(Q24678764)

inferred from title

author

Valentine Charlton-Menys

5

0 references

Robert A. Hegele

1

object named as

Robert A Hegele

0 references

author name string

Henian Cao

2

0 references

Dora M Liu

3

0 references

Gary A Costain

4

0 references

N Wilson Rodger

6

0 references

Paul N Durrington

American Journal of Human Genetics

7

0 references

language of work or name

English

0 references

publication date

August 2006

0 references

published in

0 references

volume

79

0 references

issue

2

0 references

page(s)

383-9

0 references

cites work

Lamin B1 is required for mouse development and nuclear integrity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Diseases of adipose tissue: genetic and acquired lipodystrophies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Components of the nuclear envelope and their role in human disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Intermediate filament proteins and their associated diseases

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Phenomics, lipodystrophy, and the metabolic syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Acquired and inherited lipodystrophies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Clinical features and metabolic derangements in acquired generalized lipodystrophy: case reports and review of the literature

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

A case of acquired partial lipodystrophy associated with localized scleroderma and undifferentiated connective tissue disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Fine mapping of a replication origin of human DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Characterization of human DNA sequences synthesized at the onset of S-phase

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

The gene for a novel human lamin maps at a highly transcribed locus of chromosome 19 which replicates at the onset of S-phase.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Membranoproliferative glomerulonephritis with partial lipodystrophy: discordant occurrence in identical twins

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Cephalothoracic Lipodystrophy with Hypocomplementemic Renal Disease: Discordance in Identical Twin Sisters*

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Characterization of a second highly conserved B-type lamin present in cells previously thought to contain only a single B-type lamin

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Genome-wide analysis of mouse transcripts using exon microarrays and factor graphs.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Lessons from human mutations in PPARgamma

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Noncanonical DNA elements in the lamin B2 origin of DNA replication.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Two new cases of Barraquer-Simons syndrome.

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

PPARG F388L, a transactivation-deficient mutant, in familial partial lipodystrophy

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1559499

Nephropathies in progressive lipodystrophy or Barraquer-Simons disease

28 November 2018

1 reference

12 December 2020

Partial lipodystrophy associated with juvenile dermatomyositis: report of two cases

1 reference

12 December 2020

[On lipodystrophia progressiva (Follow-up study of the case published by A. Simons in 1911 for the first time in German literature)]

1 reference

12 December 2020

LMNA mutation position predicts organ system involvement in laminopathies

1 reference

12 December 2020

Single-nucleotide polymorphisms of the nuclear lamina proteome

1 reference

12 December 2020

Cardiomyopathy in congenital complete lipodystrophy

1 reference

12 December 2020

Identifiers

DOI

10.1086/505885

1 reference

1725038

1725038

1 reference

1 reference

1 reference