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Year | Number of Results |
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2006 | 1 |
2009 | 1 |
2011 | 3 |
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2024 | 0 |
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Page 1
Mesenchymal stem cells: characteristics and clinical applications.
Folia Histochem Cytobiol. 2006;44(4):215-30.
Folia Histochem Cytobiol. 2006.
PMID: 17219716
Free article.
Review.
Identification of ADAMTS18 as a gene mutated in Knobloch syndrome.
Aldahmesh MA, Khan AO, Mohamed JY, Alkuraya H, Ahmed H, Bobis S, Al-Mesfer S, Alkuraya FS.
Aldahmesh MA, et al. Among authors: bobis s.
J Med Genet. 2011 Sep;48(9):597-601. doi: 10.1136/jmedgenet-2011-100306.
J Med Genet. 2011.
PMID: 21862674
Item in Clipboard
[Molecular basis of pigmentation disorders in skin diseases].
Drukała J, Bobis S, Zabińska-Płazak E, Wojas-Pelc A.
Drukała J, et al. Among authors: bobis s.
Przegl Lek. 2009;66(3):145-9.
Przegl Lek. 2009.
PMID: 19689040
Review.
Polish.
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Mutation of IGFBP7 causes upregulation of BRAF/MEK/ERK pathway and familial retinal arterial macroaneurysms.
Abu-Safieh L, Abboud EB, Alkuraya H, Shamseldin H, Al-Enzi S, Al-Abdi L, Hashem M, Colak D, Jarallah A, Ahmad H, Bobis S, Nemer G, Bitar F, Alkuraya FS.
Abu-Safieh L, et al. Among authors: bobis s.
Am J Hum Genet. 2011 Aug 12;89(2):313-9. doi: 10.1016/j.ajhg.2011.07.010.
Am J Hum Genet. 2011.
PMID: 21835307
Free PMC article.
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Proteomic analysis of soft tissue tumor implants treated with a novel polybisphosphonate.
Alaiya A, Fox J, Bobis S, Matic G, Shinwari Z, Barhoush E, Márquez M, Nilsson S, Holmberg AR.
Alaiya A, et al. Among authors: bobis s.
Cancer Genomics Proteomics. 2014 Jan-Feb;11(1):39-49.
Cancer Genomics Proteomics. 2014.
PMID: 24633318
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia.
Al Tassan N, Khalil D, Shinwari J, Al Sharif L, Bavi P, Abduljaleel Z, Abu Dhaim N, Magrashi A, Bobis S, Ahmed H, Alahmed S, Bohlega S.
Al Tassan N, et al. Among authors: bobis s.
Hum Mutat. 2012 Feb;33(2):351-4. doi: 10.1002/humu.21650. Epub 2011 Dec 8.
Hum Mutat. 2012.
PMID: 22065524
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