(Q38346550)

2 September 2017

title

Zebrafish gene knockdowns imply roles for human YWHAG in infantile spasms and cardiomegaly (English)

1 reference

3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide 1

2 September 2017

0 references

1 reference

GOA release 2020-03-11

Hirotomo Saitsu

10

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author name string

Yuta Komoike

1

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2 September 2017

Katsunori Fujii

2

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2 September 2017

Akira Nishimura

3

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2 September 2017

Yoko Hiraki

4

1 reference

2 September 2017

Michiko Hayashidani

5

1 reference

2 September 2017

Keiko Shimojima

6

1 reference

2 September 2017

Tsutomu Nishizawa

7

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2 September 2017

Kouji Higashi

8

1 reference

2 September 2017

Kumi Yasukawa

9

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2 September 2017

Noriko Miyake

11

1 reference

2 September 2017

Takeshi Mizuguchi

12

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2 September 2017

Naomichi Matsumoto

13

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2 September 2017

Makiko Osawa

14

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2 September 2017

Yoichi Kohno

15

1 reference

2 September 2017

Toru Higashinakagawa

16

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2 September 2017

Toshiyuki Yamamoto

17

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2 September 2017

publication date

1 April 2010

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2 September 2017

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2 September 2017

volume

48

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2 September 2017

issue

4

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2 September 2017

page(s)

233-243

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Stages of embryonic development of the zebrafish

2 September 2017

cites work

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14-3-3Gamma interacts with and is phosphorylated by multiple protein kinase C isoforms in PDGF-stimulated human vascular smooth muscle cells

21 January 2018

1 reference

7 January 2021

Expression analysis of the family of 14-3-3 proteins in zebrafish development.

1 reference

7 January 2021

Huntington's disease: roles of huntingtin-interacting protein 1 (HIP-1) and its molecular partner HIPPI in the regulation of apoptosis and transcription

1 reference

7 January 2021

An atypical deletion of the Williams-Beuren syndrome interval implicates genes associated with defective visuospatial processing and autism

1 reference

7 January 2021

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

1 reference

7 January 2021

A 1-Mb critical region in six patients with 9q34.3 terminal deletion syndrome

1 reference

7 January 2021

Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.

1 reference

7 January 2021

Unmasking 15q12 deletion using microarray-based comparative genomic hybridization in a mentally retarded boy with r(Y)

1 reference

7 January 2021

Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11.

1 reference

7 January 2021

14-3-3 proteins mediate an essential anti-apoptotic signal

1 reference

7 January 2021

Preferential paternal origin of microdeletions caused by prezygotic chromosome or chromatid rearrangements in Sotos syndrome

1 reference

7 January 2021

No detectable genomic aberrations by BAC array CGH in Kabuki make-up syndrome patients

1 reference

7 January 2021

Interstitial deletion of chromosome 7q in a patient with Williams syndrome and infantile spasms.

1 reference

7 January 2021

Infantile spasms in a patient with williams syndrome and craniosynostosis.

1 reference

7 January 2021

The 14-3-3 proteins: integrators of diverse signaling cues that impact cell fate and cancer development

1 reference

7 January 2021

Huntingtin Interacting Protein 1 mutations lead to abnormal hematopoiesis, spinal defects and cataracts

1 reference

7 January 2021

Dynamic 14-3-3/client protein interactions integrate survival and apoptotic pathways.

1 reference

7 January 2021

Reverse genetic analysis of neurogenesis in the zebrafish retina

1 reference

7 January 2021

Huntingtin interacting protein 1 Is a clathrin coat binding protein required for differentiation of late spermatogenic progenitors

1 reference

7 January 2021

Germline gain-of-function mutations in RAF1 cause Noonan syndrome

1 reference

7 January 2021

Clinical features of microdeletion 9q22.3 (pat).

1 reference

7 January 2021

TULIP1 (RALGAPA1) haploinsufficiency with brain development delay

1 reference

7 January 2021

Prevalence estimation of Williams syndrome

1 reference

7 January 2021

Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins

1 reference

7 January 2021

The zebrafish gene map defines ancestral vertebrate chromosomes

1 reference

7 January 2021

Identification of a human brain-specific gene, calneuron 1, a new member of the calmodulin superfamily

1 reference

7 January 2021

Delineation of the common critical region in Williams syndrome and clinical correlation of growth, heart defects, ethnicity, and parental origin

1 reference

7 January 2021

Identifiers

DOI

10.1002/DVG.20607

1 reference

2 September 2017

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