Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,276,776 papers from all fields of science
Search
Sign In
Create Free Account
LMNB2 gene
Known as:
LAMIN B2
, LMNB2
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
1 relation
lamin B2
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Dual strands of the miR-145 duplex (miR-145-5p and miR-145-3p) regulate oncogenes in lung adenocarcinoma pathogenesis
Shunsuke Misono
,
N. Seki
,
+7 authors
H. Inoue
Journal of Human Genetics
2018
Corpus ID: 51929117
Our original microRNA (miRNA) expression signatures (based on RNA sequencing) revealed that both strands of the miR-145 duplex…
Expand
2015
2015
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia.
John A. Damiano
,
Z. Afawi
,
+18 authors
M. Hildebrand
Human Molecular Genetics
2015
Corpus ID: 46757066
We studied a consanguineous Palestinian Arab family segregating an autosomal recessive progressive myoclonus epilepsy (PME) with…
Expand
2014
2014
Barraquer–Simons syndrome: A rare clinical entity
P. Simsek-Kiper
,
E. Roach
,
G. Utine
,
K. Boduroğlu
American Journal of Medical Genetics. Part A
2014
Corpus ID: 6515946
The Barraquer–Simons syndrome or acquired parital lipodystrophy is a rare form of partial lipodystrophy characterized by gradual…
Expand
Highly Cited
2011
Highly Cited
2011
An absence of both lamin B1 and lamin B2 in keratinocytes has no effect on cell proliferation or the development of skin and hair.
Shao H. Yang
,
Sandy Chang
,
+6 authors
S. Young
Human Molecular Genetics
2011
Corpus ID: 23996957
Nuclear lamins are usually classified as A-type (lamins A and C) or B-type (lamins B1 and B2). A-type lamins have been implicated…
Expand
Review
2009
Review
2009
Laminopathies, other progeroid disorders, and aging: Common pathogenic themes and possible treatments
E. Neilan
American Journal of Medical Genetics. Part A
2009
Corpus ID: 29770319
In this issue of the Journal, McPherson et al. [2009] describe a unique constellation of clinical findings—including premature…
Expand
Highly Cited
2006
Highly Cited
2006
Sequencing of the reannotated LMNB2 gene reveals novel mutations in patients with acquired partial lipodystrophy.
R. Hegele
,
R. Hegele
,
+5 authors
P. Durrington
American Journal of Human Genetics
2006
Corpus ID: 9737249
The etiology of acquired partial lipodystrophy (APL, also called "Barraquer-Simons syndrome") is unknown. Genomic DNA mutations…
Expand
Highly Cited
2004
Highly Cited
2004
Modular Structure of the Human Lamin B2 Replicator
Sónia Paixão
,
I. Colaluca
,
+7 authors
G. Biamonti
Molecular and Cellular Biology
2004
Corpus ID: 7414684
ABSTRACT The cis-acting elements necessary for the activity of DNA replication origins in metazoan cells are still poorly…
Expand
2001
2001
Single-nucleotide polymorphisms of the nuclear lamina proteome
R. Hegele
,
J. Yuen
,
H. Cao
Journal of Human Genetics
2001
Corpus ID: 22844448
AbstractFamilial partial lipodystrophy (FPLD) has been shown to be due to mutations in the LMNA gene encoding nuclear lamins A…
Expand
1998
1998
DNA loop anchorage region colocalizes with the replication origin located downstream to the human gene encoding lamin B2
M. Lagarkova
,
E. Svetlova
,
M. Giacca
,
A. Falaschi
,
S. Razin
Journal of Cellular Biochemistry
1998
Corpus ID: 46359928
The recently developed procedure of topoisomerase II‐mediated DNA loop excision has been used to analyze the topological…
Expand
Highly Cited
1989
Highly Cited
1989
A second higher vertebrate B-type lamin. cDNA sequence determination and in vitro processing of chicken lamin B2.
K. Vorburger
,
C. Lehner
,
G. Kitten
,
H. Eppenberger
,
E. Nigg
Journal of Molecular Biology
1989
Corpus ID: 33878634
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE