Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay.

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Implications of a Chr7q21.11 Microdeletion and the Role of the PCLO Gene in Developmental Delay.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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P1476

Implications of a Chr7q21.11 M ...... O Gene in Developmental Delay.

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P2093

Alice M George

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Donald R Love

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Fern Ashton

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Roberto L Mazzaschi

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Salim Aftimos

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P2860

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

Piccolo and bassoon maintain synaptic vesicle clustering without directly participating in vesicle exocytosis

A new imprinted cluster on the human chromosome 7q21-q31, identified by human-mouse monochromosomal hybrids

Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption

Piccolo, a presynaptic zinc finger protein structurally related to bassoon

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.

Gene expression and genetic variation data implicate PCLO in bipolar disorder.

Gene structure and genetic localization of the PCLO gene encoding the presynaptic active zone protein Piccolo.

Interactions between Piccolo and the actin/dynamin-binding protein Abp1 link vesicle endocytosis to presynaptic active zones.

Reduced transcript expression of genes affected by inherited and de novo CNVs in autism

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306-310

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scholarly article

case report

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P478

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P577

2013-05-09T00:00:00Z

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23862039

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3706123

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