Integrin alpha 7 (English Wikipedia)

"Protein sequence of human ITGA7 (Uniprot ID: Q13683)". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 24 September 2015. Retrieved 20 July 2015.

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

pubmed.ncbi.nlm.nih.gov

Wang W, Wu W, Desai T, Ward DC, Kaufman SJ (Aug 1995). "Localization of the alpha 7 integrin gene (ITGA7) on human chromosome 12q13: clustering of integrin and Hox genes implies parallel evolution of these gene families". Genomics. 26 (3): 568–70. doi:10.1016/0888-7543(95)80176-M. PMID 7607681.
Cohn RD, Mayer U, Saher G, Herrmann R, van der Flier A, Sonnenberg A, Sorokin L, Voit T (March 1999). "Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle". J. Neurol. Sci. 163 (2): 140–52. doi:10.1016/s0022-510x(99)00012-x. PMID 10371075. S2CID 53300469.
Ziober BL, Vu MP, Waleh N, Crawford J, Lin CS, Kramer RH (December 1993). "Alternative extracellular and cytoplasmic domains of the integrin alpha 7 subunit are differentially expressed during development". J. Biol. Chem. 268 (35): 26773–83. doi:10.1016/S0021-9258(19)74380-4. PMID 8253814.
Maitra N, Flink IL, Bahl JJ, Morkin E (September 2000). "Expression of alpha and beta integrins during terminal differentiation of cardiomyocytes". Cardiovasc. Res. 47 (4): 715–25. doi:10.1016/s0008-6363(00)00140-1. PMID 10974220.
Collo G, Starr L, Quaranta V (September 1993). "A new isoform of the laminin receptor integrin alpha 7 beta 1 is developmentally regulated in skeletal muscle". J. Biol. Chem. 268 (25): 19019–24. doi:10.1016/S0021-9258(17)46729-9. PMID 8360188.
Song WK, Wang W, Sato H, Bielser DA, Kaufman SJ (December 1993). "Expression of alpha 7 integrin cytoplasmic domains during skeletal muscle development: alternate forms, conformational change, and homologies with serine/threonine kinases and tyrosine phosphatases". J. Cell Sci. 106 ( Pt 4) (4): 1139–52. doi:10.1242/jcs.106.4.1139. PMID 8126096.
Ziober BL, Kramer RH (September 1996). "Identification and characterization of the cell type-specific and developmentally regulated alpha7 integrin gene promoter". J. Biol. Chem. 271 (37): 22915–22. doi:10.1074/jbc.271.37.22915. PMID 8798472.
Leung, E; Lim, SP; Berg, R; Yang, Y; Ni, J; Wang, SX; Krissansen, GW (4 February 1998). "A novel extracellular domain variant of the human integrin alpha 7 subunit generated by alternative intron splicing". Biochemical and Biophysical Research Communications. 243 (1): 317–25. doi:10.1006/bbrc.1998.8092. PMID 9473524.
Vignier N, Moghadaszadeh B, Gary F, Beckmann J, Mayer U, Guicheney P (July 1999). "Structure, genetic localization, and identification of the cardiac and skeletal muscle transcripts of the human integrin alpha7 gene (ITGA7)". Biochem. Biophys. Res. Commun. 260 (2): 357–64. doi:10.1006/bbrc.1999.0916. PMID 10403775.
Kaufman SJ, Foster RF, Haye KR, Faiman LE (June 1985). "Expression of a developmentally regulated antigen on the surface of skeletal and cardiac muscle cells". J. Cell Biol. 100 (6): 1977–87. doi:10.1083/jcb.100.6.1977. PMC 2113591. PMID 3889014.
Yao CC, Breuss J, Pytela R, Kramer RH (July 1997). "Functional expression of the alpha 7 integrin receptor in differentiated smooth muscle cells". J. Cell Sci. 110 ( Pt 13) (13): 1477–87. doi:10.1242/jcs.110.13.1477. PMID 9224765.
Velling T, Collo G, Sorokin L, Durbeej M, Zhang H, Gullberg D (December 1996). "Distinct alpha 7A beta 1 and alpha 7B beta 1 integrin expression patterns during mouse development: alpha 7A is restricted to skeletal muscle but alpha 7B is expressed in striated muscle, vasculature, and nervous system". Dev. Dyn. 207 (4): 355–71. doi:10.1002/(SICI)1097-0177(199612)207:4<355::AID-AJA1>3.0.CO;2-G. PMID 8950511.
Hynes RO (April 1992). "Integrins: versatility, modulation, and signaling in cell adhesion". Cell. 69 (1): 11–25. doi:10.1016/0092-8674(92)90115-s. PMID 1555235. S2CID 32774108.
Yao CC, Ziober BL, Sutherland AE, Mendrick DL, Kramer RH (December 1996). "Laminins promote the locomotion of skeletal myoblasts via the alpha 7 integrin receptor". J. Cell Sci. 109 ( Pt 13) (13): 3139–50. doi:10.1242/jcs.109.13.3139. PMID 9004048.
Brancaccio M, Cabodi S, Belkin AM, Collo G, Koteliansky VE, Tomatis D, Altruda F, Silengo L, Tarone G (March 1998). "Differential onset of expression of alpha 7 and beta 1D integrins during mouse heart and skeletal muscle development". Cell Adhes. Commun. 5 (3): 193–205. doi:10.3109/15419069809040291. PMID 9686317.
Samson T, Smyth N, Janetzky S, Wendler O, Müller JM, Schüle R, von der Mark H, von der Mark K, Wixler V (Jul 2004). "The LIM-only proteins FHL2 and FHL3 interact with alpha- and beta-subunits of the muscle alpha7beta1 integrin receptor". J. Biol. Chem. 279 (27): 28641–52. doi:10.1074/jbc.M312894200. PMID 15117962.
Galie PA, Khalid N, Carnahan KE, Westfall MV, Stegemann JP (2013). "Substrate stiffness affects sarcomere and costamere structure and electrophysiological function of isolated adult cardiomyocytes". Cardiovasc. Pathol. 22 (3): 219–27. doi:10.1016/j.carpath.2012.10.003. PMC 3610795. PMID 23266222.
Zolkiewska A, Moss J (1997). "The α7 Integrin as a Target Protein for Cell Surface Mono-ADP-Ribosylation in Muscle Cells". ADP-Ribosylation in Animal Tissues. Advances in Experimental Medicine and Biology. Vol. 419. pp. 297–303. doi:10.1007/978-1-4419-8632-0_39. ISBN 978-1-4613-4652-4. PMID 9193669.
Mayer U, Saher G, Fässler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Pöschl E, von der Mark K (November 1997). "Absence of integrin alpha 7 causes a novel form of muscular dystrophy". Nat. Genet. 17 (3): 318–23. doi:10.1038/ng1197-318. PMID 9354797. S2CID 23724091.
Allikian, MJ; Hack, AA; Mewborn, S; Mayer, U; McNally, EM (1 August 2004). "Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle". Journal of Cell Science. 117 (Pt 17): 3821–30. doi:10.1242/jcs.01234. PMID 15252120. S2CID 86082596.
Guo C, Willem M, Werner A, Raivich G, Emerson M, Neyses L, Mayer U (March 2006). "Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy". Hum. Mol. Genet. 15 (6): 989–98. doi:10.1093/hmg/ddl018. PMID 16476707.
Heller KN, Montgomery CL, Janssen PM, Clark KR, Mendell JR, Rodino-Klapac LR (March 2013). "AAV-mediated overexpression of human α7 integrin leads to histological and functional improvement in dystrophic mice". Mol. Ther. 21 (3): 520–5. doi:10.1038/mt.2012.281. PMC 3589167. PMID 23319059.
Mielenz D, Hapke S, Pöschl E, von Der Mark H, von Der Mark K (April 2001). "The integrin alpha 7 cytoplasmic domain regulates cell migration, lamellipodia formation, and p130CAS/Crk coupling". J. Biol. Chem. 276 (16): 13417–26. doi:10.1074/jbc.M011481200. PMID 11278916.
Hayashi YK, Chou FL, Engvall E, Ogawa M, Matsuda C, Hirabayashi S, et al. (May 1998). "Mutations in the integrin alpha7 gene cause congenital myopathy". Nat. Genet. 19 (1): 94–7. doi:10.1038/ng0598-94. PMID 9590299. S2CID 40229216.
Esposito T, Sampaolo S, Limongelli G, Varone A, Formicola D, Diodato D, et al. (June 2013). "Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy". Orphanet J Rare Dis. 8: 91. doi:10.1186/1750-1172-8-91. PMC 3695851. PMID 23800289.
Vachon PH, Xu H, Liu L, Loechel F, Hayashi Y, Arahata K, Reed JC, Wewer UM, Engvall E (October 1997). "Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy". J. Clin. Invest. 100 (7): 1870–81. doi:10.1172/JCI119716. PMC 508374. PMID 9312189.
Hodges BL, Hayashi YK, Nonaka I, Wang W, Arahata K, Kaufman SJ (November 1997). "Altered expression of the alpha7beta1 integrin in human and murine muscular dystrophies". J. Cell Sci. 110 ( Pt 22) (22): 2873–81. doi:10.1242/jcs.110.22.2873. PMID 9427295.

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: ITGA7 integrin, alpha 7".
Kaufman SJ, Foster RF, Haye KR, Faiman LE (June 1985). "Expression of a developmentally regulated antigen on the surface of skeletal and cardiac muscle cells". J. Cell Biol. 100 (6): 1977–87. doi:10.1083/jcb.100.6.1977. PMC 2113591. PMID 3889014.
Galie PA, Khalid N, Carnahan KE, Westfall MV, Stegemann JP (2013). "Substrate stiffness affects sarcomere and costamere structure and electrophysiological function of isolated adult cardiomyocytes". Cardiovasc. Pathol. 22 (3): 219–27. doi:10.1016/j.carpath.2012.10.003. PMC 3610795. PMID 23266222.
Heller KN, Montgomery CL, Janssen PM, Clark KR, Mendell JR, Rodino-Klapac LR (March 2013). "AAV-mediated overexpression of human α7 integrin leads to histological and functional improvement in dystrophic mice". Mol. Ther. 21 (3): 520–5. doi:10.1038/mt.2012.281. PMC 3589167. PMID 23319059.
Esposito T, Sampaolo S, Limongelli G, Varone A, Formicola D, Diodato D, et al. (June 2013). "Digenic mutational inheritance of the integrin alpha 7 and the myosin heavy chain 7B genes causes congenital myopathy with left ventricular non-compact cardiomyopathy". Orphanet J Rare Dis. 8: 91. doi:10.1186/1750-1172-8-91. PMC 3695851. PMID 23800289.
Vachon PH, Xu H, Liu L, Loechel F, Hayashi Y, Arahata K, Reed JC, Wewer UM, Engvall E (October 1997). "Integrins (alpha7beta1) in muscle function and survival. Disrupted expression in merosin-deficient congenital muscular dystrophy". J. Clin. Invest. 100 (7): 1870–81. doi:10.1172/JCI119716. PMC 508374. PMID 9312189.

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Cohn RD, Mayer U, Saher G, Herrmann R, van der Flier A, Sonnenberg A, Sorokin L, Voit T (March 1999). "Secondary reduction of alpha7B integrin in laminin alpha2 deficient congenital muscular dystrophy supports an additional transmembrane link in skeletal muscle". J. Neurol. Sci. 163 (2): 140–52. doi:10.1016/s0022-510x(99)00012-x. PMID 10371075. S2CID 53300469.
Hynes RO (April 1992). "Integrins: versatility, modulation, and signaling in cell adhesion". Cell. 69 (1): 11–25. doi:10.1016/0092-8674(92)90115-s. PMID 1555235. S2CID 32774108.
Mayer U, Saher G, Fässler R, Bornemann A, Echtermeyer F, von der Mark H, Miosge N, Pöschl E, von der Mark K (November 1997). "Absence of integrin alpha 7 causes a novel form of muscular dystrophy". Nat. Genet. 17 (3): 318–23. doi:10.1038/ng1197-318. PMID 9354797. S2CID 23724091.
Allikian, MJ; Hack, AA; Mewborn, S; Mayer, U; McNally, EM (1 August 2004). "Genetic compensation for sarcoglycan loss by integrin alpha7beta1 in muscle". Journal of Cell Science. 117 (Pt 17): 3821–30. doi:10.1242/jcs.01234. PMID 15252120. S2CID 86082596.
Hayashi YK, Chou FL, Engvall E, Ogawa M, Matsuda C, Hirabayashi S, et al. (May 1998). "Mutations in the integrin alpha7 gene cause congenital myopathy". Nat. Genet. 19 (1): 94–7. doi:10.1038/ng0598-94. PMID 9590299. S2CID 40229216.

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"Protein sequence of human ITGA7 (Uniprot ID: Q13683)". Cardiac Organellar Protein Atlas Knowledgebase (COPaKB). Archived from the original on 24 September 2015. Retrieved 20 July 2015.

Integrin alpha 7 (English Wikipedia)

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