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Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1996 | 1 |
1997 | 1 |
1999 | 1 |
2000 | 1 |
2002 | 1 |
2005 | 1 |
2023 | 0 |
PubMed (OMIM) for id: 347699
6 results
Results by year
Page 1
The presence of a Leu-Gly-Asn repeat-enriched protein (LGN), a putative binding partner of transducin, in ROD photoreceptors.
Invest Ophthalmol Vis Sci. 2005 Jan;46(1):383-9. doi: 10.1167/iovs.04-1006.
Invest Ophthalmol Vis Sci. 2005.
PMID: 15623799
Expression analysis and subcellular distribution of the two G-protein regulators AGS3 and LGN indicate distinct functionality. Localization of LGN to the midbody during cytokinesis.
Blumer JB, Chandler LJ, Lanier SM.
Blumer JB, et al.
J Biol Chem. 2002 May 3;277(18):15897-903. doi: 10.1074/jbc.M112185200. Epub 2002 Feb 6.
J Biol Chem. 2002.
PMID: 11832491
Free article.
Item in Clipboard
Chudley-McCullough syndrome: bilateral sensorineural deafness, hydrocephalus, and other structural brain abnormalities.
Lemire EG, Stoeber GP.
Lemire EG, et al.
Am J Med Genet. 2000 Jan 17;90(2):127-30. doi: 10.1002/(sici)1096-8628(20000117)90:2<127::aid-ajmg8>3.0.co;2-e.
Am J Med Genet. 2000.
PMID: 10607951
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Bilateral sensorineural deafness, partial agenesis of the corpus callosum, and arachnoid cysts in two sisters.
Hendriks YM, Laan LA, Vielvoye GJ, van Haeringen A.
Hendriks YM, et al.
Am J Med Genet. 1999 Sep 10;86(2):183-6.
Am J Med Genet. 1999.
PMID: 10449658
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Bilateral sensorineural deafness and hydrocephalus due to foramen of Monro obstruction in sibs: a newly described autosomal recessive disorder.
Chudley AE, McCullough C, McCullough DW.
Chudley AE, et al.
Am J Med Genet. 1997 Jan 31;68(3):350-6. doi: 10.1002/(sici)1096-8628(19970131)68:3<350::aid-ajmg19>3.0.co;2-s.
Am J Med Genet. 1997.
PMID: 9024571
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Identification and cDNA cloning of a novel human mosaic protein, LGN, based on interaction with G alpha i2.
Mochizuki N, Cho G, Wen B, Insel PA.
Mochizuki N, et al.
Gene. 1996 Nov 28;181(1-2):39-43. doi: 10.1016/s0378-1119(96)00456-8.
Gene. 1996.
PMID: 8973305
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