| 1 | TSG22A
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| Fine mapping of familial prostate cancer families narrows the interval for a susceptibility locus on chromosome 22q12.3 to 1.36 Mb.
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| Johanneson B, McDonnell SK, Karyadi DM, Hebbring SJ, Wang L, Deutsch K, McIntosh L, Kwon EM, Suuriniemi M, Stanford JL, Schaid DJ, Ostrander EA, Thibodeau SN.
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| Hum Genet 123(1):65-75. Epub 2007 Dec 8. 2008
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| 2 | TSG22A
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| Identification of recurrent regions of chromosome loss and gain in vestibular schwannomas using comparative genomic hybridisation.
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| Warren C, James LA, Ramsden RT, Wallace A, Baser ME, Varley JM, Evans DG.
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| J Med Genet 40(11):802-6. 2003
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| 3 | TSG22A
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| Loss of heterozygosity on chromosome 22 in human ependymomas.
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| Huang B, Starostik P, Kuhl J, Tonn JC, Roggendorf W.
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| Acta Neuropathol (Berl) 103(4):415-20. Epub 2002 Jan 17. 2002
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| 4 | TSG22A
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| Indications for a tumor suppressor gene at 22q11 involved in the pathogenesis of ependymal tumors and distinct from hSNF5/INI1.
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| Kraus JA, de Millas W, Sorensen N, Herbold C, Schichor C, Tonn JC, Wiestler OD, von Deimling A, Pietsch T.
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| Acta Neuropathol (Berl) 102(1):69-74. 2001
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| 5 | NF2, TSG22A
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| Frequent mutations of NF2 and allelic loss from chromosome band 22q12 in malignant mesothelioma : evidence for a two-hit mechanism of NF2 inactivation.
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| Cheng JQ, et al.
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| Genes Chromosomes Cancer 24 : 238-242. 1999
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| 6 | NF2, TSG22A
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| Merlin: the neurofibromatosis 2 tumor suppressor.
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| Gusella JF, et al.
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| Biochim Biophys Acta 1423(2):M29-36. Review. 1999
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| 7 | TSG22A, BIK
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| Mapping of a target region of allelic loss to a 0.5-cM interval on chromosome 22q13 in human colorectal cancer.
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| Castells A, Ino Y, Louis DN, Ramesh V, Gusella JF, Rustgi AK.
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| Gastroenterology 117(4):831-7. 1999
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| 8 | NF2, TSG22A
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| Tight association of loss of merlin expression with loss of heterozygosity at chromosome 22q in sporadic meningiomas.
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| Ueki K, Wen-Bin C, Narita Y, Asai A, Kirino T.
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| Cancer Res 59(23):5995-8. 1999
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| 9 | NF2, TSG22A
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| Neurofibromatosis 2 tumour suppressor schwannomin interacts with betaII-spectrin.
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| Scoles DR, et al.
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| Nat Genet 18 : 354-359. 1998
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| 10 | NF2, TSG22A
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| The involvement of calpain-dependent proteolysis of the tumor suppressor NF2 (merlin) in schwannomas and meningiomas.
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| Kimura Y, et al.
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| Nat Med 4 : 915-922. 1998
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| 11 | NF2, SCWT, TSG22A
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| Molecular analysis of the NF2 tumor-suppressor gene in schwannomatosis.
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| Jacoby LB, Jones D, Davis K, Kronn D, Short MP, Gusella J, MacCollin M.
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| Am J Hum Genet 61(6):1293-302. 1997
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| 12 | NF2, TSG22A
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| Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas.
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| Sainz J, et al.
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| Hum Genet 97 : 121-123. 1996
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| 13 | NF2, TSG22A
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| Screening for mutations in the neurofibromatosis type 2 (NF2) gene in sporadic meningiomas.
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| De Vitis LR, et al.
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| Hum Genet 97 : 632-637. 1996
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| 14 | NF2, TSG22A
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| Analysis of the neurofibromatosis type 2 gene in different human tumors of neuroectodermal origin.
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| De Vitis LR, et al.
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| Hum Genet 97 : 638-641. 1996
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| 15 | TSG22A, NF2
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| Mutational spectrum in the neurofibromatosis type 2 gene in sporadic and familial schwannomas.
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| Welling DB, et al.
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| Hum Genet 98 : 189-193. 1996
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| 16 | TSG17D, TSG22A
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| Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas.
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| von Haken MS, et al.
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| Genes Chromosomes Cancer 17 : 37-44. 1996
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| 17 | NF2, TSG22A
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| High frequency of nonsense mutations in the NF2 gene caused by C to T transitions in five CGA codons.
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| Sainz J, et al.
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| Hum Mol Genet 4 : 137-139. 1995
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| 18 | NF2, TSG22A
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| Somatic mutations in the neurofibromatosis type 2 gene in sporadic meningiomas.
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| Papi L, et al.
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| Hum Genet 95 : 347-351. 1995
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| 19 | TSG22A, NF2
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| High frequency of inactivating mutations in the neurofibromatosis type 2gene (NF2) in primary malignant mesotheliomas.
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| Bianchi AB, et al.
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| Proc Natl Acad Sci U S A 92 : 10854-10858. 1995
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| 20 | TSG22A
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| NF2 gene analysis distinguishes hemangiopericytoma from meningioma.
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| Joseph JT, et al.
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| Am J Pathol 147 : 1450-1455. 1995
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| 21 | TSG22A
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| Frequent loss of heterozygosity at telomeric loci on 22q in sporadic colorectal cancers.
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| Yana I, et al.
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| Int J Cancer 60 : 174-177. 1995
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| 22 | TSG22A, NF2
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| Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.
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| Hoang-Xuan K, et al.
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| Int J Cancer 60 : 478-481. 1995
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| 23 | TSG22A
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| Deletion mapping of the long arm of chromosome 22 in human meningiomas.
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| Akagi K, et al.
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| Int J Cancer 60 : 178-182. 1995
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| 24 | NF2, TSG22A
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| Eleven novel mutations in the NF2 tumour suppressor gene.
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| Bourn D, et al.
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| Hum Genet 95 : 572-574. 1995
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| 25 | TSG6B, KLF6, TSG13B, TSG22A, TSG17D, TSG19A
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| Molecular analysis of genetic changes in ependymomas.
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| Bijlsma EK, et al.
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| Genes Chromosomes Cancer 13 : 272-277. 1995
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| 26 | TSG22A, NF2
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| Screening for germ-line mutations in the NF2 gene.
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| Mˇrel P, et al.
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| Genes Chromosomes Cancer 12 : 117-127. 1995
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| 27 | TSG22A
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| Constitutional DNA-level aberrations in chromosome 22 in a patient with multiple meningiomas.
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| Lekanne Deprez RH, et al.
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| Genes Chromosomes Cancer 9 : 124-128. 1994
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| 28 | TSG22A
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| Abnormalities of chromosome 22 in pediatric meningiomas.
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| Biegel JA, et al.
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| Genes Chromosomes Cancer 9 : 81-87. 1994
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| 29 | TSG22A
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| Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
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| Ruttledge MH, et al.
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| Nat Genet 6 : 180-184. 1994
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| 30 | NF2, TSG22A
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| Somatic NF2 gene mutations in familial and non-familial vestibular schwannoma.
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| Irving RM, et al.
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| Hum Mol Genet 3 : 347-350. 1994
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| 31 | NF2, TSG22A
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| The neurofibromatosis type 2 gene is inactivated in schawnnomas.
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| Twist EC, et al.
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| Hum Mol Genet 3 : 147-151. 1994
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| 32 | TSG22A
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| Analysis of the neurofibromatosis 2 gene in human ependymomas and astrocytomas.
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| Rubio MP, et al.
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| Cancer Res 54 : 45-47. 1994
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| 33 | NF2, TSG22A
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| Exon scanning for mutation of the NF2 gene in schwannomas.
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| Jacoby LB, et al.
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| Hum Mol Genet 3 : 413-419. 1994
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| 34 | TSG1A, TSG22A
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| Allelic loss at Ip is associated with tumor progression of meningiomas.
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| Bello MJ, et al.
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| Genes Chromosomes Cancer 9 : 296-298. 1994
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| 35 | NF2, TSG22A
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| Alternative splicing of the NF2 gene and its mutation analysis of breast and colorectal cancers.
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| Arakawa H, et al.
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| Hum Mol Genet 3 : 565-568. 1994
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| 36 | NF2, TSG22A
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| Germline mutations in the neurofibromatosis type 2 tumour suppressor gene.
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| Bourn D, et al.
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| Hum Mol Genet 3 : 813-816. 1994
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| 37 | TSG22A, NF2
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| Mutations of the neurofibromatosis type 2 gene and lack of the gene product in vestibular schwannomas.
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| Sainz J, et al.
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| Hum Mol Genet 3 : 885-891. 1994
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| 38 | TSG22A, NF2
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| Characterization of the translocation breakpoint on chromosome 22q12.2 in a patient with neurofibromatosis type 2 (NF2).
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| Arai E, et al.
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| Hum Mol Genet 3 : 937-939. 1994
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| 39 | TSG22A
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| Deletions on chromosome 22 in sporadic meningioma.
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| Ruttledge MH, et al.
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| Genes Chromosomes Cancer 10 : 122-130. 1994
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| 40 | TSG22A, NF2
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| Frequent NF2 gene transcript mutations in sporadic meningiomas and vestibular schwannomas.
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| Lekanne Deprez RH, et al.
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| Am J Hum Genet 54 : 1022-1929. 1994
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| 41 | TSG22A, LIF
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| Analysis of chromosome 22 loci in meningioma.
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| Pergolizzi RG, et al.
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| Mol Chem Neuropathol 21 : 189-217. 1994
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| 42 | NF2, TSG22A
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| A mutation in the neurofibromatosis type 2 tumor-suppressor gene, giving rise to widely different clinical phenotypes in two unrelated individuals.
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| Bourn D, et al.
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| Am J Hum Genet 55 : 69-73. 1994
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| 43 | TSG22A, NF2
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| Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuroma.
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| Irving RM, et al.
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| Arch Otolaryngol Head Neck Surg 119 : 1222-1228. 1993
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| 44 | NF2, TSG22A
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| Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors.
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| Wolff RK, et al.
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| Am J Hum Genet 51 : 478-485. 1992
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| 45 | TSG22A
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| Molecular characterization of chromosome 22 deletions in schwannomas.
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| Bijlsma EK, et al.
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| Genes Chromosomes Cancer 5 : 201-205. 1992
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| 46 | TSG22A, TSG22D
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| Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches.
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| Rey JA, et al.
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| Cancer Genet Cytogenet 66 : 1-10. 1992
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| 47 | TSG22A, TSG22B
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| Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.
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| Tanaka N, et al.
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| Genes Chromosomes Cancer 5 : 399-403. 1992
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| 48 | MGCR, TSG22A
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| Molecular genetic analysis of chromosome 22 in 81 cases of meningioma.
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| Dumanski JP, et al.
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| Cancer Res 50 : 5863-5867. 1990
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| 49 | MGCR, TSG22A, TSG22B
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| Chromosome 22q deletions in meningiomas detected by RFLP analysis.
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| Dumanski JP, et al.
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| (HGM9) Cytogenet Cell Genet 46 : 608. 1987
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| 50 | MGCR, TSG22A, TSG22B
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| Molecular genetic approach to human meningioma : loss of genes on chromosome 22.
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| Seizinger BR, et al.
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| Proc Natl Acad Sci U S A 84 : 5419-5423. 1987
|