Alders M - Search Results

1

Genomic organization and chromosomal localization of a member of the MAP kinase phosphatase gene family to human chromosome 11p15.5 and a pseudogene to 10q11.2.

Nesbit MA, Hodges MD, Campbell L, de Meulemeester TM, Alders M, Rodrigues NR, Talbot K, Theodosiou AM, Mannens MA, Nakamura Y, Little PF, Davies KE. Nesbit MA, et al. Among authors: alders m. Genomics. 1997 Jun 1;42(2):284-94. doi: 10.1006/geno.1997.4737. Genomics. 1997. PMID: 9192849

2

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. Among authors: alders m. Cytogenet Cell Genet. 1995;68(3-4):222-5. doi: 10.1159/000133917. Cytogenet Cell Genet. 1995. PMID: 7842740

3

The human Achaete-Scute homologue 2 (ASCL2,HASH2) maps to chromosome 11p15.5, close to IGF2 and is expressed in extravillus trophoblasts.

Alders M, Hodges M, Hadjantonakis AK, Postmus J, van Wijk I, Bliek J, de Meulemeester M, Westerveld A, Guillemot F, Oudejans C, Little P, Mannens M. Alders M, et al. Hum Mol Genet. 1997 Jun;6(6):859-67. doi: 10.1093/hmg/6.6.859. Hum Mol Genet. 1997. PMID: 9175731

4

Disruption of a novel imprinted zinc-finger gene, ZNF215, in Beckwith-Wiedemann syndrome.

Alders M, Ryan A, Hodges M, Bliek J, Feinberg AP, Privitera O, Westerveld A, Little PF, Mannens M. Alders M, et al. Am J Hum Genet. 2000 May;66(5):1473-84. doi: 10.1086/302892. Epub 2000 Apr 10. Am J Hum Genet. 2000. PMID: 10762538 Free PMC article.

5

Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments.

Hoovers JM, Kalikin LM, Johnson LA, Alders M, Redeker B, Law DJ, Bliek J, Steenman M, Benedict M, Wiegant J, Lengauer C, Taillon-Miller P, Schlessinger D, Edwards MC, Elledge SJ, Ivens A, Westerveld A, Little P, Mannens M, Feinberg AP. Hoovers JM, et al. Among authors: alders m. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12456-60. doi: 10.1073/pnas.92.26.12456. Proc Natl Acad Sci U S A. 1995. PMID: 8618920 Free PMC article.

6

Genomic imprinting: concept and clinical consequences.

Mannens M, Alders M. Mannens M, et al. Among authors: alders m. Ann Med. 1999 Feb;31(1):4-11. doi: 10.3109/07853899909019258. Ann Med. 1999. PMID: 10219710 Free article. Review.

7

An integrated physical map of 210 markers assigned to the short arm of human chromosome 11.

Redeker E, Hoovers JM, Alders M, van Moorsel CJ, Ivens AC, Gregory S, Kalikin L, Bliek J, de Galan L, van den Bogaard R, et al. Redeker E, et al. Among authors: alders m. Genomics. 1994 Jun;21(3):538-50. doi: 10.1006/geno.1994.1312. Genomics. 1994. PMID: 7959730 Free article.

8

Positional cloning of genes involved in the Beckwith-Wiedemann syndrome, hemihypertrophy, and associated childhood tumors.

Mannens M, Alders M, Redeker B, Bliek J, Steenman M, Wiesmeyer C, de Meulemeester M, Ryan A, Kalikin L, Voûte T, De Kraker J, Hoovers J, Slater R, Feinberg A, Little P, Westerveld A. Mannens M, et al. Among authors: alders m. Med Pediatr Oncol. 1996 Nov;27(5):490-4. doi: 10.1002/(SICI)1096-911X(199611)27:5<490::AID-MPO17>3.0.CO;2-E. Med Pediatr Oncol. 1996. PMID: 8827079 Review.

9

Cloning of candidate genes involved in the Beckwith-Wiedemann syndrome and childhood tumors.

Alders M, Bliek J, Redeker B, Ryan A, Feinberg A, Westerveld A, Little P, Mannens M. Alders M, et al. Med Pediatr Oncol. 1996 Nov;27(5):495-7. doi: 10.1002/(SICI)1096-911X(199611)27:5<495::AID-MPO18>3.0.CO;2-9. Med Pediatr Oncol. 1996. PMID: 8827080 No abstract available.

10

Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia.

Bliek J, Maas S, Alders M, Merks JH, Mannens M. Bliek J, et al. Among authors: alders m. J Pediatr. 2008 Jul;153(1):95-100. doi: 10.1016/j.jpeds.2007.12.022. Epub 2008 Mar 7. J Pediatr. 2008. PMID: 18571544

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