Seipin deficiency alters fatty acid Delta9 desaturation and lipid droplet formation in Berardinelli-Seip congenital lipodystrophy (Q24320010)

lipid droplet organization

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Sandra Grès

Jean-Sébastien Saulnier-Blache

10

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12

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author name string

Emilie Boutet

1

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Haquima El Mourabit

2

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Matthieu Prot

3

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Mona Nemani

4

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Eliane Khallouf

5

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Odile Colard

6

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Michèle Maurice

7

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Anne-Marie Durand-Schneider

8

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Yves Chrétien

9

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Claude Wolf

11

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Jacqueline Capeau

13

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Jocelyne Magré

Rab-regulated interaction of early endosomes with lipid droplets

14

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language of work or name

English

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publication date

June 2009

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published in

Biochimie

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volume

91

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issue

6

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page(s)

796-803

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cites work

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Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13.

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AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.

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The lipodystrophy protein seipin is found at endoplasmic reticulum lipid droplet junctions and is important for droplet morphology

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Fld1p, a functional homologue of human seipin, regulates the size of lipid droplets in yeast

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