expression of histamine and vasoactive intestinal peptide (VIP) receptors in immortalized rat fetal intestinal cells

J. Feunteun, C. Gespach, E. Chastre, 1988, Agents and Actions.

A ribonuclease-resistant region of 5S RNA and its relation to the RNA binding sites of proteins L18 and L25.

R. Garrett, S. Douthwaite, R. Wagner, 1979, Nucleic acids research.

Molecular cloning of the hamster papovavirus genome in Escherichia coli plasmid vector pBR322.

W. Zimmermann, S. Scherneck, J. Feunteun, 1984, Gene.

Effect of PALB2 status on breast cancer precision medicine.

S. Delaloge, O. Caron, J. Feunteun, 2015, The Lancet Oncology.

Reuniting philosophy and science to advance cancer research

B. Daignan-Fornier, H. Clevers, C. Maley, 2023, Biological reviews of the Cambridge Philosophical Society.

Phosphorylation pattern of large T antigens in mouse cells infected by simian virus 40 wild type or deletion mutants

M. Kress, J. Feunteun, M. Resche-Rigon, 1982, Journal of virology.

5 S RNA and the assembly of bacterial ribosomes.

B. Forget, B. Jordan, J. Feunteun, 1969, Cold Spring Harbor symposia on quantitative biology.

Analysis of hamster lymphomas for the presence of hamster papovavirus DNA.

F. Vogel, W. Arnold, S. Scherneck, 1988, Acta virologica.

Early gene expression in lymphoma-associated hamster polyomavirus viral genomes.

L. Goutebroze, V. Delmas, J. Feunteun, 1992, Oncogene.

Analysis of the hamster polyomavirus infection in vitro: host-restricted productive cycle.

F. Harper, J. Feunteun, C. de la Roche Saint André, 1990, Virology.

Role of ras and gsp oncogenes in human epithelial thyroid tumorigenesis

B. Caillou, M. Schlumberger, J. Villard, 1995, Journal of endocrinological investigation.

The hamster polyomavirus transforming properties.

J. Feunteun, C. Bastien, 1988, Oncogene.

Restriction endonuclease cleavage map of the DNA of hamster papovavirus.

S. Scherneck, V. Delmas, J. Feunteun, 1985, Biomedica biochimica acta.

Isolation of transformation-defective host-range mutants of polyoma virus on normal mouse cells.

T. Benjamin, J. Feunteun, 1982, Virology.

[A paradox and three egnimas about the role of BRCA1 in breast and ovarian cancers].

J. Feunteun, 2004, Journal de la Société de Biologie.

Sex differences in cancer risk among germline p53 mutation carriers

C. Bonaïti‐pellié, A. Chompret, L. Brugières, 2004, British Journal of Cancer.

The N terminus of hamster polyomavirus middle T antigen carries a determinant for specific activation of p59c-Fyn

L. Goutebroze, J. Feunteun, K. Ballmer-Hofer, 1997, Journal of virology.

Germ-line exclusion of a single p53 allele by premature termination of translation in a Li-Fraumeni syndrome family.

C. Bonaïti‐pellié, A. Chompret, L. Brugières, 1994, Oncogene.

PEPing up preimplantation testing

G. Lenoir, N. Janin, S. Narod, 1994, Nature Genetics.

Genetic evidence of a precisely tuned dysregulation in the hypoxia signaling pathway during oncogenesis.

S. Richard, W. Kaelin, William Y. Kim, 2014, Cancer research.