Mannens MM - Search Results

1

Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in The Netherlands.

Lombardi MP, Redeker EJ, Defesche JC, Kamerling SW, Trip MD, Mannens MM, Havekes LM, Kastelein JJ. Lombardi MP, et al. Among authors: mannens mm. Clin Genet. 2000 Feb;57(2):116-24. doi: 10.1034/j.1399-0004.2000.570205.x. Clin Genet. 2000. PMID: 10735632

2

The distal region of 11p13 and associated genetic diseases.

Mannens M, Hoovers JM, Bleeker-Wagemakers EM, Redeker E, Bliek J, Overbeeke-Melkert M, Saunders G, Williams B, van Heyningen V, Junien C, et al. Mannens M, et al. Genomics. 1991 Oct;11(2):284-93. doi: 10.1016/0888-7543(91)90134-z. Genomics. 1991. PMID: 1769647

3

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.

Redeker E, Alders M, Hoovers JM, Richard CW 3rd, Westerveld A, Mannens M. Redeker E, et al. Cytogenet Cell Genet. 1995;68(3-4):222-5. doi: 10.1159/000133917. Cytogenet Cell Genet. 1995. PMID: 7842740

4

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.

Mannens M, Hoovers JM, Redeker E, Verjaal M, Feinberg AP, Little P, Boavida M, Coad N, Steenman M, Bliek J, et al. Mannens M, et al. Eur J Hum Genet. 1994;2(1):3-23. doi: 10.1159/000472337. Eur J Hum Genet. 1994. PMID: 7913866

5

TaqI and RsaI polymorphisms in the H19 gene (D11S813E).

Redeker E, Van Moorsel CJ, Feinberg A, Mannens M. Redeker E, et al. Hum Mol Genet. 1993 Jun;2(6):823. doi: 10.1093/hmg/2.6.823. Hum Mol Genet. 1993. PMID: 8102574 No abstract available.

6

High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.

Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. Hoovers JM, et al. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

7

Molecular characterisation of 10 Dutch properdin type I deficient families: mutation analysis and X-inactivation studies.

van den Bogaard R, Fijen CA, Schipper MG, de Galan L, Kuijper EJ, Mannens MM. van den Bogaard R, et al. Among authors: mannens mm. Eur J Hum Genet. 2000 Jul;8(7):513-8. doi: 10.1038/sj.ejhg.5200496. Eur J Hum Genet. 2000. PMID: 10909851

8

Chromosomal region 11p15 is associated with male factor subfertility.

Gianotten J, van der Veen F, Alders M, Leschot NJ, Tanck MW, Land JA, Kremer JA, Hoefsloot LH, Mannens MM, Lombardi MP, Hoffer MJ. Gianotten J, et al. Among authors: mannens mm. Mol Hum Reprod. 2003 Oct;9(10):587-92. doi: 10.1093/molehr/gag081. Mol Hum Reprod. 2003. PMID: 12970396

9

The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.

Alders M, Jongbloed R, Deelen W, van den Wijngaard A, Doevendans P, Ten Cate F, Regitz-Zagrosek V, Vosberg HP, van Langen I, Wilde A, Dooijes D, Mannens M. Alders M, et al. Eur Heart J. 2003 Oct;24(20):1848-53. doi: 10.1016/s0195-668x(03)00466-4. Eur Heart J. 2003. PMID: 14563344

10

Increased DNA damage sensitivity of Cornelia de Lange syndrome cells: evidence for impaired recombinational repair.

Vrouwe MG, Elghalbzouri-Maghrani E, Meijers M, Schouten P, Godthelp BC, Bhuiyan ZA, Redeker EJ, Mannens MM, Mullenders LH, Pastink A, Darroudi F. Vrouwe MG, et al. Among authors: mannens mm. Hum Mol Genet. 2007 Jun 15;16(12):1478-87. doi: 10.1093/hmg/ddm098. Epub 2007 Apr 27. Hum Mol Genet. 2007. PMID: 17468178

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