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Literature DB >> 3472611

Developmental aspects of lissencephaly and the lissencephaly syndromes.

W B Dobyns.

Abstract

Entities: Disease

Mesh：

Substances：
Tretinoin
Isotretinoin

Year: 1987 PMID： 3472611

Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN： 0547-6844

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19 in total

1. NDEL1 phosphorylation by Aurora-A kinase is essential for centrosomal maturation, separation, and TACC3 recruitment.

Authors: Daisuke Mori; Yoshihisa Yano; Kazuhito Toyo-oka; Noriyuki Yoshida; Masami Yamada; Masami Muramatsu; Dongwei Zhang; Hideyuki Saya; Yoko Y Toyoshima; Kazuhisa Kinoshita; Anthony Wynshaw-Boris; Shinji Hirotsune
Journal: Mol Cell Biol Date: 2006-10-23 Impact factor: 4.272

2. Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Authors: C E Schwartz; J P Johnson; B Holycross; T M Mandeville; T S Sears; E A Graul; J C Carey; R J Schroer; M C Phelan; J Szollar
Journal: Am J Hum Genet Date: 1988-11 Impact factor: 11.025

3. Lissencephaly with agenesis of corpus callosum: A rare anomaly.

Authors: V K Maurya; M Bhatia; R Ravikumar; K P S Senger
Journal: Med J Armed Forces India Date: 2016-05-08

4. Purinergic A2b Receptor Activation by Extracellular Cues Affects Positioning of the Centrosome and Nucleus and Causes Reduced Cell Migration.

Authors: Young Ou; Gordon Chan; Jeremy Zuo; Jerome B Rattner; Frans A van der Hoorn
Journal: J Biol Chem Date: 2016-05-13 Impact factor: 5.157

Developmental aspects of lissencephaly and the lissencephaly syndromes.

1. NDEL1 phosphorylation by Aurora-A kinase is essential for centrosomal maturation, separation, and TACC3 recruitment.

2. Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

3. Lissencephaly with agenesis of corpus callosum: A rare anomaly.

4. Purinergic A2b Receptor Activation by Extracellular Cues Affects Positioning of the Centrosome and Nucleus and Causes Reduced Cell Migration.

5. The CT and MR evaluation of migrational disorders of the brain. Part I. Lissencephaly and pachygyria.

Review 6. Emerging pharmacotherapies for neurodevelopmental disorders.

7. Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality.

8. Lissencephaly syndromes: clinical aspects.

9. Clinical manifestations and evaluation of isolated lissencephaly.

10. Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome.