Paper · 8587124

Comparative analysis of Homo sapiens and Mus musculus cyclin-dependent kinase (CDK) inhibitor genes p16 (MTS1) and p15 (MTS2).

Jiang P and 7 others. J Mol Evol, 1995. Cited by 19 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

Cite this record

ConductScience Library. Comparative analysis of Homo sapiens and Mus musculus cyclin-dependent kinase (CDK) inhibitor genes p16 (MTS1) and p15 (MTS2). Papers, record 8587124. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/8587124

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Paper

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

Title: Comparative analysis of Homo sapiens and Mus musculus cyclin-dependent kinase (CDK) inhibitor genes p16 (MTS1) and p15 (MTS2).; PubMed
Journal: J Mol Evol; PubMed
Year: 1995; PubMed
Publication types: Comparative Study, Journal Article; PubMed
PubMed: https://pubmed.ncbi.nlm.nih.gov/8587124/; PubMed
DOI: https://doi.org/10.1007/bf00173159; PubMed
The journal: https://conductscience.org/library/journal-index/0360051; PubMed
Citations, by iCite: 19; iCite
Relative citation ratio, by iCite: 0.4; iCite
Revised in PubMed: 2026-10-10; PubMed

Authors8

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

Order	Author	Forename
1	Jiang P	P
2	Stone S	S
3	Wagner R	R
4	Wang S	S
5	Dayananth P	P
6	Kozak CA	C A
7	Wold B	B
8	Kamb A	A

Source PubMed

Topics18

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

MeSH term	Major
Carrier Proteins	Major topic
Cell Cycle Proteins	Major topic
Hominidae	Major topic
Mice	Major topic
Sequence Alignment	Major topic
Tumor Suppressor Proteins	Major topic
Amino Acid Sequence
Animals
Base Sequence
Conserved Sequence
Cyclin-Dependent Kinase Inhibitor p15
Cyclin-Dependent Kinase Inhibitor p16
Enzyme Inhibitors
Evolution, Molecular
Humans
Molecular Sequence Data
Protein Kinase Inhibitors
Sequence Analysis

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.

References35

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

Order	PMID	Title	Journal	Year	In Papers	Source
1	7,729,683	Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution.	Genes Dev	1995	https://conductscience.org/library/papers/7729683	PubMed
2	8,259,215	A new regulatory motif in cell-cycle control causing specific inhibition of cyclin D/CDK4.	Nature	1993	https://conductscience.org/library/papers/8259215	PubMed
3	6,656,881	A potential donor gene for the bm1 gene conversion event in the C57BL mouse.	Nature	1983	https://conductscience.org/library/papers/6656881	PubMed
4	7,954,786	Joining the complex: cyclin-dependent kinase inhibitory proteins and the cell cycle.	Cell	1994	https://conductscience.org/library/papers/7954786	PubMed
5	7,438,203	Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes.	Cell	1980	https://conductscience.org/library/papers/7438203	PubMed
6	7,739,547	Novel INK4 proteins, p19 and p18, are specific inhibitors of the cyclin D-dependent kinases CDK4 and CDK6.	Mol Cell Biol	1995	https://conductscience.org/library/papers/7739547	PubMed
7	7,937,918	A determination of the frequency of gene conversion in unmanipulated mouse sperm.	Proc Natl Acad Sci U S A	1994	https://conductscience.org/library/papers/7937918	PubMed
8	8,033,212	Cloning of p27Kip1, a cyclin-dependent kinase inhibitor and a potential mediator of extracellular antimitogenic signals.	Cell	1994	https://conductscience.org/library/papers/8033212	PubMed
9	7,651,726	Cloning and characterization of murine p16INK4a and p15INK4b genes.	Oncogene	1995	https://conductscience.org/library/papers/7651726	PubMed
10	7,987,388	Analysis of the p16 gene (CDKN2) as a candidate for the chromosome 9p melanoma susceptibility locus.	Nat Genet	1994	https://conductscience.org/library/papers/7987388	PubMed

1 to 10 of 35

See all 35 references

Cited by3

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 19 citations.

PMID	Title	Journal	Year	In Papers	Source
11,704,876	One INK4 gene and no ARF at the Fugu equivalent of the human INK4A/ARF/INK4B tumour suppressor locus.	Oncogene	2001	https://conductscience.org/library/papers/11704876	PubMed
10,490,845	Comparative structure and characterization of a CDKN2 gene in a Xiphophorus fish melanoma model.	Oncogene	1999	https://conductscience.org/library/papers/10490845	PubMed
9,724,636	The alternative product from the human CDKN2A locus, p14(ARF), participates in a regulatory feedback loop with p53 and MDM2.	EMBO J	1998	https://conductscience.org/library/papers/9724636	PubMed

Genes3

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	Source
CDKN2A	1,029	PubTator's text mining	https://conductscience.org/library/genes/1029	NCBI Gene
CDKN2B	1,030	PubTator's text mining	https://conductscience.org/library/genes/1030	NCBI Gene
TGFB1	7,040	PubTator's text mining	https://conductscience.org/library/genes/7040	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

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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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