(Q33971550)

30 July 2017

1 reference

title

Genetic approaches to understanding brain development: holoprosencephaly as a model (English)

1 reference

30 July 2017

1 reference

Muenke M

1

1 reference

PubMed ID

10899793

30 July 2017

Cohen MM Jr

series ordinal

2

1 reference

30 July 2017

1 January 2000

1 reference

Mental Retardation and Developmental Disabilities Research Reviews

30 July 2017

1 reference

30 July 2017

6

1 reference

30 July 2017

1

1 reference

30 July 2017

15-21

1 reference

The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired.

30 July 2017

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Single central incisor in familial holoprosencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Expression of a novel murine homeobox gene in the developing cerebellar external granular layer during its proliferation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Teratogen-mediated inhibition of target tissue response to Shh signaling.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Holoprosencephaly: epidemiologic and clinical characteristics of a California population

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

FAMILIAL ALOBAR HOLOPROSENCEPHALY (ARHINENCEPHALY) WITH MEDIAN CLEFT LIP AND PALATE. REPORT OF PATIENT WITH 46 CHROMOSOMES.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Holoprosencephaly: a defect in brain patterning.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Identification and expression of six family genes in mouse retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Retinoic acid embryopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Six3 overexpression initiates the formation of ectopic retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Absence of the superior labial frenulum in holoprosencephaly: a new diagnostic sign.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Absence of the lateral philtral ridges: a clue to the structural basis of the philtrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Holoprosencephaly in human embryos: Epidemiologic studies of 150 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Human developmental disorders and the Sonic hedgehog pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Molecular cloning and expression of the human delta7-sterol reductase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations affecting segment number and polarity in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

The signaling pathway mediated by the type IIB activin receptor controls axial patterning and lateral asymmetry in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Ectopic lens induction in fish in response to the murine homeobox gene Six3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Cholesterol modification of hedgehog signaling proteins in animal development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Hedgehog patterning activity: role of a lipophilic modification mediated by the carboxy-terminal autoprocessing domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Teratogenic effect of the cholesterol synthesis inhibitor AY 9944 on rat embryos in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Holoprosencephaly: a paradigm for the complex genetics of brain development.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Teratogenic action and embryo lethality of AY 9944R: Prevention by a hypercholesterolemia-provoking diet

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

Defective forebrain development in mice lacking gp330/megalin

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

A Smad transcriptional corepressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291098-2779%282000%296%3A1%3C15%3A%3AAID-MRDD3%3E3.0.CO%3B2-8

10.1002/(SICI)1098-2779(2000)6:1<15::AID-MRDD3>3.0.CO;2-8

21 January 2018

Identifiers

DOI

1 reference

30 July 2017

1 reference

PubMed ID

10899793