(Q28594664)

Crossref

https://api.crossref.org/works/10.1007%2FS00335-004-2444-7

The recessive phenotype displayed by a dominant negative microphthalmia-associated transcription factor mutant is a result of impaired nucleation potential

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00335-004-2444-7

Aspartyl beta -hydroxylase (Asph) and an evolutionarily conserved isoform of Asph missing the catalytic domain share exons with junctin

21 January 2018

1 reference

12 December 2020

Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa

1 reference

12 December 2020

Genomic, transcriptional and mutational analysis of the mouse microphthalmia locus

1 reference

12 December 2020

Ligand specificity in the CRAL-TRIO protein family

1 reference

12 December 2020

Changing Patterns of the Retinoic Acid System in the Developing Retina

1 reference

12 December 2020

Map Manager QTX, cross-platform software for genetic mapping

1 reference

12 December 2020

Absence of post-translational aspartyl beta-hydroxylation of epidermal growth factor domains in mice leads to developmental defects and an increased incidence of intestinal neoplasia

1 reference

12 December 2020

Recessive mutations in the RLBP1 gene encoding cellular retinaldehyde-binding protein in a form of retinitis punctata albescens

1 reference

12 December 2020

PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects

1 reference

12 December 2020

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. Percin EF, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AMV, Kalnins VI, Kocak-Altintas A, Sowden JC, Trabousli E, Sarfarazi M, McInn

1 reference

12 December 2020

Gene expression of growth and differentiation factors-5, -6, and -7 in developing bovine tooth at the root forming stage.

1 reference

12 December 2020

Molecular cloning and structural analysis of the human gene encoding cellular retinaldehyde-binding protein

1 reference

12 December 2020

Mouse Otx2 functions in the formation and patterning of rostral head.

1 reference

12 December 2020

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

1 reference

12 December 2020

Mouse small eye results from mutations in a paired-like homeobox-containing gene

1 reference

12 December 2020

Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4

1 reference

12 December 2020

Novel mutation in sonic hedgehog in non-syndromic colobomatous microphthalmia.

1 reference

12 December 2020

Ocular phenotype of bothnia dystrophy, an autosomal recessive retinitis pigmentosa associated with an R234W mutation in the RLBP1 gene

1 reference

12 December 2020

Visual cycle impairment in cellular retinaldehyde binding protein (CRALBP) knockout mice results in delayed dark adaptation

1 reference

12 December 2020

Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development

1 reference

12 December 2020

EGF and TGF-alpha stimulate retinal neuroepithelial cell proliferation in vitro.

1 reference

12 December 2020

Basic local alignment search tool

1 reference

12 December 2020

Screening for PAX6 gene mutations is consistent with haploinsufficiency as the main mechanism leading to various ocular defects

1 reference

12 December 2020

Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype

1 reference

12 December 2020

Zebrafish Radar: a new member of the TGF-beta superfamily defines dorsal regions of the neural plate and the embryonic retina

1 reference

12 December 2020

Otx genes are required for tissue specification in the developing eye

1 reference

12 December 2020

The Rx homeobox gene is essential for vertebrate eye development

1 reference

12 December 2020

PAX6 in sensory development

1 reference

12 December 2020

Multiple joint and skeletal patterning defects caused by single and double mutations in the mouse Gdf6 and Gdf5 genes

1 reference

12 December 2020

Mutations in SOX2 cause anophthalmia

1 reference

12 December 2020

Dosage requirement and allelic expression of PAX6 during lens placode formation

1 reference

12 December 2020

CHD5, a new member of the chromodomain gene family, is preferentially expressed in the nervous system

1 reference

12 December 2020

Retinoic acid is necessary for development of the ventral retina in zebrafish.

1 reference

12 December 2020

Characterization of the CHD family of proteins

1 reference

12 December 2020

Mutations in a new member of the chromodomain gene family cause CHARGE syndrome

1 reference

12 December 2020

Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea

1 reference

12 December 2020

Asymmetrical retinoic acid synthesis in the dorsoventral axis of the retina

1 reference

12 December 2020

The control of cell fate in the embryonic visual system by atonal, tailless and EGFR signaling.

1 reference

12 December 2020

Xenopus GDF6, a new antagonist of noggin and a partner of BMPs

1 reference

12 December 2020

Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily

1 reference

12 December 2020

10.1007/S00335-004-2444-7

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

4002395

4002395

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference