(Q51953730)

English

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons.

scientific article published in July 2008

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

Loss of the Prader-Willi syndrome protein necdin causes defective migration, axonal outgrowth, and survival of embryonic sympathetic neurons. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

Prader–Willi syndrome

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

author name string

Alysa A Tennese

1

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

Christopher B Gee

2

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

publication date

1 July 2008

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

Developmental Dynamics

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

237

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

7

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

1935-1943

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

21 January 2018

Expression of necdin, an embryonal carcinoma-derived nuclear protein, in developing mouse brain

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of the Prader-Willi gene Necdin during mouse nervous system development correlates with neuronal differentiation and p75NTR expression.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Sensory defects in Necdin deficient mice result from a loss of sensory neurons correlated within an increase of developmental programmed cell death

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The centrosome in human genetic disease

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The MAGE proteins: emerging roles in cell cycle progression, apoptosis, and neurogenetic disease

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Two binding partners cooperate to activate the molecular motor Kinesin-1.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The Caenorhabditis elegans gene unc-76 and its human homologs define a new gene family involved in axonal outgrowth and fasciculation

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperghrelinemia does not accelerate gastric emptying in Prader-Willi syndrome patients.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Centrosome localization determines neuronal polarity.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Respiratory sinus arrhythmia in patients with Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Mice lacking brain-derived neurotrophic factor develop with sensory deficits

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Lack of neurotrophin-3 leads to deficiencies in the peripheral nervous system and loss of limb proprioceptive afferents

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Disruption of the mouse necdin gene results in early post-natal lethality

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Prader-Willi syndrome: advances in genetics, pathophysiology and treatment

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Specification of catecholaminergic and serotonergic neurons.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Salivary abnormalities in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The human necdin gene, NDN, is maternally imprinted and located in the Prader-Willi syndrome chromosomal region

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression analysis of a novel p75(NTR) signaling protein, which regulates cell cycle progression and apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Ectopic expression of necdin induces differentiation of mouse neuroblastoma cells

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Necdin downregulates CDC2 expression to attenuate neuronal apoptosis.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

A neurotrophin signaling cascade coordinates sympathetic neuron development through differential control of TrkA trafficking and retrograde signaling.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Necdin interacts with the Msx2 homeodomain protein via MAGE-D1 to promote myogenic differentiation of C2C12 cells

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Disruption of the paternal necdin gene diminishes TrkA signaling for sensory neuron survival

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Prader-Willi syndrome transcripts are expressed in phenotypically significant regions of the developing mouse brain

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Essential role for the Prader-Willi syndrome protein necdin in axonal outgrowth

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Disruption of the mouse Necdin gene results in hypothalamic and behavioral alterations reminiscent of the human Prader-Willi syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

GFR alpha3, a component of the artemin receptor, is required for migration and survival of the superior cervical ganglion

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Absence of Ndn, encoding the Prader-Willi syndrome-deleted gene necdin, results in congenital deficiency of central respiratory drive in neonatal mice

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

NRAGE, a novel MAGE protein, interacts with the p75 neurotrophin receptor and facilitates nerve growth factor-dependent apoptosis

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

NRAGE, a p75 neurotrophin receptor-interacting protein, induces caspase activation and cell death through a JNK-dependent mitochondrial pathway

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Unexpected death and critical illness in Prader-Willi syndrome: report of ten individuals

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Neuronally-expressed necdin gene: an imprinted candidate gene in Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Necdin is required for terminal differentiation and survival of primary dorsal root ganglion neurons

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

The p75 neurotrophin receptor interacts with multiple MAGE proteins

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Necdin-deficient mice do not show lethality or the obesity and infertility of Prader-Willi syndrome

1 reference

https://api.crossref.org/works/10.1002%2FDVDY.21615

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/DVDY.21615

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 April 2018

http://europepmc.org/abstract/MED/18570257

ResearchGate publication ID

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