Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication (Q24614384)

16

0 references

Francesca Antonacci

Francesca Antonacci

4

0 references

Peter H Sudmant

Peter H Sudmant

3

0 references

Maika Malig

9

Maika Malig

0 references

Xander Nuttle

2

Xander Nuttle

0 references

Jill A Rosenfeld

7

Jill A Rosenfeld

0 references

Saba Sajjadian

8

Saba Sajjadian

0 references

Holland Kotkiewicz

10

Holland Kotkiewicz

0 references

author name string

Megan Y Dennis

1

0 references

Tina A Graves

5

0 references

Mikhail Nefedov

6

0 references

Cynthia J Curry

11

0 references

Susan Shafer

12

0 references

Lisa G Shaffer

13

0 references

Pieter J de Jong

14

0 references

Richard K Wilson

De novo origin of human protein-coding genes

15

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language of work or name

English

0 references

publication date

11 May 2012

0 references

published in

Cell

0 references

volume

149

0 references

issue

4

0 references

page(s)

912-22

0 references

cites work

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srGAP2 arginine methylation regulates cell migration and cell spreading through promoting dimerization

7 April 2017

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The F-BAR domain of srGAP2 induces membrane protrusions required for neuronal migration and morphogenesis

7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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7 April 2017

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A Draft Sequence of the Neandertal Genome

7 April 2017

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7 April 2017

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7 April 2017

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Initial sequence of the chimpanzee genome and comparison with the human genome

7 April 2017

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Finishing the euchromatic sequence of the human genome

7 April 2017

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Molecular evolution of FOXP2, a gene involved in speech and language

7 April 2017

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A new hominid from the Upper Miocene of Chad, Central Africa

7 April 2017

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7 April 2017

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Alternative isoform regulation in human tissue transcriptomes

7 April 2017

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7 April 2017

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The evolutionary fate and consequences of duplicate genes

7 April 2017

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7 April 2017

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Segmental duplications and copy-number variation in the human genome

7 April 2017

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New material of the earliest hominid from the Upper Miocene of Chad

7 April 2017

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The altered evolutionary trajectories of gene duplicates

7 April 2017

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Myosin gene mutation correlates with anatomical changes in the human lineage

7 April 2017

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A candidate target for G protein action in brain

7 April 2017

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Multiple sequence alignment using ClustalW and ClustalX

7 April 2017

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A copy number variation morbidity map of developmental delay

7 April 2017

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Missing heritability and strategies for finding the underlying causes of complex disease

7 April 2017

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Recent segmental duplications in the human genome

7 April 2017

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7 April 2017

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A comparison of RNA-Seq and high-density exon array for detecting differential gene expression between closely related species

27 September 2017

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A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk

27 September 2017

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Sex-specific and lineage-specific alternative splicing in primates

27 September 2017

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Human-specific gain of function in a developmental enhancer

27 September 2017

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Characterization of the human lineage-specific pericentric inversion that distinguishes human chromosome 1 from the homologous chromosomes of the great apes

27 September 2017

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Quantifying the mechanisms for segmental duplications in mammalian genomes by statistical analysis and modeling

27 September 2017

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An Alu Transposition Model for the Origin and Expansion of Human Segmental Duplications

27 September 2017

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Geology and palaeontology of the Upper Miocene Toros-Menalla hominid locality, Chad

27 September 2017

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Segmental duplications: what's missing, misassigned, and misassembled--and should we care?

27 September 2017

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An improved approach for construction of bacterial artificial chromosome libraries.

27 September 2017

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A burst of segmental duplications in the genome of the African great ape ancestor

27 September 2017

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Miropeats: graphical DNA sequence comparisons.

30 May 2018

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Estimating errors and confidence intervals for branch lengths in phylogenetic trees by a bootstrap approach.

30 May 2018

1 reference

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Androgenetic origin of hydatidiform mole

30 May 2018

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Early infantile epileptic encephalopathy associated with the disrupted gene encoding Slit-Robo Rho GTPase activating protein 2 (SRGAP2).

30 May 2018

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Paternal Origins of Complete Hydatidiform Moles Proven by Whole Genome Single-Nucleotide Polymorphism Haplotyping

28 November 2018

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28 November 2018

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Is it Williams syndrome? GTF2IRD1 implicated in visual-spatial construction and GTF2I in sociability revealed by high resolution arrays

28 November 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/22559943

12 December 2020

inferred from PubMed ID database lookup

A human genome structural variation sequencing resource reveals insights into mutational mechanisms

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7 January 2021

Inhibition of SRGAP2 function by its human-specific paralogs induces neoteny during spine maturation

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Basic local alignment search tool

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7 January 2021

A strategy for disease gene identification through nonsense-mediated mRNA decay inhibition

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7 January 2021

Quality assessment of the human genome sequence

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7 January 2021

Fine-scale structural variation of the human genome

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mrsFAST: a cache-oblivious algorithm for short-read mapping.

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Comprehensive algorithm for quantitative real-time polymerase chain reaction

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7 January 2021

Jalview Version 2--a multiple sequence alignment editor and analysis workbench

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7 January 2021

Segmental duplications: organization and impact within the current human genome project assembly

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7 January 2021

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Identifiers

DOI

1 reference

1366317

1366317

1 reference

1 reference

1 reference