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Studies

8057 Case Reports

3198 Unclassified

1687 Reviews

1642 Research

215 Other Trials

153 Advanced Trials

68 Early Trials

9 Meta-Analysis

Guidelines

2 Guidelines

1 Cochrane

1 Consensuses

Congresses

1147 Abstracts

1

Research

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.

des Portes V, Pinard J M, Billuart P, Vinet M C, Koulakoff A ...

Cell Vol 92(1)

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Date 09 Jan 1998

Institutional score
0.00
Impact
3197.10

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Date 09 Jan 1998

Institutional score
0.00
Impact
3197.10
2

Research

Drosophila clock can generate ectopic circadian clocks.

Zhao Jie, Kilman Valerie L, Keegan Kevin P, Peng Ying, Emery Patrick ...

Cell Vol 113(6)

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Date 13 Jun 2003

Institutional score
232.44
Impact
3197.10

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Date 13 Jun 2003

Institutional score
232.44
Impact
3197.10
3

Research

Specification of neuropeptide cell identity by the integration of retrograde BMP signaling and a combinatorial transcription factor code.

Allan Douglas W, St Pierre Susan E, Miguel-Aliaga Irene, Thor Stefan

Cell Vol 113(1)

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Date 04 Apr 2003

Institutional score
1487.60
Impact
3197.10

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Date 04 Apr 2003

Institutional score
1487.60
Impact
3197.10
4

Research

Arabidopsis LEAFY COTYLEDON1 is sufficient to induce embryo development in vegetative cells.

Lotan T, Ohto M, Yee K M, West M A, Lo R ...

Cell Vol 93(7)

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Date 26 Jun 1998

Institutional score
75.13
Impact
3197.10

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Date 26 Jun 1998

Institutional score
75.13
Impact
3197.10
5

Research

Cell-Type-Specific Alternative Splicing Governs Cell Fate in the Developing Cerebral Cortex.

Zhang Xiaochang, Chen Ming Hui, Wu Xuebing, Kodani Andrew, Fan Jean ...

Cell Vol 166(5)

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Date 25 Aug 2016

Institutional score
1487.60
Impact
3197.10

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Date 25 Aug 2016

Institutional score
1487.60
Impact
3197.10
6

Research

Mutations in the HECT domain of NEDD4L lead to AKT-mTOR pathway deregulation and cause periventricular nodular heterotopia.

Broix Loïc, Jagline Hélène, Ivanova Ekaterina, Schmucker Stéphane, Drouot Nathalie ...

Nature genetics Vol 48(11)

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Date 01 Nov 2016

Institutional score
3719.00
Impact
2459.31

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Date 01 Nov 2016

Institutional score
3719.00
Impact
2459.31
7

Research

Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development.

Cappello Silvia, Gray Mary J, Badouel Caroline, Lange Simona, Einsiedler Melanie ...

Nature genetics Vol 45(11)

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Date 01 Nov 2013

Institutional score
0.00
Impact
2459.31

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Date 01 Nov 2013

Institutional score
0.00
Impact
2459.31
8

Research

Loss of WT1 function leads to ectopic myogenesis in Wilms' tumour.

Miyagawa K, Kent J, Moore A, Charlieu J P, Little M H ...

Nature genetics Vol 18(1)

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Date 01 Jan 1998

Institutional score
0.00
Impact
2459.31

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Date 01 Jan 1998

Institutional score
0.00
Impact
2459.31
9

Research

Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex.

Sheen Volney L, Ganesh Vijay S, Topcu Meral, Sebire Guillaume, Bodell Adria ...

Nature genetics Vol 36(1)

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Date 01 Jan 2004

Institutional score
30.11
Impact
2459.31

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Date 01 Jan 2004

Institutional score
30.11
Impact
2459.31
10

Research

Localized mutations in the gene encoding the cytoskeletal protein filamin A cause diverse malformations in humans.

Robertson Stephen P, Twigg Stephen R F, Sutherland-Smith Andrew J, Biancalana Valérie, Gorlin Robert J ...

Nature genetics Vol 33(4)

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Date 01 Apr 2003

Institutional score
0.00
Impact
2459.31

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Date 01 Apr 2003

Institutional score
0.00
Impact
2459.31

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