Gene inactivation as a mechanism for the expression of recessive phenotypes (Q35197581)

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English	Gene inactivation as a mechanism for the expression of recessive phenotypes	scientific article

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instance of

scholarly article

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Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

title

Gene inactivation as a mechanism for the expression of recessive phenotypes (English)

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Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

author name string

Grant SG

series ordinal

1

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stated in

Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

Campbell CE

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2

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Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

Duff C

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3

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Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

Toth SL

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

Worton RG

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

language of work or name

English

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publication date

1 October 1989

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Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

published in

American Journal of Human Genetics

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stated in

Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

volume

45

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stated in

Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

issue

4

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Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

page(s)

619-634

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Europe PubMed Central

PubMed publication ID

2491018

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7 August 2017

cites work

INTERCHROMOSOMAL EFFECTS ON SOMATIC RECOMBINATION IN DROSOPHILA MELANOGASTER

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PubMed Central

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Genetics of somatic mammalian cells. III. Long-term cultivation of euploid cells from human and animal subjects

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28 July 2018

Isolation and characterization of Chinese hamster cell mutants resistant to the cytotoxic effects of chromate

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PubMed Central

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28 July 2018

Genetic instability at the adenine phosphoribosyltransferase locus in mouse L cells

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28 July 2018

Microcell-mediated cotransfer of genes specifying methotrexate resistance, emetine sensitivity, and chromate sensitivity with Chinese hamster chromosome 2.

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28 July 2018

Ribosomal protein S14 is altered by two-step emetine resistance mutations in Chinese hamster cells

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28 July 2018

Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

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PubMed Central

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28 July 2018

High frequency "switching" at the adenine phosphoribosyltransferase locus in multipotent mouse teratocarcinoma stem cells

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PubMed Central

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28 July 2018

High-frequency structural gene deletion as the basis for functional hemizygosity of the adenine phosphoribosyltransferase locus in Chinese hamster ovary cells

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28 July 2018

A mutational assay system using the thymidine kinase locus in mouse lymphoma cells

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PubMed Central

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28 July 2018

Mutants of cultured chinese hamster cells deficient in adenine phosphoribosyl transferase

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PubMed Central

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28 July 2018

The chromosomes of CHO, an aneuploid Chinese hamster cell line: G-band, C-band, and autoradiographic analyses.

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28 July 2018

Emetine resistance of Chinese hamster cells: structures of wild-type and mutant ribosomal protein S14 mRNAs

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28 July 2018

Deletion and hypermethylation of thymidine kinase gene in V79 Chinese hamster cells resistant to bromodeoxyuridine

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PubMed Central

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28 July 2018

Review and hypotheses: somatic mosaicism: observations related to clinical genetics

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28 July 2018

Chromosome 13 homozygosity in osteosarcoma without retinoblastoma

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PubMed Central

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28 July 2018

Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition

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PubMed Central

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28 July 2018

High-frequency deletion event at aprt locus of CHO cells: detection and characterization of endpoints.

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Isolation and partial characterization of three methotrexate-resistant phenotypes from Chinese hamster ovary cells

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Proposed banding nomenclature for the Chinese hamster chromosomes (Cricetulus griseus)

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

The isolation and preliminary characterization of somatic cell mutants resistant to the protein synthesis inhibitor-emetine

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

retrieved

28 July 2018

Chromosome stability in CHO cells

1 reference

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Reversible inactivation of autosomal alleles in Chinese hamster cells

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Characterization of cell lines showing growth control isolated from both the wild type and a leucyl-tRNA synthetase mutant of chinese hamster ovary cells

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Evidence obtained by induced mutation frequency analysis for functional hemizygosity at theemt locus in CHO cells

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Meiotic and Mitotic Recombination in Aspergillus and Its Chromosomal Aberrations

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PubMed Central

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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28 July 2018

Phenotypic evolution of cells resistant to bromodeoxyuridine

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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26 September 2018

Patient with 13 Chromosome Deletion: Evidence That the Retinoblastoma Gene Is a Recessive Cancer Gene

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

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26 September 2018

Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

retrieved

26 September 2018

Genetic demonstration of mitotic recombination in cultured Chinese hamster cell hybrids.

1 reference

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683509

retrieved

26 September 2018

Random segretation of multiple genetic markers from CHO-CHO hybrids: evidence for random distribution of functional hemizygosity in the genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marker segregation without chromosome loss at the emt locus in Chinese hamster cell hybrids

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of selection and counterselection in microcell-mediated transfer of dominant genetic markers

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormalities of chromosome #13 in retinoblastomas from individuals with normal constitutional karyotypes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Induction of thymidine kinase in enzyme-deficient chinese hamster cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene for hereditary retinoblastoma assigned to human chromosome 13 by linkage to esterase D

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic inactivation of genes on chromosome 13 is a common event in retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonrandom chromosomal changes in untreated retinoblastomas

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity of chromosome 13 in retinoblastoma

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Development of homozygosity for chromosome 11p markers in Wilms' tumour

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of a Harvey ras allele in sporadic Wilms' tumour

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mitotic recombination in Wilms tumor occurs between the parathyroid hormone locus and 11p13

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Loss of heterozygosity in three embryonal tumours suggests a common pathogenetic mechanism

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bromodeoxyuridine resistance in CHO cells occurs in three discrete steps

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypomethylation and ADA gene expression in mouse CAK cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation and genetic inactivation at thymidine kinase locus: Two different mechanisms for silencing autosomal genes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Somatic mutations at a heterozygous autosomal locus in human cells occur more frequently by allele loss than by intragenic structural alterations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome loss is responsible for segregation at theHPRT locus in Chinese hamster cell hybrids

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/2491018

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

PMC publication ID

1683509

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

PubMed publication ID

2491018

1 reference

stated in

Europe PubMed Central

PubMed publication ID

2491018

retrieved

7 August 2017

 

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