van der Velden PA - Search Results

1

Accurate Quantification of T Cells in Copy Number Stable and Unstable DNA Samples Using Multiplex Digital PCR.

Nell RJ, Zoutman WH, Calbet-Llopart N, Garcia AP, Menger NV, Versluis M, Puig S, Gruis NA, van der Velden PA. Nell RJ, et al. Among authors: van der velden pa. J Mol Diagn. 2022 Jan;24(1):88-100. doi: 10.1016/j.jmoldx.2021.10.007. Epub 2021 Nov 11. J Mol Diagn. 2022. PMID: 34775028 Free article.

2

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families.

Gruis NA, Sandkuijl LA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. Melanoma Res. 1995 Jun;5(3):169-77. doi: 10.1097/00008390-199506000-00005. Melanoma Res. 1995. PMID: 7640518

3

Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds.

Gruis NA, van der Velden PA, Sandkuijl LA, Prins DE, Weaver-Feldhaus J, Kamb A, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. Nat Genet. 1995 Jul;10(3):351-3. doi: 10.1038/ng0795-351. Nat Genet. 1995. PMID: 7670475

4

Genetics of familial atypical multiple mole-melanoma (FAMMM) syndrome in The Netherlands: how far have we come?

Gruis NA, Van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. Bull Cancer. 1998 Jul;85(7):627-30. Bull Cancer. 1998. PMID: 9752270 Free article.

5

A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families.

van der Velden PA, Sandkuijl LA, Bergman W, Hille ET, Frants RR, Gruis NA. van der Velden PA, et al. Genome Res. 1999 Jun;9(6):575-80. Genome Res. 1999. PMID: 10400925 Free PMC article.

6

Familial melanoma; CDKN2A and beyond.

Gruis NA, van der Velden PA, Bergman W, Frants RR. Gruis NA, et al. Among authors: van der velden pa. J Investig Dermatol Symp Proc. 1999 Sep;4(1):50-4. doi: 10.1038/sj.jidsp.5640181. J Investig Dermatol Symp Proc. 1999. PMID: 10537008 Free article. Review.

7

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden).

Vasen HF, Gruis NA, Frants RR, van Der Velden PA, Hille ET, Bergman W. Vasen HF, et al. Among authors: van der velden pa. Int J Cancer. 2000 Sep 15;87(6):809-11. Int J Cancer. 2000. PMID: 10956390

8

Promoter hypermethylation: a common cause of reduced p16(INK4a) expression in uveal melanoma.

van der Velden PA, Metzelaar-Blok JA, Bergman W, Monique H, Hurks H, Frants RR, Gruis NA, Jager MJ. van der Velden PA, et al. Cancer Res. 2001 Jul 1;61(13):5303-6. Cancer Res. 2001. PMID: 11431374

9

Melanocortin-1 receptor variant R151C modifies melanoma risk in Dutch families with melanoma.

van der Velden PA, Sandkuijl LA, Bergman W, Pavel S, van Mourik L, Frants RR, Gruis NA. van der Velden PA, et al. Among authors: van mourik l. Am J Hum Genet. 2001 Oct;69(4):774-9. doi: 10.1086/323411. Epub 2001 Aug 7. Am J Hum Genet. 2001. PMID: 11500806 Free PMC article.

10

Homozygous germline mutation of CDKN2A/p16 and glucose-6-phosphate dehydrogenase deficiency in a multiple melanoma case.

Pavel S, Smit NP, van der Meulen H, Kolb RM, de Groot AJ, van der Velden PA, Gruis NA, Bergman W. Pavel S, et al. Among authors: van der meulen h, van der velden pa. Melanoma Res. 2003 Apr;13(2):171-8. doi: 10.1097/00008390-200304000-00010. Melanoma Res. 2003. PMID: 12690301

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