(Q35888835)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

review article

1 reference

title

Rab escort protein 1 (REP1) in intracellular traffic: a functional and pathophysiological overview (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

author name string

Markus Preising

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

publication date

1 June 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

volume

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

page(s)

101-110

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

Genetic defects of intracellular-membrane transport

1 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Heterogeneous gene expression from the inactive X chromosome: an X-linked gene that escapes X inactivation in some human cell lines but is inactivated in others

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germline.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Retrospective, longitudinal, and cross sectional study of visual acuity impairment in choroideraemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Macular pigment and lutein supplementation in choroideremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Clinical and genetic features of choroideremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Comparison of intraocular light scatter in carriers of choroideremia and X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Phenotypic variability in three carriers from a family with choroideremia and a frameshift mutation 1388delCCinsG in the REP-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

X-linked retinitis pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Gene therapy for choroideremia: in vitro rescue mediated by recombinant adenovirus

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Three RFLPs for pZ11 (DXS540) in the choroideremia gene at Xq21.2

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

REP-1 gene mutations in Japanese patients with choroideremia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Mutational analysis of patients with the diagnosis of choroideremia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Rab geranylgeranyl transferase alpha mutation in the gunmetal mouse reduces Rab prenylation and platelet synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

Defective granule exocytosis in Rab27a-deficient lymphocytes from Ashen mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F13816810490514333

10.1080/13816810490514333

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15370541%20AND%20SRC:MED&resulttype=core&format=json

1 January 2020

1 reference