LETM1 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "LETM1" in English language version.

Last modified: 05:38:07, 20 April 2026 (UTC)

Ref.Un. Ref.Website

Global rank English rank

1110nih.gov

5^th place

65doi.org

2^nd place

62ensembl.org

630^th place

326^th place

doi.org (Global: 2^nd place; English: 2^nd place)

Endele S, Fuhry M, Pak SJ, Zabel BU, Winterpacht A (Sep 1999). "LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients". Genomics. 60 (2): 218–25. doi:10.1006/geno.1999.5881. PMID 10486213.
Schlickum S, Moghekar A, Simpson JC, Steglich C, O'Brien RJ, Winterpacht A, Endele SU (Feb 2004). "LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein". Genomics. 83 (2): 254–61. doi:10.1016/j.ygeno.2003.08.013. PMID 14706454.
Waldeck-Weiermair M, Jean-Quartier C, Rost R, Khan MJ, Vishnu N, Bondarenko AI, Imamura H, Malli R, Graier WF (Aug 2011). "Leucine zipper EF hand-containing transmembrane protein 1 (Letm1) and uncoupling proteins 2 and 3 (UCP2/3) contribute to two distinct mitochondrial Ca2+ uptake pathways". The Journal of Biological Chemistry. 286 (32): 28444–55. doi:10.1074/jbc.M111.244517. PMC 3151087. PMID 21613221.
Zotova L, Aleschko M, Sponder G, Baumgartner R, Reipert S, Prinz M, Schweyen RJ, Nowikovsky K (May 2010). "Novel components of an active mitochondrial K(+)/H(+) exchange". The Journal of Biological Chemistry. 285 (19): 14399–414. doi:10.1074/jbc.M109.059956. PMC 2863244. PMID 20197279.
McQuibban AG, Joza N, Megighian A, Scorzeto M, Zanini D, Reipert S, Richter C, Schweyen RJ, Nowikovsky K (Mar 2010). "A Drosophila mutant of LETM1, a candidate gene for seizures in Wolf-Hirschhorn syndrome". Human Molecular Genetics. 19 (6): 987–1000. doi:10.1093/hmg/ddp563. PMID 20026556.

ensembl.org (Global: 630^th place; English: 326^th place)

may2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000168924 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000005299 – Ensembl, May 2017

nih.gov (Global: 5^th place; English: 5^th place)

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: leucine zipper-EF-hand containing transmembrane protein 1".
Waldeck-Weiermair M, Jean-Quartier C, Rost R, Khan MJ, Vishnu N, Bondarenko AI, Imamura H, Malli R, Graier WF (Aug 2011). "Leucine zipper EF hand-containing transmembrane protein 1 (Letm1) and uncoupling proteins 2 and 3 (UCP2/3) contribute to two distinct mitochondrial Ca2+ uptake pathways". The Journal of Biological Chemistry. 286 (32): 28444–55. doi:10.1074/jbc.M111.244517. PMC 3151087. PMID 21613221.
Zotova L, Aleschko M, Sponder G, Baumgartner R, Reipert S, Prinz M, Schweyen RJ, Nowikovsky K (May 2010). "Novel components of an active mitochondrial K(+)/H(+) exchange". The Journal of Biological Chemistry. 285 (19): 14399–414. doi:10.1074/jbc.M109.059956. PMC 2863244. PMID 20197279.

pubmed.ncbi.nlm.nih.gov

Endele S, Fuhry M, Pak SJ, Zabel BU, Winterpacht A (Sep 1999). "LETM1, a novel gene encoding a putative EF-hand Ca(2+)-binding protein, flanks the Wolf-Hirschhorn syndrome (WHS) critical region and is deleted in most WHS patients". Genomics. 60 (2): 218–25. doi:10.1006/geno.1999.5881. PMID 10486213.
Schlickum S, Moghekar A, Simpson JC, Steglich C, O'Brien RJ, Winterpacht A, Endele SU (Feb 2004). "LETM1, a gene deleted in Wolf-Hirschhorn syndrome, encodes an evolutionarily conserved mitochondrial protein". Genomics. 83 (2): 254–61. doi:10.1016/j.ygeno.2003.08.013. PMID 14706454.
Waldeck-Weiermair M, Jean-Quartier C, Rost R, Khan MJ, Vishnu N, Bondarenko AI, Imamura H, Malli R, Graier WF (Aug 2011). "Leucine zipper EF hand-containing transmembrane protein 1 (Letm1) and uncoupling proteins 2 and 3 (UCP2/3) contribute to two distinct mitochondrial Ca2+ uptake pathways". The Journal of Biological Chemistry. 286 (32): 28444–55. doi:10.1074/jbc.M111.244517. PMC 3151087. PMID 21613221.
Zotova L, Aleschko M, Sponder G, Baumgartner R, Reipert S, Prinz M, Schweyen RJ, Nowikovsky K (May 2010). "Novel components of an active mitochondrial K(+)/H(+) exchange". The Journal of Biological Chemistry. 285 (19): 14399–414. doi:10.1074/jbc.M109.059956. PMC 2863244. PMID 20197279.
McQuibban AG, Joza N, Megighian A, Scorzeto M, Zanini D, Reipert S, Richter C, Schweyen RJ, Nowikovsky K (Mar 2010). "A Drosophila mutant of LETM1, a candidate gene for seizures in Wolf-Hirschhorn syndrome". Human Molecular Genetics. 19 (6): 987–1000. doi:10.1093/hmg/ddp563. PMID 20026556.