PubMed for id: 7650

Year	Number of Results
1993	1
1998	1
2000	1
2001	1
2002	4
2003	2
2004	3
2005	5
2006	4
2007	6
2008	10
2009	10
2010	5
2011	10
2012	5
2013	7
2024	0

1

A gene expression signature of epithelial tubulogenesis and a role for ASPM in pancreatic tumor progression.

Wang WY, Hsu CC, Wang TY, Li CR, Hou YC, Chu JM, Lee CT, Liu MS, Su JJ, Jian KY, Huang SS, Jiang SS, Shan YS, Lin PW, Shen YY, Lee MT, Chan TS, Chang CC, Chen CH, Chang IS, Lee YL, Chen LT, Tsai KK. Wang WY, et al. Gastroenterology. 2013 Nov;145(5):1110-20. doi: 10.1053/j.gastro.2013.07.040. Epub 2013 Jul 27. Gastroenterology. 2013. PMID: 23896173

2

Abnormal spindle-like microcephaly gene detection in an autosomal recessive microcephalic Saudi patient with attention deficit hyperactivity disorder and mental retardation.

Mahmoud AA, Siddiqui IA. Mahmoud AA, et al. Neurosciences (Riyadh). 2013 Jul;18(3):278-80. Neurosciences (Riyadh). 2013. PMID: 23887221 No abstract available.

3

The microtubule-associated protein ASPM regulates spindle assembly and meiotic progression in mouse oocytes.

Xu XL, Ma W, Zhu YB, Wang C, Wang BY, An N, An L, Liu Y, Wu ZH, Tian JH. Xu XL, et al. PLoS One. 2012;7(11):e49303. doi: 10.1371/journal.pone.0049303. Epub 2012 Nov 13. PLoS One. 2012. PMID: 23152892 Free PMC article.

4

Exome sequencing overrides formal genetics: ASPM mutations in a case study of apparent X-linked microcephalic intellectual deficit.

Ariani F, Mari F, Amitrano S, Di Marco C, Artuso R, Scala E, Meloni I, Della Volpe R, Rossi A, van Bokhoven H, Renieri A. Ariani F, et al. Clin Genet. 2013 Mar;83(3):288-90. doi: 10.1111/j.1399-0004.2012.01901.x. Epub 2012 Jul 23. Clin Genet. 2013. PMID: 22823409 Free PMC article. No abstract available.

5

The derived allele of ASPM is associated with lexical tone perception.

Wong PC, Chandrasekaran B, Zheng J. Wong PC, et al. PLoS One. 2012;7(4):e34243. doi: 10.1371/journal.pone.0034243. Epub 2012 Apr 17. PLoS One. 2012. PMID: 22529908 Free PMC article.

6

ASPM influences DNA double-strand break repair and represents a potential target for radiotherapy.

Kato TA, Okayasu R, Jeggo PA, Fujimori A. Kato TA, et al. Int J Radiat Biol. 2011 Dec;87(12):1189-95. doi: 10.3109/09553002.2011.624152. Epub 2011 Nov 7. Int J Radiat Biol. 2011. PMID: 21923303

7

Human ASPM participates in spindle organisation, spindle orientation and cytokinesis.

Higgins J, Midgley C, Bergh AM, Bell SM, Askham JM, Roberts E, Binns RK, Sharif SM, Bennett C, Glover DM, Woods CG, Morrison EE, Bond J. Higgins J, et al. BMC Cell Biol. 2010 Nov 2;11:85. doi: 10.1186/1471-2121-11-85. BMC Cell Biol. 2010. PMID: 21044324 Free PMC article.

8

ASPM gene expression in medulloblastoma.

Vulcani-Freitas TM, Saba-Silva N, Cappellano A, Cavalheiro S, Marie SK, Oba-Shinjo SM, Malheiros SM, de Toledo SR. Vulcani-Freitas TM, et al. Childs Nerv Syst. 2011 Jan;27(1):71-4. doi: 10.1007/s00381-010-1252-5. Epub 2010 Aug 6. Childs Nerv Syst. 2011. PMID: 20694558

9

Mutation analysis of the ASPM gene in 18 Pakistani families with autosomal recessive primary microcephaly.

Kousar R, Nawaz H, Khurshid M, Ali G, Khan SU, Mir H, Ayub M, Wali A, Ali N, Jelani M, Basit S, Ahmad W, Ansar M. Kousar R, et al. J Child Neurol. 2010 Jun;25(6):715-20. doi: 10.1177/0883073809346850. Epub 2009 Oct 6. J Child Neurol. 2010. PMID: 19808985

10

Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations.

Passemard S, Titomanlio L, Elmaleh M, Afenjar A, Alessandri JL, Andria G, de Villemeur TB, Boespflug-Tanguy O, Burglen L, Del Giudice E, Guimiot F, Hyon C, Isidor B, Mégarbané A, Moog U, Odent S, Hernandez K, Pouvreau N, Scala I, Schaer M, Gressens P, Gerard B, Verloes A. Passemard S, et al. Neurology. 2009 Sep 22;73(12):962-9. doi: 10.1212/WNL.0b013e3181b8799a. Neurology. 2009. PMID: 19770472

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