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Items: 1 to 20 of 112

1.

Chromosome 21: a small land of fascinating disorders with unknown pathophysiology.

Antonarakis SE, Lyle R, Deutsch S, Reymond A.

Int J Dev Biol. 2002 Jan;46(1):89-96. Review.

2.

Chromosome 21: from sequence to applications.

Antonarakis SE.

Curr Opin Genet Dev. 2001 Jun;11(3):241-6. Review.

PMID:
11377958
3.

10 years of Genomics, chromosome 21, and Down syndrome.

Antonarakis SE.

Genomics. 1998 Jul 1;51(1):1-16. Review.

PMID:
9693027
4.

The DNA sequence of human chromosome 21.

Hattori M, Fujiyama A, Taylor TD, Watanabe H, Yada T, Park HS, Toyoda A, Ishii K, Totoki Y, Choi DK, Groner Y, Soeda E, Ohki M, Takagi T, Sakaki Y, Taudien S, Blechschmidt K, Polley A, Menzel U, Delabar J, Kumpf K, Lehmann R, Patterson D, Reichwald K, Rump A, Schillhabel M, Schudy A, Zimmermann W, Rosenthal A, Kudoh J, Schibuya K, Kawasaki K, Asakawa S, Shintani A, Sasaki T, Nagamine K, Mitsuyama S, Antonarakis SE, Minoshima S, Shimizu N, Nordsiek G, Hornischer K, Brant P, Scharfe M, Schon O, Desario A, Reichelt J, Kauer G, Blocker H, Ramser J, Beck A, Klages S, Hennig S, Riesselmann L, Dagand E, Haaf T, Wehrmeyer S, Borzym K, Gardiner K, Nizetic D, Francis F, Lehrach H, Reinhardt R, Yaspo ML; Chromosome 21 mapping and sequencing consortium..

Nature. 2000 May 18;405(6784):311-9. Erratum in: Nature 2000 Sep 7;407(6800):110.

PMID:
10830953
5.

Chromosome 21 and down syndrome: from genomics to pathophysiology.

Antonarakis SE, Lyle R, Dermitzakis ET, Reymond A, Deutsch S.

Nat Rev Genet. 2004 Oct;5(10):725-38. Review.

PMID:
15510164
6.

Mapping of a novel SH3 domain protein and two proteins of unknown function to human chromosome 21.

Katsanis N, Beck JA, Fisher EM.

Hum Genet. 1997 Sep;100(3-4):477-80.

PMID:
9272176
7.

Differential gene expression studies to explore the molecular pathophysiology of Down syndrome.

Antonarakis SE, Lyle R, Chrast R, Scott HS.

Brain Res Brain Res Rev. 2001 Oct;36(2-3):265-74. Review.

PMID:
11690624
8.
9.

Genetic mechanisms involved in the phenotype of Down syndrome.

Patterson D.

Ment Retard Dev Disabil Res Rev. 2007;13(3):199-206. Review.

PMID:
17910086
10.

Human chromosome 21: genome mapping and exploration, circa 1993.

Antonarakis SE.

Trends Genet. 1993 Apr;9(4):142-8. Review.

PMID:
8516850
11.

Human chromosome 21/Down syndrome gene function and pathway database.

Nikolaienko O, Nguyen C, Crinc LS, Cios KJ, Gardiner K.

Gene. 2005 Dec 30;364:90-8. Epub 2005 Nov 28.

PMID:
16310977
12.

Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis.

Gardiner K, Slavov D, Bechtel L, Davisson M.

Genomics. 2002 Jun;79(6):833-43.

PMID:
12036298
13.

Allelic dosage analysis with genotyping microarrays.

Ishikawa S, Komura D, Tsuji S, Nishimura K, Yamamoto S, Panda B, Huang J, Fukayama M, Jones KW, Aburatani H.

Biochem Biophys Res Commun. 2005 Aug 12;333(4):1309-14.

PMID:
15982637
14.

A population-based LD map of the human chromosome 6p.

Yu HX, Chia JM, Bourque G, Wong MV, Chan SH, Ren EC.

Immunogenetics. 2005 Sep;57(8):559-65. Epub 2005 Sep 29.

PMID:
16133449
15.

Physical mapping of chromosome 21.

Patterson D, Rahmani Z, Donaldson D, Gardiner K, Jones C.

Prog Clin Biol Res. 1993;384:33-50. Review.

PMID:
8115406
16.

Down syndrome: advances in molecular biology and the neurosciences.

Capone GT.

J Dev Behav Pediatr. 2001 Feb;22(1):40-59. Review.

PMID:
11265922
17.

Isolation and analysis of chromosome 21 genes potentially involved in Down syndrome.

Gosset P, Ait-Ghezala G, Sinet PM, Créau N.

J Neural Transm Suppl. 1999;57:197-209. Review. No abstract available.

PMID:
10666676
19.

Protein levels of genes encoded on chromosome 21 in fetal Down syndrome brain: challenging the gene dosage effect hypothesis (Part III).

Cheon MS, Kim SH, Ovod V, Kopitar Jerala N, Morgan JI, Hatefi Y, Ijuin T, Takenawa T, Lubec G.

Amino Acids. 2003;24(1-2):127-34.

PMID:
12624744
20.

Molecular approaches to trisomy 21.

Jankowski S, Stewart GD, Buraczynska M, Galt J, Van Keuren M, Kurnit DM.

Prog Clin Biol Res. 1990;360:79-88. Review. No abstract available.

PMID:
2147291

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