The Opitz syndrome gene product, MID1, associates with microtubules-Reference-Cited by-同舟云学术

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The Opitz syndrome gene product, MID1, associates with microtubules

Published:1999-03-16 Issue:6 Volume:96 Page:2794-2799
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Schweiger S.,Foerster J.,Lehmann T.,Suckow V.,Muller Y. A.,Walter G.,Davies T.,Porter H.,van Bokhoven H.,Lunt P. W.,Traub P.,Ropers H.-H.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference32 articles.

1. Opitz G/BBB syndrome: Clinical comparisons of families linked to Xp22 and 22Q and a review of the literature

2. Opitz syndrome is genetically heterogeneous, with one locus on Xp22, and a second locus on 22q11.2

3. Chromosomal deletion complexes in mice by radiation of embryonic stem cells

4. A novel zinc finger coiled-coil domain in a family of nuclear proteins

5. A novel gysteine-rich sequence motif

Cited by 116 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. TRIM Proteins and Antiviral Microtubule Reorganization: A Novel Component in Innate Immune Responses?;Viruses;2024-08-20

2. A unique missense mutation in the RING domain impairs MID1 E3 ubiquitin ligase activity and localisation and is associated with uncommon Opitz Syndrome-like signs;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-04

3. Absence of the RING domain inMID1results in patterning defects in the developing human brain;Life Science Alliance;2024-01-18

4. Skeletal Muscle Receptors;Skeletal Muscle Physiology;2024

5. Dynamic X-chromosomal reactivation enhances female brain resilience;2023-06-21

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