(Q21092495)

15 August 2022

4

Fowzan S Alkuraya

Fowzan S

Alkuraya

1 reference

15 August 2022

27

James F Gusella

James F

Gusella

1 reference

15 August 2022

20

Christopher A Walsh

Christopher A

Walsh

1 reference

15 August 2022

Fabiola Quintero-Rivera

2

object named as

Fabiola Quintero-Rivera

Fabiola

Quintero-Rivera

1 reference

15 August 2022

6

Qiongchao Xi

Qiongchao

Xi

1 reference

15 August 2022

3

Yanli Fan

Yanli

Fan

1 reference

15 August 2022

Diana J Donovan

5

Diana J

Donovan

1 reference

15 August 2022

Annick Turbe-Doan

7

Annick

Turbe-Doan

1 reference

15 August 2022

Qing-Gang Li

8

Qing-Gang

Li

1 reference

15 August 2022

Craig G Campbell

9

Craig G

Campbell

1 reference

15 August 2022

Alan L Shanske

10

Alan L

Shanske

1 reference

15 August 2022

Elliott H Sherr

11

Elliott H

Sherr

1 reference

15 August 2022

Ayesha Ahmad

12

Ayesha

Ahmad

1 reference

15 August 2022

Roxana Peters

13

Roxana

Peters

1 reference

15 August 2022

Benedict Rilliet

14

Benedict

Rilliet

1 reference

15 August 2022

Paloma Parvex

15

Paloma

Parvex

1 reference

15 August 2022

Alexander G Bassuk

16

Alexander G

Bassuk

1 reference

15 August 2022

David J Harris

17

David J

Harris

1 reference

15 August 2022

Heather Ferguson

18

Heather

Ferguson

1 reference

15 August 2022

Chantal Kelly

19

Chantal

Kelly

1 reference

15 August 2022

Richard M Gronostajski

21

Richard M

Gronostajski

1 reference

15 August 2022

Koenraad Devriendt

22

Koenraad

Devriendt

1 reference

15 August 2022

Anne Higgins

23

Anne

Higgins

1 reference

15 August 2022

Azra H Ligon

24

Azra H

Ligon

1 reference

15 August 2022

Bradley J Quade

25

Bradley J

Quade

1 reference

15 August 2022

Cynthia C Morton

26

Cynthia C

Morton

1 reference

15 August 2022

Richard L Maas

28

Richard L

Maas

1 reference

Creative Commons Attribution 4.0 International

15 August 2022

language of work or name

English

0 references

publication date

25 May 2007

0 references

published in

PLOS Genetics

0 references

volume

3

0 references

issue

5

0 references

page(s)

e80

0 references

copyright license

start time

25 May 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Disruption of ROBO2 is associated with urinary tract anomalies and confers risk of vesicoureteral reflux

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

SLIT2-mediated ROBO2 signaling restricts kidney induction to a single site

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactyly

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Disruption of the murine nuclear factor I-A gene (Nfia) results in perinatal lethality, hydrocephalus, and agenesis of the corpus callosum

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Absence makes the search grow longer

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Conserved roles for Slit and Robo proteins in midline commissural axon guidance

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Essential role for NFI-C/CTF transcription-replication factor in tooth root development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Slit proteins prevent midline crossing and determine the dorsoventral position of major axonal pathways in the mammalian forebrain

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Deficient outgrowth of the ureteric bud underlies the renal agenesis phenotype in mice manifesting the limb deformity (ld) mutation

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

The transcription factor gene Nfib is essential for both lung maturation and brain development

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Mouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expression

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Multiple roles for slits in the control of cell migration in the rostral migratory stream

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Eya1-deficient mice lack ears and kidneys and show abnormal apoptosis of organ primordia

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Characterization of a novel rat brain glycosylphosphatidylinositol-anchored protein (Kilon), a member of the IgLON cell adhesion molecule family

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Adult syringomielia. Classification, pathogenesis and therapeutic approaches

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Long-range control of gene expression: emerging mechanisms and disruption in disease

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Pathophysiology of tethered cord syndrome and other complex factors

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

History, anatomic forms, and pathogenesis of Chiari I malformations

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Slit2 guides both precrossing and postcrossing callosal axons at the midline in vivo.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Abnormal development of forebrain midline glia and commissural projections in Nfia knock-out mice.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Roles of the NFI/CTF gene family in transcription and development

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Brain anomalies, retardation of mentality and growth, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, ear deformity and deafness, eye hypoplasia, cleft palate, cryptorchidism, and kidney dysplasia/hypoplasia (BRESEK/BRESHECK): ne

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Hypoplasia of the corpus callosum: a study of 445 consecutive MRI scans

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Development of the corpus callosum and cavum septi in man.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Orofaciodigital syndrome type I associated with polycystic kidneys and agenesis of the corpus callosum

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Agenesis of the corpus callosum. Its associated anomalies and syndromes with special reference to the Apert syndrome.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Real-time analysis of ureteric bud branching morphogenesis in vitro

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Abnormalities of corpus callosum in patients with inherited metabolic diseases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Frequency of agenesis of the corpus callosum in the developmentally disabled population as determined by computerized tomography.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Interstitial deletion of chromosome 2q associated with ovarian dysgenesis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

The transcription factor NFIA controls the onset of gliogenesis in the developing spinal cord.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Robo1 regulates the development of major axon tracts and interneuron migration in the forebrain.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Major brain lesions detected on sonographic screening of apparently normal term neonates.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Trends in elective terminations of pregnancy between 1989 and 2000 in a French county (the Isère).

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Renal size and function in patients with neuropathic bladder due to myelomeningocele: the role of growth hormone

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Interstitial microdeletion of chromosome 1p in two siblings.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Renal failure in patients with neurogenic lower urinary tract dysfunction

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Cortical axon guidance by the glial wedge during the development of the corpus callosum.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Expression of green fluorescent protein in the ureteric bud of transgenic mice: a new tool for the analysis of ureteric bud morphogenesis.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Axonal guidance during development of the great cerebral commissures: descriptive and experimental studies, in vivo, on the role of preformed glial pathways.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Postnatally induced formation of the corpus callosum in acallosal mice on glia-coated cellulose bridges

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1877820

Detection of an interstitial deletion of 2q21-22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation

29 November 2018

1 reference

12 December 2020

Urologic aspects of tethered cord

1 reference

12 December 2020

Interstitial deletion 2q14q21

1 reference

12 December 2020

De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report

1 reference

12 December 2020

Position effect in human genetic disease

1 reference

12 December 2020

10.1371/JOURNAL.PGEN.0030080

Identifiers

DOI

0 references

PMC publication ID

1877820

0 references