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Abdel-Monem M, Dürwald H, Hoffmann-Berling H (June 1976). "Enzymic unwinding of DNA. 2. Chain separation by an ATP-dependent DNA unwinding enzyme". Eur. J. Biochem.65 (2): 441–9. PMID133023. doi:10.1111/j.1432-1033.1976.tb10359.x.
Hotta Y, Stern H (May 1978). "DNA unwinding protein from meiotic cells of Lilium". Biochemistry17 (10): 1872–80. PMID207302. doi:10.1021/bi00603a011.
Tuteja N, Tuteja R (May 2004). "Prokaryotic and eukaryotic DNA helicases. Essential molecular motor proteins for cellular machinery". Eur. J. Biochem.271 (10): 1835–48. PMID15128294. doi:10.1111/j.1432-1033.2004.04093.x.
Tuteja N, Phan TN, Tewari KK (May 1996). "Purification and characterization of a DNA helicase from pea chloroplast that translocates in the 3'-to-5' direction". Eur. J. Biochem.238 (1): 54–63. PMID8665952. doi:10.1111/j.1432-1033.1996.0054q.x.
Tuteja R, Malhotra P, Song P, Tuteja N, Chauhan VS (2002). "Isolation and characterization of an eIF-4A homologue from Plasmodium cynomolgi". Mol. Biochem. Parasitol.124 (1–2): 79–83. PMID12387853. doi:10.1016/S0166-6851(02)00205-0.
Martin Singleton, Mark S. Dillingham, and Dale B. Wigley (2007). "Structure and mechanism of Helicases and Nucleic Acid Translocases". The Annual Review of Biochemistry76: 23–50. PMID17506634. doi:10.1146/annurev.biochem.76.052305.115300.
Koonin EV, Aravind L, Leipe DD, Iyer LM (2004). "Evolutionary history and higher order classification of AAA+ ATPases". J. Struct. Biol.146 (1–2): 11–31. PMID15037234. doi:10.1016/j.jsb.2003.10.010.
Gibbons RJ, Picketts DJ, Villard L, Higgs DR (March 1995). "Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia ATR-X syndrome". Cell80 (6): 837–45. PMID7697714. doi:10.1016/0092-8674(95)90287-2.
Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ (December 1996). "ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome". Hum. Mol. Genet.5 (12): 1899–907. PMID8968741. doi:10.1093/hmg/5.12.1899.
Gibbons RJ, Picketts DJ, Villard L, Higgs DR (March 1995). "Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)". Cell80 (6): 837–45. PMID7697714. doi:10.1016/0092-8674(95)90287-2.
Tirode F, Busso D, Coin F, Egly JM (January 1999). "Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7". Mol. Cell3 (1): 87–95. PMID10024882. doi:10.1016/S1097-2765(00)80177-X.
Sung P, Bailly V, Weber C, Thompson LH, Prakash L, Prakash S (October 1993). "Human xeroderma pigmentosum group D gene encodes a DNA helicase". Nature365 (6449): 852–5. PMID8413672. doi:10.1038/365852a0.
Schaeffer L, Roy R, Humbert S, Moncollin V, Vermeulen W, Hoeijmakers JH, Chambon P, Egly JM (April 1993). "DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor". Science260 (5104): 58–63. PMID8465201. doi:10.1126/science.8465201.
Opresko PL, Cheng WH, Bohr VA (April 2004). "Junction of RecQ helicase biochemistry and human disease". J. Biol. Chem.279 (18): 18099–102. PMID15023996. doi:10.1074/jbc.R300034200.
Ouyang KJ, Woo LL, Ellis NA (2008). "Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases". Mech. Ageing Dev.129 (7–8): 425–40. PMID18430459. doi:10.1016/j.mad.2008.03.003.
Ellis NA, Groden J, Ye TZ, Straughen J, Lennon DJ, Ciocci S, Proytcheva M, German J (November 1995). "The Bloom's syndrome gene product is homologous to RecQ helicases". Cell83 (4): 655–66. PMID7585968. doi:10.1016/0092-8674(95)90105-1.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA (September 1997). "The Werner syndrome protein is a DNA helicase". Nat. Genet.17 (1): 100–3. PMID9288107. doi:10.1038/ng0997-100.
Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y (May 1999). "Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome". Nat. Genet.22 (1): 82–4. PMID10319867. doi:10.1038/8788.
Yang Q, Del Campo M, Lambowitz AM, Jankowsky E (October 2007). "DEAD-box proteins unwind duplexes by local strand separation". Mol. Cell28 (2): 253–63. PMID17964264. doi:10.1016/j.molcel.2007.08.016.
Abdel-Monem M, Dürwald H, Hoffmann-Berling H (June 1976). "Enzymic unwinding of DNA. 2. Chain separation by an ATP-dependent DNA unwinding enzyme". Eur. J. Biochem.65 (2): 441–9. PMID133023. doi:10.1111/j.1432-1033.1976.tb10359.x.
Hotta Y, Stern H (May 1978). "DNA unwinding protein from meiotic cells of Lilium". Biochemistry17 (10): 1872–80. PMID207302. doi:10.1021/bi00603a011.
Tuteja N, Tuteja R (May 2004). "Prokaryotic and eukaryotic DNA helicases. Essential molecular motor proteins for cellular machinery". Eur. J. Biochem.271 (10): 1835–48. PMID15128294. doi:10.1111/j.1432-1033.2004.04093.x.
Tuteja N, Phan TN, Tewari KK (May 1996). "Purification and characterization of a DNA helicase from pea chloroplast that translocates in the 3'-to-5' direction". Eur. J. Biochem.238 (1): 54–63. PMID8665952. doi:10.1111/j.1432-1033.1996.0054q.x.
Tuteja R, Malhotra P, Song P, Tuteja N, Chauhan VS (2002). "Isolation and characterization of an eIF-4A homologue from Plasmodium cynomolgi". Mol. Biochem. Parasitol.124 (1–2): 79–83. PMID12387853. doi:10.1016/S0166-6851(02)00205-0.
Martin Singleton, Mark S. Dillingham, and Dale B. Wigley (2007). "Structure and mechanism of Helicases and Nucleic Acid Translocases". The Annual Review of Biochemistry76: 23–50. PMID17506634. doi:10.1146/annurev.biochem.76.052305.115300.
Koonin EV, Aravind L, Leipe DD, Iyer LM (2004). "Evolutionary history and higher order classification of AAA+ ATPases". J. Struct. Biol.146 (1–2): 11–31. PMID15037234. doi:10.1016/j.jsb.2003.10.010.
Gibbons RJ, Picketts DJ, Villard L, Higgs DR (March 1995). "Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia ATR-X syndrome". Cell80 (6): 837–45. PMID7697714. doi:10.1016/0092-8674(95)90287-2.
Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ (December 1996). "ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome". Hum. Mol. Genet.5 (12): 1899–907. PMID8968741. doi:10.1093/hmg/5.12.1899.
Pagon RA, Bird TD, Dolan CR, Stephens K, Adam MP, Stevenson RE (1993). "Alpha-Thalassemia X-Linked Intellectual Disability Syndrome". PMID20301622.
Gibbons RJ, Picketts DJ, Villard L, Higgs DR (March 1995). "Mutations in a putative global transcriptional regulator cause X-linked mental retardation with alpha-thalassemia (ATR-X syndrome)". Cell80 (6): 837–45. PMID7697714. doi:10.1016/0092-8674(95)90287-2.
Tirode F, Busso D, Coin F, Egly JM (January 1999). "Reconstitution of the transcription factor TFIIH: assignment of functions for the three enzymatic subunits, XPB, XPD, and cdk7". Mol. Cell3 (1): 87–95. PMID10024882. doi:10.1016/S1097-2765(00)80177-X.
Sung P, Bailly V, Weber C, Thompson LH, Prakash L, Prakash S (October 1993). "Human xeroderma pigmentosum group D gene encodes a DNA helicase". Nature365 (6449): 852–5. PMID8413672. doi:10.1038/365852a0.
Schaeffer L, Roy R, Humbert S, Moncollin V, Vermeulen W, Hoeijmakers JH, Chambon P, Egly JM (April 1993). "DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor". Science260 (5104): 58–63. PMID8465201. doi:10.1126/science.8465201.
Opresko PL, Cheng WH, Bohr VA (April 2004). "Junction of RecQ helicase biochemistry and human disease". J. Biol. Chem.279 (18): 18099–102. PMID15023996. doi:10.1074/jbc.R300034200.
Ouyang KJ, Woo LL, Ellis NA (2008). "Homologous recombination and maintenance of genome integrity: cancer and aging through the prism of human RecQ helicases". Mech. Ageing Dev.129 (7–8): 425–40. PMID18430459. doi:10.1016/j.mad.2008.03.003.
Ellis NA, Groden J, Ye TZ, Straughen J, Lennon DJ, Ciocci S, Proytcheva M, German J (November 1995). "The Bloom's syndrome gene product is homologous to RecQ helicases". Cell83 (4): 655–66. PMID7585968. doi:10.1016/0092-8674(95)90105-1.
Gray MD, Shen JC, Kamath-Loeb AS, Blank A, Sopher BL, Martin GM, Oshima J, Loeb LA (September 1997). "The Werner syndrome protein is a DNA helicase". Nat. Genet.17 (1): 100–3. PMID9288107. doi:10.1038/ng0997-100.
Kitao S, Shimamoto A, Goto M, Miller RW, Smithson WA, Lindor NM, Furuichi Y (May 1999). "Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome". Nat. Genet.22 (1): 82–4. PMID10319867. doi:10.1038/8788.
Jankowsky, A.; Guenther, U. -P.; Jankowsky, E. (2010). "The RNA helicase database". Nucleic Acids Research 39 (Database issue): D338–D341. doi:10.1093/nar/gkq1002. PMC 3013637. PMID 21112871.
Steimer, L.; Klostermeier, D. (2012). "RNA helicases in infection and disease". RNA Biology 9 (6): 751–771. doi:10.4161/rna.20090. PMID 22699555.
Ranji, A.; Boris-Lawrie, K. (2010). "RNA helicases: Emerging roles in viral replication and the host innate response". RNA Biology 7 (6): 775–787. doi:10.4161/rna.7.6.14249. PMC 3073335. PMID 21173576.
Harald Dürr, Andrew Flaus, Tom Owen-Hughes, e Karl-Peter Hopfner. Snf2 family ATPases and DExx box helicases: differences and unifying concepts from high-resolution crystal structures. Nucleic Acids Res. 2006 Sep; 34(15): 4160–4167.
Published online 2006 Aug 25. doi 10.1093/nar/gkl540. [1]
Yang Q, Del Campo M, Lambowitz AM, Jankowsky E (October 2007). "DEAD-box proteins unwind duplexes by local strand separation". Mol. Cell28 (2): 253–63. PMID17964264. doi:10.1016/j.molcel.2007.08.016.