Mutations in mouse Aspm (abnormal spindle-like microcephaly associated) cause not only microcephaly but also major defects in the germline (Q28586392)

GOA release 2020-03-11

author

Svante Pääbo

14

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Jarosław Bryk

2

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Johannes Vogt

10

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Bianca Habermann

9

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Wieland B Huttner

15

object named as

Wieland B. Huttner

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31 January 2017

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13

Wolfgang Enard

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31 January 2017

Jeremy N. Pulvers

1

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31 January 2017

Jennifer L. Fish

3

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31 January 2017

Michaela Wilsch-Bräuninger

4

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31 January 2017

Yoko Arai

5

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31 January 2017

Dora Schreier

6

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31 January 2017

Ronald Naumann

7

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31 January 2017

Jussi Helppi

8

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31 January 2017

Robert Nitsch

11

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31 January 2017

Attila Tóth

Proceedings of the National Academy of Sciences of the United States of America

12

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31 January 2017

language of work or name

English

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publication date

21 September 2010

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31 January 2017

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31 January 2017

107

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31 January 2017

38

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31 January 2017

16595–16600

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31 January 2017

on focus list of Wikimedia project

ScienceSource

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cites work

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Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family

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ASPM and citron kinase co-localize to the midbody ring during cytokinesis

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Analysis of oncogenic signaling networks in glioblastoma identifies ASPM as a molecular target

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Expression analysis of the autosomal recessive primary microcephaly genes MCPH1 (microcephalin) and MCPH5 (ASPM, abnormal spindle-like, microcephaly associated) in human malignant gliomas.

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A novel domain suggests a ciliary function for ASPM, a brain size determining gene

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inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1073/PNAS.1010494107

1 reference

1658038

ADS bibcode

2010PNAS..10716595P

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1658038

1 reference

1 reference

1 reference