(Q28209433)

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Bone dysplasias in man: molecular insights

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Mutations in the p53 homolog p63: allele-specific developmental syndromes in humans.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Molecular diagnosis of cystic fibrosis

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Lumping and splitting: molecular biology in the genetics clinic

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Lamin a truncation in Hutchinson-Gilford progeria.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

A progeroid syndrome in mice is caused by defects in A-type lamins

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Zmpste24 deficiency in mice causes spontaneous bone fractures, muscle weakness, and a prelamin A processing defect.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

The nuclear envelope, muscular dystrophy and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Nuclear lamin A/C R482Q mutation in canadian kindreds with Dunnigan-type familial partial lipodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Life at the edge: the nuclear envelope and human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

The carboxyl-terminal region common to lamins A and C contains a DNA binding domain.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

In vivo and in vitro interaction between human transcription factor MOK2 and nuclear lamin A/C.

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Effects of expressing lamin A mutant protein causing Emery-Dreifuss muscular dystrophy and familial partial lipodystrophy in HeLa cells

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Mitotic misregulation and human aging

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021

Zinc metalloproteinase, ZMPSTE24, is mutated in mandibuloacral dysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900162-X

7 January 2021