نتایج جستجو برای: von hippel

تعداد نتایج: 96670  

Journal: :Internal Medicine and Medical Investigation Journal 2017

Journal: :Current Genetic Medicine Reports 2019

Journal: :The Journal of Clinical Endocrinology & Metabolism 2003

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1965
S W Englander J J Englander

1 Bradbury, E. M., W. C. Price, and G. R. Wilkinson, J. Mol. Biol., 4, 39 (1962). 2 von Hippel, P. H., and G. Felsenfeld, Biochemistry, 3, 27 (1964). 3 Englander, S. W., Biochemistry, 2, 798 (1963). 4Englander, S. W., and J. J. Englander, these PROCEEDINGS, 53, 370 (1965). 5 Bray, G. A., Anal. Biochem., 1, 279 (1960). 6 Flodin, P., J. Chromatoq., 6, 103 (1961). 7 Doty, P., B. B. McGill, and S. ...

Journal: :Turkish neurosurgery 2013
Bulent Tucer Mehmet Ali Ekici Burak Kazanci Bulent Guclu

We report a 41-year-old man who presented with low back pain, lower extremity paresthesia, urinary retention and constipation. Magnetic resonance imaging showed a vascular intradural-extramedullary lesion at the second lumbar vertebral level. His medical history revealed that he had undergone surgery for a cerebellar hemangioblastoma 5 years ago. The patient underwent a spinal operation and a v...

2016
Suzanne S. Fei Asia D. Mitchell Michael B. Heskett Cathy D. Vocke Christopher J. Ricketts Myron Peto Nicholas J. Wang Kemal Sönmez W. Marston Linehan Paul T. Spellman

Cancer development is presumed to be an evolutionary process that is influenced by genetic background and environment. In laboratory animals, genetics and environment are variables that can largely be held constant. In humans, it is possible to compare independent tumours that have developed in the same patient, effectively constraining genetic and environmental variation and leaving only stoch...

Journal: :The Medical journal of Malaysia 2006
A G Rohana M K Norazmi M Norlaila

Pheochromocytoma is a rare catecholamine-secreting tumour typically arising within the adrenal medulla. It may occur sporadically or be associated as part of a tumour syndrome including Von Hippel Lindau (VHL), Multiple Endocrine Neoplasia (MEN) 2 and Neurofibromatosis Type 1. VHL is associated with multi-organ involvement of benign and malignant tumours characterized by the presence of retinal...

Journal: :Folia neuropathologica 2009
Karol Krzysztolik C Cybulski L Sagan P Nowacki J Lubiński

Endolymphatic sac tumours (ELST) are aggressive papillary tumours of the temporal bone. The name was finally determined after the endolymphatic sac was determined as the site of their origin. They should be considered in patients with tumours eroding the petrous part of the temporal bone, extending to the cerebellopontine angle or other adjacent structures. These very rare tumours in the genera...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Aurélie Mousnier Nicole Kubat Aurélie Massias-Simon Emmanuel Ségéral Jean-Christophe Rain Richard Benarous Stéphane Emiliani Catherine Dargemont

HIV-1 integrase, the viral enzyme responsible for provirus integration into the host genome, can be actively degraded by the ubiquitin-proteasome pathway. Here, we identify von Hippel-Lindau binding protein 1(VBP1), a subunit of the prefoldin chaperone, as an integrase cellular binding protein that bridges interaction between integrase and the cullin2 (Cul2)-based von Hippel-Lindau (VHL) ubiqui...

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