(Q24322628)

multicellular organism development

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

nail-patella syndrome

1 reference

D Vollrath

1

0 references

V L Jaramillo-Babb

2

0 references

M V Clough

3

0 references

I McIntosh

4

0 references

K M Scott

5

0 references

P R Lichter

6

0 references

J E Richards

Gene targeting in kidney development

7

0 references

language of work or name

English

0 references

publication date

July 1998

0 references

published in

Human Molecular Genetics

0 references

volume

7

0 references

issue

7

0 references

page(s)

1091-8

0 references

cites work

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

DeLIMiting development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Paralogy mapping: identification of a region in the human MHC triplicated onto human chromosomes 1 and 9 allows the prediction and isolation of novel PBX and NOTCH loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2: tissue-specific expression and linkage mapping on chromosome 9

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Hereditary Osteo-Onychodysplasia

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Induction of the LIM homeobox gene Lmx1 by WNT6a establishes dorsoventral pattern in the vertebrate limb

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

The LIM domain: a new structural motif found in zinc-finger-like proteins.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Multiplex DNA deletion detection and exon sequencing of the hypoxanthine phosphoribosyltransferase gene in Lesch-Nyhan families

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Cosegregation of open-angle glaucoma and the nail-patella syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Renal dysplasia in a family with multiple hereditary abnormalities including iliac horns

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Transcription factors in disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Dorsalizing signal Wnt-7a required for normal polarity of D-V and A-P axes of mouse limb

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Requirement for Lim1 in head-organizer function

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Dorsal cell fate specified by chick Lmx1 during vertebrate limb development

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Mutations in the PAX3 gene causing Waardenburg syndrome type 1 and type 2

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies and vesicoureteral reflux.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

No linkage to chromosome 14 in Swedish Alzheimer's disease families.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Synergistic activation of the insulin gene by a LIM-homeo domain protein and a basic helix-loop-helix protein: building a functional insulin minienhancer complex

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Genetical linkage between the ABO and nail-patella loci

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Nail-patella syndrome: evidence for modification by alleles at the main locus.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Identification of a gene that causes primary open angle glaucoma.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Cooperative interactions between the Caenorhabditis elegans homeoproteins UNC-86 and MEC-3.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021

Transcriptional synergy between LIM-homeodomain proteins and basic helix-loop-helix proteins: the LIM2 domain determines specificity

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2F7.7.1091

7 January 2021