Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis (Q24337705)

GOA release 2020-03-11

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30

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Janai R. Carr

Janai R Carr

5

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Mustafa A. Salih

Mustafa A M Salih

12

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Irene Gottlob

20

Irene Gottlob

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Robert W. Baloh

34

Robert W Baloh

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Joanna C Jen

1

Joanna C Jen

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Stanley F Nelson

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Stanley F Nelson

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author name string

Wai-Man Chan

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Thomas M Bosley

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Jijun Wan

4

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Udo Rüb

6

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David Shattuck

7

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Georges Salamon

8

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Lili C Kudo

9

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Jing Ou

10

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Doris D M Lin

11

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Tülay Kansu

13

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Hesham Al Dhalaan

14

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Zayed Al Zayed

15

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David B MacDonald

16

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Bent Stigsby

17

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Andreas Plaitakis

18

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Emmanuel K Dretakis

19

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Christina Pieh

21

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Elias I Traboulsi

22

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Qing Wang

23

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Lejin Wang

24

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Caroline Andrews

25

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Koki Yamada

26

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Joseph L Demer

27

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Shaheen Karim

28

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Jeffry R Alger

29

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Thomas Deller

31

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Nancy L Sicotte

32

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Elizabeth C Engle

on focus list of Wikimedia project

35

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language of work or name

English

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publication date

4 June 2004

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published in

Science

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volume

304

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issue

5676

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page(s)

1509-13

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ScienceSource

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cites work

Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family

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Directional guidance of neuronal migration in the olfactory system by the protein Slit

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Slit proteins bind Robo receptors and have an evolutionarily conserved role in repulsive axon guidance

19 March 2017

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Roundabout controls axon crossing of the CNS midline and defines a novel subfamily of evolutionarily conserved guidance receptors

19 March 2017

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The divergent Robo family protein rig-1/Robo3 is a negative regulator of slit responsiveness required for midline crossing by commissural axons

19 March 2017

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Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25

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Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2

19 March 2017

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Hierarchical organization of guidance receptors: silencing of netrin attraction by slit through a Robo/DCC receptor complex

19 March 2017

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Cloning and functional studies of a novel gene aberrantly expressed in RB-deficient embryos

19 March 2017

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Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

19 March 2017

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Axon guidance: the cytoplasmic tail

27 September 2017

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astray, a zebrafish roundabout homolog required for retinal axon guidance

27 September 2017

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Selecting a longitudinal pathway: Robo receptors specify the lateral position of axons in the Drosophila CNS.

27 September 2017

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Mutations affecting growth cone guidance in Drosophila: genes necessary for guidance toward or away from the midline

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A Leu7Pro mutation in the signal peptide of platelet glycoprotein (GP)IX in a case of Bernard-Soulier syndrome abolishes surface expression of the GPIb-V-IX complex

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Rig-1 a new member of Robo family genes exhibits distinct pattern of expression during mouse development

30 May 2018

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Brainstem hypoplasia in familial horizontal gaze palsy and scoliosis

29 November 2018

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29 November 2018

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29 November 2018

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Familial paralysis of horizontal gaze: Associated with pendular nystagmus, progressive scoliosis, and facial contraction with myokymia

29 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15105459

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The source of 'paradoxical lateralization' of cortical evoked potentials to posterior tibial nerve stimulation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15105459

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Familial congenital horizontal gaze paralysis and kyphoscoliosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15105459

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1126/SCIENCE.1096437

1 reference

1 reference

1 reference

PubMed publication ID

15105459

1 reference