Pascal Cousin

Publications | Mémoires et thèses

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25 publications

2023 | 2022 | 2021 | 2019 | 2018 | 2017 | 2015 | 2012 | 2010 | 2006 | 2004 | 2002 | 2001 | 2000 | 1995 |
2023
 
Chromosome-level organization of the regulatory genome in the Drosophila nervous system.
Mohana G., Dorier J., Li X., Mouginot M., Smith R.C., Malek H., Leleu M., Rodriguez D., Khadka J., Rosa P. et al., 2023/08/31. Cell, 186 (18) pp. 3826-3844.e26. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_B8B0A2EC720F]
 
Contrasting effects of whole-body and hepatocyte-specific deletion of the RNA polymerase III repressor Maf1 in the mouse.
Willemin G., Mange F., Praz V., Lorrain S., Cousin P., Roger C., Willis I.M., Hernandez N., 2023. Frontiers in molecular biosciences, 10 p. 1297800. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_83067C6358E5]
2022
Essential role of Cp190 in physical and regulatory boundary formation.
Kaushal A., Dorier J., Wang B., Mohana G., Taschner M., Cousin P., Waridel P., Iseli C., Semenova A., Restrepo S. et al., 2022/05/13. Science advances, 8 (19) pp. eabl8834. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_EEEA9AFE8EED]
2021
CTCF loss has limited effects on global genome architecture in Drosophila despite critical regulatory functions.
Kaushal A., Mohana G., Dorier J., Özdemir I., Omer A., Cousin P., Semenova A., Taschner M., Dergai O., Marzetta F. et al., 2021/02/12. Nature communications, 12 (1) p. 1011. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_6E8BCA9FDAE9]
2019
Differential regulation of RNA polymerase III genes during liver regeneration.
Yeganeh M., Praz V., Carmeli C., Villeneuve D., Rib L., Guex N., Herr W., Delorenzi M., Hernandez N., CycliX consortium, 2019/02/28. Nucleic Acids Research, 47 (4) pp. 1786-1796. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_014840C5C9E3]
2018
Mechanism of selective recruitment of RNA polymerases II and III to snRNA gene promoters.
Dergai O., Cousin P., Gouge J., Satia K., Praz V., Kuhlman T., Lhôte P., Vannini A., Hernandez N., 2018/05/01. Genes & development, 32 (9-10) pp. 711-722. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_A9F33414833D]
2017
Molecular mechanisms of Bdp1 in TFIIIB assembly and RNA polymerase III transcription initiation.
Gouge J., Guthertz N., Kramm K., Dergai O., Abascal-Palacios G., Satia K., Cousin P., Hernandez N., Grohmann D., Vannini A., 2017/07/25. Nature communications, 8 (1) p. 130. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_F5A355864C55]
Transcriptional interference by RNA polymerase III affects expression of the Polr3e gene.
Yeganeh M., Praz V., Cousin P., Hernandez N., 2017. Genes and Development, 31 (4) pp. 413-421. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_9C06585B158C]
2015
Redox Signaling by the RNA Polymerase III TFIIB-Related Factor Brf2.
Gouge J., Satia K., Guthertz N., Widya M., Thompson A.J., Cousin P., Dergai O., Hernandez N., Vannini A., 2015. Cell, 163 (6) pp. 1375-1387.
[URN][DOI][WoS][Pmid][serval:BIB_E29E6F7F6BE0]
2012
A multiplicity of factors contributes to selective RNA polymerase III occupancy of a subset of RNA polymerase III genes in mouse liver.
Canella D., Bernasconi D., Gilardi F., LeMartelot G., Migliavacca E., Praz V., Cousin P., Delorenzi M., Hernandez N., CycliX Consortium, 2012. Genome Research, 22 (4) pp. 666-680. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_AFFF7604F2F3]
 
Nanopore detection of single molecule RNAP-DNA transcription complex.
Raillon C., Cousin P., Traversi F., Garcia-Cordero E., Hernandez N., Radenovic A., 2012. Nano Letters, 12 (3) pp. 1157-1164.
[DOI][WoS][Pmid][serval:BIB_846A9ACCE57B]
2010
Defining the RNA polymerase III transcriptome: Genome-wide localization of the RNA polymerase III transcription machinery in human cells.
Canella D., Praz V., Reina J.H., Cousin P., Hernandez N., 2010. Genome Research, 20 (6) pp. 710-721. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_CDA7B1F5A872]
2006
 
Synthetic chemokines directly labeled with a fluorescent dye as tools for studying chemokine and chemokine receptor interactions.
Strong A.E., Thierry A.C., Cousin P., Moulon C., Demotz S., 2006/03. European cytokine network, 17 (1) pp. 49-59. Peer-reviewed.
[WoS][Pmid][serval:BIB_D38622EA57AC]
2004
 
A recombinant rubella virus E1 glycoprotein as a rubella vaccine candidate.
Perrenoud G., Messerli F., Thierry A.C., Beltraminelli N., Cousin P., Fasel N., Vallet V., Demotz S., Duchosal M.A., Moulon C., 2004. Vaccine, 23 (4) pp. 480-488.
[DOI][WoS][Pmid][serval:BIB_AFA406FAAEB9]
2002
 
Large Family With Maturity-Onset Diabetes of the Young and a Novel V121I Mutation in HNF4A
Monney C.T., Kaltenrieder V., Cousin P., Bonny C, Schorderet D.F., 2002/05. Human Mutation, 20 (3) p. 230.
[Pmid][serval:BIB_416EFB13A593]
 
BIGH3 mutation spectrum in corneal dystrophies.
Munier F.L., Frueh B.E., Othenin-Girard P., Uffer S., Cousin P., Wang M.X., Héon E., Black G.C., Blasi M.A., Balestrazzi E. et al., 2002. Investigative Ophthalmology and Visual Science, 43 (4) pp. 949-954.
[WoS][Pmid][serval:BIB_EAC5576BC35D]
2001
 
MYOC mutation frequency in primary open-angle glaucoma patients from Western Switzerland
Mataftsi A., Achache F., Heon E., Mermoud A., Cousin P., Metthez G., Schorderet D. F., Munier F. L., 2001/12. Ophthalmic Genetics, 22 (4) pp. 225-31.
[Pmid][serval:BIB_A45FC41B05C6]
Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy
Biswas S., Munier F. L., Yardley J., Hart-Holden N., Perveen R., Cousin P., Sutphin J. E., Noble B., Batterbury M., Kielty C. et al., 2001/10. Human Molecular Genetics, 10 (21) pp. 2415-23.
[URN][DOI][WoS][Pmid][serval:BIB_1B7B96B25B4E]
 
Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies
Lavanchy L., Munier F. L., Cousin P., Gaide A. C., Thonney F., Schorderet D. F., 2001/03. Ophthalmic Genetics, 22 (1) pp. 1-10.
[Pmid][serval:BIB_A12922FB3702]
 
A novel highly informative polyA microsatellite on the telomeric side of the INK4a/ARF locus
Chaubert P., Burri N., Cousin P., Shaw P., 2001. Molecular and Cellular Probes, 15 (3) pp. 183-185.
[DOI][WoS][Pmid][serval:BIB_BDB1D4B729F8]
 
Fatal outcome in a female monozygotic twin with X-linked hypohydrotic ectodermal dysplasia (XLHED) due to a de novo t(X;9) translocation with probable disruption of the EDA gene.
Zankl A., Addor M.C., Cousin P., Gaide A.C., Gudinchet F., Schorderet D.F., 2001. European Journal of Pediatrics, 160 (5) pp. 296-299.
[DOI][WoS][Pmid][serval:BIB_ABE4579D86A5]
2000
 
Complex chromosome rearrangement in a girl with an incomplete form of Beckwith-Wiedemann syndrome.
Zankl A., Addor M.C., Gaide A.C., Thonney F., Cousin P., Schorderet D.F., Gudinchet F., Nenadov-Beck M., 2000. American Journal of Medical Genetics, 95 (5) pp. 510-512.
[DOI][WoS][Pmid][serval:BIB_6DBE546CD6CE]
 
Mutation in the gene for connexin 30.3 in a family with erythrokeratodermia variabilis.
Macari F., Landau M., Cousin P., Mevorah B., Brenner S., Panizzon R., Schorderet D.F., Hohl D., Huber M., 2000. American journal of human genetics, 67 (5) pp. 1296-301. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_15267]
 
Physical map of 17p13 and the genes adjacent to p53
Cousin P., Billotte J., Chaubert P., Shaw P., 2000. Genomics, 63 (1) pp. 60-68.
[DOI][WoS][Pmid][serval:BIB_B47DB5A03734]
1995
 
Transient inhibition of angiotensinogen production in transgenic mice bearing an antisense angiotensinogen gene.
Pedrazzini T., Cousin P., Aubert J.F., Brunner H.R., 1995. Kidney International, 47 (6) pp. 1638-1346. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_0765AFF9B27A]
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