Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids (Q35200986)

7 August 2017

title

Regional localization of DNA sequences on chromosome 21 using somatic cell hybrids (English)

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7 August 2017

J F Gusella

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7 August 2017

M L Van Keuren

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7 August 2017

P C Watkins

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7 August 2017

H A Drabkin

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7 August 2017

E W Jabs

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7 August 2017

D Patterson

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7 August 2017

language of work or name

English

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publication date

1 June 1986

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American Journal of Human Genetics

7 August 2017

published in

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7 August 2017

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7 August 2017

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7 August 2017

page(s)

793-804

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Construction and characterization of genomic libraries from specific human chromosomes

7 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Isolation of repetitive DNA sequences from human chromosome 21

28 July 2018

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Characterization of a cloned DNA sequence that is present at centromeres of all human autosomes and the X chromosome and shows polymorphic variation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Assignment of the gene for cystathionine beta-synthase to human chromosome 21 in somatic cell hybrids

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Structural gene coding for multifunctional protein carrying orotate phosphoribosyltransferase and OMP decarboxylase activity is located on long arm of human chromosome 3.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Assignment of the human gene for liver-type 6-phosphofructokinase isozyme (PFKL) to chromosome 21 by using somatic cell hybrids and monoclonal anti-L antibody

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the down syndrome

28 July 2018

1 reference

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Human cytoplasmic superoxide dismutase cDNA clone: a probe for studying the molecular biology of Down syndrome

28 July 2018

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Down's syndrome phenotype and autosomal gene inactivation in a child with presumed (X;21) de novo translocation

28 July 2018

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Receptors for human alpha and beta interferon but not for gamma interferon are specified by human chromosome 21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

[Overactivity of the indophenol oxidase (form dimeric) in the trisomy 21, secondary to triplicated gene (author's transl)].

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Induction and isolation of auxotrophic mutants in mammalian cells

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

The linkage of genes for the human interferon-induced antiviral protein and indophenol oxidase-B traits to chromosome G-21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Down's syndrome. The possibility of a pathogenetic segment on chromosome no. 21.

28 July 2018

1 reference

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Presenile dementia in Down's syndrome. Ultrastructural identity with Alzheimer's disease

28 July 2018

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Presenile dementia and Alzheimer's disease in mongolism

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Isolation of polymorphic DNA segments from human chromosome 21.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Chromosomal localization of several families of repetitive sequences by in situ hybridization

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Complete structure of the alpha B-crystallin gene: conservation of the exon-intron distribution in the two nonlinked alpha-crystallin genes

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Isolation and analysis of the 21q+ chromosome in the acute myelogenous leukemia 8;21 translocation: evidence that c-mos is not translocated

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Detection of specific sequences among DNA fragments separated by gel electrophoresis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Synteny between glycinamide ribonucleotide synthetase and superoxide dismutase (soluble).

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Biochemical genetics of Chinese hamster cell mutants with deviant purine metabolism: characterization of Chinese hamster cell mutants defective in phosphoribosylpyrophosphate amidotransferase and phosphoribosylglycinamide synthetase and an examinati

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Characterization and Localization of the Human Genes for Ribosomal Ribonucleic Acid

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Precise localization of human beta-globin gene complex on chromosome 11

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Dosage effects for superoxide dismutase-1 in nucleated cells aneuploid for chromosome 21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Partial trisomy 21. Further evidence that trisomy of band 21q22 is essential for Down's phenotype

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Partial trisomies of chromosome 21 in man. Two new observations due to translocations 19;21 and 4;21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Down syndrome due to partial trisomy 21q

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Partial trisomy 21 (21q21 - 21q22.2)

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Familial Down syndrome due to t(10;21) translocation: evidence that the Down phenotype is related to trisomy of a specific segment of chromosome 21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

A sequential staining technique for the chromosomal analysis of interspecific mouse/hamster and mouse/human somatic cell hybrids

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Demonstration, by somatic cell genetics, of coordinate regulation of genes for two enzymes of purine synthesis assigned to human chromosome 21.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Isolation and regional localization by in situ hybridization of a unique gene segment to chromosome 21.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Prenatal detection of an unstable ring 21 chromosome.

26 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1684850

Cardiac malformation in mongolism: a prospective study of 184 mongoloid children

26 September 2018

1 reference

12 December 2020

Cardiac malformations associated with Down's syndrome

1 reference

12 December 2020

Trisomy 21 and superoxide dismutase-1 (IPO-A). Tentative localization of sub-band 21Q22.1

1 reference

12 December 2020

Differential staining of interspecific chromosomes in somatic cell hybrids by alkaline Giemsa stain

1 reference

12 December 2020

Simultaneous identification of chromatid replication and of human chromosomes in metaphases of man-mouse somatic cell hybrids

1 reference

12 December 2020

Gene dosage effect for glycinamide ribonucleotide synthetase in human fibroblasts trisomic for chromosome 21

1 reference

12 December 2020

Trisomy 21 for the region 21q223: identification by high-resolution R-banding patterns

1 reference

12 December 2020

Down's syndrome. Recent trends in the United States

1 reference

12 December 2020

Down Syndrome and acute leukaemia: increased risk may be due to trisomy 21

1 reference

12 December 2020

Moderate Down's syndrome in three siblings having partial trisomy 21q22.2?qter and therefore no SOD-1 excess

1 reference

12 December 2020

Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments

1 reference

12 December 2020

Direct evidence that the gene product of the human chromosome 21 locus, IFRC, is the interferon-α receptor

1 reference

12 December 2020

Leukemia and other Cancers, Anomalies and Infections as Causes of Death in Down's Syndrome in the United States during 1976

1 reference

12 December 2020

Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome

1 reference

12 December 2020

Assignment of human phosphoribosylglycinamide synthetase locus to region 21q221

1 reference

12 December 2020

Cystathionine beta synthase: gene dosage effect in trisomy 21

1 reference

12 December 2020

Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunion

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

Identifiers

PMC publication ID

1684850

1 reference

7 August 2017

1 reference