van der Burgt C - Search Results

1

ATF3 and Fra1 have opposite functions in JNK- and ERK-dependent DNA damage responses.

Hamdi M, Popeijus HE, Carlotti F, Janssen JM, van der Burgt C, Cornelissen-Steijger P, van de Water B, Hoeben RC, Matsuo K, van Dam H. Hamdi M, et al. Among authors: van der burgt c. DNA Repair (Amst). 2008 Mar 1;7(3):487-96. doi: 10.1016/j.dnarep.2007.12.004. Epub 2008 Jan 30. DNA Repair (Amst). 2008. PMID: 18249159

2

JNK-Dependent cJun Phosphorylation Mitigates TGFβ- and EGF-Induced Pre-Malignant Breast Cancer Cell Invasion by Suppressing AP-1-Mediated Transcriptional Responses.

Sundqvist A, Voytyuk O, Hamdi M, Popeijus HE, van der Burgt CB, Janssen J, Martens JWM, Moustakas A, Heldin CH, Ten Dijke P, van Dam H. Sundqvist A, et al. Among authors: van der burgt cb. Cells. 2019 Nov 21;8(12):1481. doi: 10.3390/cells8121481. Cells. 2019. PMID: 31766464 Free PMC article.

3

DNA damage in transcribed genes induces apoptosis via the JNK pathway and the JNK-phosphatase MKP-1.

Hamdi M, Kool J, Cornelissen-Steijger P, Carlotti F, Popeijus HE, van der Burgt C, Janssen JM, Yasui A, Hoeben RC, Terleth C, Mullenders LH, van Dam H. Hamdi M, et al. Among authors: van der burgt c. Oncogene. 2005 Nov 3;24(48):7135-44. doi: 10.1038/sj.onc.1208875. Oncogene. 2005. PMID: 16044158

4

Growth factors can activate ATF2 via a two-step mechanism: phosphorylation of Thr71 through the Ras-MEK-ERK pathway and of Thr69 through RalGDS-Src-p38.

Ouwens DM, de Ruiter ND, van der Zon GC, Carter AP, Schouten J, van der Burgt C, Kooistra K, Bos JL, Maassen JA, van Dam H. Ouwens DM, et al. Among authors: van der burgt c. EMBO J. 2002 Jul 15;21(14):3782-93. doi: 10.1093/emboj/cdf361. EMBO J. 2002. PMID: 12110590 Free PMC article.

5

Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?

Raaijmakers R, Noordam C, Noonan JA, Croonen EA, van der Burgt CJ, Draaisma JM. Raaijmakers R, et al. Among authors: van der burgt cj. Eur J Pediatr. 2008 Dec;167(12):1363-7. doi: 10.1007/s00431-008-0670-9. Epub 2008 Feb 13. Eur J Pediatr. 2008. PMID: 18270737

6

[The Noonan syndrome from a pediatric perspective].

Noordam C, Thoonen G, van der Burgt CJ. Noordam C, et al. Among authors: van der burgt cj. Ned Tijdschr Geneeskd. 2003 Apr 5;147(14):644-8. Ned Tijdschr Geneeskd. 2003. PMID: 12712646 Review. Dutch.

7

A female patient with neurological, facial, digital and renal abnormalities: another case of the neurofaciodigitorenal (NFDR) syndrome?

Rump P, Gruijters MY, Van der Burgt CJ. Rump P, et al. Among authors: van der burgt cj. Clin Dysmorphol. 1997 Oct;6(4):337-40. doi: 10.1097/00019605-199710000-00006. Clin Dysmorphol. 1997. PMID: 9354842

8

T cell subsets and T cell function in cartilage-hair hypoplasia.

Kooijman R, van der Burgt CJ, Weemaes CM, Haraldsson A, Scholtens EJ, Zegers BJ. Kooijman R, et al. Among authors: van der burgt cj. Scand J Immunol. 1997 Aug;46(2):209-15. doi: 10.1046/j.1365-3083.1997.d01-112.x. Scand J Immunol. 1997. PMID: 9584003 Free article.

9

Myopathology in patients with a Noonan phenotype.

de Boode WP, Semmekrot BA, ter Laak HJ, van der Burgt CJ, Draaisma JM, Lommen EJ, Sengers RC, van Wijk-Hoek JM. de Boode WP, et al. Among authors: van der burgt cj. Acta Neuropathol. 1996 Dec;92(6):597-602. doi: 10.1007/s004010050566. Acta Neuropathol. 1996. PMID: 8960317

10

Ectrodactyly of lower limbs, congenital heart defect and characteristic facies in four unrelated Dutch patients: a new association.

Van Den Ende JJ, Van Der Burgt CJ, Jansweijer MC, Hamel BC, Brunner HG. Van Den Ende JJ, et al. Among authors: van der burgt cj. Clin Dysmorphol. 1996 Jan;5(1):1-7. doi: 10.1097/00019605-199601000-00001. Clin Dysmorphol. 1996. PMID: 8867653

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