(Q51834193)

English

Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21).

scientific article published in October 2003

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Disruption of a novel gene, DIRC3, and expression of DIRC3-HSPBAP1 fusion transcripts in a case of familial renal cell cancer and t(2;3)(q35;q21). (English)

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

author name string

Daniëlle Bodmer

1

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Marga Schepens

2

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Marc J Eleveld

3

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Eric F P M Schoenmakers

4

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Ad Geurts van Kessel

5

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

publication date

1 October 2003

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

Genes, Chromosomes and Cancer

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

38

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

2

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

107-116

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

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bic, a novel gene activated by proviral insertions in avian leukosis virus-induced lymphomas, is likely to function through its noncoding RNA

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A Novel Synapse-Associated Noncoding RNA

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Clinical and genetic studies of renal cell carcinomas in a family with a constitutional chromosome 3;8 translocation. Genetics of familial renal carcinoma

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Evidence of domain swapping within the jumonji family of transcription factors

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An alternative route for multistep tumorigenesis in a novel case of hereditary renal cell cancer and a t(2;3)(q35;q21) chromosome translocation

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Disruption of a novel MFS transporter gene, DIRC2, by a familial renal cell carcinoma-associated t(2;3)(q35;q21).

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Cytogenetic and molecular analysis of early stage renal cell carcinomas in a family with a translocation (2;3)(q35;q21)

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Understanding familial and non-familial renal cell cancer

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The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

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JmjC: cupin metalloenzyme-like domains in jumonji, hairless and phospholipase A2β

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Hereditary Renal-Cell Carcinoma Associated with a Chromosomal Translocation

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The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

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7 January 2021

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Microbial relatives of the seed storage proteins of higher plants: conservation of structure and diversification of function during evolution of the cupin superfamily

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Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

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The hereditary renal cell carcinoma 3;8 translocation fuses FHIT to a patched-related gene, TRC8

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The TRC8 hereditary kidney cancer gene suppresses growth and functions with VHL in a common pathway

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Renal Cell Cancer: Chromosome 3 Translocations as Risk Factors

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Altered neural cell fates and medulloblastoma in mouse patched mutants

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Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome

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Tumour-suppressor activity of H19 RNA

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A novel nuclear protein, 5qNCA (LOC51780) is a candidate for the myeloid leukemia tumor suppressor gene on chromosome 5 band q31.

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7 January 2021

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Molecular cloning and characterization of a novel human gene (HSPBAP1) from human fetal brain

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7 January 2021

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Human homolog of patched, a candidate gene for the basal cell nevus syndrome

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Association of a novel constitutional translocation t(1q;3q) with familial renal cell carcinoma

1 reference

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7 January 2021

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A familial case of renal cell carcinoma and a t(2;3) chromosome translocation

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Tissue-specific expression of a constitutional 3;6 translocation: development of multiple bilateral renal-cell carcinomas

1 reference

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A steroid receptor coactivator, SRA, functions as an RNA and is present in an SRC-1 complex

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Identification and characterization of a novel protein from Sertoli cells, PASS1, that associates with mammalian small stress protein hsp27.

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The FHIT gene, spanning the chromosome 3p14.2 fragile site and renal carcinoma-associated t(3;8) breakpoint, is abnormal in digestive tract cancers

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Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15

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Identifiers

10.1002/GCC.10243

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

13 April 2018

http://europepmc.org/abstract/MED/12939738

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