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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.
Highly Cited
2013
Highly Cited
2013
LMX1B mutations cause hereditary FSGS without extrarenal involvement.
O. Boyer
,
S. Woerner
,
+19 authors
C. Antignac
Journal of the American Society of Nephrology
2013
Corpus ID: 207258169
LMX1B encodes a homeodomain-containing transcription factor that is essential during development. Mutations in LMX1B cause nail…
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Highly Cited
2005
Highly Cited
2005
Genotype–phenotype studies in nail-patella syndrome show that LMX1B mutation location is involved in the risk of developing nephropathy
E. Bongers
,
F. Huysmans
,
+15 authors
N. Knoers
European Journal of Human Genetics
2005
Corpus ID: 22625954
Nail-patella syndrome (NPS) is characterized by developmental defects of dorsal limb structures, nephropathy, and glaucoma and is…
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Highly Cited
2003
Highly Cited
2003
Lmx1b is essential for the development of serotonergic neurons
Yu-Qiang Ding
,
Ulrika Marklund
,
+6 authors
Zhou-Feng Chen
Nature Neuroscience
2003
Corpus ID: 31114893
The specification and differentiation of serotonergic (5-HT) neurons require both extrinsic signaling molecules and intrinsic…
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Review
2003
Review
2003
Nail patella syndrome: a review of the phenotype aided by developmental biology
E. Sweeney
,
A. Fryer
,
R. Mountford
,
A. Green
,
I. Mcintosh
Journal of Medical Genetics
2003
Corpus ID: 13512508
Nail patella syndrome (NPS) is an autosomal dominant condition affecting the nails, skeletal system, kidneys, and eyes. Skeletal…
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Highly Cited
2003
Highly Cited
2003
Lmx1b, Pet-1, and Nkx2.2 Coordinately Specify Serotonergic Neurotransmitter Phenotype
Le-ping Cheng
,
Chih-Li Chen
,
+4 authors
Qiufu Ma
Journal of Neuroscience
2003
Corpus ID: 38855748
Serotonergic (5-HT) neurons in the brainstem modulate a wide range of physiological processes and behaviors. Two transcription…
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Highly Cited
2000
Highly Cited
2000
A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b
M. Smidt
,
C. Asbreuk
,
J. J. Cox
,
Haixu Chen
,
Randy L. Johnson
,
J. Burbach
Nature Neuroscience
2000
Corpus ID: 30508899
We identified the LIM homeodomain transcription factor Lmx1b in the mesencephalic dopamine (mesDA) systems of embryos and adults…
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Highly Cited
2000
Highly Cited
2000
lmx1b, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye
C. Pressman
,
Haixu Chen
,
Randy L. Johnson
Genesis
2000
Corpus ID: 36083333
Summary: Proper development of the anterior segment of the mammalian eye is critical for normal ocular function. Indeed, several…
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Highly Cited
1998
Highly Cited
1998
Limb and kidney defects in Lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome
Haixu Chen
,
Y. Lun
,
+6 authors
Randy L. Johnson
Nature Genetics
1998
Corpus ID: 27786730
Dorsal-ventral limb patterning in vertebrates is thought to be controlled by the LIM-homeodomain protein Lmx1b which is expressed…
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Highly Cited
1998
Highly Cited
1998
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndrome.
Douglas Vollrath
,
V. L. Jaramillo-Babb
,
+4 authors
Julia E. Richards
Human Molecular Genetics
1998
Corpus ID: 22161511
Nail-patella syndrome (NPS) is an inherited developmental disorder most commonly involving maldevelopment of the fingernails…
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Highly Cited
1998
Highly Cited
1998
Mutation analysis of LMX1B gene in nail-patella syndrome patients.
I. Mcintosh
,
Sandra D. Dreyer
,
+14 authors
Brendan H. Lee
American Journal of Human Genetics
1998
Corpus ID: 31187735
Nail-patella syndrome (NPS), a pleiotropic disorder exhibiting autosomal dominant inheritance, has been studied for >100 years…
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