TMEM43 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "TMEM43" in Arabic language version.

Last modified: 06:24:00, 22 July 2026 (UTC)

Ref.Un. Ref.Website

Global rank Arabic rank

1111nih.gov

5^th place

6^th place

77doi.org

2^nd place

4^th place

55web.archive.org

1^st place

22uniprot.org

2,402^nd place

3,713^th place

11omim.org

3,900^th place

2,000^th place

11proteinatlas.org

low place

doi.org (Global: 2^nd place; Arabic: 4^th place)

Wiemann S، Weil B، Wellenreuther R، وآخرون (مارس 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research. ج. 11 ع. 3: 422–35. DOI:10.1101/gr.GR1547R. PMC:311072. PMID:11230166.
Merner ND، Hodgkinson KA، Haywood AF، وآخرون (أبريل 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. ج. 82 ع. 4: 809–21. DOI:10.1016/j.ajhg.2008.01.010. PMC:2427209. PMID:18313022.
Haywood AF، Merner ND، Hodgkinson KA، وآخرون (أبريل 2013). "Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada". European Heart Journal. ج. 34 ع. 13: 1002–11. DOI:10.1093/eurheartj/ehs383. PMID:23161701.
Franke WW، Dörflinger Y، Kuhn C، وآخرون (يوليو 2014). "Protein LUMA is a cytoplasmic plaque constituent of various epithelial adherens junctions and composite junctions of myocardial intercalated disks: a unifying finding for cell biology and cardiology". Cell and Tissue Research. ج. 357 ع. 1: 159–72. DOI:10.1007/s00441-014-1865-1. PMID:24770932.
Baskin B، Skinner JR، Sanatani S، وآخرون (نوفمبر 2013). "TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations". Human Genetics. ج. 132 ع. 11: 1245–52. DOI:10.1007/s00439-013-1323-2. PMID:23812740.
Christensen AH، Andersen CB، Tybjaerg-Hansen A، Haunso S، Svendsen JH (سبتمبر 2011). "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy". Clinical Genetics. ج. 80 ع. 3: 256–64. DOI:10.1111/j.1399-0004.2011.01623.x. PMID:21214875.
Merner، ND (2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. ج. 82 ع. 4: 809–821. DOI:10.1016/j.ajhg.2008.01.017. PMID:18313022.

nih.gov (Global: 5^th place; Arabic: 6^th place)

pubmed.ncbi.nlm.nih.gov

Wiemann S، Weil B، Wellenreuther R، وآخرون (مارس 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research. ج. 11 ع. 3: 422–35. DOI:10.1101/gr.GR1547R. PMC:311072. PMID:11230166.
Merner ND، Hodgkinson KA، Haywood AF، وآخرون (أبريل 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. ج. 82 ع. 4: 809–21. DOI:10.1016/j.ajhg.2008.01.010. PMC:2427209. PMID:18313022.
Haywood AF، Merner ND، Hodgkinson KA، وآخرون (أبريل 2013). "Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada". European Heart Journal. ج. 34 ع. 13: 1002–11. DOI:10.1093/eurheartj/ehs383. PMID:23161701.
Franke WW، Dörflinger Y، Kuhn C، وآخرون (يوليو 2014). "Protein LUMA is a cytoplasmic plaque constituent of various epithelial adherens junctions and composite junctions of myocardial intercalated disks: a unifying finding for cell biology and cardiology". Cell and Tissue Research. ج. 357 ع. 1: 159–72. DOI:10.1007/s00441-014-1865-1. PMID:24770932.
Baskin B، Skinner JR، Sanatani S، وآخرون (نوفمبر 2013). "TMEM43 mutations associated with arrhythmogenic right ventricular cardiomyopathy in non-Newfoundland populations". Human Genetics. ج. 132 ع. 11: 1245–52. DOI:10.1007/s00439-013-1323-2. PMID:23812740.
Christensen AH، Andersen CB، Tybjaerg-Hansen A، Haunso S، Svendsen JH (سبتمبر 2011). "Mutation analysis and evaluation of the cardiac localization of TMEM43 in arrhythmogenic right ventricular cardiomyopathy". Clinical Genetics. ج. 80 ع. 3: 256–64. DOI:10.1111/j.1399-0004.2011.01623.x. PMID:21214875.
Merner، ND (2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. ج. 82 ع. 4: 809–821. DOI:10.1016/j.ajhg.2008.01.017. PMID:18313022.

ncbi.nlm.nih.gov

EntrezGene 79188
Wiemann S، Weil B، Wellenreuther R، وآخرون (مارس 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Research. ج. 11 ع. 3: 422–35. DOI:10.1101/gr.GR1547R. PMC:311072. PMID:11230166.
Merner ND، Hodgkinson KA، Haywood AF، وآخرون (أبريل 2008). "Arrhythmogenic right ventricular cardiomyopathy type 5 is a fully penetrant, lethal arrhythmic disorder caused by a missense mutation in the TMEM43 gene". American Journal of Human Genetics. ج. 82 ع. 4: 809–21. DOI:10.1016/j.ajhg.2008.01.010. PMC:2427209. PMID:18313022.
"TMEM43 gene - NCBI". المركز الوطني لمعلومات التقنية الحيوية (NCBI). مؤرشف من الأصل في 2025-02-08. اطلع عليه بتاريخ 2025-05-10.

omim.org (Global: 3,900^th place; Arabic: 2,000^th place)

"OMIM Entry #614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7". omim.org. مؤرشف من الأصل في 2019-10-23. اطلع عليه بتاريخ 2017-08-29.

proteinatlas.org (Global: low place; Arabic: low place)

"TMEM43 - The Human Protein Atlas". Human Protein Atlas. مؤرشف من الأصل في 2022-11-12. اطلع عليه بتاريخ 2025-05-10.

uniprot.org (Global: 2,402^nd place; Arabic: 3,713^th place)

"TMEM43_HUMAN - UniProt". UniProt. مؤرشف من الأصل في 2025-04-19. اطلع عليه بتاريخ 2025-05-10.
"TMEM43_HUMAN – Transmembrane protein 43". UniProt. مؤرشف من الأصل في 2025-04-19. اطلع عليه بتاريخ 2025-05-10.

web.archive.org (Global: 1^st place; Arabic: 1^st place)

"OMIM Entry #614302 EMERY-DREIFUSS MUSCULAR DYSTROPHY 7, AUTOSOMAL DOMINANT; EDMD7". omim.org. مؤرشف من الأصل في 2019-10-23. اطلع عليه بتاريخ 2017-08-29.
"TMEM43 gene - NCBI". المركز الوطني لمعلومات التقنية الحيوية (NCBI). مؤرشف من الأصل في 2025-02-08. اطلع عليه بتاريخ 2025-05-10.
"TMEM43_HUMAN - UniProt". UniProt. مؤرشف من الأصل في 2025-04-19. اطلع عليه بتاريخ 2025-05-10.
"TMEM43 - The Human Protein Atlas". Human Protein Atlas. مؤرشف من الأصل في 2022-11-12. اطلع عليه بتاريخ 2025-05-10.
"TMEM43_HUMAN – Transmembrane protein 43". UniProt. مؤرشف من الأصل في 2025-04-19. اطلع عليه بتاريخ 2025-05-10.

TMEM43 (Arabic Wikipedia)

doi.org (Global: 2nd place; Arabic: 4th place)

nih.gov (Global: 5th place; Arabic: 6th place)