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CNTNAP1 protein, human
Known as:
CNTNAP1 Protein
, Neurexin 4
, Neurexin IV
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Contactin-associated protein 1 (1384 aa, ~156 kDa) is encoded by the human CNTNAP1 gene. This protein is involved in neuronal signaling.
National Institutes of Health
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Related topics
Related topics
22 relations
Brain
CNTNAP1 gene
Caspr protein, rat
Colon structure (body structure)
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Broader (1)
Cell Adhesion Molecules, Neuronal
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Chemogenetic Synaptic Silencing of Neural Circuits Localizes a Hypothalamus→Midbrain Pathway for Feeding Behavior
T. Stachniak
,
Anirvan Ghosh
,
S. Sternson
Neuron
2014
Corpus ID: 10562233
Highly Cited
2013
Highly Cited
2013
Antibodies to contactin‐1 in chronic inflammatory demyelinating polyneuropathy
L. Querol
,
G. Nogales-Gadea
,
+7 authors
I. Illa
Annals of Neurology
2013
Corpus ID: 22718318
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a frequent autoimmune neuropathy with a heterogeneous…
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Highly Cited
2008
Highly Cited
2008
No Evidence for Chronic Demyelination in Spared Axons after Spinal Cord Injury in a Mouse
J. Lasiene
,
L. Shupe
,
S. Perlmutter
,
P. Horner
Journal of Neuroscience
2008
Corpus ID: 16675910
The pattern of remyelination after traumatic spinal cord injury remains elusive, with animal and human studies reporting partial…
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Highly Cited
2005
Highly Cited
2005
Distinct patterns of hematopoietic stem cell involvement in acute lymphoblastic leukemia
A. Castor
,
L. Nilsson
,
+13 authors
S. Jacobsen
Nature Network Boston
2005
Corpus ID: 387525
The cellular targets of primary mutations and malignant transformation remain elusive in most cancers. Here, we show that…
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Highly Cited
2005
Highly Cited
2005
Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes
Mohammed Sunbulli
,
I. Zak
,
S. Chaturvedi
Neurology
2005
Corpus ID: 26220889
Fabry disease is associated with increased risk of premature stroke and presumptive ischemic cerebral lesions. In 57 consecutive…
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Highly Cited
1999
Highly Cited
1999
The P190, P210, and P230 Forms of the BCR/ABL Oncogene Induce a Similar Chronic Myeloid Leukemia–like Syndrome in Mice but Have Different Lymphoid Leukemogenic Activity
Shaoguang Li
,
R. Ilaria
,
R. Million
,
G. Daley
,
R. V. van Etten
Journal of Experimental Medicine
1999
Corpus ID: 14892220
The product of the Philadelphia chromosome (Ph) translocation, the BCR/ABL oncogene, exists in three principal forms (P190, P210…
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Highly Cited
1995
Highly Cited
1995
BCR/ABL P210 and P190 cause distinct leukemia in transgenic mice.
J. Voncken
,
V. Kaartinen
,
P. Pattengale
,
W. Germeraad
,
J. Groffen
,
N. Heisterkamp
Blood
1995
Corpus ID: 13414484
DNA constructs encoding BCR/ABL P210 have been introduced into the mouse germ line using microinjection of one-cell fertilized…
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Highly Cited
1992
Highly Cited
1992
Primary structure and cellular localization of chicken brain myosin-V (p190), an unconventional myosin with calmodulin light chains
E. M. Espreafico
,
Richard E. Cheney
,
+4 authors
M. Mooseker
Journal of Cell Biology
1992
Corpus ID: 5228052
Recent biochemical studies of p190, a calmodulin (CM)-binding protein purified from vertebrate brain, have demonstrated that this…
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Highly Cited
1992
Highly Cited
1992
Association between GTPase activators for Rho and Ras families
J. Settleman
,
C. Albright
,
L. Foster
,
R. Weinberg
Nature
1992
Corpus ID: 4271554
THE ras-related low-molecular-mass GTPases participate in signal transduction involving a variety of cellular functions…
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Highly Cited
1991
Highly Cited
1991
Signal transduction by normal isoforms and W mutant variants of the Kit receptor tyrosine kinase.
Alastair
,
D. Reithl
,
+7 authors
Pawson
EMBO Journal
1991
Corpus ID: 7596859
Germline mutations at the Dominant White Spotting (W) and Steel (Sl) loci have provided conclusive genetic evidence that c‐kit…
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