Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome (Q24337580)

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English	Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome	scientific article

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23 September 2019

Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome (English)

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23 September 2019

Ribosomal protein S4 X-linked

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GOA release 2020-03-11

Turner syndrome

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based on heuristic

inferred from title

4

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23 September 2019

Frederick R Bieber

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23 September 2019

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E M Fisher

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23 September 2019

P Beer-Romero

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23 September 2019

L G Brown

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23 September 2019

J A McNeil

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23 September 2019

J B Lawrence

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23 September 2019

H F Willard

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23 September 2019

D C Page

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23 September 2019

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1 December 1990

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23 September 2019

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23 September 2019

63

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23 September 2019

6

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23 September 2019

1205-1218

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23 September 2019

Spreading of inactivation in an (X;14) translocation

1 reference

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7 January 2021

based on heuristic

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Somatic cell hybrid studies of fragile (X) expression in a carrier female and transmitting male

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Ullrich-Turner syndrome in an XY female fetus with deletion of the sex-determining portion of the Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Identification by RNA-protein cross-linking of ribosomal proteins located at the interface between the small and the large subunits of mammalian ribosomes

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Sequence of the amino-terminal region of rat liver ribosomal proteins S4, S6, S8, L6, L7a, L18, L27, L30, L37, L37a, and L39

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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The similarity of phenotypic effects caused by Xp and Xq deletions in the human female: a hypothesis

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Structural anomalies of the X chromosome and inactivation center

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

X chromosome constitution and the human female phenotype

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Restriction site polymorphism in the phosphoglycerate kinase gene on the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytologic evidence for three human X-chromosomal segments escaping inactivation

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Position of the human X inactivation center on Xq

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Interstitial deletion in the "critical region" of the long arm of the X chromosome in a mentally retarded boy and his normal mother.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of an abundantly expressed sequence from the human X chromosome by differential screening

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

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7 January 2021

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Organization and structure of the Methanococcus transcriptional unit homologous to the Escherichia coli "spectinomycin operon". Implications for the evolutionary relationship of 70 S and 80 S ribosomes

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https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Isolation of cloned DNA sequences containing ribosomal protein genes from saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Mammals have multiple genes for individual ribosomal proteins

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Chromosomal distribution of ribosomal protein genes in the mouse

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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The sequence 5'-AAUAAA-3'forms parts of the recognition site for polyadenylation of late SV40 mRNAs

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

The gene family encoding the mouse ribosomal protein L32 contains a uniquely expressed intron-containing gene and an unmutated processed gene

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

The sex-determining region of the human Y chromosome encodes a finger protein.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Sensitive, high-resolution chromatin and chromosome mapping in situ: presence and orientation of two closely integrated copies of EBV in a lymphoma line

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

ZFX has a gene structure similar to ZFY, the putative human sex determinant, and escapes X inactivation

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

The spatial arrangement of the complex between eukaryotic initiation factor eIF-3 and 40 S ribosomal subunit. Cross-linking between factor and ribosomal proteins

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

A simple and very efficient method for generating cDNA libraries

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

The transcriptionally active human ribosomal protein S17 gene

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Turner syndrome resulting from partial deletion of Y chromosome short arm: localization of male determinants

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Establishing homologies in protein sequences

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7 January 2021

based on heuristic

inferred from DOI database lookup

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Isolation of seventeen proteins and amino-terminal amino acid sequences of eight proteins from cytoplasmic ribosomes of yeast

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7 January 2021

based on heuristic

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A human quantitative polymorphism related to Xg blood groups

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7 January 2021

based on heuristic

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Differential expression of steroid sulphatase locus on active and inactive human X chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

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Occurrence of a transposition from the X-chromosome long arm to the Y-chromosome short arm during human evolution

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7 January 2021

based on heuristic

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A Drosophila Minute gene encodes a ribosomal protein.

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7 January 2021

based on heuristic

inferred from DOI database lookup

The pseudoautosomal boundary in man is defined by an Alu repeat sequence inserted on the Y chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Putative transcription activator with alternative isoforms encoded by human ZFX gene

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the human GM-CSF receptor gene to the X-Y pseudoautosomal region.

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Additional deletion in sex-determining region of human Y chromosome resolves paradox of X,t(Y;22) female

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Familial Syndrome of Streak Gonads and Normal Male Karyotype in Five Phenotypic Females

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Equipotent mouse ribosomal protein promoters have a similar architecture that includes internal sequence elements

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

49,XYYYY. A case report.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical and cytogenetic aspects of X-chromosome deletions

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Non-inactivation of an X-Chromosome Locus in Man

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Interphase and metaphase resolution of different distances within the human dystrophin gene

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

A pseudoautosomal gene in man

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Reactivation of an inactive human X chromosome: evidence for X inactivation by DNA methylation

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes

1 reference

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7 January 2021

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inferred from DOI database lookup

Complete sequence of three alpha-tubulin cDNAs in Chinese hamster ovary cells: each encodes a distinct alpha-tubulin isoprotein

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7 January 2021

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KARYOTYPE-PHENOTYPE CORRELATIONS IN GONADAL DYSGENESIS AND THEIR BEARING ON THE PATHOGENESIS OF MALFORMATIONS

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

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inferred from DOI database lookup

The Structure and Function of Eukaryotic Ribosomes

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

Report of the committee on the genetic constitution of the X chromosome

1 reference

https://api.crossref.org/works/10.1016%2F0092-8674%2890%2990416-C

7 January 2021

based on heuristic

inferred from DOI database lookup

A SYNDROME OF INFANTILISM, CONGENITAL WEBBED NECK, AND CUBITUS VALGUS1

1 reference

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based on heuristic

inferred from DOI database lookup

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10.1016/0092-8674(90)90416-C

2 references

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23 September 2019

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2124517%20AND%20SRC:MED&resulttype=core&format=json

23 September 2019

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