A region of common deletion in 22q13.3 in human glioma associated with astrocytoma progression

Autor: Oskam, N. T., Bijleveld, E. H., Hulsebos, T. J.

Publikováno v: International journal of cancer. Journal international du cancer, 85(3), 336-339. Wiley-Liss Inc.

Loss of heterozygosity for chromosome 22 (LOH 22) occurs in gliomas of all malignancy grades. Neurofibromatosis type 2 (NF2) patients are at increased risk of developing a glioma. However, the NF2 gene in 22q12.2 is not involved in glioma tumorigenes

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https://pure.amc.nl/en/publications/a-region-of-common-deletion-in-22q133-in-human-glioma-associated-with-astrocytoma-progression(09fa01ff-4256-4ec5-85ab-20c9e74c2638).html

The Influence of Gene Aberrations on Survival in Resected IDH Wildtype Glioblastoma Patients: A Single-Institution Study.

Autor: Kalita, Ondrej¹ ondrej.kalita@fnol.cz, Sporikova, Zuzana² sporikovaz@gmail.com, Hajduch, Marian² marian.hajduch@fnol.cz, Houdova, Magdalena Megova² magdalena.houdova-megova@lf1.cuni.cz, Slavkovsky, Rastislav² rastislav.slavskovsky@upol.cz, Hrabalek, Lumir¹ lumir.hrabalek@fnol.cz, Halaj, Matej¹ matej.halaj@fnol.cz, Klementova, Yvona³ yvona.klementova@fnol.cz, Dolezel, Martin³ martin.dolezel@fnol.cz, Drabek, Jiri² jiri.drabek@upol.cz, Tuckova, Lucie⁴ lucie.tuckova@fnol.cz, Ehrmann Jr., Jiri⁴ jiri.ehrmann2@fnol.cz, Vrbkova, Jana² jana.vrbkova@upol.cz, Trojanec, Radek² radek.trojanec@fnol.cz, Vaverka, Miroslav¹ miroslav.vaverka@fnol.cz

Publikováno v: Current Oncology. Apr2021, Vol. 28 Issue 2, p1280-1293. 14p.

Neuropsychological Function in Adults With Von Recklinghausen's Neurofibromatosis.

Autor: Pavol, Marykay¹ mpavol@siuh.edu, Hiscock, Merrill², Massman, Paul², Moore, III, Bartlett³, Foorman, Barbara⁴, Meyers, Christina³

Publikováno v: Developmental Neuropsychology. 2006, Vol. 29 Issue 3, p509-526. 18p. 6 Charts.

Gene conversion is a likely cause of mutation in PKD1.

Autor: Watnick, Terry J., Gandolph, Michael A., Weber, Horst, Neumann, Hartmut P. H., Germino, Gregory G.

Publikováno v: Human Molecular Genetics; Aug98, Vol. 7 Issue 8, p1239, 5p

Evidence for an ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2

Autor: N.C. Oskam, A. M. W. Van Den Ouweland, C.C. Tijssen, M.A.J.A. Hermsen, Andries Westerveld, Theo J. M. Hulsebos, Engelien H. Bijleveld, Ben C.J. Hamel

Publikováno v: British journal of cancer, 81(7), 1150-1154. Nature Publishing Group
British Journal of Cancer
British Journal of Cancer, 81, 1150-1154. Nature Publishing Group
Hulsebos, T J M, Oskam, N C, Bijleveld, E H, Westerveld, A, Hermsen, M A J A, van den Ouweland, A M W, Hamel, B C & Tijssen, C C 1999, ' Evidence for a ependymoma tumour suppressor gene in chromosome region 22pter-22q11.2. ', British Journal of Cancer, vol. 81, pp. 1150-1154 . https://doi.org/10.1038/sj.bjc.6690822
British Journal of Cancer, 81(7), 1150-1154. Nature Publishing Group

Ependymomas are glial tumours of the brain and spinal cord. The most frequent genetic change in sporadic ependymoma is monosomy 22, suggesting the presence of an ependymoma tumour suppressor gene on that chromosome. Clustering of ependymomas has been

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https://pure.amc.nl/en/publications/evidence-for-an-ependymoma-tumour-suppressor-gene-in-chromosome-region-22pter22q112(22395a74-ec17-4da7-ba6c-d4f40a1b3ad7).html