케라틴 14 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "케라틴 14" in Korean language version.

refsWebsite

Global rank Korean rank

8nih.gov

4^th place

5doi.org

2^nd place

3^rd place

3semanticscholar.org

11^th place

310^th place

2ensembl.org

1,626^th place

501^st place

1zenodo.org

621^st place

732^nd place

doi.org

dx.doi.org

Hanukoglu I, Fuchs E (November 1982). “The cDNA sequence of a human epidermal keratin: divergence of sequence but conservation of structure among intermediate filament proteins”. 《Cell》 31 (1): 243–52. doi:10.1016/0092-8674(82)90424-X. PMID 6186381. S2CID 35796315.
Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E (September 1991). “Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses”. 《Cell》 66 (6): 1301–11. doi:10.1016/0092-8674(91)90051-Y. PMID 1717157. S2CID 11965913.
Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, 외. (July 2006). “New consensus nomenclature for mammalian keratins”. 《The Journal of Cell Biology》 174 (2): 169–74. doi:10.1083/jcb.200603161. PMC 2064177. PMID 16831889.
Bardhan A, Bruckner-Tuderman L, Chapple IL, Fine JD, Harper N, Has C, 외. (September 2020). “Epidermolysis bullosa”. 《Nature Reviews. Disease Primers》 6 (1): 78. doi:10.1038/s41572-020-0210-0. PMID 32973163. S2CID 221861310.
Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, 외. (October 2006). “Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14”. 《American Journal of Human Genetics》 79 (4): 724–30. doi:10.1086/507792. PMC 1592572. PMID 16960809.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000186847 - 앙상블, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000045545 - 앙상블, May 2017

nih.gov

ncbi.nlm.nih.gov

“Human PubMed Reference:”. 《National Center for Biotechnology Information, U.S. National Library of Medicine》.
“Mouse PubMed Reference:”. 《National Center for Biotechnology Information, U.S. National Library of Medicine》.
Hanukoglu I, Fuchs E (November 1982). “The cDNA sequence of a human epidermal keratin: divergence of sequence but conservation of structure among intermediate filament proteins”. 《Cell》 31 (1): 243–52. doi:10.1016/0092-8674(82)90424-X. PMID 6186381. S2CID 35796315.
Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E (September 1991). “Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses”. 《Cell》 66 (6): 1301–11. doi:10.1016/0092-8674(91)90051-Y. PMID 1717157. S2CID 11965913.
Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, 외. (July 2006). “New consensus nomenclature for mammalian keratins”. 《The Journal of Cell Biology》 174 (2): 169–74. doi:10.1083/jcb.200603161. PMC 2064177. PMID 16831889.
“Entrez Gene: KRT14 keratin 14 (epidermolysis bullosa simplex, Dowling-Meara, Koebner)”.
Bardhan A, Bruckner-Tuderman L, Chapple IL, Fine JD, Harper N, Has C, 외. (September 2020). “Epidermolysis bullosa”. 《Nature Reviews. Disease Primers》 6 (1): 78. doi:10.1038/s41572-020-0210-0. PMID 32973163. S2CID 221861310.
Lugassy J, Itin P, Ishida-Yamamoto A, Holland K, Huson S, Geiger D, 외. (October 2006). “Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: two allelic ectodermal dysplasias caused by dominant mutations in KRT14”. 《American Journal of Human Genetics》 79 (4): 724–30. doi:10.1086/507792. PMC 1592572. PMID 16960809.

semanticscholar.org

api.semanticscholar.org

Hanukoglu I, Fuchs E (November 1982). “The cDNA sequence of a human epidermal keratin: divergence of sequence but conservation of structure among intermediate filament proteins”. 《Cell》 31 (1): 243–52. doi:10.1016/0092-8674(82)90424-X. PMID 6186381. S2CID 35796315.
Coulombe PA, Hutton ME, Letai A, Hebert A, Paller AS, Fuchs E (September 1991). “Point mutations in human keratin 14 genes of epidermolysis bullosa simplex patients: genetic and functional analyses”. 《Cell》 66 (6): 1301–11. doi:10.1016/0092-8674(91)90051-Y. PMID 1717157. S2CID 11965913.
Bardhan A, Bruckner-Tuderman L, Chapple IL, Fine JD, Harper N, Has C, 외. (September 2020). “Epidermolysis bullosa”. 《Nature Reviews. Disease Primers》 6 (1): 78. doi:10.1038/s41572-020-0210-0. PMID 32973163. S2CID 221861310.

zenodo.org

Hanukoglu I, Fuchs E (November 1982). “The cDNA sequence of a human epidermal keratin: divergence of sequence but conservation of structure among intermediate filament proteins”. 《Cell》 31 (1): 243–52. doi:10.1016/0092-8674(82)90424-X. PMID 6186381. S2CID 35796315.