Presenilin 1 is essential for cardiac morphogenesis (Q28592290)

31 January 2017

title

Presenilin 1 is essential for cardiac morphogenesis (English)

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31 January 2017

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GOA release 2020-03-11

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Mitsunari Nakajima

1

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31 January 2017

Eiko Moriizumi

series ordinal

2

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31 January 2017

Haruhiko Koseki

series ordinal

3

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31 January 2017

Takuji Shirasawa

series ordinal

4

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31 January 2017

publication date

1 August 2004

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31 January 2017

published in

Developmental Dynamics

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31 January 2017

volume

230

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31 January 2017

issue

4

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31 January 2017

page(s)

795–799

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Molecular genetics of Alzheimer's disease

31 January 2017

cites work

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https://api.crossref.org/works/10.1002%2FDVDY.20098

7 January 2021

Presenilin mutations in Alzheimer's disease

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7 January 2021

Mice lacking both presenilin genes exhibit early embryonic patterning defects

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A RIP tide in neuronal signal transduction

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Familial Tetralogy of Fallot caused by mutation in the jagged1 gene

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7 January 2021

Genetic basis of syndromes associated with congenital heart disease

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Congenital heart disease: incidence and inheritance.

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Incidence of congenital heart disease: I. Postnatal incidence.

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7 January 2021

Physical disorders and causes of death in relatives of Alzheimer's disease patients.

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7 January 2021

Jagged1 mutations in patients ascertained with isolated congenital heart defects

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7 January 2021

Expression of presenilin 1 and 2 (PS1 and PS2) in human and murine tissues

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7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

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7 January 2021

Epidemiology of cardiovascular malformations: prevalence and risk factors

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7 January 2021

A presenilin-1/gamma-secretase cleavage releases the E-cadherin intracellular domain and regulates disassembly of adherens junctions

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7 January 2021

Outcome of congenital heart defects--a population-based study

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7 January 2021

Abnormal blood vessel development in mice lacking presenilin-1.

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7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

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7 January 2021

Skeletal and CNS defects in Presenilin-1-deficient mice

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7 January 2021

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

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7 January 2021

Presenilin 1 is required for Notch1 and DII1 expression in the paraxial mesoderm

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7 January 2021

Embryonic lethality and vascular defects in mice lacking the Notch ligand Jagged1

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7 January 2021

Impaired cell cycle control of neuronal precursor cells in the neocortical primordium of presenilin-1-deficient mice

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7 January 2021

Identifiers

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31 January 2017

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