Literature DB >> 7872647

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

S Povey1, J Armour, P Farndon, J L Haines, M Knowles, F Olopade, A Pilz, J A White, D J Kwiatkowski.   

Abstract

Mesh：

Year:  1994        PMID： 7872647     DOI： 10.1111/j.1469-1809.1994.tb01887.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN： 0003-4800            Impact factor:   1.670


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  9 in total

1.  Report of a critical recombination further narrowing the TSC1 region.

Authors:  K S Au; J Murrell; A Buckler; S H Blanton; H Northrup
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

2.  Loss of tuberin in both subependymal giant cell astrocytomas and angiomyolipomas supports a two-hit model for the pathogenesis of tuberous sclerosis tumors.

Authors:  E P Henske; L L Wessner; J Golden; B W Scheithauer; A O Vortmeyer; Z Zhuang; A J Klein-Szanto; D J Kwiatkowski; R S Yeung
Journal:  Am J Pathol       Date:  1997-12       Impact factor: 4.307

3.  Tuberous sclerosis-associated renal cell carcinoma. Clinical, pathological, and genetic features.

Authors:  J Bjornsson; M P Short; D J Kwiatkowski; E P Henske
Journal:  Am J Pathol       Date:  1996-10       Impact factor: 4.307

4.  Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesions.

Authors:  E P Henske; B W Scheithauer; M P Short; R Wollmann; J Nahmias; N Hornigold; M van Slegtenhorst; C T Welsh; D J Kwiatkowski
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

5.  Loss of heterozygosity in tuberous sclerosis hamartomas.

Authors:  T Sepp; J R Yates; A J Green
Journal:  J Med Genet       Date:  1996-11       Impact factor: 6.318

6.  Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.

Authors:  M Piantanida; E Buscarini; C Dellavecchia; A Minelli; A Rossi; L Buscarini; C Danesino
Journal:  J Med Genet       Date:  1996-06       Impact factor: 6.318

7.  The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma.

Authors:  R Cowan; P Hoban; A Kelsey; J M Birch; R Gattamaneni; D G Evans
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

8.  Differential allele loss on chromosome 9q22.3 in human non-melanoma skin cancer.

Authors:  E Holmberg; B L Rozell; R Toftgård
Journal:  Br J Cancer       Date:  1996-07       Impact factor: 7.640

9.  High frequency of chromosome 9 deletion in ovarian cancer: evidence for three tumour-suppressor loci.

Authors:  J Devlin; P A Elder; H Gabra; C M Steel; M A Knowles
Journal:  Br J Cancer       Date:  1996-02       Impact factor: 7.640
  9 in total

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