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Items: 1 to 20 of 94

1.

A transcriptome profile in hepatocellular carcinomas based on integrated analysis of microarray studies.

Wang F, Wang R, Li Q, Qu X, Hao Y, Yang J, Zhao H, Wang Q, Li G, Zhang F, Zhang H, Zhou X, Peng X, Bian Y, Xiao W.

Diagn Pathol. 2017 Jan 13;12(1):4. doi: 10.1186/s13000-016-0596-x.

2.

A novel splice-site mutation in the ASPM gene underlies autosomal recessive primary microcephaly.

Hashmi JA, Al-Harbi KM, Ramzan K, Albalawi AM, Mehmood A, Samman MI, Basit S.

Ann Saudi Med. 2016 Nov-Dec;36(6):391-396.

3.

Frameshift Mutation of ASPM Gene in Colorectal Cancers with Regional Heterogeneity.

Choi EJ, Kim MS, Yoo NJ, Lee SH.

Pathol Oncol Res. 2016 Oct;22(4):877-9. doi: 10.1007/s12253-016-0108-z. Epub 2016 Aug 29. No abstract available.

PMID:
27571986
4.

CO-OCCURRENCE OF PRIMARY MICROCEPHALY CAUSED BY A NOVEL HOMOZYGOUS ASPM MUTATION ALONG WITH X-LINKED ICHTHYOSIS IN THE SAME PATIENT.

Abdel-Hamid MS, Ismail MF, Darwish HA, Effat LK, Zaki MS, Abdel-Salam GM.

Genet Couns. 2016;27(1):25-33.

PMID:
27192889
5.

Whole-exome sequencing is a powerful approach for establishing the etiological diagnosis in patients with intellectual disability and microcephaly.

Rump P, Jazayeri O, van Dijk-Bos KK, Johansson LF, van Essen AJ, Verheij JB, Veenstra-Knol HE, Redeker EJ, Mannens MM, Swertz MA, Alizadeh BZ, van Ravenswaaij-Arts CM, Sinke RJ, Sikkema-Raddatz B.

BMC Med Genomics. 2016 Feb 4;9:7. doi: 10.1186/s12920-016-0167-8.

6.

Abnormal spindle-like microcephaly-associated (ASPM) mutations strongly disrupt neocortical structure but spare the hippocampus and long-term memory.

Passemard S, Verloes A, Billette de Villemeur T, Boespflug-Tanguy O, Hernandez K, Laurent M, Isidor B, Alberti C, Pouvreau N, Drunat S, Gérard B, El Ghouzzi V, Gallego J, Elmaleh-Bergès M, Huttner WB, Eliez S, Gressens P, Schaer M.

Cortex. 2016 Jan;74:158-76. doi: 10.1016/j.cortex.2015.10.010. Epub 2015 Oct 31.

PMID:
26691732
7.

ASPM regulates symmetric stem cell division by tuning Cyclin E ubiquitination.

Capecchi MR, Pozner A.

Nat Commun. 2015 Nov 19;6:8763. doi: 10.1038/ncomms9763.

8.
9.

Genome-wide analysis of the oxyntic proliferative isthmus zone reveals ASPM as a possible gastric stem/progenitor cell marker over-expressed in cancer.

Vange P, Bruland T, Beisvag V, Erlandsen SE, Flatberg A, Doseth B, Sandvik AK, Bakke I.

J Pathol. 2015 Dec;237(4):447-59. doi: 10.1002/path.4591. Epub 2015 Aug 26.

10.

Estrogen regulation of microcephaly genes and evolution of brain sexual dimorphism in primates.

Shi L, Lin Q, Su B.

BMC Evol Biol. 2015 Jun 30;15:127. doi: 10.1186/s12862-015-0398-x.

11.

Accurate Prediction and Validation of Response to Endocrine Therapy in Breast Cancer.

Turnbull AK, Arthur LM, Renshaw L, Larionov AA, Kay C, Dunbier AK, Thomas JS, Dowsett M, Sims AH, Dixon JM.

J Clin Oncol. 2015 Jul 10;33(20):2270-8. doi: 10.1200/JCO.2014.57.8963. Epub 2015 Jun 1.

PMID:
26033813
12.

Molecular genetics of human primary microcephaly: an overview.

Faheem M, Naseer MI, Rasool M, Chaudhary AG, Kumosani TA, Ilyas AM, Pushparaj P, Ahmed F, Algahtani HA, Al-Qahtani MH, Saleh Jamal H.

BMC Med Genomics. 2015;8 Suppl 1:S4. doi: 10.1186/1755-8794-8-S1-S4. Epub 2015 Jan 15. Review.

13.

Global analysis of chromosome 1 genes among patients with lung adenocarcinoma, squamous carcinoma, large-cell carcinoma, small-cell carcinoma, or non-cancer.

Zhang Y, Wang H, Wang J, Bao L, Wang L, Huo J, Wang X.

Cancer Metastasis Rev. 2015 Jun;34(2):249-64. doi: 10.1007/s10555-015-9558-0. Review.

PMID:
25937073
14.

Extramedullary relapse of multiple myeloma defined as the highest risk group based on deregulated gene expression data.

Sevcikova S, Paszekova H, Besse L, Sedlarikova L, Kubaczkova V, Almasi M, Pour L, Hajek R.

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2015 Jun;159(2):288-93. doi: 10.5507/bp.2015.014. Epub 2015 Apr 16.

15.

Expression and clinical significance of genes frequently mutated in small cell lung cancers defined by whole exome/RNA sequencing.

Iwakawa R, Kohno T, Totoki Y, Shibata T, Tsuchihara K, Mimaki S, Tsuta K, Narita Y, Nishikawa R, Noguchi M, Harris CC, Robles AI, Yamaguchi R, Imoto S, Miyano S, Totsuka H, Yoshida T, Yokota J.

Carcinogenesis. 2015 Jun;36(6):616-21. doi: 10.1093/carcin/bgv026. Epub 2015 Apr 11.

16.

Enhancement of tumor initiation and expression of KCNMA1, MORF4L2 and ASPM genes in the adenocarcinoma of lung xenograft after vorinostat treatment.

Kuo WY, Wu CY, Hwu L, Lee JS, Tsai CH, Lin KP, Wang HE, Chou TY, Tsai CM, Gelovani J, Liu RS.

Oncotarget. 2015 Apr 20;6(11):8663-75.

17.

Primary microcephaly with anterior predominant pachygyria caused by novel compound heterozygous mutations in ASPM.

Nakamura K, Inui T, Miya F, Kanemura Y, Okamoto N, Saitoh S, Yamasaki M, Tsunoda T, Kosaki K, Tanaka S, Kato M.

Pediatr Neurol. 2015 May;52(5):e7-8. doi: 10.1016/j.pediatrneurol.2015.01.019. Epub 2015 Feb 7. No abstract available.

PMID:
25765464
18.

Genome resequencing and bioinformatic analysis of SNP containing candidate genes in the autoimmune vitiligo Smyth line chicken model.

Jang HM, Erf GF, Rowland KC, Kong BW.

BMC Genomics. 2014 Aug 23;15:707. doi: 10.1186/1471-2164-15-707.

19.

Simplified gyral pattern in severe developmental microcephalies? New insights from allometric modeling for spatial and spectral analysis of gyrification.

Germanaud D, Lefèvre J, Fischer C, Bintner M, Curie A, des Portes V, Eliez S, Elmaleh-Bergès M, Lamblin D, Passemard S, Operto G, Schaer M, Verloes A, Toro R, Mangin JF, Hertz-Pannier L.

Neuroimage. 2014 Nov 15;102 Pt 2:317-31. doi: 10.1016/j.neuroimage.2014.07.057. Epub 2014 Aug 6.

PMID:
25107856
20.

Microcephaly genes evolved adaptively throughout the evolution of eutherian mammals.

Montgomery SH, Mundy NI.

BMC Evol Biol. 2014 Jun 5;14:120. doi: 10.1186/1471-2148-14-120.

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