Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

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P1476

Utilizing lymphatic cell markers to visualize human lymphatic abnormalities.

@en

P2860

GJC2 missense mutations cause human lymphedema

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome

Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasia

Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans

FOXC2 controls formation and maturation of lymphatic collecting vessels through cooperation with NFATc1

Functionally specialized junctions between endothelial cells of lymphatic vessels

Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies

Pressing the right buttons: signaling in lymphangiogenesis

Plasticity of blood- and lymphatic endothelial cells and marker identification

Lymphatic and other vascular malformative/overgrowth disorders are caused by somatic mutations in PIK3CA

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scholarly article

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10.1002/JBIO.201700117

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Zerina Lokmic

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2017-09-04T00:00:00Z

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P698

28869350

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