Type |
Details |
Score |
Publication |
First Author: |
Melzer S |
Year: |
2021 |
Journal: |
bioRxiv |
Title: |
Bombesin-like peptide recruits disinhibitory cortical circuits and enhances fear memories |
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•
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•
•
|
Protein Domain |
Type: |
Family |
Description: |
G protein-coupled receptors (GPCRs) constitute a vast protein family that encompasses a wide range of functions, including various autocrine, paracrine and endocrine processes. They show considerable diversity at the sequence level, on the basis of which they can be separated into distinct groups []. The term clan can be used to describe the GPCRs, as they embrace a group of families for which there are indications of evolutionary relationship, but between which there is no statistically significant similarity in sequence []. The currently known clan members include rhodopsin-like GPCRs (Class A, GPCRA), secretin-like GPCRs (Class B, GPCRB), metabotropic glutamate receptor family (Class C, GPCRC), fungal mating pheromone receptors (Class D, GPCRD), cAMP receptors (Class E, GPCRE) and frizzled/smoothened (Class F, GPCRF) [, , , , ]. GPCRs are major drug targets, and are consequently the subject of considerable research interest. It has been reported that the repertoire of GPCRs for endogenous ligands consists of approximately 400 receptors in humans and mice []. Most GPCRs are identified on the basis of their DNA sequences, rather than the ligand they bind, those that are unmatched to known natural ligands are designated by as orphan GPCRs, or unclassified GPCRs [].The rhodopsin-like GPCRs (GPCRA) represent a widespread protein family that includes hormone, neurotransmitter and light receptors, all of which transduce extracellular signals through interaction with guanine nucleotide-binding (G) proteins. Although their activating ligands vary widely in structure and character, the amino acid sequences of the receptors are very similar and are believed to adopt a common structural framework comprising 7 transmembrane (TM) helices [, , ].Bombesins are peptide neurotransmitters whose biological activity residesin a common C-terminal sequence, WAXGHXM. In the periphery, bombesin-related peptides stimulate smooth muscle and glandular secretion. In thebrain, these peptides are believed to play a role in homeostasis, thermoregulation and metabolism, and have been reported to elicit analgesia andexcessive grooming, together with central regulation of a variety ofperipheral effects.Mammalian bombesins are encoded by 2 genes. The preproGRP gene transcriptencodes a precursor of 147 amino acids, which gives GRP and GRP18-27. ThepreproNMB gene transcript encodes a precursor of 117 amino acids, which ismetabolised to neuromedin B. Receptors for these peptides have widespreaddistribution in peripheral tissue. High levels are found in smooth muscleand in the brain.The gastrin-releasing peptide receptor has a wide distribution in peripheraltissue. High levels are found in smooth muscle (e.g., intestine, stomachand bladder) and in secretory glands (e.g., pancreas). In the brain, it isfound in high levels in the hypothalamus, and is present in other areas inlower levels (e.g., the olfactory tract, dendate gyrus and cortex). Itis also found in various cell lines (e.g., Swiss 3T3 fibroblasts and small-cell lung carcinomas). GRP receptors activate the phosphoinositidepathway via a pertussis-toxin-insensitive G-protein, probably of the Gq/G11class. |
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•
•
•
•
•
|
Publication |
First Author: |
Battey JF |
Year: |
1991 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Molecular cloning of the bombesin/gastrin-releasing peptide receptor from Swiss 3T3 cells. |
Volume: |
88 |
Issue: |
2 |
Pages: |
395-9 |
|
•
•
•
•
•
|
Publication |
First Author: |
Le Jeune M |
Year: |
2010 |
Journal: |
Exp Cell Res |
Title: |
Identification of four alternatively spliced transcripts of the Ucma/GRP gene, encoding a new Gla-containing protein. |
Volume: |
316 |
Issue: |
2 |
Pages: |
203-15 |
|
•
•
•
•
•
|
Publication |
First Author: |
Freyburger M |
Year: |
2016 |
Journal: |
Sleep |
Title: |
EphA4 is Involved in Sleep Regulation but Not in the Electrophysiological Response to Sleep Deprivation. |
Volume: |
39 |
Issue: |
3 |
Pages: |
613-24 |
|
•
•
•
•
•
|
Publication |
First Author: |
Mathews JA |
Year: |
2018 |
Journal: |
Am J Respir Cell Mol Biol |
Title: |
Augmented Responses to Ozone in Obese Mice Require IL-17A and Gastrin-Releasing Peptide. |
Volume: |
58 |
Issue: |
3 |
Pages: |
341-351 |
|
•
•
•
•
•
|
Publication |
First Author: |
Osada N |
Year: |
2009 |
Journal: |
Neurochem Int |
Title: |
Apolipoprotein E-deficient mice are more vulnerable to ER stress after transient forebrain ischemia. |
Volume: |
54 |
Issue: |
7 |
Pages: |
403-9 |
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•
•
•
•
•
|
Publication |
First Author: |
Walton NM |
Year: |
2014 |
Journal: |
Stem Cells |
Title: |
Gastrin-releasing peptide contributes to the regulation of adult hippocampal neurogenesis and neuronal development. |
Volume: |
32 |
Issue: |
9 |
Pages: |
2454-66 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhao ZQ |
Year: |
2014 |
Journal: |
J Neurosci |
Title: |
Cross-inhibition of NMBR and GRPR signaling maintains normal histaminergic itch transmission. |
Volume: |
34 |
Issue: |
37 |
Pages: |
12402-14 |
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•
•
•
•
•
|
Publication |
First Author: |
Carroll RE |
Year: |
2000 |
Journal: |
Cell Growth Differ |
Title: |
Gastrin-releasing peptide is a mitogen and a morphogen in murine colon cancer. |
Volume: |
11 |
Issue: |
7 |
Pages: |
385-93 |
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•
•
•
•
•
|
Publication |
First Author: |
Sakamoto H |
Year: |
2014 |
Journal: |
Neurosci Lett |
Title: |
Androgen regulates development of the sexually dimorphic gastrin-releasing peptide neuron system in the lumbar spinal cord: evidence from a mouse line lacking androgen receptor in the nervous system. |
Volume: |
558 |
|
Pages: |
109-14 |
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•
•
•
•
•
|
Publication |
First Author: |
Haidet-Phillips AM |
Year: |
2015 |
Journal: |
Exp Neurol |
Title: |
Human glial progenitor engraftment and gene expression is independent of the ALS environment. |
Volume: |
264 |
|
Pages: |
188-99 |
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•
•
•
•
•
|
Publication |
First Author: |
Kozlowska U |
Year: |
2021 |
Journal: |
Cells |
Title: |
Assessment of Immunological Potential of Glial Restricted Progenitor Graft In Vivo-Is Immunosuppression Mandatory? |
Volume: |
10 |
Issue: |
7 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Ashour K |
Year: |
2006 |
Journal: |
Am J Respir Crit Care Med |
Title: |
Bombesin inhibits alveolarization and promotes pulmonary fibrosis in newborn mice. |
Volume: |
173 |
Issue: |
12 |
Pages: |
1377-85 |
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•
•
•
•
•
|
Publication |
First Author: |
Ohki-Hamazaki H |
Year: |
1999 |
Journal: |
J Neurosci |
Title: |
Functional properties of two bombesin-like peptide receptors revealed by the analysis of mice lacking neuromedin B receptor. |
Volume: |
19 |
Issue: |
3 |
Pages: |
948-54 |
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•
•
•
•
•
|
Publication |
First Author: |
Karatsoreos IN |
Year: |
2006 |
Journal: |
Eur J Neurosci |
Title: |
Diurnal regulation of the gastrin-releasing peptide receptor in the mouse circadian clock. |
Volume: |
23 |
Issue: |
4 |
Pages: |
1047-53 |
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•
•
•
•
•
|
Publication |
First Author: |
Persson K |
Year: |
2002 |
Journal: |
Endocrinology |
Title: |
Islet function phenotype in gastrin-releasing peptide receptor gene-deficient mice. |
Volume: |
143 |
Issue: |
10 |
Pages: |
3717-26 |
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•
•
•
•
•
|
Publication |
First Author: |
Varadarajan S |
Year: |
2018 |
Journal: |
eNeuro |
Title: |
Connectome of the Suprachiasmatic Nucleus: New Evidence of the Core-Shell Relationship. |
Volume: |
5 |
Issue: |
5 |
|
|
•
•
•
•
•
|
Publication |
First Author: |
Liu Y |
Year: |
2004 |
Journal: |
Dev Biol |
Title: |
CD44 expression identifies astrocyte-restricted precursor cells. |
Volume: |
276 |
Issue: |
1 |
Pages: |
31-46 |
|
•
•
•
•
•
|
Publication |
First Author: |
Zhang ZJ |
Year: |
2023 |
Journal: |
EMBO Rep |
Title: |
Descending dopaminergic pathway facilitates itch signal processing via activating spinal GRPR(+) neurons. |
Volume: |
24 |
Issue: |
10 |
Pages: |
e56098 |
|
•
•
•
•
•
|
Publication |
First Author: |
Patricio ES |
Year: |
2015 |
Journal: |
J Invest Dermatol |
Title: |
Mechanisms Underlying the Scratching Behavior Induced by the Activation of Proteinase-Activated Receptor-4 in Mice. |
Volume: |
135 |
Issue: |
10 |
Pages: |
2484-2491 |
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•
•
•
•
•
|
Publication |
First Author: |
Bell AM |
Year: |
2020 |
Journal: |
Sci Rep |
Title: |
Expression of green fluorescent protein defines a specific population of lamina II excitatory interneurons in the GRP::eGFP mouse. |
Volume: |
10 |
Issue: |
1 |
Pages: |
13176 |
|
•
•
•
•
•
|
Publication |
First Author: |
Drouyer E |
Year: |
2010 |
Journal: |
J Comp Neurol |
Title: |
Specializations of gastrin-releasing peptide cells of the mouse suprachiasmatic nucleus. |
Volume: |
518 |
Issue: |
8 |
Pages: |
1249-63 |
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•
•
•
•
•
|
Publication |
First Author: |
Yao Y |
Year: |
2023 |
Journal: |
Curr Biol |
Title: |
A carotid body-brainstem neural circuit mediates sighing in hypoxia. |
Volume: |
33 |
Issue: |
5 |
Pages: |
827-837.e4 |
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•
•
•
•
•
|
Publication |
First Author: |
Kiguchi N |
Year: |
2021 |
Journal: |
Pharmacol Res Perspect |
Title: |
Chemogenetic activation of central gastrin-releasing peptide-expressing neurons elicits itch-related scratching behavior in male and female mice. |
Volume: |
9 |
Issue: |
3 |
Pages: |
e00790 |
|
•
•
•
•
•
|
Publication |
First Author: |
Barnes JA |
Year: |
1999 |
Journal: |
Cell Stress Chaperones |
Title: |
Expression of glucose-regulated proteins (GRP78 and GRP94) in hearts and fore-limb buds of mouse embryos exposed to hypoglycemia in vitro. |
Volume: |
4 |
Issue: |
4 |
Pages: |
250-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kusano K |
Year: |
1993 |
Journal: |
Am J Physiol |
Title: |
Receptor-activated currents in mouse fibroblasts expressing transfected bombesin receptor subtype cDNAs. |
Volume: |
265 |
Issue: |
4 Pt 1 |
Pages: |
C869-76 |
|
•
•
•
•
•
|
Publication |
First Author: |
Otto C |
Year: |
1997 |
Journal: |
J Biol Chem |
Title: |
Absence of glucocorticoid receptor-beta in mice. |
Volume: |
272 |
Issue: |
42 |
Pages: |
26665-8 |
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•
•
•
•
|
Publication |
First Author: |
Kamichi S |
Year: |
2005 |
Journal: |
Brain Res |
Title: |
Immunohistochemical localization of gastrin-releasing peptide receptor in the mouse brain. |
Volume: |
1032 |
Issue: |
1-2 |
Pages: |
162-70 |
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•
•
•
•
•
|
Publication |
First Author: |
Nakagawa T |
Year: |
2005 |
Journal: |
Biochem Pharmacol |
Title: |
Identification of key amino acids in the gastrin-releasing peptide receptor (GRPR) responsible for high affinity binding of gastrin-releasing peptide (GRP). |
Volume: |
69 |
Issue: |
4 |
Pages: |
579-93 |
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•
•
•
•
•
|
Publication |
First Author: |
Benali-Furet NL |
Year: |
2005 |
Journal: |
Oncogene |
Title: |
Hepatitis C virus core triggers apoptosis in liver cells by inducing ER stress and ER calcium depletion. |
Volume: |
24 |
Issue: |
31 |
Pages: |
4921-33 |
|
•
•
•
•
•
|
Publication |
First Author: |
Czepielewski RS |
Year: |
2012 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
Gastrin-releasing peptide receptor (GRPR) mediates chemotaxis in neutrophils. |
Volume: |
109 |
Issue: |
2 |
Pages: |
547-52 |
|
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•
•
•
•
|
Publication |
First Author: |
Wang J |
Year: |
2013 |
Journal: |
J Neurosci |
Title: |
Oligodendrocyte/type-2 astrocyte progenitor cells and glial-restricted precursor cells generate different tumor phenotypes in response to the identical oncogenes. |
Volume: |
33 |
Issue: |
42 |
Pages: |
16805-17 |
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•
•
•
•
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Publication |
First Author: |
Kaminski MT |
Year: |
2014 |
Journal: |
Biochim Biophys Acta |
Title: |
Glucose-induced dissociation of glucokinase from its regulatory protein in the nucleus of hepatocytes prior to nuclear export. |
Volume: |
1843 |
Issue: |
3 |
Pages: |
554-64 |
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•
•
•
•
|
Publication |
First Author: |
Abu-Toamih Atamni HJ |
Year: |
2019 |
Journal: |
Animal Model Exp Med |
Title: |
Efficient protocols and methods for high-throughput utilization of the Collaborative Cross mouse model for dissecting the genetic basis of complex traits. |
Volume: |
2 |
Issue: |
3 |
Pages: |
137-149 |
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•
•
•
•
•
|
Publication |
First Author: |
Takanami K |
Year: |
2023 |
Journal: |
Front Mol Neurosci |
Title: |
Function of gastrin-releasing peptide receptors in ocular itch transmission in the mouse trigeminal sensory system. |
Volume: |
16 |
|
Pages: |
1280024 |
|
•
•
•
•
•
|
Publication |
First Author: |
Chaperon F |
Year: |
2012 |
Journal: |
PLoS One |
Title: |
Gastrin-releasing peptide signaling plays a limited and subtle role in amygdala physiology and aversive memory. |
Volume: |
7 |
Issue: |
4 |
Pages: |
e34963 |
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•
•
•
•
•
|
Publication |
First Author: |
Albisetti GW |
Year: |
2019 |
Journal: |
J Neurosci |
Title: |
Dorsal Horn Gastrin-Releasing Peptide Expressing Neurons Transmit Spinal Itch But Not Pain Signals. |
Volume: |
39 |
Issue: |
12 |
Pages: |
2238-2250 |
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•
•
•
•
|
Publication |
First Author: |
Gutierrez-Mecinas M |
Year: |
2016 |
Journal: |
Mol Pain |
Title: |
A quantitative study of neurochemically defined excitatory interneuron populations in laminae I-III of the mouse spinal cord. |
Volume: |
12 |
|
|
|
•
•
•
•
•
|
Publication |
First Author: |
Yuan XS |
Year: |
2018 |
Journal: |
Front Neurosci |
Title: |
Whole-Brain Monosynaptic Afferent Projections to the Cholecystokinin Neurons of the Suprachiasmatic Nucleus. |
Volume: |
12 |
|
Pages: |
807 |
|
•
•
•
•
•
|
Publication |
First Author: |
Blum M |
Year: |
2007 |
Journal: |
Differentiation |
Title: |
Ciliation and gene expression distinguish between node and posterior notochord in the mammalian embryo. |
Volume: |
75 |
Issue: |
2 |
Pages: |
133-46 |
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•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
G protein-coupled receptors (GPCRs) constitute a vast protein family that encompasses a wide range of functions, including various autocrine, paracrine and endocrine processes. They show considerable diversity at the sequence level, on the basis of which they can be separated into distinct groups []. The term clan can be used to describe the GPCRs, as they embrace a group of families for which there are indications of evolutionary relationship, but between which there is no statistically significant similarity in sequence []. The currently known clan members include rhodopsin-like GPCRs (Class A, GPCRA), secretin-like GPCRs (Class B, GPCRB), metabotropic glutamate receptor family (Class C, GPCRC), fungal mating pheromone receptors (Class D, GPCRD), cAMP receptors (Class E, GPCRE) and frizzled/smoothened (Class F, GPCRF) [, , , , ]. GPCRs are major drug targets, and are consequently the subject of considerable research interest. It has been reported that the repertoire of GPCRs for endogenous ligands consists of approximately 400 receptors in humans and mice []. Most GPCRs are identified on the basis of their DNA sequences, rather than the ligand they bind, those that are unmatched to known natural ligands are designated by as orphan GPCRs, or unclassified GPCRs [].The rhodopsin-like GPCRs (GPCRA) represent a widespread protein family that includes hormone, neurotransmitter and light receptors, all of which transduce extracellular signals through interaction with guanine nucleotide-binding (G) proteins. Although their activating ligands vary widely in structure and character, the amino acid sequences of the receptors are very similar and are believed to adopt a common structural framework comprising 7 transmembrane (TM) helices [, , ].Bombesins are peptide neurotransmitters whose biological activity residesin a common C-terminal sequence, WAXGHXM. In the periphery, bombesin-related peptides stimulate smooth muscle and glandular secretion. In thebrain, these peptides are believed to play a role in homeostasis, thermoregulation and metabolism, and have been reported to elicit analgesia andexcessive grooming, together with central regulation of a variety ofperipheral effects.Mammalian bombesins are encoded by 2 genes. The preproGRP gene transcriptencodes a precursor of 147 amino acids, which gives GRP and GRP18-27. ThepreproNMB gene transcript encodes a precursor of 117 amino acids, which ismetabolised to neuromedin B. Receptors for these peptides have widespreaddistribution in peripheral tissue. High levels are found in smooth muscleand in the brain.The neuromedin B receptor has been characterised in rat oesophagus and raturinary bladder. It is widespread in the CNS, and is found in highlevels in olfactory nucleus and thalamic regions, and in lower levels inthe frontal cortex, dendate gyrus, amygdala and dorsal raphe. Thereceptor activates the phosphoinositide pathway through a pertussis-toxin-insensitive G-protein, probably of the Gq/G11 class. |
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•
•
•
•
•
|
Protein Domain |
Type: |
Family |
Description: |
G protein-coupled receptors (GPCRs) constitute a vast protein family that encompasses a wide range of functions, including various autocrine, paracrine and endocrine processes. They show considerable diversity at the sequence level, on the basis of which they can be separated into distinct groups []. The term clan can be used to describe the GPCRs, as they embrace a group of families for which there are indications of evolutionary relationship, but between which there is no statistically significant similarity in sequence []. The currently known clan members include rhodopsin-like GPCRs (Class A, GPCRA), secretin-like GPCRs (Class B, GPCRB), metabotropic glutamate receptor family (Class C, GPCRC), fungal mating pheromone receptors (Class D, GPCRD), cAMP receptors (Class E, GPCRE) and frizzled/smoothened (Class F, GPCRF) [, , , , ]. GPCRs are major drug targets, and are consequently the subject of considerable research interest. It has been reported that the repertoire of GPCRs for endogenous ligands consists of approximately 400 receptors in humans and mice []. Most GPCRs are identified on the basis of their DNA sequences, rather than the ligand they bind, those that are unmatched to known natural ligands are designated by as orphan GPCRs, or unclassified GPCRs [].The rhodopsin-like GPCRs (GPCRA) represent a widespread protein family that includes hormone, neurotransmitter and light receptors, all of which transduce extracellular signals through interaction with guanine nucleotide-binding (G) proteins. Although their activating ligands vary widely in structure and character, the amino acid sequences of the receptors are very similar and are believed to adopt a common structural framework comprising 7 transmembrane (TM) helices [, , ].Bombesins are peptide neurotransmitters whose biological activity residesin a common C-terminal sequence, WAXGHXM. In the periphery, bombesin-related peptides stimulate smooth muscle and glandular secretion. In thebrain, these peptides are believed to play a role in homeostasis, thermo-regulation and metabolism, and have been reported to elicit analgesia andexcessive grooming, together with central regulation of a variety ofperipheral effects.Mammalian bombesins are encoded by 2 genes. The preproGRP gene transcriptencodes a precursor of 147 amino acids, which gives GRP and GRP18-27. ThepreproNMB gene transcript encodes a precursor of 117 amino acids, which ismetabolised to neuromedin B. Receptors for these peptides have widespreaddistribution in peripheral tissue. High levels are found in smooth muscleand in the brain.The recently-identified BRS-3 bombesin receptor subtype is found in germcells in testis and in uteri of pregnant animals; it is also present in avariety of lung carcinoma cell lines. The receptor is believed to playa role in sperm cell division and maturation. Its action is mediated byassociation with G-proteins that activate a phosphatidylinositol-calciumsecond messenger system. |
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•
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Protein |
Organism: |
Mus musculus/domesticus |
Length: |
384
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
399
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
390
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
179
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
257
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Protein |
Organism: |
Mus musculus/domesticus |
Length: |
390
 |
Fragment?: |
false |
|
•
•
•
•
•
|
Publication |
First Author: |
Birnbaumer L |
Year: |
1990 |
Journal: |
Annu Rev Pharmacol Toxicol |
Title: |
G proteins in signal transduction. |
Volume: |
30 |
|
Pages: |
675-705 |
|
•
•
•
•
•
|
Publication |
First Author: |
Casey PJ |
Year: |
1988 |
Journal: |
J Biol Chem |
Title: |
G protein involvement in receptor-effector coupling. |
Volume: |
263 |
Issue: |
6 |
Pages: |
2577-80 |
|
•
•
•
•
•
|
Publication |
First Author: |
Attwood TK |
Year: |
1993 |
Journal: |
Protein Eng |
Title: |
Design of a discriminating fingerprint for G-protein-coupled receptors. |
Volume: |
6 |
Issue: |
2 |
Pages: |
167-76 |
|
•
•
•
•
•
|
Publication |
First Author: |
Vassilatis DK |
Year: |
2003 |
Journal: |
Proc Natl Acad Sci U S A |
Title: |
The G protein-coupled receptor repertoires of human and mouse. |
Volume: |
100 |
Issue: |
8 |
Pages: |
4903-8 |
|
•
•
•
•
•
|
Publication |
First Author: |
Attwood TK |
Year: |
1994 |
Journal: |
Protein Eng |
Title: |
Fingerprinting G-protein-coupled receptors. |
Volume: |
7 |
Issue: |
2 |
Pages: |
195-203 |
|
•
•
•
•
•
|
Publication |
First Author: |
Kolakowski LF Jr |
Year: |
1994 |
Journal: |
Receptors Channels |
Title: |
GCRDb: a G-protein-coupled receptor database. |
Volume: |
2 |
Issue: |
1 |
Pages: |
1-7 |
|
•
•
•
•
•
|
Publication |
First Author: |
Foord SM |
Year: |
2005 |
Journal: |
Pharmacol Rev |
Title: |
International Union of Pharmacology. XLVI. G protein-coupled receptor list. |
Volume: |
57 |
Issue: |
2 |
Pages: |
279-88 |
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•
•
•
•
|
Publication |
First Author: |
Harmar AJ |
Year: |
2009 |
Journal: |
Nucleic Acids Res |
Title: |
IUPHAR-DB: the IUPHAR database of G protein-coupled receptors and ion channels. |
Volume: |
37 |
Issue: |
Database issue |
Pages: |
D680-5 |
|
•
•
•
•
•
|
Publication |
First Author: |
Bjarnadóttir TK |
Year: |
2006 |
Journal: |
Genomics |
Title: |
Comprehensive repertoire and phylogenetic analysis of the G protein-coupled receptors in human and mouse. |
Volume: |
88 |
Issue: |
3 |
Pages: |
263-73 |
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Publication |
First Author: |
Civelli O |
Year: |
2013 |
Journal: |
Annu Rev Pharmacol Toxicol |
Title: |
G protein-coupled receptor deorphanizations. |
Volume: |
53 |
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Pages: |
127-46 |
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