Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.
about
A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3Neuroblastoma tumour genetics: clinical and biological aspects.Gain of chromosome arm 17q is associated with unfavourable prognosis in neuroblastoma, but does not involve mutations in the somatostatin receptor 2(SSTR2) gene at 17q24.The emerging molecular pathogenesis of neuroblastoma: implications for improved risk assessment and targeted therapy.Escape from het-6 incompatibility in Neurospora crassa partial diploids involves preferential deletion within the ectopic segment.
P2860
Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.
description
1994 nî lūn-bûn
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1994年の論文
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1994年論文
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1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
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1994年論文
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1994年论文
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1994年论文
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1994年论文
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name
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@en
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@nl
type
label
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@en
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@nl
prefLabel
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@en
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@nl
P2093
P2860
P1476
Recurrent 1;17 translocations ...... sm for loss of heterozygosity.
@en
P2093
Speleman F
Versteeg R
Westerveld A
de Kraker J
van Sluis P
P2860
P304
P407
P577
1994-08-01T00:00:00Z