Evidence map›Paper›PMID 40765230›Full record

ArticleJournal of veterinary science2025

PCR-based detection of hereditary mutations in

Mingue Kang, Byeongyong Ahn, Jaeyeol Shin, Chankyu Park

Abstract read
In one paragraph

Article in Journal of veterinary science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Mingue KangDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea.ORCID https://orcid.org/0000-0001-8564-9455
Byeongyong AhnDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea.ORCID https://orcid.org/0000-0001-5933-7028
Jaeyeol ShinDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea.ORCID https://orcid.org/0009-0008-4307-5770
Chankyu ParkDepartment of Stem Cell and Regenerative Biotechnology, Konkuk University, Seoul 05029, Korea. chankyu@konkuk.ac.kr.ORCID https://orcid.org/0000-0003-4855-2210

Funding

Konkuk UniversityRural Development Administration PJ01456801
6 · The paper itself

Abstract

importanceUnderstanding the susceptibility of native Korean dogs to genetic diseases is important for animal welfare and breeding. However, little is known regarding the segregation of genetic variations associated with genetic diseases among native Korean dog breeds, highlighting the need for further research in this area.

objectiveA genome-wide analysis was conducted using the available whole genome sequencing (WGS) results of DongGyeongi, Sapsaree, and Jindo dogs to evaluate the presence of disease-associated mutations and develop polymerase chain reaction (PCR)-based typing methods.

methodsUsing WGS data from 32 individuals of DongGyeongi, Sapsaree, and Jindo dogs, variant calling was used to identify variants associated with canine genetic diseases in Online Mendelian Inheritance in Animals. Additionally, allele-specific PCR-based typing methods for the identified mutations were developed.

resultsFour different variants were identified: NC_006583.3:g.54192143C>G in the CONCLUSIONS AND RELEVANCE: Genome-wide analysis was conducted to identify the causative mutations of genetic diseases in native Korean dogs. The observed frequencies of the identified variants differed among native Korean dog breeds. The typing methods used to detect variant alleles in this study will contribute to improving the genetic robustness of native Korean dog breeds.

Indexed as

Dog DiseasesGlucose Transport Proteins, FacilitativePolymerase Chain ReactionAnimalsDogsFemaleGenetic Predisposition to DiseaseMaleMutationRepublic of KoreaWhole Genome SequencingGlucose Transport Proteins, Facilitativeallele-specific PCRDog genomegenetic diseasesmutationswhole genome sequencing

Identifiers

PMID40765230
PMCPMC12329054

What Socratic holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.