Rottier RJ - Search Results

1

The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins.

Edel GG, van Kempen M, Munck AB, Huisman CN, Naalden CAP, Brouwer RWW, Koornneef S, van IJcken WFJ, Wijnen RMH, Rottier RJ. Edel GG, et al. Among authors: rottier rj. J Biomed Sci. 2024 Nov 4;31(1):100. doi: 10.1186/s12929-024-01088-5. J Biomed Sci. 2024. PMID: 39497128 Free PMC article.

2

Early origins of lung disease: towards an interdisciplinary approach.

Ubags NDJ, Alejandre Alcazar MA, Kallapur SG, Knapp S, Lanone S, Lloyd CM, Morty RE, Pattaroni C, Reynaert NL, Rottier RJ, Smits HH, de Steenhuijsen Piters WAA, Strickland DH, Collins JJP. Ubags NDJ, et al. Among authors: rottier rj. Eur Respir Rev. 2020 Oct 1;29(157):200191. doi: 10.1183/16000617.0191-2020. Print 2020 Sep 30. Eur Respir Rev. 2020. PMID: 33004528 Free PMC article. Review.

3

Distal angiogenesis: a new concept for lung vascular morphogenesis.

Parera MC, van Dooren M, van Kempen M, de Krijger R, Grosveld F, Tibboel D, Rottier R. Parera MC, et al. Am J Physiol Lung Cell Mol Physiol. 2005 Jan;288(1):L141-9. doi: 10.1152/ajplung.00148.2004. Epub 2004 Sep 17. Am J Physiol Lung Cell Mol Physiol. 2005. PMID: 15377499 Free article.

4

Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes.

Engelen E, Akinci U, Bryne JC, Hou J, Gontan C, Moen M, Szumska D, Kockx C, van Ijcken W, Dekkers DH, Demmers J, Rijkers EJ, Bhattacharya S, Philipsen S, Pevny LH, Grosveld FG, Rottier RJ, Lenhard B, Poot RA. Engelen E, et al. Among authors: rottier rj. Nat Genet. 2011 Jun;43(6):607-11. doi: 10.1038/ng.825. Epub 2011 May 1. Nat Genet. 2011. PMID: 21532573

5

Hypoxia-inducible factor 2α plays a critical role in the formation of alveoli and surfactant.

Huang Y, Kempen MB, Munck AB, Swagemakers S, Driegen S, Mahavadi P, Meijer D, van Ijcken W, van der Spek P, Grosveld F, Günther A, Tibboel D, Rottier RJ. Huang Y, et al. Among authors: rottier rj. Am J Respir Cell Mol Biol. 2012 Feb;46(2):224-32. doi: 10.1165/rcmb.2011-0024OC. Am J Respir Cell Mol Biol. 2012. PMID: 22298531

6

SOX2 redirects the developmental fate of the intestinal epithelium toward a premature gastric phenotype.

Raghoebir L, Bakker ER, Mills JC, Swagemakers S, Kempen MB, Munck AB, Driegen S, Meijer D, Grosveld F, Tibboel D, Smits R, Rottier RJ. Raghoebir L, et al. Among authors: rottier rj. J Mol Cell Biol. 2012 Dec;4(6):377-85. doi: 10.1093/jmcb/mjs030. Epub 2012 Jun 7. J Mol Cell Biol. 2012. PMID: 22679103 Free PMC article.

7

Hypoxia inducible factor 3α plays a critical role in alveolarization and distal epithelial cell differentiation during mouse lung development.

Huang Y, Kapere Ochieng J, Kempen MB, Munck AB, Swagemakers S, van Ijcken W, Grosveld F, Tibboel D, Rottier RJ. Huang Y, et al. Among authors: rottier rj. PLoS One. 2013;8(2):e57695. doi: 10.1371/journal.pone.0057695. Epub 2013 Feb 25. PLoS One. 2013. PMID: 23451260 Free PMC article.

8

Disturbed balance between SOX2 and CDX2 in human vitelline duct anomalies and intestinal duplications.

Raghoebir L, Biermann K, Buscop-van Kempen M, Wijnen RM, Tibboel D, Smits R, Rottier RJ. Raghoebir L, et al. Among authors: rottier rj. Virchows Arch. 2013 May;462(5):515-22. doi: 10.1007/s00428-013-1405-5. Epub 2013 Apr 9. Virchows Arch. 2013. PMID: 23568430

9

Sox2 regulates the emergence of lung basal cells by directly activating the transcription of Trp63.

Ochieng JK, Schilders K, Kool H, Boerema-De Munck A, Buscop-Van Kempen M, Gontan C, Smits R, Grosveld FG, Wijnen RM, Tibboel D, Rottier RJ. Ochieng JK, et al. Among authors: rottier rj. Am J Respir Cell Mol Biol. 2014 Aug;51(2):311-22. doi: 10.1165/rcmb.2013-0419OC. Am J Respir Cell Mol Biol. 2014. PMID: 24669837

10

Clinical and etiological heterogeneity in patients with tracheo-esophageal malformations and associated anomalies.

Brosens E, Ploeg M, van Bever Y, Koopmans AE, IJsselstijn H, Rottier RJ, Wijnen R, Tibboel D, de Klein A. Brosens E, et al. Among authors: rottier rj. Eur J Med Genet. 2014 Aug;57(8):440-52. doi: 10.1016/j.ejmg.2014.05.009. Epub 2014 Jun 13. Eur J Med Genet. 2014. PMID: 24931924 Review.

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