(Q38309940)

2 September 2017

title

Functional conservation of zinc-finger homeodomain gene zfh1/SIP1 in Drosophila heart development (English)

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2 September 2017

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Margaret Liu

1

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2 September 2017

Mingtsan Su

series ordinal

2

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2 September 2017

Gary E Lyons

series ordinal

3

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2 September 2017

Rolf Bodmer

series ordinal

4

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2 September 2017

publication date

7 September 2006

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Development Genes and Evolution

2 September 2017

published in

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2 September 2017

volume

216

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2 September 2017

issue

11

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2 September 2017

page(s)

683-693

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Neural crest and cardiovascular patterning.

2 September 2017

cites work

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00427-006-0096-1

The delta-crystallin enhancer-binding protein delta EF1 is a repressor of E2-box-mediated gene activation

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00427-006-0096-1

DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages

21 January 2018

1 reference

12 December 2020

Sizing up the heart: development redux in disease.

1 reference

12 December 2020

Enteric nervous system development: analysis of the selective developmental potentialities of vagal and sacral neural crest cells using quail-chick chimeras.

1 reference

12 December 2020

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

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12 December 2020

The gene tinman is required for specification of the heart and visceral muscles in Drosophila

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12 December 2020

SIP1, a novel zinc finger/homeodomain repressor, interacts with Smad proteins and binds to 5'-CACCT sequences in candidate target genes

1 reference

12 December 2020

The expression of myosin genes in developing skeletal muscle in the mouse embryo

1 reference

12 December 2020

Slit and Robo control cardiac cell polarity and morphogenesis

1 reference

12 December 2020

Generation of the floxed allele of the SIP1 (Smad-interacting protein 1) gene for Cre-mediated conditional knockout in the mouse.

1 reference

12 December 2020

Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease

1 reference

12 December 2020

Delta-crystallin enhancer binding protein delta EF1 is a zinc finger-homeodomain protein implicated in postgastrulation embryogenesis

1 reference

12 December 2020

Pleiotropic and diverse expression of ZFHX1B gene transcripts during mouse and human development supports the various clinical manifestations of the "Mowat-Wilson" syndrome

1 reference

12 December 2020

?Mowat-Wilson? syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

1 reference

12 December 2020

Hirschsprung's disease: genetic mutations in mice and men.

1 reference

12 December 2020

Characterization and localization of the even-skipped protein of Drosophila

1 reference

12 December 2020

Nonsense and frameshift mutations in ZFHX1B, encoding Smad-interacting protein 1, cause a complex developmental disorder with a great variety of clinical features

1 reference

12 December 2020

Parsing the heart: genetic modules for organ assembly

1 reference

12 December 2020

Further delineation of the phenotype associated with heterozygous mutations in ZFHX1B.

1 reference

12 December 2020

Neuromancer Tbx20-related genes (H15/midline) promote cell fate specification and morphogenesis of the Drosophila heart

1 reference

12 December 2020

ZEB, a vertebrate homolog of Drosophila Zfh-1, is a negative regulator of muscle differentiation

1 reference

12 December 2020

Molecular screening of the ZFHX1B gene in prenatally diagnosed isolated agenesis of the corpus callosum

1 reference

12 December 2020

Function of alternative splicing

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12 December 2020

Signalling interactions during facial development

1 reference

12 December 2020

Hirschsprung disease, mental retardation, characteristic facial features, and mutation in the gene ZFHX1B (SIP1): confirmation of the Mowat-Wilson syndrome.

1 reference

12 December 2020

The embryonic expression patterns of zfh-1 and zfh-2, two Drosophila genes encoding novel zinc-finger homeodomain proteins

1 reference

12 December 2020

Interactions of the Drosophila gap gene giant with maternal and zygotic pattern-forming genes

1 reference

12 December 2020

Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures.

1 reference

12 December 2020

New mode of DNA binding of multi-zinc finger transcription factors: deltaEF1 family members bind with two hands to two target sites

1 reference

12 December 2020

Genome-wide detection of tissue-specific alternative splicing in the human transcriptome

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12 December 2020

Alternative neural crest cell fates are instructively promoted by TGFbeta superfamily members

1 reference

12 December 2020

The Drosophila melanogaster T-box genes midline and H15 are conserved regulators of heart development

1 reference

12 December 2020

The patterns of wingless, decapentaplegic, and tinman position the Drosophila heart.

1 reference

12 December 2020

Sacral neural crest cells colonise aganglionic hindgut in vivo but fail to compensate for lack of enteric ganglia

1 reference

12 December 2020

Heart development in Drosophila and vertebrates: conservation of molecular mechanisms.

1 reference

12 December 2020

Frameshift mutation of the zinc finger homeo box 1 B gene in syndromic corpus callosum agenesis (Mowat-Wilson syndrome).

1 reference

12 December 2020

Loss-of-function mutations in SIP1 Smad interacting protein 1 result in a syndromic Hirschsprung disease

1 reference

12 December 2020

Loss of function of the Drosophila zfh-1 gene results in abnormal development of mesodermally derived tissues

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12 December 2020

Expression of the SMADIP1 gene during early human development

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12 December 2020

Mechanisms of alternative pre-messenger RNA splicing

1 reference

12 December 2020

Heart development in Drosophila and its relationship to vertebrates.

1 reference

12 December 2020

SIP1 (Smad interacting protein 1) and deltaEF1 (delta-crystallin enhancer binding factor) are structurally similar transcriptional repressors

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12 December 2020

Requirement of MADS domain transcription factor D-MEF2 for muscle formation in Drosophila

1 reference

12 December 2020

Homeotic genes autonomously specify one aspect of pattern in the Drosophila mesoderm.

1 reference

12 December 2020

Hirschsprung's disease: a review

1 reference

12 December 2020

An alternative-exon database and its statistical analysis

1 reference

12 December 2020

The two-handed E box binding zinc finger protein SIP1 downregulates E-cadherin and induces invasion

1 reference

12 December 2020

V. Genes, lineages, and tissue interactions in the development of the enteric nervous system

1 reference

12 December 2020

Mowat-Wilson syndrome

1 reference

12 December 2020

zfh-1 is required for germ cell migration and gonadal mesoderm development in Drosophila.

1 reference

12 December 2020

Imaging neuronal subsets and other cell types in whole-mount Drosophila embryos and larvae using antibody probes.

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12 December 2020

Embryonic even skipped-dependent muscle and heart cell fates are required for normal adult activity, heart function, and lifespan.

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12 December 2020

T-box transcription factors and their roles in regulatory hierarchies in the developing heart

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12 December 2020

Laminin is required for heart, somatic muscles, and gut development in the Drosophila embryo.

1 reference

12 December 2020

Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome

1 reference

12 December 2020

The Drosophila homeobox genes zfh-1 and even-skipped are required for cardiac-specific differentiation of a numb-dependent lineage decision.

1 reference

12 December 2020

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12 December 2020

Impairment of T cell development in deltaEF1 mutant mice

1 reference

12 December 2020

"Mowat-Wilson" syndrome with and without Hirschsprung disease is a distinct, recognizable multiple congenital anomalies-mental retardation syndrome caused by mutations in the zinc finger homeo box 1B gene

1 reference

12 December 2020

10.1007/S00427-006-0096-1

Identifiers

DOI

1 reference

2 September 2017

1 reference