(Q46755743)

24 December 2017

title

A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice (English)

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24 December 2017

author

Fudi Wang

5

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24 December 2017

Nancy Andrews

8

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24 December 2017

Mark D Fleming

object named as

Mark D Fleming

7

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author name string

Jackie E Lim

1

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24 December 2017

Ou Jin

2

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24 December 2017

Carolyn Bennett

3

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24 December 2017

Kelly Morgan

4

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24 December 2017

Cameron C Trenor

6

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24 December 2017

language of work or name

English

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publication date

16 October 2005

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24 December 2017

published in

Nature Genetics

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24 December 2017

volume

37

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24 December 2017

issue

11

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24 December 2017

page(s)

1270-1273

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24 December 2017

https://scigraph.springernature.com/pub.10.1038/ng1659

exact match

0 references

cites work

Balancing acts: molecular control of mammalian iron metabolism

1 reference

Transferrin receptor is necessary for development of erythrocytes and the nervous system

21 January 2018

1 reference

Hemoglobin deficit: an inherited hypochromic anemia in the mouse

21 January 2018

1 reference

The hemoglobin-deficit mutation is located on mouse chromosome 19.

21 January 2018

1 reference

Sec6/8 complex is recruited to cell-cell contacts and specifies transport vesicle delivery to the basal-lateral membrane in epithelial cells

21 January 2018

1 reference

Exocyst is involved in cystogenesis and tubulogenesis and acts by modulating synthesis and delivery of basolateral plasma membrane and secretory proteins

21 January 2018

1 reference

Mechanism of recruiting Sec6/8 (exocyst) complex to the apical junctional complex during polarization of epithelial cells

21 January 2018

1 reference

Sec15 is an effector for the Rab11 GTPase in mammalian cells

21 January 2018

1 reference

The secretory protein Sec8 is required for paraxial mesoderm formation in the mouse

21 January 2018

1 reference

Mutations in the exocyst component Sec5 disrupt neuronal membrane traffic, but neurotransmitter release persists

21 January 2018

1 reference

Drosophila sec10 is required for hormone secretion but not general exocytosis or neurotransmission

21 January 2018

1 reference

Mutations in Drosophila sec15 reveal a function in neuronal targeting for a subset of exocyst components

21 January 2018

1 reference

The brain exocyst complex interacts with RalA in a GTP-dependent manner: identification of a novel mammalian Sec3 gene and a second Sec15 gene

21 January 2018

1 reference

The exocyst is an effector for Sec4p, targeting secretory vesicles to sites of exocytosis

21 January 2018

1 reference

Hydrolysis of GTP on rab11 is required for the direct delivery of transferrin from the pericentriolar recycling compartment to the cell surface but not from sorting endosomes

21 January 2018

1 reference

Rab11 regulates recycling through the pericentriolar recycling endosome

21 January 2018

1 reference

Rab11 promotes docking and fusion of multivesicular bodies in a calcium-dependent manner

21 January 2018

1 reference

Receptor-mediated endocytosis of transferrin and recycling of the transferrin receptor in rat reticulocytes

21 January 2018

1 reference

Constitutively activated FGFR3 mutants signal through PLCgamma-dependent and -independent pathways for hematopoietic transformation.

21 January 2018

1 reference

Constitutive activation of the MEK/ERK pathway mediates all effects of oncogenic H-ras expression in primary erythroid progenitors

21 January 2018

1 reference

The molecular defect in hypotransferrinemic mice

21 January 2018

1 reference

7 January 2021

Iron homeostasis: insights from genetics and animal models

1 reference

7 January 2021

Exosome formation during maturation of mammalian and avian reticulocytes: evidence that exosome release is a major route for externalization of obsolete membrane proteins

1 reference

7 January 2021

Stat5 is essential for the myelo- and lymphoproliferative disease induced by TEL/JAK2

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG1659

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24 December 2017

PubMed ID

16227995

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24 December 2017