Radiographic analysis of zebrafish skeletal defects (Q47074000)

5 January 2018

title

Radiographic analysis of zebrafish skeletal defects (English)

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

3 April 2024

0 references

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

3 April 2024

author name string

Shannon Fisher

1

1 reference

5 January 2018

Pudur Jagadeeswaran

2

1 reference

5 January 2018

Marnie E. Halpern

3

1 reference

PubMed ID

14623232

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14623232

3 April 2024

language of work or name

English

0 references

publication date

1 December 2003

1 reference

5 January 2018

full work available at URL

number of pages

13

1 reference

based on heuristic

inferred from page(s)

https://doi.org/10.1016/s0012-1606(03)00399-3

online access status

open access

1 reference

PubMed ID

14623232

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A14623232

https://api.elsevier.com/content/article/PII:S0012160603003993?httpAccept=text/xml

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

https://api.elsevier.com/content/article/PII:S0012160603003993?httpAccept=text/plain

3 April 2024

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

3 April 2024

published in

Developmental Biology

1 reference

5 January 2018

volume

264

1 reference

5 January 2018

issue

1

1 reference

5 January 2018

page(s)

64-76

1 reference

5 January 2018

Transgenic mouse model of the mild dominant form of osteogenesis imperfecta

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Noggin, cartilage morphogenesis, and joint formation in the mammalian skeleton

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfecta

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Development of the cranium and paired fins in the zebrafish Danio rerio (Ostariophysi, Cyprinidae)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Haploinsufficient phenotypes in Bmp4 heterozygous null mice and modification by mutations in Gli3 and Alx4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Mutations of the TWIST gene in the Saethre-Chotzen syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Patterning the zebrafish axial skeleton requires early chordin function

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Use of the Cre/lox recombination system to develop a non-lethal knock-in murine model for osteogenesis imperfecta with an alpha1(I) G349C substitution. Variability in phenotype in BrtlIV mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Bone dysplasias in man: molecular insights

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Mutations affecting pigmentation and shape of the adult zebrafish

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Insertion of retrovirus into the first intron of alpha 1(I) collagen gene to embryonic lethal mutation in mice

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

7 January 2021

A skeletal gene database

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Genome-wide, large-scale production of mutant mice by ENU mutagenesis.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Radiation hybrid mapping of the zebrafish genome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

The LN54 radiation hybrid map of zebrafish expressed sequences

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vessels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

The morbid anatomy of the human genome: chromosomal location of mutations causing disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

The morbid anatomy of the human genome: chromosomal location of mutations causing disease (update 1 December 1993).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Large-scale mutagenesis in the zebrafish: in search of genes controlling development in a vertebrate.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Transgenic mice expressing a partially deleted gene for type I procollagen (COL1A1). A breeding line with a phenotype of spontaneous fractures and decreased bone collagen and mineral

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

A genetic linkage map for the zebrafish

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Complete primary structure of rainbow trout type I collagen consisting of alpha1(I)alpha2(I)alpha3(I) heterotrimers

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Genetic analysis of craniofacial development in the vertebrate embryo

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Production of clones of homozygous diploid zebra fish (Brachydanio rerio)

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Teleost HoxD and HoxA genes: comparison with tetrapods and functional evolution of the HOXD complex.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

Novel regulators of bone formation: molecular clones and activities

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0012-1606%2803%2900399-3

A genetic screen for mutations affecting embryogenesis in zebrafish

7 January 2021

5

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio

3 April 2024

13

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Sclerotome development and peripheral nervous system segmentation in embryonic zebrafish

3 April 2024

29

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Segmental relationship between somites and vertebral column in zebrafish

3 April 2024

30

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Mutations affecting craniofacial development in zebrafish

3 April 2024

33

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Jaw and branchial arch mutants in zebrafish II: anterior arches and cartilage differentiation

3 April 2024

37

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Segment and cell type lineage restrictions during pharyngeal arch development in the zebrafish embryo

3 April 2024

42

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

Jaw and branchial arch mutants in zebrafish I: branchial arches

3 April 2024

43

1 reference

https://api.crossref.org/works/10.1016/S0012-1606(03)00399-3

3 April 2024

Identifiers

1 reference

5 January 2018

PubMed ID

14623232

1 reference

5 January 2018