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LMX1B gene
Known as:
LIM Homeobox Transcription Factor 1, Beta Gene
, LIM HOMEOBOX TRANSCRIPTION FACTOR 1, BETA
, LMX1B
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This gene plays a role in both transcriptional regulation and the mediation of limb development.
National Institutes of Health
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Related topics
Related topics
8 relations
Cell Differentiation process
Homo sapiens
LIM homeobox transcription factor 1 beta
Limb Development
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LMX1B wt Allele
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.
M. Mukai
,
Harumi Fujita
,
+6 authors
A. Kubo
Journal of dermatological science (Amsterdam)
2017
Corpus ID: 3849122
2014
2014
LIM homeobox transcription factor 1B expression affects renal interstitial fibrosis and apoptosis in unilateral ureteral obstructed rats.
Tian-biao Zhou
,
C. Ou
,
Yuan-Han Qin
,
Feng-ying Lei
,
Wei-Fang Huang
,
G. Drummen
AJP - Renal Physiology
2014
Corpus ID: 6139380
LIM homeobox transcription factor 1B (LMX1B) is a transcription factor of the LIM homeodomain type and has been implicated in the…
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2013
2013
Lmx1b controls peptide phenotypes in serotonergic and dopaminergic neurons.
Rui Yan
,
Tianwen Huang
,
+4 authors
Le-ping Cheng
Acta Biochimica et Biophysica Sinica
2013
Corpus ID: 1622443
Serotonin (5-HT) neurons synthesize a variety of peptides. How these peptides are controlled during development remains unclear…
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2011
2011
c.194 A>C (Q65P) mutation in the LMX1B gene in patients with nail-patella syndrome associated with glaucoma
Pablo Romero
,
F. Sanhueza
,
P. López
,
Loreto Reyes
,
L. Herrera
Molecular Vision
2011
Corpus ID: 1637770
Purpose To report the clinical, ophthalmic, extraophthalmic, and genetic characteristics of nail-patella syndrome (NPS) in a…
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2011
2011
LMX1B gene mutation in a Saudi patient with bilateral symmetrical hypoplastic nails of the hands
I. Abdulkareem
,
S. Abdi
,
Mohammed Fawaz
,
M. Balwi
2011
Corpus ID: 15390295
Nail-patella syndrome (NPS) is a rare autosomal dominant disorder that is highly penetrant with marked phonotypical variability…
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2009
2009
A Synonymous Genetic Alteration of LMX1B in a Family with Nail-Patella Syndrome
J. Ham
,
S. Shin
,
+7 authors
Eui-Jin Choi
The Korean Journal of Internal Medicine
2009
Corpus ID: 17712375
The gene responsible for nail-patella syndrome, LMX1B, has recently been identified on chromosome 9q. Here we present a patient…
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2004
2004
Characterization of migration behavior of myogenic precursor cells in the limb bud with respect to Lmx1b expression
H. Schweizer
,
R. L. Johnson
,
B. Brand-Saberi
Anatomy and Embryology
2004
Corpus ID: 24982408
Limb buds develop from lateral plate-derived stationary mesenchyme and are invaded by cells from extrinsic regions. The largest…
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Review
2003
Review
2003
[From gene to disease; the nail-patella syndrome and the LMX1B gene].
E. Bongers
,
N. Knoers
Nederlandsch tijdschrift voor geneeskunde
2003
Corpus ID: 10517670
Nail-patella syndrome (NPS) is an autosomal dominant hereditary disorder characterised by nail dysplasia, patellar apoplasia…
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2003
2003
LMX1B 17-bp Deletion and A3243G mtDNA Transition in a Previously Described Patient
J. Finsterer
,
C. Stöllberger
European Neurology
2003
Corpus ID: 37995437
Recently, we described a 45-year-old man with the typical phenotypic features of nail-patella syndrome (NPS, dysplastic nails…
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2002
2002
Meier-Gorlin syndrome (ear-patella-short stature syndrome) in an Italian patient: clinical evaluation and analysis of possible candidate genes.
A. Cohen
,
R. Mulas
,
+5 authors
G. Camera
American journal of medical genetics
2002
Corpus ID: 6127485
We report on an Italian boy with the Meier-Gorlin syndrome (ear-patella-short stature syndrome). This rare autosomal recessive…
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