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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 4
1995 2
1996 1
1997 1
1998 1
1999 1
2001 1
2002 1
2003 1
2004 1
2005 1
2006 3
2007 6
2008 5
2009 3
2010 2
2011 4
2012 1
2014 2
2015 6
2016 3
2017 2
2019 3
2020 6
2021 4
2022 6
2023 5
2024 5
2025 5
2026 0

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76 results

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Page 1
Impaired Kupffer Cell Self-Renewal Alters the Liver Response to Lipid Overload during Non-alcoholic Steatohepatitis.
Tran S, Baba I, Poupel L, Dussaud S, Moreau M, Gélineau A, Marcelin G, Magréau-Davy E, Ouhachi M, Lesnik P, Boissonnas A, Le Goff W, Clausen BE, Yvan-Charvet L, Sennlaub F, Huby T, Gautier EL. Tran S, et al. Among authors: huby t. Immunity. 2020 Sep 15;53(3):627-640.e5. doi: 10.1016/j.immuni.2020.06.003. Epub 2020 Jun 19. Immunity. 2020. PMID: 32562600 Free article.
Cholesterol efflux pathways hinder KRAS-driven lung tumor progenitor cell expansion.
Guilbaud E, Barouillet T, Ilie M, Borowczyk C, Ivanov S, Sarrazy V, Vaillant N, Ayrault M, Castiglione A, Rignol G, Brest P, Bazioti V, Zaitsev K, Lebrigand K, Dussaud S, Magnone V, Bertolotto C, Marchetti S, Irondelle M, Goldberg I, Huby T, Westerterp M, Gautier EL, Mari B, Barbry P, Hofman P, Yvan-Charvet L. Guilbaud E, et al. Among authors: huby t. Cell Stem Cell. 2023 Jun 1;30(6):800-817.e9. doi: 10.1016/j.stem.2023.05.005. Cell Stem Cell. 2023. PMID: 37267915 Free article.
Epidermal maintenance of Langerhans cells relies on autophagy-regulated lipid metabolism.
Arbogast F, Sal-Carro R, Boufenghour W, Frenger Q, Bouis D, Filippi De La Palavesa L, Fauny JD, Griso O, Puccio H, Fima R, Huby T, Gautier EL, Molitor A, Carapito R, Bahram S, Romani N, Clausen BE, Voisin B, Mueller CG, Gros F, Flacher V. Arbogast F, et al. Among authors: huby t. J Cell Biol. 2025 Feb 3;224(2):e202403178. doi: 10.1083/jcb.202403178. Epub 2024 Nov 13. J Cell Biol. 2025. PMID: 39535446 Free PMC article.
Prenatal and neonatal phenotype of Larsen of La Réunion Island syndrome (B4GALT7-linkeropathy).
Alessandri JL, Celse T, Spodenkiewicz M, Calaya A, Dumont C, Jacquemont ML, Bertaut-Nativel B, Boumahni B, Rémy M, Ferroul F, Guilly S, Huby T, Irabé M, Laurens T, Munier P, Morel G, Payet F, Randrianaivo H, Doray B, Dospeux J. Alessandri JL, et al. Among authors: huby t. Eur J Med Genet. 2024 Jun;69:104940. doi: 10.1016/j.ejmg.2024.104940. Epub 2024 May 3. Eur J Med Genet. 2024. PMID: 38705458 Free article.
Rare features in Feingold syndrome type 1.
Ferroul F, Snanoudj S, Leterme G, Mezouaghi K, Kieffer-Traversier M, Celse T, Dospeux J, Huby T, Marzin P, Morel G, Payet F, Remy M, Sennsfelder L, Spondenkiewicz M, Roy-Doray B, Amiel J, Pingault V, Alessandri JL. Ferroul F, et al. Among authors: huby t. Eur J Med Genet. 2025 Dec;78:105049. doi: 10.1016/j.ejmg.2025.105049. Epub 2025 Sep 24. Eur J Med Genet. 2025. PMID: 41005613 Free article.
76 results