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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1993 | 2 |
2003 | 1 |
2006 | 1 |
2015 | 3 |
2024 | 0 |
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7 results
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Page 1
Transport of proline and hydroxyproline by the neutral amino-acid exchanger ASCT1.
J Membr Biol. 2003 Sep 1;195(1):27-32. doi: 10.1007/s00232-003-2041-9.
J Membr Biol. 2003.
PMID: 14502423
Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.
Chi A, Valencia JC, Hu ZZ, Watabe H, Yamaguchi H, Mangini NJ, Huang H, Canfield VA, Cheng KC, Yang F, Abe R, Yamagishi S, Shabanowitz J, Hearing VJ, Wu C, Appella E, Hunt DF.
Chi A, et al.
J Proteome Res. 2006 Nov;5(11):3135-44. doi: 10.1021/pr060363j.
J Proteome Res. 2006.
PMID: 17081065
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A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly.
Srour M, Hamdan FF, Gan-Or Z, Labuda D, Nassif C, Oskoui M, Gana-Weisz M, Orr-Urtreger A, Rouleau GA, Michaud JL.
Srour M, et al.
Clin Genet. 2015 Jul;88(1):e1-4. doi: 10.1111/cge.12605. Epub 2015 May 28.
Clin Genet. 2015.
PMID: 25930971
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Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination.
Damseh N, Simonin A, Jalas C, Picoraro JA, Shaag A, Cho MT, Yaacov B, Neidich J, Al-Ashhab M, Juusola J, Bale S, Telegrafi A, Retterer K, Pappas JG, Moran E, Cappell J, Anyane Yeboa K, Abu-Libdeh B, Hediger MA, Chung WK, Elpeleg O, Edvardson S.
Damseh N, et al.
J Med Genet. 2015 Aug;52(8):541-7. doi: 10.1136/jmedgenet-2015-103104. Epub 2015 Jun 3.
J Med Genet. 2015.
PMID: 26041762
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SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosum.
Heimer G, Marek-Yagel D, Eyal E, Barel O, Oz Levi D, Hoffmann C, Ruzzo EK, Ganelin-Cohen E, Lancet D, Pras E, Rechavi G, Nissenkorn A, Anikster Y, Goldstein DB, Ben Zeev B.
Heimer G, et al.
Clin Genet. 2015 Oct;88(4):327-35. doi: 10.1111/cge.12637. Epub 2015 Jul 28.
Clin Genet. 2015.
PMID: 26138499
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Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family.
Arriza JL, Kavanaugh MP, Fairman WA, Wu YN, Murdoch GH, North RA, Amara SG.
Arriza JL, et al.
J Biol Chem. 1993 Jul 25;268(21):15329-32.
J Biol Chem. 1993.
PMID: 8101838
Free article.
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Cloning and expression of a novel Na(+)-dependent neutral amino acid transporter structurally related to mammalian Na+/glutamate cotransporters.
Shafqat S, Tamarappoo BK, Kilberg MS, Puranam RS, McNamara JO, Guadaño-Ferraz A, Fremeau RT Jr.
Shafqat S, et al.
J Biol Chem. 1993 Jul 25;268(21):15351-5.
J Biol Chem. 1993.
PMID: 8340364
Free article.
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