118 related articles for article (PubMed ID: 9878243)
1. Conserved chromosomal location and genomic structure of human and mouse fatty-acid amide hydrolase genes and evaluation of clasper as a candidate neurological mutation.
Wan M; Cravatt BF; Ring HZ; Zhang X; Francke U
Genomics; 1998 Dec; 54(3):408-14. PubMed ID: 9878243
[TBL] [Abstract][Full Text] [Related]
2. Canavan disease: genomic organization and localization of human ASPA to 17p13-ter and conservation of the ASPA gene during evolution.
Kaul R; Balamurugan K; Gao GP; Matalon R
Genomics; 1994 May; 21(2):364-70. PubMed ID: 8088831
[TBL] [Abstract][Full Text] [Related]
3. Genomic characterization of the lysophosphatidic acid receptor gene, lp(A2)/Edg4, and identification of a frameshift mutation in a previously characterized cDNA.
Contos JJ; Chun J
Genomics; 2000 Mar; 64(2):155-69. PubMed ID: 10729222
[TBL] [Abstract][Full Text] [Related]
4. Genomic cloning of mouse MIF (macrophage inhibitory factor) and genetic mapping of the human and mouse expressed gene and nine mouse pseudogenes.
Kozak CA; Adamson MC; Buckler CE; Segovia L; Paralkar V; Wistow G
Genomics; 1995 Jun; 27(3):405-11. PubMed ID: 7558020
[TBL] [Abstract][Full Text] [Related]
5. Human and mouse chromosomal mapping of Stac, a neuron-specific protein with an SH3 domain.
Kawai J; Suzuki H; Hara A; Hirose K; Watanabe S
Genomics; 1998 Jan; 47(1):140-2. PubMed ID: 9465308
[TBL] [Abstract][Full Text] [Related]
6. Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.
Johnson KR; Smith L; Johnson DK; Rhodes J; Rinchik EM; Thayer M; Lewis EJ
Genomics; 1996 May; 33(3):527-31. PubMed ID: 8661014
[TBL] [Abstract][Full Text] [Related]
7. Calcium channel beta 4 (CACNB4): human ortholog of the mouse epilepsy gene lethargic.
Escayg A; Jones JM; Kearney JA; Hitchcock PF; Meisler MH
Genomics; 1998 May; 50(1):14-22. PubMed ID: 9628818
[TBL] [Abstract][Full Text] [Related]
8. Structure of the human gene (COX6A2) for the heart/muscle isoform of cytochrome c oxidase subunit VIa and its chromosomal location in humans, mice, and cattle.
Bachman NJ; Riggs PK; Siddiqui N; Makris GJ; Womack JE; Lomax MI
Genomics; 1997 May; 42(1):146-51. PubMed ID: 9177785
[TBL] [Abstract][Full Text] [Related]
9. Characterization of the mouse loricrin gene: linkage with profilaggrin and the flaky tail and soft coat mutant loci on chromosome 3.
Rothnagel JA; Longley MA; Bundman DS; Naylor SL; Lalley PA; Jenkins NA; Gilbert DJ; Copeland NG; Roop DR
Genomics; 1994 Sep; 23(2):450-6. PubMed ID: 7835895
[TBL] [Abstract][Full Text] [Related]
10. The human acid ceramidase gene (ASAH): structure, chromosomal location, mutation analysis, and expression.
Li CM; Park JH; He X; Levy B; Chen F; Arai K; Adler DA; Disteche CM; Koch J; Sandhoff K; Schuchman EH
Genomics; 1999 Dec; 62(2):223-31. PubMed ID: 10610716
[TBL] [Abstract][Full Text] [Related]
11. Mapping of the phenol sulfotransferase gene (STP) to human chromosome 16p12.1-p11.2 and to mouse chromosome 7.
Dooley TP; Obermoeller RD; Leiter EH; Chapman HD; Falany CN; Deng Z; Siciliano MJ
Genomics; 1993 Nov; 18(2):440-3. PubMed ID: 8288252
[TBL] [Abstract][Full Text] [Related]
12. Rapid screening for potentially relevant polymorphisms in the human fatty acid amide hydrolase gene using Pyrosequencing.
Doehring A; Geisslinger G; Lötsch J
Prostaglandins Other Lipid Mediat; 2007 Nov; 84(3-4):128-37. PubMed ID: 17991615
[TBL] [Abstract][Full Text] [Related]
13. Gene structure, chromosomal localization, and expression pattern of Capn12, a new member of the calpain large subunit gene family.
Dear TN; Meier NT; Hunn M; Boehm T
Genomics; 2000 Sep; 68(2):152-60. PubMed ID: 10964513
[TBL] [Abstract][Full Text] [Related]
14. Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter.
Chen H; Gos A; Morris MA; Antonarakis SE
Genomics; 1996 Aug; 35(3):620-4. PubMed ID: 8812505
[TBL] [Abstract][Full Text] [Related]
15. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO.
Griffith AJ; Burgess DL; Kohrman DC; Yu J; Blaschak J; Blanton SH; Boehnke M; Hecht JT; Overhauser J; Meisler MH
Genomics; 1996 Jun; 34(3):299-303. PubMed ID: 8786128
[TBL] [Abstract][Full Text] [Related]
16. Assignment of the beta B1 crystallin gene (CRYBB1) to human chromosome 22 and mouse chromosome 5.
Hulsebos TJ; Gilbert DJ; Delattre O; Smink LJ; Dunham I; Westerveld A; Thomas G; Jenkins NA; Copeland NG
Genomics; 1995 Oct; 29(3):712-8. PubMed ID: 8575764
[TBL] [Abstract][Full Text] [Related]
17. Fatty acid amide hydrolase in brain ventricular epithelium: mutually exclusive patterns of expression in mouse and rat.
Egertová M; Michael GJ; Cravatt BF; Elphick MR
J Chem Neuroanat; 2004 Nov; 28(3):171-81. PubMed ID: 15482903
[TBL] [Abstract][Full Text] [Related]
18. Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
Pasteris NG; Gorski JL
Genomics; 1999 Aug; 60(1):57-66. PubMed ID: 10458911
[TBL] [Abstract][Full Text] [Related]
19. An intron capture strategy used to identify and map a lysyl oxidase-like gene on chromosome 9 in the mouse.
Wydner KS; Kim Y; Csiszar K; Boyd CD; Passmore HC
Genomics; 1997 Mar; 40(2):342-5. PubMed ID: 9119402
[TBL] [Abstract][Full Text] [Related]
20. Chromosomal localization and genomic organization of genes encoding guanylyl cyclase receptors expressed in olfactory sensory neurons and retina.
Yang RB; Fülle HJ; Garbers DL
Genomics; 1996 Feb; 31(3):367-72. PubMed ID: 8838319
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
