Literature DB >> 6704944

Involvement of band 3p14 in t(3;8) hereditary renal carcinoma.

N Wang, K L Perkins.   

Abstract

High resolution prometaphase G-banding analysis was applied to three translocation carriers from the t(3;8) hereditary renal cell carcinoma family. It was clearly illustrated that the chromosomal rearrangement is reciprocal with breakpoints occurring at the subbands 3p14.2 (instead of 3p21) and 8q24.1.

Entities:  

Mesh：

Year:  1984        PMID： 6704944     DOI： 10.1016/0165-4608(84)90028-1

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN： 0165-4608


  19 in total

Review 1.  The new biomedical technology.

Authors:  C H Scoggin
Journal:  West J Med       Date:  1985-12

2.  Human class III POU genes, POU3F1 and POU3F3, map to chromosomes 1p34.1 and 3p14.2.

Authors:  K Sumiyama; K Washio-Watanabe; T Ono; M C Yoshida; T Hayakawa; S Ueda
Journal:  Mamm Genome       Date:  1998-02       Impact factor: 2.957

3.  Identification of two cosmids derived from within chromosomal band 3p21.1 that contain clusters of rare restriction sites and evolutionarily conserved sequences.

Authors:  D I Smith; W Golembieski; H Drabkin; S Kiousis
Journal:  Am J Hum Genet       Date:  1989-09       Impact factor: 11.025

4.  Regional localization of chromosome 3-specific DNA fragments by using a hybrid cell deletion mapping panel.

Authors:  M J Gerber; H A Drabkin; C Firnhaber; Y E Miller; C H Scoggin; D I Smith
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

5.  Statistical analysis of the two stage mutation model in von Hippel-Lindau disease, and in sporadic cerebellar haemangioblastoma and renal cell carcinoma.

Authors:  E R Maher; J R Yates; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1990-05       Impact factor: 6.318

6.  Cytogenetic studies on three pheochromocytomas derived from patients with von Hippel-Lindau syndrome.

Authors:  M Kiechle-Schwarz; H P Neumann; H J Decker; C Dietrich; B Wullich; W Schempp
Journal:  Hum Genet       Date:  1989-05       Impact factor: 4.132

7.  Positional cloning of the hereditary renal carcinoma 3;8 chromosome translocation breakpoint.

Authors:  F L Boldog; R M Gemmill; C M Wilke; T W Glover; A S Nilsson; S C Chandrasekharappa; R S Brown; F P Li; H A Drabkin
Journal:  Proc Natl Acad Sci U S A       Date:  1993-09-15       Impact factor: 11.205

Review 8.  [Molecular diagnostics of renal diseases with underlying genetic predisposition].

Authors:  K Junker
Journal:  Urologe A       Date:  2003-04-08       Impact factor: 0.639

9.  The most common fragile site in man is 3p14.

Authors:  D F Smeets; J M Scheres; T W Hustinx
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

Review 10.  Origin of renal cell carcinomas.

Authors:  Manuel Valladares Ayerbes; Guadalupe Aparicio Gallego; Silvia Díaz Prado; Paula Jiménez Fonseca; Rosario García Campelo; Luis Miguel Antón Aparicio
Journal:  Clin Transl Oncol       Date:  2008-11       Impact factor: 3.405
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