Ferlins (English Wikipedia)

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

refsWebsite

Global rank English rank

52nih.gov

4^th place

31doi.org

2^nd place

3harvard.edu

18^th place

17^th place

3semanticscholar.org

11^th place

8^th place

1bbk.ac.uk

low place

7,925^th place

1jain-foundation.org

low place

1embl-heidelberg.de

low place

1xfam.org

low place

1ulg.ac.be

7,875^th place

8,199^th place

bbk.ac.uk (Global: low place; English: 7,925^th place)

eprints.bbk.ac.uk

Patel P, Harris R, Geddes SM, Strehle EM, Watson JD, Bashir R, Bushby K, Driscoll PC, Keep NH (June 2008). "Solution structure of the inner DysF domain of myoferlin and implications for limb girdle muscular dystrophy type 2b" (PDF). Journal of Molecular Biology. 379 (5): 981–90. doi:10.1016/j.jmb.2008.04.046. PMID 18495154.

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

Eisenberg MC, Kim Y, Li R, Ackerman WE, Kniss DA, Friedman A (December 2011). "Mechanistic modeling of the effects of myoferlin on tumor cell invasion". Proceedings of the National Academy of Sciences of the United States of America. 108 (50): 20078–83. Bibcode:2011PNAS..10820078E. doi:10.1073/pnas.1116327108. PMC 3250187. PMID 22135466.
Kumar B, Brown NV, Swanson BJ, Schmitt AC, Old M, Ozer E, Agrawal A, Schuller DE, Teknos TN, Kumar P (April 2016). "High expression of myoferlin is associated with poor outcome in oropharyngeal squamous cell carcinoma patients and is inversely associated with HPV-status". Oncotarget. 7 (14): 18665–77. doi:10.18632/oncotarget.7625. PMC 4951318. PMID 26919244.
Bansal D, Campbell KP (April 2004). "Dysferlin and the plasma membrane repair in muscular dystrophy". Trends in Cell Biology. 14 (4): 206–13. doi:10.1016/j.tcb.2004.03.001. PMID 15066638.
Coleman BI, Saha S, Sato S, Engelberg K, Ferguson DJ, Coppens I, Lodoen MB, Gubbels MJ (October 2018). "A Member of the Ferlin Calcium Sensor Family Is Essential for Toxoplasma gondii Rhoptry Secretion". mBio. 9 (5). doi:10.1128/mBio.01510-18. PMC 6168857. PMID 30279285.
Patel P, Harris R, Geddes SM, Strehle EM, Watson JD, Bashir R, Bushby K, Driscoll PC, Keep NH (June 2008). "Solution structure of the inner DysF domain of myoferlin and implications for limb girdle muscular dystrophy type 2b" (PDF). Journal of Molecular Biology. 379 (5): 981–90. doi:10.1016/j.jmb.2008.04.046. PMID 18495154.
Harsini FM, Chebrolu S, Fuson KL, White MA, Rice AM, Sutton RB (July 2018). "FerA is a Membrane-Associating Four-Helix Bundle Domain in the Ferlin Family of Membrane-Fusion Proteins". Scientific Reports. 8 (1) 10949. Bibcode:2018NatSR...810949H. doi:10.1038/s41598-018-29184-1. PMC 6053371. PMID 30026467.
Lek A, Lek M, North KN, Cooper ST (July 2010). "Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins". BMC Evolutionary Biology. 10 231. doi:10.1186/1471-2148-10-231. PMC 2923515. PMID 20667140.
Achanzar WE, Ward S (May 1997). "A nematode gene required for sperm vesicle fusion". Journal of Cell Science. 110 (Pt 9) (9): 1073–81. doi:10.1242/jcs.110.9.1073. PMID 9175703.
Staub E, Fiziev P, Rosenthal A, Hinzmann B (May 2004). "Insights into the evolution of the nucleolus by an analysis of its protein domain repertoire". BioEssays. 26 (5): 567–81. doi:10.1002/bies.20032. PMID 15112237.
Rizo J, Südhof TC (June 1998). "C2-domains, structure and function of a universal Ca2+-binding domain". The Journal of Biological Chemistry. 273 (26): 15879–82. doi:10.1074/jbc.273.26.15879. PMID 9632630.
Nalefski EA, Wisner MA, Chen JZ, Sprang SR, Fukuda M, Mikoshiba K, Falke JJ (March 2001). "C2 domains from different Ca2+ signaling pathways display functional and mechanistic diversity". Biochemistry. 40 (10): 3089–100. doi:10.1021/bi001968a. PMC 3862187. PMID 11258923.
Sula A, Cole AR, Yeats C, Orengo C, Keep NH (January 2014). "Crystal structures of the human Dysferlin inner DysF domain". BMC Structural Biology. 14 3. doi:10.1186/1472-6807-14-3. PMC 3898210. PMID 24438169.
Lek A, Evesson FJ, Sutton RB, North KN, Cooper ST (February 2012). "Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair". Traffic. 13 (2): 185–94. doi:10.1111/j.1600-0854.2011.01267.x. PMID 21838746. S2CID 25445442.
Washington NL, Ward S (June 2006). "FER-1 regulates Ca2+ -mediated membrane fusion during C. elegans spermatogenesis". Journal of Cell Science. 119 (Pt 12): 2552–62. doi:10.1242/jcs.02980. PMID 16735442.
Oulhen N, Onorato TM, Ramos I, Wessel GM (April 2014). "Dysferlin is essential for endocytosis in the sea star oocyte". Developmental Biology. 388 (1): 94–102. doi:10.1016/j.ydbio.2013.12.018. PMC 3982204. PMID 24368072.
Cooper ST, Head SI (December 2015). "Membrane Injury and Repair in the Muscular Dystrophies". The Neuroscientist. 21 (6): 653–68. doi:10.1177/1073858414558336. PMID 25406223. S2CID 29751207.
Demonbreun AR, Quattrocelli M, Barefield DY, Allen MV, Swanson KE, McNally EM (June 2016). "An actin-dependent annexin complex mediates plasma membrane repair in muscle". The Journal of Cell Biology. 213 (6): 705–18. doi:10.1083/jcb.201512022. PMC 4915191. PMID 27298325.
Pangršič T, Reisinger E, Moser T (November 2012). "Otoferlin: a multi-C2 domain protein essential for hearing". Trends in Neurosciences. 35 (11): 671–80. doi:10.1016/j.tins.2012.08.002. PMID 22959777. S2CID 12329992.
Smith MK, Wakimoto BT (March 2007). "Complex regulation and multiple developmental functions of misfire, the Drosophila melanogaster ferlin gene". BMC Developmental Biology. 7 21. doi:10.1186/1471-213X-7-21. PMC 1853072. PMID 17386097.
Urtizberea JA, Bassez G, Leturcq F, Nguyen K, Krahn M, Levy N (2008). "Dysferlinopathies". Neurology India. 56 (3): 289–97. doi:10.4103/0028-3886.43447. PMID 18974555.
Cacciottolo M, Numitone G, Aurino S, Caserta IR, Fanin M, Politano L, Minetti C, Ricci E, Piluso G, Angelini C, Nigro V (September 2011). "Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations". European Journal of Human Genetics. 19 (9): 974–80. doi:10.1038/ejhg.2011.70. PMC 3179367. PMID 21522182.
Jin SQ, Yu M, Zhang W, Lyu H, Yuan Y, Wang ZX (October 2016). "Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy". Chinese Medical Journal. 129 (19): 2287–93. doi:10.4103/0366-6999.190671. PMC 5040013. PMID 27647186.
Matsuda C, Miyake K, Kameyama K, Keduka E, Takeshima H, Imamura T, Araki N, Nishino I, Hayashi Y (November 2012). "The C2A domain in dysferlin is important for association with MG53 (TRIM72)". PLOS Currents. 4 e5035add8caff4. doi:10.1371/5035add8caff4 (inactive 12 July 2025). PMC 3493068. PMID 23145354.{{cite journal}}: CS1 maint: DOI inactive as of July 2025 (link)
Ramakrishnan NA, Drescher MJ, Morley BJ, Kelley PM, Drescher DG (March 2014). "Calcium regulates molecular interactions of otoferlin with soluble NSF attachment protein receptor (SNARE) proteins required for hair cell exocytosis". The Journal of Biological Chemistry. 289 (13): 8750–66. doi:10.1074/jbc.M113.480533. PMC 3979417. PMID 24478316.
Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB (March 2009). "Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan". Clinical Genetics. 75 (3): 237–43. doi:10.1111/j.1399-0004.2008.01128.x. PMC 3461579. PMID 19250381.
Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ (July 2006). "OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele". Journal of Medical Genetics. 43 (7): 576–81. doi:10.1136/jmg.2005.038612. PMC 2593030. PMID 16371502.
Doherty KR, Cave A, Davis DB, Delmonte AJ, Posey A, Earley JU, Hadhazy M, McNally EM (December 2005). "Normal myoblast fusion requires myoferlin". Development. 132 (24): 5565–75. doi:10.1242/dev.02155. PMC 4066872. PMID 16280346.
Song DH, Ko GH, Lee JH, Lee JS, Lee GW, Kim HC, Yang JW, Heo RW, Roh GS, Han SY, Kim DC (February 2016). "Myoferlin expression in non-small cell lung cancer: Prognostic role and correlation with VEGFR-2 expression". Oncology Letters. 11 (2): 998–1006. doi:10.3892/ol.2015.3988. PMC 4734036. PMID 26893682.
Turtoi A, Blomme A, Bellahcène A, Gilles C, Hennequière V, Peixoto P, Bianchi E, Noel A, De Pauw E, Lifrange E, Delvenne P, Castronovo V (September 2013). "Myoferlin is a key regulator of EGFR activity in breast cancer" (PDF). Cancer Research. 73 (17): 5438–48. doi:10.1158/0008-5472.CAN-13-1142. PMID 23864327.
Rademaker G, Hennequière V, Brohée L, Nokin MJ, Lovinfosse P, Durieux F, Gofflot S, Bellier J, Costanza B, Herfs M, Peiffer R, Bettendorff L, Deroanne C, Thiry M, Delvenne P, Hustinx R, Bellahcène A, Castronovo V, Peulen O (August 2018). "Myoferlin controls mitochondrial structure and activity in pancreatic ductal adenocarcinoma, and affects tumor aggressiveness". Oncogene. 37 (32): 4398–4412. doi:10.1038/s41388-018-0287-z. PMC 6085282. PMID 29720728.
Li R, Ackerman WE, Mihai C, Volakis LI, Ghadiali S, Kniss DA (2012). "Myoferlin depletion in breast cancer cells promotes mesenchymal to epithelial shape change and stalls invasion". PLOS ONE. 7 (6) e39766. Bibcode:2012PLoSO...739766L. doi:10.1371/journal.pone.0039766. PMC 3384637. PMID 22761893.

embl-heidelberg.de (Global: low place; English: low place)

smart.embl-heidelberg.de

"SMART: FerA domain annotation". smart.embl-heidelberg.de. Retrieved 2018-11-17.

harvard.edu (Global: 18^th place; English: 17^th place)

ui.adsabs.harvard.edu

Eisenberg MC, Kim Y, Li R, Ackerman WE, Kniss DA, Friedman A (December 2011). "Mechanistic modeling of the effects of myoferlin on tumor cell invasion". Proceedings of the National Academy of Sciences of the United States of America. 108 (50): 20078–83. Bibcode:2011PNAS..10820078E. doi:10.1073/pnas.1116327108. PMC 3250187. PMID 22135466.
Harsini FM, Chebrolu S, Fuson KL, White MA, Rice AM, Sutton RB (July 2018). "FerA is a Membrane-Associating Four-Helix Bundle Domain in the Ferlin Family of Membrane-Fusion Proteins". Scientific Reports. 8 (1) 10949. Bibcode:2018NatSR...810949H. doi:10.1038/s41598-018-29184-1. PMC 6053371. PMID 30026467.
Li R, Ackerman WE, Mihai C, Volakis LI, Ghadiali S, Kniss DA (2012). "Myoferlin depletion in breast cancer cells promotes mesenchymal to epithelial shape change and stalls invasion". PLOS ONE. 7 (6) e39766. Bibcode:2012PLoSO...739766L. doi:10.1371/journal.pone.0039766. PMC 3384637. PMID 22761893.

jain-foundation.org (Global: low place; English: low place)

"Which Ferlin protein was discovered first? | Jain Foundation". www.jain-foundation.org. Retrieved 2018-11-18.

nih.gov (Global: 4^th place; English: 4^th place)

pubmed.ncbi.nlm.nih.gov

Eisenberg MC, Kim Y, Li R, Ackerman WE, Kniss DA, Friedman A (December 2011). "Mechanistic modeling of the effects of myoferlin on tumor cell invasion". Proceedings of the National Academy of Sciences of the United States of America. 108 (50): 20078–83. Bibcode:2011PNAS..10820078E. doi:10.1073/pnas.1116327108. PMC 3250187. PMID 22135466.
Kumar B, Brown NV, Swanson BJ, Schmitt AC, Old M, Ozer E, Agrawal A, Schuller DE, Teknos TN, Kumar P (April 2016). "High expression of myoferlin is associated with poor outcome in oropharyngeal squamous cell carcinoma patients and is inversely associated with HPV-status". Oncotarget. 7 (14): 18665–77. doi:10.18632/oncotarget.7625. PMC 4951318. PMID 26919244.
Bansal D, Campbell KP (April 2004). "Dysferlin and the plasma membrane repair in muscular dystrophy". Trends in Cell Biology. 14 (4): 206–13. doi:10.1016/j.tcb.2004.03.001. PMID 15066638.
Coleman BI, Saha S, Sato S, Engelberg K, Ferguson DJ, Coppens I, Lodoen MB, Gubbels MJ (October 2018). "A Member of the Ferlin Calcium Sensor Family Is Essential for Toxoplasma gondii Rhoptry Secretion". mBio. 9 (5). doi:10.1128/mBio.01510-18. PMC 6168857. PMID 30279285.
Patel P, Harris R, Geddes SM, Strehle EM, Watson JD, Bashir R, Bushby K, Driscoll PC, Keep NH (June 2008). "Solution structure of the inner DysF domain of myoferlin and implications for limb girdle muscular dystrophy type 2b" (PDF). Journal of Molecular Biology. 379 (5): 981–90. doi:10.1016/j.jmb.2008.04.046. PMID 18495154.
Harsini FM, Chebrolu S, Fuson KL, White MA, Rice AM, Sutton RB (July 2018). "FerA is a Membrane-Associating Four-Helix Bundle Domain in the Ferlin Family of Membrane-Fusion Proteins". Scientific Reports. 8 (1) 10949. Bibcode:2018NatSR...810949H. doi:10.1038/s41598-018-29184-1. PMC 6053371. PMID 30026467.
Lek A, Lek M, North KN, Cooper ST (July 2010). "Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins". BMC Evolutionary Biology. 10 231. doi:10.1186/1471-2148-10-231. PMC 2923515. PMID 20667140.
Achanzar WE, Ward S (May 1997). "A nematode gene required for sperm vesicle fusion". Journal of Cell Science. 110 (Pt 9) (9): 1073–81. doi:10.1242/jcs.110.9.1073. PMID 9175703.
Staub E, Fiziev P, Rosenthal A, Hinzmann B (May 2004). "Insights into the evolution of the nucleolus by an analysis of its protein domain repertoire". BioEssays. 26 (5): 567–81. doi:10.1002/bies.20032. PMID 15112237.
Rizo J, Südhof TC (June 1998). "C2-domains, structure and function of a universal Ca2+-binding domain". The Journal of Biological Chemistry. 273 (26): 15879–82. doi:10.1074/jbc.273.26.15879. PMID 9632630.
Nalefski EA, Wisner MA, Chen JZ, Sprang SR, Fukuda M, Mikoshiba K, Falke JJ (March 2001). "C2 domains from different Ca2+ signaling pathways display functional and mechanistic diversity". Biochemistry. 40 (10): 3089–100. doi:10.1021/bi001968a. PMC 3862187. PMID 11258923.
Sula A, Cole AR, Yeats C, Orengo C, Keep NH (January 2014). "Crystal structures of the human Dysferlin inner DysF domain". BMC Structural Biology. 14 3. doi:10.1186/1472-6807-14-3. PMC 3898210. PMID 24438169.
Lek A, Evesson FJ, Sutton RB, North KN, Cooper ST (February 2012). "Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair". Traffic. 13 (2): 185–94. doi:10.1111/j.1600-0854.2011.01267.x. PMID 21838746. S2CID 25445442.
Washington NL, Ward S (June 2006). "FER-1 regulates Ca2+ -mediated membrane fusion during C. elegans spermatogenesis". Journal of Cell Science. 119 (Pt 12): 2552–62. doi:10.1242/jcs.02980. PMID 16735442.
Oulhen N, Onorato TM, Ramos I, Wessel GM (April 2014). "Dysferlin is essential for endocytosis in the sea star oocyte". Developmental Biology. 388 (1): 94–102. doi:10.1016/j.ydbio.2013.12.018. PMC 3982204. PMID 24368072.
Cooper ST, Head SI (December 2015). "Membrane Injury and Repair in the Muscular Dystrophies". The Neuroscientist. 21 (6): 653–68. doi:10.1177/1073858414558336. PMID 25406223. S2CID 29751207.
Demonbreun AR, Quattrocelli M, Barefield DY, Allen MV, Swanson KE, McNally EM (June 2016). "An actin-dependent annexin complex mediates plasma membrane repair in muscle". The Journal of Cell Biology. 213 (6): 705–18. doi:10.1083/jcb.201512022. PMC 4915191. PMID 27298325.
Pangršič T, Reisinger E, Moser T (November 2012). "Otoferlin: a multi-C2 domain protein essential for hearing". Trends in Neurosciences. 35 (11): 671–80. doi:10.1016/j.tins.2012.08.002. PMID 22959777. S2CID 12329992.
Smith MK, Wakimoto BT (March 2007). "Complex regulation and multiple developmental functions of misfire, the Drosophila melanogaster ferlin gene". BMC Developmental Biology. 7 21. doi:10.1186/1471-213X-7-21. PMC 1853072. PMID 17386097.
Urtizberea JA, Bassez G, Leturcq F, Nguyen K, Krahn M, Levy N (2008). "Dysferlinopathies". Neurology India. 56 (3): 289–97. doi:10.4103/0028-3886.43447. PMID 18974555.
Cacciottolo M, Numitone G, Aurino S, Caserta IR, Fanin M, Politano L, Minetti C, Ricci E, Piluso G, Angelini C, Nigro V (September 2011). "Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations". European Journal of Human Genetics. 19 (9): 974–80. doi:10.1038/ejhg.2011.70. PMC 3179367. PMID 21522182.
Jin SQ, Yu M, Zhang W, Lyu H, Yuan Y, Wang ZX (October 2016). "Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy". Chinese Medical Journal. 129 (19): 2287–93. doi:10.4103/0366-6999.190671. PMC 5040013. PMID 27647186.
Matsuda C, Miyake K, Kameyama K, Keduka E, Takeshima H, Imamura T, Araki N, Nishino I, Hayashi Y (November 2012). "The C2A domain in dysferlin is important for association with MG53 (TRIM72)". PLOS Currents. 4 e5035add8caff4. doi:10.1371/5035add8caff4 (inactive 12 July 2025). PMC 3493068. PMID 23145354.{{cite journal}}: CS1 maint: DOI inactive as of July 2025 (link)
Ramakrishnan NA, Drescher MJ, Morley BJ, Kelley PM, Drescher DG (March 2014). "Calcium regulates molecular interactions of otoferlin with soluble NSF attachment protein receptor (SNARE) proteins required for hair cell exocytosis". The Journal of Biological Chemistry. 289 (13): 8750–66. doi:10.1074/jbc.M113.480533. PMC 3979417. PMID 24478316.
Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB (March 2009). "Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan". Clinical Genetics. 75 (3): 237–43. doi:10.1111/j.1399-0004.2008.01128.x. PMC 3461579. PMID 19250381.
Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ (July 2006). "OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele". Journal of Medical Genetics. 43 (7): 576–81. doi:10.1136/jmg.2005.038612. PMC 2593030. PMID 16371502.
Doherty KR, Cave A, Davis DB, Delmonte AJ, Posey A, Earley JU, Hadhazy M, McNally EM (December 2005). "Normal myoblast fusion requires myoferlin". Development. 132 (24): 5565–75. doi:10.1242/dev.02155. PMC 4066872. PMID 16280346.
Song DH, Ko GH, Lee JH, Lee JS, Lee GW, Kim HC, Yang JW, Heo RW, Roh GS, Han SY, Kim DC (February 2016). "Myoferlin expression in non-small cell lung cancer: Prognostic role and correlation with VEGFR-2 expression". Oncology Letters. 11 (2): 998–1006. doi:10.3892/ol.2015.3988. PMC 4734036. PMID 26893682.
Turtoi A, Blomme A, Bellahcène A, Gilles C, Hennequière V, Peixoto P, Bianchi E, Noel A, De Pauw E, Lifrange E, Delvenne P, Castronovo V (September 2013). "Myoferlin is a key regulator of EGFR activity in breast cancer" (PDF). Cancer Research. 73 (17): 5438–48. doi:10.1158/0008-5472.CAN-13-1142. PMID 23864327.
Rademaker G, Hennequière V, Brohée L, Nokin MJ, Lovinfosse P, Durieux F, Gofflot S, Bellier J, Costanza B, Herfs M, Peiffer R, Bettendorff L, Deroanne C, Thiry M, Delvenne P, Hustinx R, Bellahcène A, Castronovo V, Peulen O (August 2018). "Myoferlin controls mitochondrial structure and activity in pancreatic ductal adenocarcinoma, and affects tumor aggressiveness". Oncogene. 37 (32): 4398–4412. doi:10.1038/s41388-018-0287-z. PMC 6085282. PMID 29720728.
Li R, Ackerman WE, Mihai C, Volakis LI, Ghadiali S, Kniss DA (2012). "Myoferlin depletion in breast cancer cells promotes mesenchymal to epithelial shape change and stalls invasion". PLOS ONE. 7 (6) e39766. Bibcode:2012PLoSO...739766L. doi:10.1371/journal.pone.0039766. PMC 3384637. PMID 22761893.

ncbi.nlm.nih.gov

Eisenberg MC, Kim Y, Li R, Ackerman WE, Kniss DA, Friedman A (December 2011). "Mechanistic modeling of the effects of myoferlin on tumor cell invasion". Proceedings of the National Academy of Sciences of the United States of America. 108 (50): 20078–83. Bibcode:2011PNAS..10820078E. doi:10.1073/pnas.1116327108. PMC 3250187. PMID 22135466.
Kumar B, Brown NV, Swanson BJ, Schmitt AC, Old M, Ozer E, Agrawal A, Schuller DE, Teknos TN, Kumar P (April 2016). "High expression of myoferlin is associated with poor outcome in oropharyngeal squamous cell carcinoma patients and is inversely associated with HPV-status". Oncotarget. 7 (14): 18665–77. doi:10.18632/oncotarget.7625. PMC 4951318. PMID 26919244.
Coleman BI, Saha S, Sato S, Engelberg K, Ferguson DJ, Coppens I, Lodoen MB, Gubbels MJ (October 2018). "A Member of the Ferlin Calcium Sensor Family Is Essential for Toxoplasma gondii Rhoptry Secretion". mBio. 9 (5). doi:10.1128/mBio.01510-18. PMC 6168857. PMID 30279285.
Harsini FM, Chebrolu S, Fuson KL, White MA, Rice AM, Sutton RB (July 2018). "FerA is a Membrane-Associating Four-Helix Bundle Domain in the Ferlin Family of Membrane-Fusion Proteins". Scientific Reports. 8 (1) 10949. Bibcode:2018NatSR...810949H. doi:10.1038/s41598-018-29184-1. PMC 6053371. PMID 30026467.
Lek A, Lek M, North KN, Cooper ST (July 2010). "Phylogenetic analysis of ferlin genes reveals ancient eukaryotic origins". BMC Evolutionary Biology. 10 231. doi:10.1186/1471-2148-10-231. PMC 2923515. PMID 20667140.
Nalefski EA, Wisner MA, Chen JZ, Sprang SR, Fukuda M, Mikoshiba K, Falke JJ (March 2001). "C2 domains from different Ca2+ signaling pathways display functional and mechanistic diversity". Biochemistry. 40 (10): 3089–100. doi:10.1021/bi001968a. PMC 3862187. PMID 11258923.
Sula A, Cole AR, Yeats C, Orengo C, Keep NH (January 2014). "Crystal structures of the human Dysferlin inner DysF domain". BMC Structural Biology. 14 3. doi:10.1186/1472-6807-14-3. PMC 3898210. PMID 24438169.
Riddle DL, Blumenthal T, Meyer BJ, Priess JR (1997). Organelle Morphogenesis During Spermatogenesis. Cold Spring Harbor Laboratory Press.
Oulhen N, Onorato TM, Ramos I, Wessel GM (April 2014). "Dysferlin is essential for endocytosis in the sea star oocyte". Developmental Biology. 388 (1): 94–102. doi:10.1016/j.ydbio.2013.12.018. PMC 3982204. PMID 24368072.
Demonbreun AR, Quattrocelli M, Barefield DY, Allen MV, Swanson KE, McNally EM (June 2016). "An actin-dependent annexin complex mediates plasma membrane repair in muscle". The Journal of Cell Biology. 213 (6): 705–18. doi:10.1083/jcb.201512022. PMC 4915191. PMID 27298325.
Smith MK, Wakimoto BT (March 2007). "Complex regulation and multiple developmental functions of misfire, the Drosophila melanogaster ferlin gene". BMC Developmental Biology. 7 21. doi:10.1186/1471-213X-7-21. PMC 1853072. PMID 17386097.
Cacciottolo M, Numitone G, Aurino S, Caserta IR, Fanin M, Politano L, Minetti C, Ricci E, Piluso G, Angelini C, Nigro V (September 2011). "Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations". European Journal of Human Genetics. 19 (9): 974–80. doi:10.1038/ejhg.2011.70. PMC 3179367. PMID 21522182.
Jin SQ, Yu M, Zhang W, Lyu H, Yuan Y, Wang ZX (October 2016). "Dysferlin Gene Mutation Spectrum in a Large Cohort of Chinese Patients with Dysferlinopathy". Chinese Medical Journal. 129 (19): 2287–93. doi:10.4103/0366-6999.190671. PMC 5040013. PMID 27647186.
Matsuda C, Miyake K, Kameyama K, Keduka E, Takeshima H, Imamura T, Araki N, Nishino I, Hayashi Y (November 2012). "The C2A domain in dysferlin is important for association with MG53 (TRIM72)". PLOS Currents. 4 e5035add8caff4. doi:10.1371/5035add8caff4 (inactive 12 July 2025). PMC 3493068. PMID 23145354.{{cite journal}}: CS1 maint: DOI inactive as of July 2025 (link)
Ramakrishnan NA, Drescher MJ, Morley BJ, Kelley PM, Drescher DG (March 2014). "Calcium regulates molecular interactions of otoferlin with soluble NSF attachment protein receptor (SNARE) proteins required for hair cell exocytosis". The Journal of Biological Chemistry. 289 (13): 8750–66. doi:10.1074/jbc.M113.480533. PMC 3979417. PMID 24478316.
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ulg.ac.be (Global: 7,875^th place; English: 8,199^th place)

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xfam.org (Global: low place; English: low place)

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"Family: FerA (PF08165)". Retrieved 2018-11-17.

Ferlins (English Wikipedia)

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