(Q24336077)

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Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus

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scholarly article

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Chromosomal locations of three human nuclear genes (RPSM12, TUFM, and AFG3L1) specifying putative components of the mitochondrial gene expression apparatus (English)

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Mitochondrial ribosomal protein S12

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GOA release 2020-03-11

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object named as

Z H Shah

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Thomas B. Friedman

5

object named as

T B Friedman

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author name string

V Migliosi

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S C Miller

3

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A Wang

4

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H T Jacobs

6

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language of work or name

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publication date

15 March 1998

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48

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3

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384-8

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A novel mitochondrial point mutation in a maternal pedigree with sensorineural deafness.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

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Mutants of elongation factor Tu promote ribosomal frameshifting and nonsense readthrough.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

New regional localisations for HAGH and PGP on human chromosome 16

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

The role of protein degradation in mitochondrial function and biogenesis.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

A mitochondrial elongation factor-like protein is over-expressed in tumours and differentially expressed in normal tissues

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

The tko locus, site of a behavioral mutation in D. melanogaster, codes for a protein homologous to prokaryotic ribosomal protein S12.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning, sequence analysis and expression of mammalian mitochondrial protein synthesis elongation factor Tu.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Metazoan nuclear genes for mitoribosomal protein S12.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene for congenital, recessive deafness DFNB3 maps to the pericentromeric region of chromosome 17.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

MtDNA mutation in MERRF syndrome causes defective aminoacylation of tRNA(Lys) and premature translation termination

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

An accuracy center in the ribosome conserved over 2 billion years

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage of a gene for dominant non-syndromic deafness to chromosome 19.

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

A radiation hybrid map of the human genome

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

A monoclonal antibody recognizing a cell surface antigen coded for by a gene on human chromosome 17

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA(Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Protein import into mitochondria

1 reference

https://api.crossref.org/works/10.1006%2FGENO.1997.5166

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1006/GENO.1997.5166

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