(Q36767457)

16 August 2017

title

Rapid evolution of the sex determining locus in Old World mice and rats (English)

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16 August 2017

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Tucker PK

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16 August 2017

Lundrigan BL

series ordinal

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16 August 2017

language of work or name

English

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publication date

1 August 1993

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16 August 2017

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16 August 2017

volume

364

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16 August 2017

issue

6439

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16 August 2017

page(s)

715-717

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A gene from the human sex-determining region encodes a protein with homology to a conserved DNA-binding motif

16 August 2017

cites work

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7 January 2021

Genetic evidence equating SRY and the testis-determining factor

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7 January 2021

A human XY female with a frame shift mutation in the candidate testis-determining gene SRY.

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7 January 2021

A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes

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7 January 2021

Male development of chromosomally female mice transgenic for Sry.

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7 January 2021

Evolution of sex determination and the Y chromosome: SRY-related sequences in marsupials

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7 January 2021

Rapid sequence evolution of the mammalian sex-determining gene SRY.

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7 January 2021

The molecular clock ticks regularly in muroid rodents and hamsters

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7 January 2021

Sex determining gene expression during embryogenesis

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7 January 2021

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

1 reference

7 January 2021

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

1 reference

7 January 2021

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

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7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

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7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

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7 January 2021

Cloning of the essential myotonic dystrophy region and mapping of the putative defect

1 reference

7 January 2021

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

1 reference

7 January 2021

Detection of an unstable fragment of DNA specific to individuals with myotonic dystrophy

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7 January 2021

An unstable triplet repeat in a gene related to myotonic muscular dystrophy

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7 January 2021

Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy

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7 January 2021

Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene

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7 January 2021

Evolution of Protein Molecules

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7 January 2021

Comparative studies of mammalian Y chromosome

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7 January 2021

Inverted repeat structure of the Sry locus in mice

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7 January 2021

Geographic origin of the Y chromosomes in "old" inbred strains of mice

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7 January 2021

Optimal sequence alignment using affine gap costs

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7 January 2021

Identifiers

DOI

10.1038/364715A0

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Dimensions Publication ID

16 August 2017

1026959884

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