84 related articles for article (PubMed ID: 10749990)
1. The mouse neurological mutant flailer expresses a novel hybrid gene derived by exon shuffling between Gnb5 and Myo5a.
Jones JM; Huang JD; Mermall V; Hamilton BA; Mooseker MS; Escayg A; Copeland NG; Jenkins NA; Meisler MH
Hum Mol Genet; 2000 Mar; 9(5):821-8. PubMed ID: 10749990
[TBL] [Abstract][Full Text] [Related]
2. Identification of a novel myosin-Va mutation in an ataxic mutant rat, dilute-opisthotonus.
Futaki S; Takagishi Y; Hayashi Y; Ohmori S; Kanou Y; Inouye M; Oda S; Seo H; Iwaikawa Y; Murata Y
Mamm Genome; 2000 Aug; 11(8):649-55. PubMed ID: 10920234
[TBL] [Abstract][Full Text] [Related]
3. The human Nramp2 gene: characterization of the gene structure, alternative splicing, promoter region and polymorphisms.
Lee PL; Gelbart T; West C; Halloran C; Beutler E
Blood Cells Mol Dis; 1998 Jun; 24(2):199-215. PubMed ID: 9642100
[TBL] [Abstract][Full Text] [Related]
4. The Gnb5 gene is a novel beta-transducin homolog transcribed from a divergent promoter located immediately upstream of the Syrian hamster p53 P1 promoter.
Albor A; Notario V
Mamm Genome; 1995 Apr; 6(4):236-41. PubMed ID: 7613025
[TBL] [Abstract][Full Text] [Related]
5. Myosin Va mutation in rats is an animal model for the human hereditary neurological disease, Griscelli syndrome type 1.
Takagishi Y; Murata Y
Ann N Y Acad Sci; 2006 Nov; 1086():66-80. PubMed ID: 17185506
[TBL] [Abstract][Full Text] [Related]
6. Loss of heterozygosity at the dilute-short ear (Myo5a-Bmp5) region of the mouse: mitotic recombination or double non-disjunction?
Favor J; Neuhäuser-Klaus A
Genet Res; 1998 Dec; 72(3):199-204. PubMed ID: 10036975
[TBL] [Abstract][Full Text] [Related]
7. Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
Ménasché G; Pastural E; Feldmann J; Certain S; Ersoy F; Dupuis S; Wulffraat N; Bianchi D; Fischer A; Le Deist F; de Saint Basile G
Nat Genet; 2000 Jun; 25(2):173-6. PubMed ID: 10835631
[TBL] [Abstract][Full Text] [Related]
8. Synthetic lethality screen identifies a novel yeast myosin I gene (MYO5): myosin I proteins are required for polarization of the actin cytoskeleton.
Goodson HV; Anderson BL; Warrick HM; Pon LA; Spudich JA
J Cell Biol; 1996 Jun; 133(6):1277-91. PubMed ID: 8682864
[TBL] [Abstract][Full Text] [Related]
9. A Ufd2/D4Cole1e chimeric protein and overexpression of Rbp7 in the slow Wallerian degeneration (WldS) mouse.
Conforti L; Tarlton A; Mack TG; Mi W; Buckmaster EA; Wagner D; Perry VH; Coleman MP
Proc Natl Acad Sci U S A; 2000 Oct; 97(21):11377-82. PubMed ID: 11027338
[TBL] [Abstract][Full Text] [Related]
10. Identification of five mouse mu-opioid receptor (MOR) gene (Oprm1) splice variants containing a newly identified alternatively spliced exon.
Doyle GA; Sheng XR; Lin SS; Press DM; Grice DE; Buono RJ; Ferraro TN; Berrettini WH
Gene; 2007 Jun; 395(1-2):98-107. PubMed ID: 17398041
[TBL] [Abstract][Full Text] [Related]
11. Myosin Va Brain-Specific Mutation Alters Mouse Behavior and Disrupts Hippocampal Synapses.
Pandian S; Zhao JP; Murata Y; Bustos FJ; Tunca C; Almeida RD; Constantine-Paton M
eNeuro; 2020; 7(6):. PubMed ID: 33229412
[TBL] [Abstract][Full Text] [Related]
12. New insights into the melanophilin (MLPH) gene controlling coat color phenotypes in American mink.
Cirera S; Markakis MN; Christensen K; Anistoroaei R
Gene; 2013 Sep; 527(1):48-54. PubMed ID: 23747352
[TBL] [Abstract][Full Text] [Related]
13. KIAA1735 gene on human chromosome 11q23.1 encodes a novel protein with myosine-tail homologous domain and C-terminal DIX domain.
Katoh M; Katoh M
Int J Oncol; 2003 Jul; 23(1):145-50. PubMed ID: 12792787
[TBL] [Abstract][Full Text] [Related]
14. Genomic organization of the mouse Msh4 gene producing bicistronic, chimeric and antisense mRNA.
Hirano M; Noda T
Gene; 2004 Nov; 342(1):165-77. PubMed ID: 15527976
[TBL] [Abstract][Full Text] [Related]
15. Myosin-VIIb, a novel unconventional myosin, is a constituent of microvilli in transporting epithelia.
Chen ZY; Hasson T; Zhang DS; Schwender BJ; Derfler BH; Mooseker MS; Corey DP
Genomics; 2001 Mar; 72(3):285-96. PubMed ID: 11401444
[TBL] [Abstract][Full Text] [Related]
16. Cloning, structural characterization, and chromosomal localization of the human orthologue of Saccharomyces cerevisiae MSH5 gene.
Her C; Doggett NA
Genomics; 1998 Aug; 52(1):50-61. PubMed ID: 9740671
[TBL] [Abstract][Full Text] [Related]
17. The mouse DNA binding protein Rc for the kappa B motif of transcription and for the V(D)J recombination signal sequences contains composite DNA-protein interaction domains and belongs to a new family of large transcriptional proteins.
Wu LC; Liu Y; Strandtmann J; Mak CH; Lee B; Li Z; Yu CY
Genomics; 1996 Aug; 35(3):415-24. PubMed ID: 8812474
[TBL] [Abstract][Full Text] [Related]
18. Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
Ménasché G; Ho CH; Sanal O; Feldmann J; Tezcan I; Ersoy F; Houdusse A; Fischer A; de Saint Basile G
J Clin Invest; 2003 Aug; 112(3):450-6. PubMed ID: 12897212
[TBL] [Abstract][Full Text] [Related]
19. The cloning and developmental expression of unconventional myosin IXA (MYO9A) a gene in the Bardet-Biedl syndrome (BBS4) region at chromosome 15q22-q23.
Gorman SW; Haider NB; Grieshammer U; Swiderski RE; Kim E; Welch JW; Searby C; Leng S; Carmi R; Sheffield VC; Duhl DM
Genomics; 1999 Jul; 59(2):150-60. PubMed ID: 10409426
[TBL] [Abstract][Full Text] [Related]
20. The mouse mutants recoil wobbler and nmf373 represent a series of Grm1 mutations.
Sachs AJ; Schwendinger JK; Yang AW; Haider NB; Nystuen AM
Mamm Genome; 2007 Nov; 18(11):749-56. PubMed ID: 17934773
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]