T J Hulsebos
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Explore the profile of T J Hulsebos including associated specialties, affiliations and a list of published articles.
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40
Citations
483
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Recent Articles
1.
Vandeputte D, Meije C, van Dartel M, Leenstra S, Das P, Troost D, et al.
Biochem Biophys Res Commun
. 2001 Aug;
286(3):574-9.
PMID: 11511098
Serial analysis of gene expression (SAGE) was used to identify a gene named GOA (gene overexpressed in astrocytoma), which codes for a novel Ring finger B-box coiled-coil (RBCC) protein. Northern...
2.
Luijten M, Redeker S, Minoshima S, Shimizu N, Westerveld A, Hulsebos T
Hum Genet
. 2001 Aug;
109(1):109-16.
PMID: 11479742
Numerous NF1 pseudogenes have been identified in the human genome. Those in 2q21, 14q11, and 22q11 form a subset with a similar genomic organization and a high sequence homology. We...
3.
Luijten M, Fahsold R, Mischung C, Westerveld A, Nurnberg P, Hulsebos T
J Med Genet
. 2001 Jul;
38(7):481-5.
PMID: 11476066
No abstract available.
4.
Aronica E, Leenstra S, van Veelen C, van Rijen P, Hulsebos T, Tersmette A, et al.
Epilepsy Res
. 2001 Mar;
43(3):179-91.
PMID: 11248530
The present study intends to identify factors that predict postoperative clinical outcome in patients with gangliogliomas (GG) and dysembryoplastic neuroepithelial tumors (DNT). We evaluated the medical records of 45 patients...
5.
Luijten M, Redeker S, van Noesel M, Troost D, Westerveld A, Hulsebos T
Eur J Hum Genet
. 2001 Feb;
8(12):939-45.
PMID: 11175282
Neurofibromatosis type 1 (NF1) is a frequent hereditary disorder. One of the characteristic features of this disease is the development of neurofibromas. Since the NF1 gene is supposed to be...
6.
Grimmond S, Larder R, Van Hateren N, Siggers P, Hulsebos T, Arkell R, et al.
Genomics
. 2000 Nov;
70(1):74-81.
PMID: 11087664
The epidermal growth factor (EGF) superfamily comprises a diverse group of proteins that function as secreted signaling molecules, growth factors, and components of the extracellular matrix, many with a role...
7.
Luijten M, Wang Y, Smith B, Westerveld A, Smink L, Dunham I, et al.
Eur J Hum Genet
. 2000 Apr;
8(3):209-14.
PMID: 10780787
Neurofibromatosis type 1 (NF1) is a frequent hereditary disorder that involves tissues derived from the embryonic neural crest. Besides the functional gene on chromosome arm 17q, NF1-related sequences (pseudogenes) are...
8.
Oskam N, Bijleveld E, Hulsebos T
Int J Cancer
. 2000 Feb;
85(3):336-9.
PMID: 10652423
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...
9.
Hulsebos T, Oskam N, Bijleveld E, Westerveld A, Hermsen M, van den Ouweland A, et al.
Br J Cancer
. 1999 Dec;
81(7):1150-4.
PMID: 10584875
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...
10.
Hulsebos T, Oskam N, Troost D, Leenstra S, Bijleveld E
Genes Chromosomes Cancer
. 1998 Sep;
23(2):153-8.
PMID: 9739018
We investigated the dynamics of the genetic changes that are associated with two types of glioma recurrence, that is, progression from a lower-grade to a high-grade tumor (7 cases) and...