Prelamin-A/C (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Prelamin-A/C" in English language version.

refsWebsite

Global rank English rank

37nih.gov

4^th place

26doi.org

2^nd place

6semanticscholar.org

11^th place

8^th place

2ensembl.org

1,626^th place

1,007^th place

1harvard.edu

18^th place

17^th place

doi.org

Lin F, Worman HJ (August 1993). "Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C". The Journal of Biological Chemistry. 268 (22): 16321–16326. doi:10.1016/S0021-9258(19)85424-8. PMID 8344919.
Kamat AK, Rocchi M, Smith DI, Miller OJ (March 1993). "Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10". Somatic Cell and Molecular Genetics. 19 (2): 203–208. doi:10.1007/BF01233534. PMID 8511676. S2CID 32913788.
Wydner KL, McNeil JA, Lin F, Worman HJ, Lawrence JB (March 1996). "Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1, and LBR by fluorescence in situ hybridization". Genomics. 32 (3): 474–478. doi:10.1006/geno.1996.0146. PMID 8838815.
Buxboim A, Swift J, Irianto J, Spinler KR, Dingal PC, Athirasala A, et al. (August 2014). "Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin". Current Biology. 24 (16): 1909–1917. Bibcode:2014CBio...24.1909B. doi:10.1016/j.cub.2014.07.001. PMC 4373646. PMID 25127216.
Coutinho HD, Falcão-Silva VS, Gonçalves GF, da Nóbrega RB (April 2009). "Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model". Immunity & Ageing. 6: 4. doi:10.1186/1742-4933-6-4. PMC 2674425. PMID 19379495.
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, et al. (November 2012). "A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome". European Journal of Human Genetics. 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. PMC 3476705. PMID 22549407.
Capell BC, Collins FS (December 2006). "Human laminopathies: nuclei gone genetically awry". Nature Reviews. Genetics. 7 (12): 940–952. doi:10.1038/nrg1906. PMID 17139325. S2CID 13438737.
Rankin J, Ellard S (October 2006). "The laminopathies: a clinical review". Clinical Genetics. 70 (4): 261–274. doi:10.1111/j.1399-0004.2006.00677.x. PMID 16965317. S2CID 7234475.
Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, et al. (April 2008). "Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy". American Journal of Medical Genetics. Part A. 146A (8): 1049–1054. doi:10.1002/ajmg.a.32259. PMID 18348272. S2CID 205309256.
Cao H, Hegele RA (January 2000). "Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy". Human Molecular Genetics. 9 (1): 109–112. doi:10.1093/hmg/9.1.109. PMID 10587585.
Agarwal AK, Kazachkova I, Ten S, Garg A (December 2008). "Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation". The Journal of Clinical Endocrinology and Metabolism. 93 (12): 4617–4623. doi:10.1210/jc.2008-0123. PMC 2626450. PMID 18796515.
Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK (September 2005). "A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia". The Journal of Clinical Endocrinology and Metabolism. 90 (9): 5259–5264. doi:10.1210/jc.2004-2560. PMID 15998779.
Redwood AB, Perkins SM, Vanderwaal RP, Feng Z, Biehl KJ, Gonzalez-Suarez I, et al. (August 2011). "A dual role for A-type lamins in DNA double-strand break repair". Cell Cycle. 10 (15): 2549–2560. doi:10.4161/cc.10.15.16531. PMC 3180193. PMID 21701264.
Gonzalo S, Kreienkamp R (June 2015). "DNA repair defects and genome instability in Hutchinson-Gilford Progeria Syndrome". Current Opinion in Cell Biology. 34: 75–83. doi:10.1016/j.ceb.2015.05.007. PMC 4522337. PMID 26079711.
Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, et al. (July 2005). "Genomic instability in laminopathy-based premature aging". Nature Medicine. 11 (7): 780–785. doi:10.1038/nm1266. PMID 15980864. S2CID 11798376.
Tang K, Finley RL, Nie D, Honn KV (March 2000). "Identification of 12-lipoxygenase interaction with cellular proteins by yeast two-hybrid screening". Biochemistry. 39 (12): 3185–3191. doi:10.1021/bi992664v. PMID 10727209.
Wilkinson FL, Holaska JM, Zhang Z, Sharma A, Manilal S, Holt I, et al. (June 2003). "Emerin interacts in vitro with the splicing-associated factor, YT521-B". European Journal of Biochemistry. 270 (11): 2459–2466. doi:10.1046/j.1432-1033.2003.03617.x. PMID 12755701. S2CID 5963743.
Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, et al. (April 2003). "Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts". Biochemical and Biophysical Research Communications. 303 (3): 764–770. doi:10.1016/S0006-291X(03)00415-7. PMID 12670476.
Sakaki M, Koike H, Takahashi N, Sasagawa N, Tomioka S, Arahata K, Ishiura S (February 2001). "Interaction between emerin and nuclear lamins". Journal of Biochemistry. 129 (2): 321–327. doi:10.1093/oxfordjournals.jbchem.a002860. PMID 11173535.
Clements L, Manilal S, Love DR, Morris GE (January 2000). "Direct interaction between emerin and lamin A". Biochemical and Biophysical Research Communications. 267 (3): 709–714. doi:10.1006/bbrc.1999.2023. PMID 10673356.
Barton RM, Worman HJ (October 1999). "Prenylated prelamin A interacts with Narf, a novel nuclear protein". The Journal of Biological Chemistry. 274 (42): 30008–30018. doi:10.1074/jbc.274.42.30008. PMID 10514485.
Lloyd DJ, Trembath RC, Shackleton S (April 2002). "A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies". Human Molecular Genetics. 11 (7): 769–777. doi:10.1093/hmg/11.7.769. PMID 11929849.
Markiewicz E, Dechat T, Foisner R, Quinlan RA, Hutchison CJ (December 2002). "Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein". Molecular Biology of the Cell. 13 (12): 4401–4413. doi:10.1091/mbc.E02-07-0450. PMC 138642. PMID 12475961.
Dechat T, Korbei B, Vaughan OA, Vlcek S, Hutchison CJ, Foisner R (October 2000). "Lamina-associated polypeptide 2alpha binds intranuclear A-type lamins". Journal of Cell Science. 113 (19): 3473–3484. doi:10.1242/jcs.113.19.3473. PMID 10984438.
Dreuillet C, Tillit J, Kress M, Ernoult-Lange M (November 2002). "In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C". Nucleic Acids Research. 30 (21): 4634–4642. doi:10.1093/nar/gkf587. PMC 135794. PMID 12409453.
Liu B, Ghosh S, Yang X, Zheng H, Liu X, Wang Z, et al. (December 2012). "Resveratrol rescues SIRT1-dependent adult stem cell decline and alleviates progeroid features in laminopathy-based progeria". Cell Metabolism. 16 (6): 738–750. doi:10.1016/j.cmet.2012.11.007. PMID 23217256.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000160789 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000028063 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Buxboim A, Swift J, Irianto J, Spinler KR, Dingal PC, Athirasala A, et al. (August 2014). "Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin". Current Biology. 24 (16): 1909–1917. Bibcode:2014CBio...24.1909B. doi:10.1016/j.cub.2014.07.001. PMC 4373646. PMID 25127216.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lin F, Worman HJ (August 1993). "Structural organization of the human gene encoding nuclear lamin A and nuclear lamin C". The Journal of Biological Chemistry. 268 (22): 16321–16326. doi:10.1016/S0021-9258(19)85424-8. PMID 8344919.
Kamat AK, Rocchi M, Smith DI, Miller OJ (March 1993). "Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10". Somatic Cell and Molecular Genetics. 19 (2): 203–208. doi:10.1007/BF01233534. PMID 8511676. S2CID 32913788.
Wydner KL, McNeil JA, Lin F, Worman HJ, Lawrence JB (March 1996). "Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1, and LBR by fluorescence in situ hybridization". Genomics. 32 (3): 474–478. doi:10.1006/geno.1996.0146. PMID 8838815.
Buxboim A, Swift J, Irianto J, Spinler KR, Dingal PC, Athirasala A, et al. (August 2014). "Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin". Current Biology. 24 (16): 1909–1917. Bibcode:2014CBio...24.1909B. doi:10.1016/j.cub.2014.07.001. PMC 4373646. PMID 25127216.
Coutinho HD, Falcão-Silva VS, Gonçalves GF, da Nóbrega RB (April 2009). "Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model". Immunity & Ageing. 6: 4. doi:10.1186/1742-4933-6-4. PMC 2674425. PMID 19379495.
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, et al. (November 2012). "A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome". European Journal of Human Genetics. 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. PMC 3476705. PMID 22549407.
Capell BC, Collins FS (December 2006). "Human laminopathies: nuclei gone genetically awry". Nature Reviews. Genetics. 7 (12): 940–952. doi:10.1038/nrg1906. PMID 17139325. S2CID 13438737.
Rankin J, Ellard S (October 2006). "The laminopathies: a clinical review". Clinical Genetics. 70 (4): 261–274. doi:10.1111/j.1399-0004.2006.00677.x. PMID 16965317. S2CID 7234475.
Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, et al. (April 2008). "Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy". American Journal of Medical Genetics. Part A. 146A (8): 1049–1054. doi:10.1002/ajmg.a.32259. PMID 18348272. S2CID 205309256.
Cao H, Hegele RA (January 2000). "Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy". Human Molecular Genetics. 9 (1): 109–112. doi:10.1093/hmg/9.1.109. PMID 10587585.
Agarwal AK, Kazachkova I, Ten S, Garg A (December 2008). "Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation". The Journal of Clinical Endocrinology and Metabolism. 93 (12): 4617–4623. doi:10.1210/jc.2008-0123. PMC 2626450. PMID 18796515.
Garg A, Cogulu O, Ozkinay F, Onay H, Agarwal AK (September 2005). "A novel homozygous Ala529Val LMNA mutation in Turkish patients with mandibuloacral dysplasia". The Journal of Clinical Endocrinology and Metabolism. 90 (9): 5259–5264. doi:10.1210/jc.2004-2560. PMID 15998779.
Redwood AB, Perkins SM, Vanderwaal RP, Feng Z, Biehl KJ, Gonzalez-Suarez I, et al. (August 2011). "A dual role for A-type lamins in DNA double-strand break repair". Cell Cycle. 10 (15): 2549–2560. doi:10.4161/cc.10.15.16531. PMC 3180193. PMID 21701264.
Gonzalo S, Kreienkamp R (June 2015). "DNA repair defects and genome instability in Hutchinson-Gilford Progeria Syndrome". Current Opinion in Cell Biology. 34: 75–83. doi:10.1016/j.ceb.2015.05.007. PMC 4522337. PMID 26079711.
Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, et al. (July 2005). "Genomic instability in laminopathy-based premature aging". Nature Medicine. 11 (7): 780–785. doi:10.1038/nm1266. PMID 15980864. S2CID 11798376.
Tang K, Finley RL, Nie D, Honn KV (March 2000). "Identification of 12-lipoxygenase interaction with cellular proteins by yeast two-hybrid screening". Biochemistry. 39 (12): 3185–3191. doi:10.1021/bi992664v. PMID 10727209.
Wilkinson FL, Holaska JM, Zhang Z, Sharma A, Manilal S, Holt I, et al. (June 2003). "Emerin interacts in vitro with the splicing-associated factor, YT521-B". European Journal of Biochemistry. 270 (11): 2459–2466. doi:10.1046/j.1432-1033.2003.03617.x. PMID 12755701. S2CID 5963743.
Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, et al. (April 2003). "Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts". Biochemical and Biophysical Research Communications. 303 (3): 764–770. doi:10.1016/S0006-291X(03)00415-7. PMID 12670476.
Sakaki M, Koike H, Takahashi N, Sasagawa N, Tomioka S, Arahata K, Ishiura S (February 2001). "Interaction between emerin and nuclear lamins". Journal of Biochemistry. 129 (2): 321–327. doi:10.1093/oxfordjournals.jbchem.a002860. PMID 11173535.
Clements L, Manilal S, Love DR, Morris GE (January 2000). "Direct interaction between emerin and lamin A". Biochemical and Biophysical Research Communications. 267 (3): 709–714. doi:10.1006/bbrc.1999.2023. PMID 10673356.
Barton RM, Worman HJ (October 1999). "Prenylated prelamin A interacts with Narf, a novel nuclear protein". The Journal of Biological Chemistry. 274 (42): 30008–30018. doi:10.1074/jbc.274.42.30008. PMID 10514485.
Lloyd DJ, Trembath RC, Shackleton S (April 2002). "A novel interaction between lamin A and SREBP1: implications for partial lipodystrophy and other laminopathies". Human Molecular Genetics. 11 (7): 769–777. doi:10.1093/hmg/11.7.769. PMID 11929849.
Markiewicz E, Dechat T, Foisner R, Quinlan RA, Hutchison CJ (December 2002). "Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein". Molecular Biology of the Cell. 13 (12): 4401–4413. doi:10.1091/mbc.E02-07-0450. PMC 138642. PMID 12475961.
Dechat T, Korbei B, Vaughan OA, Vlcek S, Hutchison CJ, Foisner R (October 2000). "Lamina-associated polypeptide 2alpha binds intranuclear A-type lamins". Journal of Cell Science. 113 (19): 3473–3484. doi:10.1242/jcs.113.19.3473. PMID 10984438.
Dreuillet C, Tillit J, Kress M, Ernoult-Lange M (November 2002). "In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C". Nucleic Acids Research. 30 (21): 4634–4642. doi:10.1093/nar/gkf587. PMC 135794. PMID 12409453.
Liu B, Ghosh S, Yang X, Zheng H, Liu X, Wang Z, et al. (December 2012). "Resveratrol rescues SIRT1-dependent adult stem cell decline and alleviates progeroid features in laminopathy-based progeria". Cell Metabolism. 16 (6): 738–750. doi:10.1016/j.cmet.2012.11.007. PMID 23217256.

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.
Buxboim A, Swift J, Irianto J, Spinler KR, Dingal PC, Athirasala A, et al. (August 2014). "Matrix elasticity regulates lamin-A,C phosphorylation and turnover with feedback to actomyosin". Current Biology. 24 (16): 1909–1917. Bibcode:2014CBio...24.1909B. doi:10.1016/j.cub.2014.07.001. PMC 4373646. PMID 25127216.
Coutinho HD, Falcão-Silva VS, Gonçalves GF, da Nóbrega RB (April 2009). "Molecular ageing in progeroid syndromes: Hutchinson-Gilford progeria syndrome as a model". Immunity & Ageing. 6: 4. doi:10.1186/1742-4933-6-4. PMC 2674425. PMID 19379495.
"Entrez Gene: LMNA lamin A/C".
Al-Haggar M, Madej-Pilarczyk A, Kozlowski L, Bujnicki JM, Yahia S, Abdel-Hadi D, et al. (November 2012). "A novel homozygous p.Arg527Leu LMNA mutation in two unrelated Egyptian families causes overlapping mandibuloacral dysplasia and progeria syndrome". European Journal of Human Genetics. 20 (11): 1134–1140. doi:10.1038/ejhg.2012.77. PMC 3476705. PMID 22549407.
Agarwal AK, Kazachkova I, Ten S, Garg A (December 2008). "Severe mandibuloacral dysplasia-associated lipodystrophy and progeria in a young girl with a novel homozygous Arg527Cys LMNA mutation". The Journal of Clinical Endocrinology and Metabolism. 93 (12): 4617–4623. doi:10.1210/jc.2008-0123. PMC 2626450. PMID 18796515.
Redwood AB, Perkins SM, Vanderwaal RP, Feng Z, Biehl KJ, Gonzalez-Suarez I, et al. (August 2011). "A dual role for A-type lamins in DNA double-strand break repair". Cell Cycle. 10 (15): 2549–2560. doi:10.4161/cc.10.15.16531. PMC 3180193. PMID 21701264.
Gonzalo S, Kreienkamp R (June 2015). "DNA repair defects and genome instability in Hutchinson-Gilford Progeria Syndrome". Current Opinion in Cell Biology. 34: 75–83. doi:10.1016/j.ceb.2015.05.007. PMC 4522337. PMID 26079711.
Markiewicz E, Dechat T, Foisner R, Quinlan RA, Hutchison CJ (December 2002). "Lamin A/C binding protein LAP2alpha is required for nuclear anchorage of retinoblastoma protein". Molecular Biology of the Cell. 13 (12): 4401–4413. doi:10.1091/mbc.E02-07-0450. PMC 138642. PMID 12475961.
Dreuillet C, Tillit J, Kress M, Ernoult-Lange M (November 2002). "In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C". Nucleic Acids Research. 30 (21): 4634–4642. doi:10.1093/nar/gkf587. PMC 135794. PMID 12409453.

semanticscholar.org

api.semanticscholar.org

Kamat AK, Rocchi M, Smith DI, Miller OJ (March 1993). "Lamin A/C gene and a related sequence map to human chromosomes 1q12.1-q23 and 10". Somatic Cell and Molecular Genetics. 19 (2): 203–208. doi:10.1007/BF01233534. PMID 8511676. S2CID 32913788.
Capell BC, Collins FS (December 2006). "Human laminopathies: nuclei gone genetically awry". Nature Reviews. Genetics. 7 (12): 940–952. doi:10.1038/nrg1906. PMID 17139325. S2CID 13438737.
Rankin J, Ellard S (October 2006). "The laminopathies: a clinical review". Clinical Genetics. 70 (4): 261–274. doi:10.1111/j.1399-0004.2006.00677.x. PMID 16965317. S2CID 7234475.
Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, et al. (April 2008). "Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy". American Journal of Medical Genetics. Part A. 146A (8): 1049–1054. doi:10.1002/ajmg.a.32259. PMID 18348272. S2CID 205309256.
Liu B, Wang J, Chan KM, Tjia WM, Deng W, Guan X, et al. (July 2005). "Genomic instability in laminopathy-based premature aging". Nature Medicine. 11 (7): 780–785. doi:10.1038/nm1266. PMID 15980864. S2CID 11798376.
Wilkinson FL, Holaska JM, Zhang Z, Sharma A, Manilal S, Holt I, et al. (June 2003). "Emerin interacts in vitro with the splicing-associated factor, YT521-B". European Journal of Biochemistry. 270 (11): 2459–2466. doi:10.1046/j.1432-1033.2003.03617.x. PMID 12755701. S2CID 5963743.