Similar articles for PMID: 12119096

Year	Number of Results
1991	2
1992	1
1995	3
1997	1
1998	6
1999	9
2000	22
2001	22
2002	9
2003	2
2004	6
2005	2
2007	2
2010	2
2014	1
2015	1
2022	2
2023	3
2024	0

1

The human gamma-aminobutyric acid A receptor delta (GABRD) gene: molecular characterisation and tissue-specific expression.

Windpassinger C, Kroisel PM, Wagner K, Petek E. Windpassinger C, et al. Gene. 2002 Jun 12;292(1-2):25-31. doi: 10.1016/s0378-1119(02)00649-2. Gene. 2002. PMID: 12119096

2

Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit.

Berti L, Mittler G, Przemeck GK, Stelzer G, Günzler B, Amati F, Conti E, Dallapiccola B, Hrabé de Angelis M, Novelli G, Meisterernst M. Berti L, et al. Genomics. 2001 Jun 15;74(3):320-32. doi: 10.1006/geno.2001.6566. Genomics. 2001. PMID: 11414760

3

Gene structure, chromosomal localization, cDNA cloning and expression of the mouse ATP-gated ionotropic receptor P2X5 subunit.

Cox JA, Barmina O, Voigt MM. Cox JA, et al. Gene. 2001 May 30;270(1-2):145-52. doi: 10.1016/s0378-1119(01)00484-x. Gene. 2001. PMID: 11404011

4

Cloning, expression patterns, and chromosome localization of three human and two mouse homologues of GABA(A) receptor-associated protein.

Xin Y, Yu L, Chen Z, Zheng L, Fu Q, Jiang J, Zhang P, Gong R, Zhao S. Xin Y, et al. Genomics. 2001 Jun 15;74(3):408-13. doi: 10.1006/geno.2001.6555. Genomics. 2001. PMID: 11414770

5

Molecular cloning, genomic organization, chromosomal mapping and subcellular localization of mouse PAP7: a PBR and PKA-RIalpha associated protein.

Liu J, Cavalli LR, Haddad BR, Papadopoulos V. Liu J, et al. Gene. 2003 Apr 10;308:1-10. doi: 10.1016/s0378-1119(03)00453-0. Gene. 2003. PMID: 12711385

6

Complex RNA processing of TDRKH, a novel gene encoding the putative RNA-binding tudor and KH domains.

Lamb FS, Barna TJ, Goud C, Marenholz I, Mischke D, Schutte BC. Lamb FS, et al. Gene. 2000 Apr 4;246(1-2):209-18. doi: 10.1016/s0378-1119(00)00087-1. Gene. 2000. PMID: 10767542

7

Human homologue of a gene mutated in the slow Wallerian degeneration (C57BL/Wld(s)) mouse.

Fernando FS, Conforti L, Tosi S, Smith AD, Coleman MP. Fernando FS, et al. Gene. 2002 Feb 6;284(1-2):23-9. doi: 10.1016/s0378-1119(02)00394-3. Gene. 2002. PMID: 11891043

8

Epilepsy and neurological findings in 11 individuals with 1p36 deletion syndrome.

Kurosawa K, Kawame H, Okamoto N, Ochiai Y, Akatsuka A, Kobayashi M, Shimohira M, Mizuno S, Wada K, Fukushima Y, Kawawaki H, Yamamoto T, Masuno M, Imaizumi K, Kuroki Y. Kurosawa K, et al. Brain Dev. 2005 Aug;27(5):378-82. doi: 10.1016/j.braindev.2005.02.004. Epub 2005 Apr 13. Brain Dev. 2005. PMID: 16023556

9

Refinement of causative genes in monosomy 1p36 through clinical and molecular cytogenetic characterization of small interstitial deletions.

Rosenfeld JA, Crolla JA, Tomkins S, Bader P, Morrow B, Gorski J, Troxell R, Forster-Gibson C, Cilliers D, Hislop RG, Lamb A, Torchia B, Ballif BC, Shaffer LG. Rosenfeld JA, et al. Am J Med Genet A. 2010 Aug;152A(8):1951-9. doi: 10.1002/ajmg.a.33516. Am J Med Genet A. 2010. PMID: 20635359

10

Characterization of a novel gene, C21orf6, mapping to a critical region of chromosome 21q22.1 involved in the monosomy 21 phenotype and of its murine ortholog, orf5.

Orti R, Rachidi M, Vialard F, Toyama K, Lopes C, Taudien S, Rosenthal A, Yaspo ML, Sinet PM, Delabar JM. Orti R, et al. Genomics. 2000 Mar 1;64(2):203-10. doi: 10.1006/geno.1999.6109. Genomics. 2000. PMID: 10729227

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