Molecular biology and genetics of embryonic eyelid development.

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Meibomian gland morphogenesis requires developmental eyelid closure and lid fusion.Early Development of Network Oscillations in the Ferret Visual Cortex.

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P2860

Molecular biology and genetics of embryonic eyelid development.

Item

http://www.wikidata.org/entity/Q53178607

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

@zh-hant

name

Molecular biology and genetics of embryonic eyelid development.

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Molecular biology and genetics of embryonic eyelid development.

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Molecular biology and genetics of embryonic eyelid development.

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Molecular biology and genetics of embryonic eyelid development.

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Molecular biology and genetics of embryonic eyelid development.

@en

Molecular biology and genetics of embryonic eyelid development.

@nl

P1476

Molecular biology and genetics of embryonic eyelid development.

@en

P2093

Adam C Weber

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Elias I Traboulsi

http://www.w3.org/2001/XMLSchema#string

Tal J Rubinstein

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P2860

The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome

R-spondins function as ligands of the orphan receptors LGR4 and LGR5 to regulate Wnt/beta-catenin signaling

The unique and cooperative roles of the Grainy head-like transcription factors in epidermal development reflect unexpected target gene specificity

DeltaNp63 knockdown mice: A mouse model for AEC syndrome

Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

P63 alpha mutations lead to aberrant splicing of keratinocyte growth factor receptor in the Hay-Wells syndrome

Identification of a novel cell-adhesive protein spatiotemporally expressed in the basement membrane of mouse developing hair follicle

Spectrum of p63 mutations in a selected patient cohort affected with ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (AEC)

Mutations in GRIP1 cause Fraser syndrome

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252-259

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scholarly article

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10.3109/13816810.2015.1071409

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2016-02-11T00:00:00Z

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26863902

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Molecular biology and genetics of embryonic eyelid development.

about

P2860

P2860

Molecular biology and genetics of embryonic eyelid development.

description

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P698