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Page 1
Origin, specification and differentiation of a rare supporting-like lineage in the developing mouse gonad.
Mayère C, Regard V, Perea-Gomez A, Bunce C, Neirijnck Y, Djari C, Bellido-Carreras N, Sararols P, Reeves R, Greenaway S, Simon M, Siggers P, Condrea D, Kühne F, Gantar I, Tang F, Stévant I, Batti L, Ghyselinck NB, Wilhelm D, Greenfield A, Capel B, Chaboissier MC, Nef S. Mayère C, et al. Among authors: kuhne f. Sci Adv. 2022 May 27;8(21):eabm0972. doi: 10.1126/sciadv.abm0972. Epub 2022 May 25. Sci Adv. 2022. PMID: 35613264 Free PMC article.
Loss of Dicer in Sertoli cells has a major impact on the testicular proteome of mice.
Papaioannou MD, Lagarrigue M, Vejnar CE, Rolland AD, Kühne F, Aubry F, Schaad O, Fort A, Descombes P, Neerman-Arbez M, Guillou F, Zdobnov EM, Pineau C, Nef S. Papaioannou MD, et al. Among authors: kuhne f. Mol Cell Proteomics. 2011 Apr;10(4):M900587MCP200. doi: 10.1074/mcp.M900587-MCP200. Epub 2010 May 13. Mol Cell Proteomics. 2011. PMID: 20467044 Free PMC article.
Loss of function mutation in the palmitoyl-transferase HHAT leads to syndromic 46,XY disorder of sex development by impeding Hedgehog protein palmitoylation and signaling.
Callier P, Calvel P, Matevossian A, Makrythanasis P, Bernard P, Kurosaka H, Vannier A, Thauvin-Robinet C, Borel C, Mazaud-Guittot S, Rolland A, Desdoits-Lethimonier C, Guipponi M, Zimmermann C, Stévant I, Kuhne F, Conne B, Santoni F, Lambert S, Huet F, Mugneret F, Jaruzelska J, Faivre L, Wilhelm D, Jégou B, Trainor PA, Resh MD, Antonarakis SE, Nef S. Callier P, et al. Among authors: kuhne f. PLoS Genet. 2014 May 1;10(5):e1004340. doi: 10.1371/journal.pgen.1004340. eCollection 2014 May. PLoS Genet. 2014. PMID: 24784881 Free PMC article.
Insulin and IGF1 receptors are essential for the development and steroidogenic function of adult Leydig cells.
Neirijnck Y, Calvel P, Kilcoyne KR, Kühne F, Stévant I, Griffeth RJ, Pitetti JL, Andric SA, Hu MC, Pralong F, Smith LB, Nef S. Neirijnck Y, et al. Among authors: kuhne f. FASEB J. 2018 Jun;32(6):3321-3335. doi: 10.1096/fj.201700769RR. Epub 2018 Jan 24. FASEB J. 2018. PMID: 29401624
-Neirijnck, Y., Calvel, P., Kilcoyne, K. R., Kuhne, F., Stevant, I., Griffeth, R. J., Pitetti, J.-L., Andric, S. A., Hu, M.-C., Pralong, F., Smith, L. ...
-Neirijnck, Y., Calvel, P., Kilcoyne, K. R., Kuhne, F., Stevant, I., Griffeth, R. J., Pitetti, J.-L., Andric, S. A., Hu, M.-C. …
Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B.
Cazin C, Neirijnck Y, Loeuillet C, Wehrli L, Kühne F, Lordey I, Mustapha SFB, Bouker A, Zouari R, Thierry-Mieg N, Nef S, Arnoult C, Ray PF, Kherraf ZE. Cazin C, et al. Among authors: kuhne f. Cells. 2021 Dec 30;11(1):118. doi: 10.3390/cells11010118. Cells. 2021. PMID: 35011680 Free PMC article.
148 results