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Items: 1 to 20 of 175

1.

Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome.

Dahmane N, Ghezala GA, Gosset P, Chamoun Z, Dufresne-Zacharia MC, Lopes C, Rabatel N, Gassanova-Maugenre S, Chettouh Z, Abramowski V, Fayet E, Yaspo ML, Korn B, Blouin JL, Lehrach H, Poutska A, Antonarakis SE, Sinet PM, Créau N, Delabar JM.

Genomics. 1998 Feb 15;48(1):12-23.

PMID:
9503011
2.

Model for a transcript map of human chromosome 21: isolation of new coding sequences from exon and enriched cDNA libraries.

Yaspo ML, Gellen L, Mott R, Korn B, Nizetic D, Poustka AM, Lehrach H.

Hum Mol Genet. 1995 Aug;4(8):1291-304.

PMID:
7581366
3.

A 1.6-Mb P1-based physical map of the Down syndrome region on chromosome 21.

Ohira M, Ichikawa H, Suzuki E, Iwaki M, Suzuki K, Saito-Ohara F, Ikeuchi T, Chumakov I, Tanahashi H, Tashiro K, Sakaki Y.

Genomics. 1996 Apr 1;33(1):65-74.

PMID:
8617511
4.

A transcript map of the Down syndrome critical region on chromosome 21.

Peterson A, Patil N, Robbins C, Wang L, Cox DR, Myers RM.

Hum Mol Genet. 1994 Oct;3(10):1735-42.

PMID:
7849696
5.

Cosmid contig and transcriptional map of three regions of human chromosome 21q22: identification of 37 novel transcripts by direct selection.

Guimera J, Pucharcós C, Domènech A, Casas C, Solans A, Gallardo T, Ashley J, Lovett M, Estivill X, Pritchard M.

Genomics. 1997 Oct 1;45(1):59-67.

PMID:
9339361
6.

Localization of 102 exons to a 2.5 Mb region involved in Down syndrome.

Lucente D, Chen HM, Shea D, Samec SN, Rutter M, Chrast R, Rossier C, Buckler A, Antonarakis SE, McCormick MK.

Hum Mol Genet. 1995 Aug;4(8):1305-11.

PMID:
7581367
7.

Localization of 16 exons to a 450-kb region involved in the autoimmune polyglandular disease type I (APECED) on human chromosome 21q22.3.

Kudoh J, Nagamine K, Asakawa S, Abe I, Kawasaki K, Maeda H, Tsujimoto S, Minoshima S, Ito F, Shimizu N.

DNA Res. 1997 Feb 28;4(1):45-52.

PMID:
9179495
8.

YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome.

Nadal M, Milà M, Pritchard M, Mur A, Pujals J, Blouin JL, Antonarakis SE, Ballesta F, Estivill X.

Hum Genet. 1996 Oct;98(4):460-6.

PMID:
8792823
9.

An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region.

Osoegawa K, Susukida R, Okano S, Kudoh J, Minoshima S, Shimizu N, de Jong PJ, Groet J, Ives J, Lehrach H, Nizetic D, Soeda E.

Genomics. 1996 Mar 15;32(3):375-87.

PMID:
8838801
10.

3.6-Mb genomic and YAC physical map of the Down syndrome chromosome region on chromosome 21.

Dufresne-Zacharia MC, Dahmane N, Theophile D, Orti R, Chettouh Z, Sinet PM, Delabar JM.

Genomics. 1994 Feb;19(3):462-9.

PMID:
8188288
11.

A new human gene from the Down syndrome critical region encodes a proline-rich protein highly expressed in fetal brain and heart.

Fuentes JJ, Pritchard MA, Planas AM, Bosch A, Ferrer I, Estivill X.

Hum Mol Genet. 1995 Oct;4(10):1935-44.

PMID:
8595418
12.

Isolation of the human BACH1 transcription regulator gene, which maps to chromosome 21q22.1.

Blouin JL, Duriaux Saïl G, Guipponi M, Rossier C, Pappasavas MP, Antonarakis SE.

Hum Genet. 1998 Mar;102(3):282-8.

PMID:
9544839
13.

Gene identification in 1.6-Mb region of the Down syndrome region on chromosome 21.

Ohira M, Seki N, Nagase T, Suzuki E, Nomura N, Ohara O, Hattori M, Sakaki Y, Eki T, Murakami Y, Saito T, Ichikawa H, Ohki M.

Genome Res. 1997 Jan;7(1):47-58.

14.

Mapping the Down syndrome chromosome region. Establishment of a YAC contig spanning 1.2 megabases.

Crété N, Gosset P, Théophile D, Duterque-Coquillaud M, Blouin JL, Vayssettes C, Sinet PM, Créau-Goldberg N.

Eur J Hum Genet. 1993;1(1):51-63.

PMID:
8069651
15.

A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21.

Patil N, Peterson A, Rothman A, de Jong PJ, Myers RM, Cox DR.

Hum Mol Genet. 1994 Oct;3(10):1811-7.

PMID:
7849705
16.

Identification of a novel human gene containing the tetratricopeptide repeat domain from the Down syndrome region of chromosome 21.

Ohira M, Ootsuyama A, Suzuki E, Ichikawa H, Seki N, Nagase T, Nomura N, Ohki M.

DNA Res. 1996 Feb 29;3(1):9-16.

PMID:
8724848
17.

Down syndrome-critical region contains a gene homologous to Drosophila sim expressed during rat and human central nervous system development.

Dahmane N, Charron G, Lopes C, Yaspo ML, Maunoury C, Decorte L, Sinet PM, Bloch B, Delabar JM.

Proc Natl Acad Sci U S A. 1995 Sep 26;92(20):9191-5.

18.

High resolution physical mapping and identification of transcribed sequences in the Down syndrome region-2.

Vidal-Taboada JM, Bergoñón S, Sánchez M, López-Acedo C, Groet J, Nizetic D, Egeo A, Scartezzini P, Katsanis N, Fisher EM, Delabar JM, Oliva R.

Biochem Biophys Res Commun. 1998 Feb 13;243(2):572-8.

PMID:
9480850
19.

High-resolution physical map and identification of potentially regulatory sequences of the human SH3BGR located in the Down syndrome chromosomal region.

Vidal-Taboada JM, Bergoñon S, Scartezzini P, Egeo A, Nizetic D, Oliva R.

Biochem Biophys Res Commun. 1997 Dec 18;241(2):321-6.

PMID:
9425270
20.

Mapping of a novel human carbonyl reductase, CBR3, and ribosomal pseudogenes to human chromosome 21q22.2.

Watanabe K, Sugawara C, Ono A, Fukuzumi Y, Itakura S, Yamazaki M, Tashiro H, Osoegawa K, Soeda E, Nomura T.

Genomics. 1998 Aug 15;52(1):95-100.

PMID:
9740676

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