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24 results

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Page 1
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder.
Pérez Baca MDR, Palomares-Bralo M, Vanhooydonck M, Hamerlinck L, D'haene E, Leimbacher S, Jacobs EZ, De Cock L, D'haenens E, Dheedene A, Malfait Z, Vantomme L, Silva A, Rooney K, Zhao X, Saeidian AH, Owen NM, Santos-Simarro F, Lleuger-Pujol R, García-Miñaúr S, Losantos-García I, Menten B, Gestri G, Ragge N; ZFHX4 consortium; Sadikovic B, Bogaert E, Vleminckx K, Naert T, Syx D, Callewaert B, Vergult S. Pérez Baca MDR, et al. Among authors: naert t. Am J Hum Genet. 2025 Jun 5;112(6):1388-1414. doi: 10.1016/j.ajhg.2025.04.008. Epub 2025 May 13. Am J Hum Genet. 2025. PMID: 40367947
Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development.
Ceroni F, Cicekdal MB, Holt R, Sorokina E, Chassaing N, Clokie S, Naert T, Talbot LV, Muheisen S, Bax DA, Kesim Y, Kivuva EC, Vincent-Delorme C, Lienkamp SS, Plaisancié J, De Baere E, Calvas P, Vleminckx K, Semina EV, Ragge NK. Ceroni F, et al. Among authors: naert t. Nat Commun. 2024 Oct 26;15(1):9245. doi: 10.1038/s41467-024-53553-2. Nat Commun. 2024. PMID: 39455595 Free PMC article.
Benchtop mesoSPIM: a next-generation open-source light-sheet microscope for cleared samples.
Vladimirov N, Voigt FF, Naert T, Araujo GR, Cai R, Reuss AM, Zhao S, Schmid P, Hildebrand S, Schaettin M, Groos D, Mateos JM, Bethge P, Yamamoto T, Aerne V, Roebroeck A, Ertürk A, Aguzzi A, Ziegler U, Stoeckli E, Baudis L, Lienkamp SS, Helmchen F. Vladimirov N, et al. Among authors: naert t. Nat Commun. 2024 Mar 27;15(1):2679. doi: 10.1038/s41467-024-46770-2. Nat Commun. 2024. PMID: 38538644 Free PMC article.
The Benchtop mesoSPIM: a next-generation open-source light-sheet microscope for large cleared samples.
Vladimirov N, Voigt FF, Naert T, Araujo GR, Cai R, Reuss AM, Zhao S, Schmid P, Hildebrand S, Schaettin M, Groos D, Mateos JM, Bethge P, Yamamoto T, Aerne V, Roebroeck A, Ertürk A, Aguzzi A, Ziegler U, Stoeckli E, Baudis L, Lienkamp SS, Helmchen F. Vladimirov N, et al. Among authors: naert t. bioRxiv [Preprint]. 2023 Dec 12:2023.06.16.545256. doi: 10.1101/2023.06.16.545256. bioRxiv. 2023. Update in: Nat Commun. 2024 Mar 27;15(1):2679. doi: 10.1038/s41467-024-46770-2. PMID: 38168219 Free PMC article. Updated. Preprint.
Reflective multi-immersion microscope objectives inspired by the Schmidt telescope.
Voigt FF, Reuss AM, Naert T, Hildebrand S, Schaettin M, Hotz AL, Whitehead L, Bahl A, Neuhauss SCF, Roebroeck A, Stoeckli ET, Lienkamp SS, Aguzzi A, Helmchen F. Voigt FF, et al. Among authors: naert t. Nat Biotechnol. 2024 Jan;42(1):65-71. doi: 10.1038/s41587-023-01717-8. Epub 2023 Mar 30. Nat Biotechnol. 2024. PMID: 36997681 Free PMC article.
HNF1B Alters an Evolutionarily Conserved Nephrogenic Program of Target Genes.
Grand K, Stoltz M, Rizzo L, Röck R, Kaminski MM, Salinas G, Getwan M, Naert T, Pichler R, Lienkamp SS. Grand K, et al. Among authors: naert t. J Am Soc Nephrol. 2023 Mar 1;34(3):412-432. doi: 10.1681/ASN.2022010076. Epub 2022 Dec 15. J Am Soc Nephrol. 2023. PMID: 36522156 Free PMC article.
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and Frogs.
Klämbt V, Buerger F, Wang C, Naert T, Richter K, Nauth T, Weiss AC, Sieckmann T, Lai E, Connaughton DM, Seltzsam S, Mann N, Majmundar AJ, Wu CW, Onuchic-Whitford AC, Shril S, Schneider S, Schierbaum L, Dai R, Bekheirnia MR, Joosten M, Shlomovitz O, Vivante A, Banne E, Mane S, Lifton RP, Kirschner KM, Kispert A, Rosenberger G, Fischer KD, Lienkamp SS, Zegers MMP, Hildebrandt F. Klämbt V, et al. Among authors: naert t. J Am Soc Nephrol. 2023 Feb 1;34(2):273-290. doi: 10.1681/ASN.2022010050. Epub 2023 Nov 22. J Am Soc Nephrol. 2023. PMID: 36414417 Free PMC article.
24 results