Paper · 7723741

Divergent structural requirements exist for calcitonin receptor binding specificity and adenylate cyclase activation.

Houssami S and 9 others. Mol Pharmacol, 1995. Cited by 42 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Divergent structural requirements exist for calcitonin receptor binding specificity and adenylate cyclase activation. Papers, record 7723741. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/7723741

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title: Divergent structural requirements exist for calcitonin receptor binding specificity and adenylate cyclase activation.; PubMed
Journal: Mol Pharmacol; PubMed
Year: 1995; PubMed
Publication types: Journal Article, Research Support, Non-U.S. Gov't; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/7723741/; PubMed
The journal: https://conductscience.org/library/journal-index/0035623; PubMed
Citations, by iCite: 42; iCite
Relative citation ratio, by iCite: 1.22; iCite
Revised in PubMed: 2015-11-19; PubMed

Authors10

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

Order	Author	Forename
1	Houssami S	S
2	Findlay DM	D M
3	Brady CL	C L
4	Martin TJ	T J
5	Epand RM	R M
6	Moore EE	E E
7	Murayama E	E
8	Tamura T	T
9	Orlowski RC	R C
10	Sexton PM	P M

Source PubMed

Topics13

NLM's MeSH indexing of the paper, its major topics first.

MeSH term	Major
Adenylyl Cyclases	Major topic
Calcitonin	Major topic
Receptors, Calcitonin	Major topic
Amino Acid Sequence
Animals
Binding, Competitive
Cells, Cultured
Cyclic AMP
Enzyme Activation
Humans
Molecular Sequence Data
Sensitivity and Specificity
Structure-Activity Relationship

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References0

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

None in this release.

Cited by7

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 42 citations.

PMID	Title	Journal	Year	In Papers	Source
32,219,215	The Molecular Control of Calcitonin Receptor Signaling.	ACS Pharmacol Transl Sci	2019	https://conductscience.org/library/papers/32219215	PubMed
28,437,792	Phase-plate cryo-EM structure of a class B GPCR-G-protein complex.	Nature	2017	https://conductscience.org/library/papers/28437792	PubMed
24,643,196	Prolonged calcitonin receptor signaling by salmon, but not human calcitonin, reveals ligand bias.	PLoS One	2014	https://conductscience.org/library/papers/24643196	PubMed
21,864,311	Lifting the lid on GPCRs: the role of extracellular loops.	Br J Pharmacol	2012	https://conductscience.org/library/papers/21864311	PubMed
21,649,645	Calcitonin and calcitonin receptor-like receptors: common themes with family B GPCRs?	Br J Pharmacol	2012	https://conductscience.org/library/papers/21649645	PubMed
17,906,370	A synthetic peptide derived from mouse pituitary calcitonin cDNA sequence exhibits potent inhibition of prolactin secretion and prolactin mRNA abundance in primary mouse pituitary cells.	Endocrine	2007	https://conductscience.org/library/papers/17906370	PubMed
17,109,213	Aqueous-soluble, non-reversible lipid conjugate of salmon calcitonin: synthesis, characterization and in vivo activity.	Pharm Res	2007	https://conductscience.org/library/papers/17109213	PubMed

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

Gene	NCBI Gene ID	Linked by	In Genes
CALCR	799	PubTator's text mining	https://conductscience.org/library/genes/799

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed: 2026-11-06; PubMed
iCite: 2026-11-05; iCite
PMC's ID file: 2026-11-05; PMC's ID file
NIH RePORTER's grant and paper links: 2026-11-01; NIH RePORTER's grant and paper links
Trials: 2026-11-12
Gene search: 2026-11-11
Pipelines: 2026-09-18

Sources 11

ChEMBL, through Open TargetsCC BY-SA 3.0
ClinicalTrials.govNo license stated
HGNCCC0
iCiteCC BY 4.0
NCBI GenePublic domain (US government)
NIH RePORTER's grant and paper linksPublic domain
Open TargetsCC0 1.0
PMC's ID filePublic domain (US government)
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0

Each source's terms

ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
ClinicalTrials.govnone stated
HGNCCC0: https://www.genenames.org/about/license/
iCiteCC BY 4.0
NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
PubMedNLM's terms
PubTator 3Public domain
UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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