(Q73588818)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12833090%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

title

Cloned lambs--lessons from pathology (English)

1 reference

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5 November 2019

3

1 reference

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5 November 2019

5

William Wallace

1 reference

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5 November 2019

7

Ian Wilmut

1 reference

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5 November 2019

author name string

Susan M Rhind

1

1 reference

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5 November 2019

Tim J King

2

1 reference

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5 November 2019

Chris Bellamy

4

1 reference

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5 November 2019

Paul DeSousa

6

1 reference

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5 November 2019

publication date

1 July 2003

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5 November 2019

1 reference

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5 November 2019

volume

21

1 reference

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5 November 2019

issue

7

1 reference

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5 November 2019

page(s)

744-745

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https://scigraph.springernature.com/pub.10.1038/nbt0703-744

5 November 2019

exact match

0 references

cites work

The health profile of cloned animals.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Large offspring syndrome in cattle and sheep

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Mutations in the human Jagged1 gene are responsible for Alagille syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Alagille syndrome is caused by mutations in human Jagged1, which encodes a ligand for Notch1

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Clinical and pathologic features of cloned transgenic calves and fetuses (13 case studies).

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Production of alpha-1,3-galactosyltransferase knockout pigs by nuclear transfer cloning.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Congenital misalignment of pulmonary veins with alveolar capillary dysplasia causing persistent neonatal pulmonary hypertension: report of two affected siblings

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Congenital misalignment of pulmonary vessels: an unusual syndrome associated with PPHN.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Fatal persistent pulmonary hypertension presenting late in the neonatal period

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Evaluation of gestational deficiencies in cloned sheep fetuses and placentae.

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Deletion of the alpha(1,3)galactosyl transferase (GGTA1) gene and the prion protein (PrP) gene in sheep

1 reference

https://api.crossref.org/works/10.1038%2FNBT0703-744

7 January 2021

Identifiers

DOI

10.1038/NBT0703-744

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12833090%20AND%20SRC:MED&resulttype=core&format=json

5 November 2019

1 reference