(Q48329447)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

title

FGFR1 and anosmin-1 underlying genetically distinct forms of Kallmann syndrome are co-expressed and interact in olfactory bulbs (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

1 reference

1 reference

Nadia Soussi-Yanicostas

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

author name string

Besma Ayari

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

publication date

21 December 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

Development Genes and Evolution

23 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

volume

217

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

page(s)

169-175

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00427-006-0125-0

23 December 2019

exact match

0 references

cites work

Initial characterization of anosmin-1, a putative extracellular matrix protein synthesized by definite neuronal cell populations in the central nervous system

1 reference

12 December 2020

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

1 reference

12 December 2020

Cell signaling by receptor tyrosine kinases

1 reference

12 December 2020

Role of heparan sulfate in fibroblast growth factor signalling: a structural view

1 reference

12 December 2020

Heparan sulfate proteoglycan-dependent induction of axon branching and axon misrouting by the Kallmann syndrome gene kal-1.

1 reference

12 December 2020

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.

1 reference

12 December 2020

Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndrome.

1 reference

12 December 2020

Topographic organization of sensory projections to the olfactory bulb

1 reference

12 December 2020

Anosmin-1, defective in the X-linked form of Kallmann syndrome, promotes axonal branch formation from olfactory bulb output neurons.

1 reference

12 December 2020

Effect of Purified Luteinizing Hormone Releasing Factor on Normal and Hypogonadotrophic Anosmic Men

1 reference

12 December 2020

Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome

1 reference

12 December 2020

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

1 reference

12 December 2020

Studies in cranio-encephalic dysraphia. I. Agenesia of the olfactory lobe (lateral telencephaloschisis) and of the callous and anterior commissures (median telencephaloschisis); olfacto-genital dysplasia

1 reference

12 December 2020

Increased expression of fibroblast growth factor 6 in human prostatic intraepithelial neoplasia and prostate cancer

1 reference

12 December 2020

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

1 reference

12 December 2020

Anosmin-1 underlying the X chromosome-linked Kallmann syndrome is an adhesion molecule that can modulate neurite growth in a cell-type specific manner

1 reference

12 December 2020

FGF signaling through FGFR1 is required for olfactory bulb morphogenesis.

1 reference

12 December 2020

Genetic tracing reveals a stereotyped sensory map in the olfactory cortex

1 reference

12 December 2020

10.1007/S00427-006-0125-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17186267%20AND%20SRC:MED&resulttype=core&format=json

23 December 2019

1 reference