(Q38359413)

2 September 2017

title

Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease (English)

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2 September 2017

Namik Kaya

1

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2 September 2017

Faiqa Imtiaz

2

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2 September 2017

Dilek Colak

3

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2 September 2017

Moeenaldeen Al-Sayed

4

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2 September 2017

Ali Al-Odaib

5

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2 September 2017

Fatma Al-Zahrani

6

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2 September 2017

Bashayer R Al-Mubarak

7

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2 September 2017

Mohammad Al-Owain

8

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2 September 2017

Hesham Al-Dhalaan

9

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2 September 2017

Aziza Chedrawi

10

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2 September 2017

Zuhair Al-Hassnan

11

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2 September 2017

Serdar Coskun

12

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2 September 2017

Nadia Sakati

13

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2 September 2017

Pinar Ozand

14

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2 September 2017

Brian F Meyer

15

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2 September 2017

language of work or name

English

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publication date

1 September 2008

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2 September 2017

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2 September 2017

volume

10

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2 September 2017

issue

9

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2 September 2017

page(s)

675-684

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Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with canavan disease

2 September 2017

cites work

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Aspartoacylase deficiency and Canavan disease in Saudi Arabia

21 January 2018

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Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease

21 January 2018

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Structure of aspartoacylase, the brain enzyme impaired in Canavan disease

21 January 2018

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Identification of the zinc binding ligands and the catalytic residue in human aspartoacylase, an enzyme involved in Canavan disease

21 January 2018

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Mutational analysis of aspartoacylase: implications for Canavan disease

21 January 2018

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Mild-onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene

21 January 2018

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21 January 2018

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Canavan disease and the role of N-acetylaspartate in myelin synthesis

21 January 2018

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Metabolic changes in the knockout mouse for Canavan's disease: implications for patients with Canavan's disease

21 January 2018

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Canavan disease: a monogenic trait with complex genomic interaction.

21 January 2018

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Expression of glutamate transporter, GABRA6, serine proteinase inhibitor 2 and low levels of glutamate and GABA in the brain of knock-out mouse for Canavan disease

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Neuropilin is a receptor for the axonal chemorepellent Semaphorin III

21 January 2018

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21 January 2018

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Neuropilin-1 promotes human glioma progression through potentiating the activity of the HGF/SF autocrine pathway

21 January 2018

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A cricket Gene Index: a genomic resource for studying neurobiology, speciation, and molecular evolution

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Aspartoacylase gene knockout results in severe vacuolation in the white matter and gray matter of the spinal cord in the mouse

21 January 2018

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Aspartoacylase deficiency does not affect N-acetylaspartylglutamate level or glutamate carboxypeptidase II activity in the knockout mouse brain

21 January 2018

1 reference

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Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiency.

21 January 2018

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Molecular basis of Canavan's disease: from human to mouse

21 January 2018

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The gene for neuronal apoptosis inhibitory protein is partially deleted in individuals with spinal muscular atrophy

21 January 2018

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Heterotypic interactions among NACHT domains: implications for regulation of innate immune responses

21 January 2018

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Neuronal apoptosis-inhibitory protein does not interact with Smac and requires ATP to bind caspase-9

21 January 2018

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Mutation analysis of the aspartoacylase gene in non-Jewish patients with Canavan disease

21 January 2018

1 reference

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10.1097/GIM.0B013E31818337A8

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

2 September 2017

1002691653

0 references

1 reference