Morris MA - Search Results

1

Characterization and chromosomal localization of a human P2X receptor from the urinary bladder.

Valera S, Talabot F, Evans RJ, Gos A, Antonarakis SE, Morris MA, Buell GN. Valera S, et al. Among authors: morris ma. Recept Channels. 1995;3(4):283-9. Recept Channels. 1995. PMID: 8834001

2

Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.

Chen H, Gos A, Morris MA, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genomics. 1996 Aug 1;35(3):620-4. doi: 10.1006/geno.1996.0411. Genomics. 1996. PMID: 8812505

3

Gene structure and chromosomal localization of the human P2X7 receptor.

Buell GN, Talabot F, Gos A, Lorenz J, Lai E, Morris MA, Antonarakis SE. Buell GN, et al. Among authors: morris ma. Recept Channels. 1998;5(6):347-54. Recept Channels. 1998. PMID: 9826911

4

A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y.

Chen H, Rossier C, Morris MA, Scott HS, Gos A, Bairoch A, Antonarakis SE. Chen H, et al. Among authors: morris ma. Hum Genet. 1999 Nov;105(5):399-409. doi: 10.1007/s004390051122. Hum Genet. 1999. PMID: 10598804

5

The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3.

Lalioti MD, Gos A, Green MR, Rossier C, Morris MA, Antonarakis SE. Lalioti MD, et al. Among authors: morris ma. Genomics. 1996 Apr 15;33(2):298-300. doi: 10.1006/geno.1996.0196. Genomics. 1996. PMID: 8660980

6

Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21.

Blouin JL, Duriaux-Sail G, Chen H, Gos A, Morris MA, Rossier C, Antonarakis SE. Blouin JL, et al. Among authors: morris ma. Genomics. 1996 Apr 15;33(2):309-12. doi: 10.1006/geno.1996.0199. Genomics. 1996. PMID: 8660983

7

Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping.

Chen H, Chrast R, Rossier C, Morris MA, Lalioti MD, Antonarakis SE. Chen H, et al. Among authors: morris ma. Genome Res. 1996 Aug;6(8):747-60. doi: 10.1101/gr.6.8.747. Genome Res. 1996. PMID: 8858350 Free article.

8

Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.

Eliez S, Morris MA, Dahoun-Hadorn S, DeLozier-Blanchet CD, Gos A, Sizonenko P, Antonarakis SE. Eliez S, et al. Among authors: morris ma. Am J Med Genet. 1997 Jun 13;70(3):222-8. doi: 10.1002/(sici)1096-8628(19970613)70:3<222::aid-ajmg3>3.0.co;2-y. Am J Med Genet. 1997. PMID: 9188657

9

Analysis of mutations and chromosomal localisation of the gene encoding RFX5, a novel transcription factor affected in major histocompatibility complex class II deficiency.

Villard J, Reith W, Barras E, Gos A, Morris MA, Antonarakis SE, Van den Elsen PJ, Mach B. Villard J, et al. Among authors: morris ma. Hum Mutat. 1997;10(6):430-5. doi: 10.1002/(SICI)1098-1004(1997)10:6<430::AID-HUMU3>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9401005

10

Isolation and characterization of the mouse Aire gene.

Mittaz L, Rossier C, Heino M, Peterson P, Krohn KJ, Gos A, Morris MA, Kudoh J, Shimizu N, Antonarakis SE, Scott HS. Mittaz L, et al. Among authors: morris ma. Biochem Biophys Res Commun. 1999 Feb 16;255(2):483-90. doi: 10.1006/bbrc.1999.0223. Biochem Biophys Res Commun. 1999. PMID: 10049735

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

536 results

Search Page

Filters