ASPM Antibodies

Lin, Liang, Dong, Ren, Zhao, Li: "Identification of Abnormal Spindle Microtubule Assembly as a Promising Therapeutic Target for Osteosarcoma." in: Orthopaedic surgery, Vol. 12, Issue 6, pp. 1963-1970, (2021) (PubMed).

Chinen, Yamamoto, Takeda, Watanabe, Kuroki, Hashimoto, Takao, Kitagawa: "NuMA assemblies organize microtubule asters to establish spindle bipolarity in acentrosomal human cells." in: The EMBO journal, Vol. 39, Issue 2, pp. e102378, (2020) (PubMed).

Yuan, Sun, Gao, Yin, Yuan, Xu: "Abnormal spindle-like microcephaly-associated protein (ASPM) contributes to the progression of Lung Squamous Cell Carcinoma (LSCC) by regulating CDK4." in: Journal of Cancer, Vol. 11, Issue 18, pp. 5413-5423, (2020) (PubMed).

Gemble, Simon, Pennetier, Dumont, Hervé, Meitinger, Oegema, Rodriguez, Almouzni, Fachinetti, Basto: "Centromere Dysfunction Compromises Mitotic Spindle Pole Integrity." in: Current biology : CB, Vol. 29, Issue 18, pp. 3072-3080.e5, (2019) (PubMed).

Raman, Maddipati, Lim, Tozeren: "Pancreatic cancer survival analysis defines a signature that predicts outcome." in: PLoS ONE, Vol. 13, Issue 8, pp. e0201751, (2018) (PubMed).

Sgourdou, Mishra-Gorur, Saotome, Henagariu, Tuysuz, Campos, Ishigame, Giannikou, Quon, Sestan, Caglayan, Gunel, Louvi: "Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly." in: Scientific reports, Vol. 7, pp. 43708, (2017) (PubMed).

Jiang, Rezabkova, Hua, Liu, Capitani, Altelaar, Heck, Kammerer, Steinmetz, Akhmanova: "Microtubule minus-end regulation at spindle poles by an ASPM-katanin complex." in: Nature cell biology, Vol. 19, Issue 5, pp. 480-492, (2017) (PubMed).

Bainer, Veneris, Yamada, Montag, Lingen, Gilad, Rinker-Schaeffer: "Time-dependent transcriptional profiling links gene expression to mitogen-activated protein kinase kinase 4 (MKK4)-mediated suppression of omental metastatic colonization." in: Clinical & experimental metastasis, Vol. 29, Issue 5, pp. 397-408, (2012) (PubMed).

Griffith, Walker, Martin, Vagnarelli, Stiff, Vernay, Al Sanna, Saggar, Hamel, Earnshaw, Jeggo, Jackson, ODriscoll: "Mutations in pericentrin cause Seckel syndrome with defective ATR-dependent DNA damage signaling." in: Nature genetics, Vol. 40, Issue 2, pp. 232-6, (2008) (PubMed).