متلازمات شبيهة الشياخ (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "متلازمات شبيهة الشياخ" in Arabic language version.

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19nih.gov

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3arxiv.org

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1rarediseases.org

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archive.org

Hanada، K.؛ Hickson، I. D. (2007). "Molecular genetics of RecQ helicase disorders". Cellular and Molecular Life Sciences. ج. 64 ع. 17: 2306–22. DOI:10.1007/s00018-007-7121-z. PMID:17571213. S2CID:29287970.

arxiv.org

A bot will complete this citation soon. Click here to jump the queue أرخايف:0904.0575.
A bot will complete this citation soon. Click here to jump the queue أرخايف:1503.07163.
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doi.org

Gordon، Leslie B.؛ Cao، Kan؛ Collins، Francis S. (2012). "Progeria: Translational insights from cell biology". J Cell Biol. ج. 199 ع. 1: 9–13. DOI:10.1083/jcb.201207072. PMC:3461511. PMID:23027899.
Navarro، CL؛ Cau، P؛ Lévy، N (2006). "Molecular bases of progeroid syndromes". Human Molecular Genetics. 15 Spec No 2: R151–61. DOI:10.1093/hmg/ddl214. PMID:16987878.
Kaneko، H؛ Fukao، T؛ Kondo، N (2004). "The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining". Advances in Biophysics. ج. 38 ع. Complete: 45–64. DOI:10.1016/S0065-227X(04)80061-3. PMID:15493327.
Mohaghegh، P؛ Hickson، ID (2001). "DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders". Human Molecular Genetics. ج. 10 ع. 7: 741–6. DOI:10.1093/hmg/10.7.741. PMID:11257107.
Ouyang، KJ؛ Woo، LL؛ Ellis، NA (2008). "Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases". Mechanisms of Ageing and Development. ج. 129 ع. 7–8: 425–40. DOI:10.1016/j.mad.2008.03.003. PMID:18430459. S2CID:6804631.
Hanada، K.؛ Hickson، I. D. (2007). "Molecular genetics of RecQ helicase disorders". Cellular and Molecular Life Sciences. ج. 64 ع. 17: 2306–22. DOI:10.1007/s00018-007-7121-z. PMID:17571213. S2CID:29287970.
Hirai، M؛ Ohbayashi، T؛ Horiguchi، M (2007). "Fibulin-5/DANCE has an elastogenic organizer activity that is abrogated by proteolytic cleavage in vivo". J Cell Biol. ج. 176 ع. 7: 1061–71. DOI:10.1083/jcb.200611026. PMC:2064089. PMID:17371835.
Lanske، B؛ Razzaque، MS (2007). "Premature aging in klotho mutant mice: cause or consequence?". Ageing Res Rev. ج. 6 ع. 1: 73–9. DOI:10.1016/j.arr.2007.02.002. PMC:2896497. PMID:17353153.
Arboleda، H؛ Quintero، L؛ Yunis، E (1997). "Wiedemann–Rautenstrauch neonatal progeroid syndrome: Report of three new patients". Journal of Medical Genetics. ج. 34 ع. 5: 433–7. DOI:10.1136/jmg.34.5.433. PMC:1050956. PMID:9152846.
Toriello، HV (1990). "Wiedemann–Rautenstrauch syndrome". Journal of Medical Genetics. ج. 27 ع. 4: 256–7. DOI:10.1136/jmg.27.4.256. PMC:1017029. PMID:2325106.
Puzianowska-Kuznicka، M؛ Kuznicki، J (2005). "Genetic alterations in accelerated ageing syndromes. Do they play a role in natural ageing?". The International Journal of Biochemistry & Cell Biology. ج. 37 ع. 5: 947–60. DOI:10.1016/j.biocel.2004.10.011. PMID:15743670.

nih.gov

pubmed.ncbi.nlm.nih.gov

Sinha، Jitendra Kumar؛ Ghosh، Shampa؛ Raghunath، Manchala (مايو 2014). "Progeria: a rare genetic premature ageing disorder". Indian J Med Res. ج. 139 ع. 5: 667–74. PMC:4140030. PMID:25027075.
Gordon، Leslie B.؛ Cao، Kan؛ Collins، Francis S. (2012). "Progeria: Translational insights from cell biology". J Cell Biol. ج. 199 ع. 1: 9–13. DOI:10.1083/jcb.201207072. PMC:3461511. PMID:23027899.
Navarro، CL؛ Cau، P؛ Lévy، N (2006). "Molecular bases of progeroid syndromes". Human Molecular Genetics. 15 Spec No 2: R151–61. DOI:10.1093/hmg/ddl214. PMID:16987878.
Kaneko، H؛ Fukao، T؛ Kondo، N (2004). "The function of RecQ helicase gene family (especially BLM) in DNA recombination and joining". Advances in Biophysics. ج. 38 ع. Complete: 45–64. DOI:10.1016/S0065-227X(04)80061-3. PMID:15493327.
Mohaghegh، P؛ Hickson، ID (2001). "DNA helicase deficiencies associated with cancer predisposition and premature ageing disorders". Human Molecular Genetics. ج. 10 ع. 7: 741–6. DOI:10.1093/hmg/10.7.741. PMID:11257107.
Goode، EL؛ Ulrich، CM؛ Potter، JD (2002). "Polymorphisms in DNA repair genes and associations with cancer risk". Cancer Epidemiology, Biomarkers & Prevention. ج. 11 ع. 12: 1513–30. PMID:12496039.
Ouyang، KJ؛ Woo، LL؛ Ellis، NA (2008). "Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases". Mechanisms of Ageing and Development. ج. 129 ع. 7–8: 425–40. DOI:10.1016/j.mad.2008.03.003. PMID:18430459. S2CID:6804631.
Hanada، K.؛ Hickson، I. D. (2007). "Molecular genetics of RecQ helicase disorders". Cellular and Molecular Life Sciences. ج. 64 ع. 17: 2306–22. DOI:10.1007/s00018-007-7121-z. PMID:17571213. S2CID:29287970.
Hirai، M؛ Ohbayashi، T؛ Horiguchi، M (2007). "Fibulin-5/DANCE has an elastogenic organizer activity that is abrogated by proteolytic cleavage in vivo". J Cell Biol. ج. 176 ع. 7: 1061–71. DOI:10.1083/jcb.200611026. PMC:2064089. PMID:17371835.
Lanske، B؛ Razzaque، MS (2007). "Premature aging in klotho mutant mice: cause or consequence?". Ageing Res Rev. ج. 6 ع. 1: 73–9. DOI:10.1016/j.arr.2007.02.002. PMC:2896497. PMID:17353153.
Arboleda، H؛ Quintero، L؛ Yunis، E (1997). "Wiedemann–Rautenstrauch neonatal progeroid syndrome: Report of three new patients". Journal of Medical Genetics. ج. 34 ع. 5: 433–7. DOI:10.1136/jmg.34.5.433. PMC:1050956. PMID:9152846.
Toriello، HV (1990). "Wiedemann–Rautenstrauch syndrome". Journal of Medical Genetics. ج. 27 ع. 4: 256–7. DOI:10.1136/jmg.27.4.256. PMC:1017029. PMID:2325106.
Puzianowska-Kuznicka، M؛ Kuznicki، J (2005). "Genetic alterations in accelerated ageing syndromes. Do they play a role in natural ageing?". The International Journal of Biochemistry & Cell Biology. ج. 37 ع. 5: 947–60. DOI:10.1016/j.biocel.2004.10.011. PMID:15743670.

ncbi.nlm.nih.gov

Sinha، Jitendra Kumar؛ Ghosh، Shampa؛ Raghunath، Manchala (مايو 2014). "Progeria: a rare genetic premature ageing disorder". Indian J Med Res. ج. 139 ع. 5: 667–74. PMC:4140030. PMID:25027075.
Gordon، Leslie B.؛ Cao، Kan؛ Collins، Francis S. (2012). "Progeria: Translational insights from cell biology". J Cell Biol. ج. 199 ع. 1: 9–13. DOI:10.1083/jcb.201207072. PMC:3461511. PMID:23027899.
Hirai، M؛ Ohbayashi، T؛ Horiguchi، M (2007). "Fibulin-5/DANCE has an elastogenic organizer activity that is abrogated by proteolytic cleavage in vivo". J Cell Biol. ج. 176 ع. 7: 1061–71. DOI:10.1083/jcb.200611026. PMC:2064089. PMID:17371835.
Lanske، B؛ Razzaque، MS (2007). "Premature aging in klotho mutant mice: cause or consequence?". Ageing Res Rev. ج. 6 ع. 1: 73–9. DOI:10.1016/j.arr.2007.02.002. PMC:2896497. PMID:17353153.
Arboleda، H؛ Quintero، L؛ Yunis، E (1997). "Wiedemann–Rautenstrauch neonatal progeroid syndrome: Report of three new patients". Journal of Medical Genetics. ج. 34 ع. 5: 433–7. DOI:10.1136/jmg.34.5.433. PMC:1050956. PMID:9152846.
Toriello، HV (1990). "Wiedemann–Rautenstrauch syndrome". Journal of Medical Genetics. ج. 27 ع. 4: 256–7. DOI:10.1136/jmg.27.4.256. PMC:1017029. PMID:2325106.

orpha.net

"Wiedemann–Rautenstrauch syndrome". Orphanet. مؤرشف من الأصل في 2020-11-12. اطلع عليه بتاريخ 2013-03-16.

rarediseases.org

"Wiedemann Rautenstrauch Syndrome". NORD Rare Disease Report Abstract. مؤرشف من الأصل في 2013-03-27. اطلع عليه بتاريخ 2013-03-16.

semanticscholar.org

api.semanticscholar.org

Ouyang، KJ؛ Woo، LL؛ Ellis، NA (2008). "Homologous recombination and maintenance of genome integrity: Cancer and aging through the prism of human RecQ helicases". Mechanisms of Ageing and Development. ج. 129 ع. 7–8: 425–40. DOI:10.1016/j.mad.2008.03.003. PMID:18430459. S2CID:6804631.
Hanada، K.؛ Hickson، I. D. (2007). "Molecular genetics of RecQ helicase disorders". Cellular and Molecular Life Sciences. ج. 64 ع. 17: 2306–22. DOI:10.1007/s00018-007-7121-z. PMID:17571213. S2CID:29287970.

tools.wmflabs.org

A bot will complete this citation soon. Click here to jump the queue أرخايف:0904.0575.
A bot will complete this citation soon. Click here to jump the queue أرخايف:1503.07163.
A bot will complete this citation soon. Click here to jump the queue أرخايف:1505.03905.

web.archive.org

"Wiedemann Rautenstrauch Syndrome". NORD Rare Disease Report Abstract. مؤرشف من الأصل في 2013-03-27. اطلع عليه بتاريخ 2013-03-16.
"Wiedemann–Rautenstrauch syndrome". Orphanet. مؤرشف من الأصل في 2020-11-12. اطلع عليه بتاريخ 2013-03-16.