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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1999 | 1 |
2002 | 1 |
2015 | 1 |
2020 | 1 |
2022 | 1 |
2024 | 1 |
PubMed for id: 160333222
6 results
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Page 1
Touch sensation requires the mechanically gated ion channel ELKIN1.
Science. 2024 Mar;383(6686):992-998. doi: 10.1126/science.adl0495. Epub 2024 Feb 29.
Science. 2024.
PMID: 38422143
Structure of the GOLD-domain seven-transmembrane helix protein family member TMEM87A.
Hoel CM, Zhang L, Brohawn SG.
Hoel CM, et al.
Elife. 2022 Nov 14;11:e81704. doi: 10.7554/eLife.81704.
Elife. 2022.
PMID: 36373655
Free PMC article.
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TMEM87a/Elkin1, a component of a novel mechanoelectrical transduction pathway, modulates melanoma adhesion and migration.
Patkunarajah A, Stear JH, Moroni M, Schroeter L, Blaszkiewicz J, Tearle JL, Cox CD, Fürst C, Sánchez-Carranza O, Ocaña Fernández MDÁ, Fleischer R, Eravci M, Weise C, Martinac B, Biro M, Lewin GR, Poole K.
Patkunarajah A, et al.
Elife. 2020 Apr 1;9:e53308. doi: 10.7554/eLife.53308.
Elife. 2020.
PMID: 32228863
Free PMC article.
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Post-Golgi anterograde transport requires GARP-dependent endosome-to-TGN retrograde transport.
Hirata T, Fujita M, Nakamura S, Gotoh K, Motooka D, Murakami Y, Maeda Y, Kinoshita T.
Hirata T, et al.
Mol Biol Cell. 2015 Sep 1;26(17):3071-84. doi: 10.1091/mbc.E14-11-1568. Epub 2015 Jul 8.
Mol Biol Cell. 2015.
PMID: 26157166
Free PMC article.
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Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.
Dgany O, Avidan N, Delaunay J, Krasnov T, Shalmon L, Shalev H, Eidelitz-Markus T, Kapelushnik J, Cattan D, Pariente A, Tulliez M, Crétien A, Schischmanoff PO, Iolascon A, Fibach E, Koren A, Rössler J, Le Merrer M, Yaniv I, Zaizov R, Ben-Asher E, Olender T, Lancet D, Beckmann JS, Tamary H.
Dgany O, et al.
Am J Hum Genet. 2002 Dec;71(6):1467-74. doi: 10.1086/344781. Epub 2002 Nov 14.
Am J Hum Genet. 2002.
PMID: 12434312
Free PMC article.
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Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).
Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH.
Christian SL, et al.
Hum Mol Genet. 1999 Jun;8(6):1025-37. doi: 10.1093/hmg/8.6.1025.
Hum Mol Genet. 1999.
PMID: 10332034
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