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1 to 25 of 32  Show
  1. 1
    "Cloning and characterization of multiple human genes and cDNAs encoding highly related type II keratin 6 isoforms."
    Takahashi K., Paladini R.D., Coulombe P.A.
    J. Biol. Chem. 270:18581-18592(1995) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA], VARIANTS ASN-227 AND ILE-481.
    Category: Sequences.
    Tissue: Skin.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 2 other entries.

  2. 2
    "The finished DNA sequence of human chromosome 12."
    Scherer S.E., Muzny D.M., Buhay C.J., Chen R., Cree A., Ding Y., Dugan-Rocha S., Gill R., Gunaratne P., Harris R.A., Hawes A.C., Hernandez J., Hodgson A.V., Hume J., Jackson A., Khan Z.M., Kovar-Smith C., Lewis L.R.
    , Lozado R.J., Metzker M.L., Milosavljevic A., Miner G.R., Montgomery K.T., Morgan M.B., Nazareth L.V., Scott G., Sodergren E., Song X.-Z., Steffen D., Lovering R.C., Wheeler D.A., Worley K.C., Yuan Y., Zhang Z., Adams C.Q., Ansari-Lari M.A., Ayele M., Brown M.J., Chen G., Chen Z., Clerc-Blankenburg K.P., Davis C., Delgado O., Dinh H.H., Draper H., Gonzalez-Garay M.L., Havlak P., Jackson L.R., Jacob L.S., Kelly S.H., Li L., Li Z., Liu J., Liu W., Lu J., Maheshwari M., Nguyen B.-V., Okwuonu G.O., Pasternak S., Perez L.M., Plopper F.J.H., Santibanez J., Shen H., Tabor P.E., Verduzco D., Waldron L., Wang Q., Williams G.A., Zhang J., Zhou J., Allen C.C., Amin A.G., Anyalebechi V., Bailey M., Barbaria J.A., Bimage K.E., Bryant N.P., Burch P.E., Burkett C.E., Burrell K.L., Calderon E., Cardenas V., Carter K., Casias K., Cavazos I., Cavazos S.R., Ceasar H., Chacko J., Chan S.N., Chavez D., Christopoulos C., Chu J., Cockrell R., Cox C.D., Dang M., Dathorne S.R., David R., Davis C.M., Davy-Carroll L., Deshazo D.R., Donlin J.E., D'Souza L., Eaves K.A., Egan A., Emery-Cohen A.J., Escotto M., Flagg N., Forbes L.D., Gabisi A.M., Garza M., Hamilton C., Henderson N., Hernandez O., Hines S., Hogues M.E., Huang M., Idlebird D.G., Johnson R., Jolivet A., Jones S., Kagan R., King L.M., Leal B., Lebow H., Lee S., LeVan J.M., Lewis L.C., London P., Lorensuhewa L.M., Loulseged H., Lovett D.A., Lucier A., Lucier R.L., Ma J., Madu R.C., Mapua P., Martindale A.D., Martinez E., Massey E., Mawhiney S., Meador M.G., Mendez S., Mercado C., Mercado I.C., Merritt C.E., Miner Z.L., Minja E., Mitchell T., Mohabbat F., Mohabbat K., Montgomery B., Moore N., Morris S., Munidasa M., Ngo R.N., Nguyen N.B., Nickerson E., Nwaokelemeh O.O., Nwokenkwo S., Obregon M., Oguh M., Oragunye N., Oviedo R.J., Parish B.J., Parker D.N., Parrish J., Parks K.L., Paul H.A., Payton B.A., Perez A., Perrin W., Pickens A., Primus E.L., Pu L.-L., Puazo M., Quiles M.M., Quiroz J.B., Rabata D., Reeves K., Ruiz S.J., Shao H., Sisson I., Sonaike T., Sorelle R.P., Sutton A.E., Svatek A.F., Svetz L.A., Tamerisa K.S., Taylor T.R., Teague B., Thomas N., Thorn R.D., Trejos Z.Y., Trevino B.K., Ukegbu O.N., Urban J.B., Vasquez L.I., Vera V.A., Villasana D.M., Wang L., Ward-Moore S., Warren J.T., Wei X., White F., Williamson A.L., Wleczyk R., Wooden H.S., Wooden S.H., Yen J., Yoon L., Yoon V., Zorrilla S.E., Nelson D., Kucherlapati R., Weinstock G., Gibbs R.A.
    Nature 440:346-351(2006) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
    Category: Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 3853 other entries.

  3. 3
    "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
    The MGC Project Team
    Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
    Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT GLN-182.
    Category: Sequences.
    Tissue: Skin.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 50494 other entries.

  4. 4
    Bienvenut W.V., Vousden K.H., Lukashchuk N.
    Submitted (MAR-2008) to UniProtKB
    Cited for: PROTEIN SEQUENCE OF 2-9; 16-24; 31-40; 43-86; 169-189; 195-204; 208-222; 224-369; 376-386; 425-436; 456-475 AND 534-550, CLEAVAGE OF INITIATOR METHIONINE, ACETYLATION AT ALA-2, IDENTIFICATION BY MASS SPECTROMETRY.
    Category: PTM / Processing, Sequences.
    Tissue: Lung carcinoma.
    Source: UniProtKB/Swiss-Prot (reviewed).
  5. 5
    "Genes for intermediate filament proteins and the draft sequence of the human genome: novel keratin genes and a surprisingly high number of pseudogenes related to keratin genes 8 and 18."
    Hesse M., Magin T.M., Weber K.
    J. Cell Sci. 114:2569-2575(2001) [PubMed] [Europe PMC] [Abstract]
    Cited for: IDENTIFICATION.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 4 other entries.

  6. 6
    "Phosphorylation of human keratin 8 in vivo at conserved head domain serine 23 and at epidermal growth factor-stimulated tail domain serine 431."
    Ku N.-O., Omary M.B.
    J. Biol. Chem. 272:7556-7564(1997) [PubMed] [Europe PMC] [Abstract]
    Cited for: PHOSPHORYLATION AT SER-60.
    Category: PTM / Processing.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is cited by 1 other entry.

  7. 7
    Cited for: INVOLVEMENT IN PPKNEFD, VARIANT PPKNEFD ASN-172 DEL.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 1 other entry.

  8. 8
    Cited for: INVOLVEMENT IN PPKNEFD, VARIANT PPKNEFD LYS-472.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).
  9. 9
    "Collapse of the keratin filament network through the expression of mutant keratin 6c observed in a case of focal plantar keratoderma."
    Kubo A., Oura Y., Hirano T., Aoyama Y., Sato S., Nakamura K., Takae Y., Amagai M.
    J. Dermatol. 40:553-557(2013) [PubMed] [Europe PMC] [Abstract]
    Cited for: VARIANT PPKNEFD LYS-472, CHARACTERIZATION OF VARIANT PPKNEFD LYS-472.
    Category: Pathology & Biotech, Sequences.
    Source: UniProtKB/Swiss-Prot (reviewed).

    This publication is mapped to 1 other entry.

  10. 10
    "Use of immunohistochemical markers can refine prognosis in triple negative breast cancer."
    Tischkowitz M., Brunet J.S., Begin L.R., Huntsman D.G., Cheang M.C., Akslen L.A., Nielsen T.O., Foulkes W.D.
    BMC Cancer 7:134-134(2007) [PubMed] [Europe PMC] [Abstract]
    Annotation: CK5/6 and/or EGFR expressing tumor types have a persistently poorer prognosis over the longer term.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 52 other entries.

  11. 11
    Annotation: Four new missense and five known mutations in K6a one new deletion and three previously identified missense mutations in K16 plus one known mutation in K17 are reported in pachyonychia congenita.Imported.
    Source: GeneRIF:3853.

    This publication is cited by 2 and mapped to 9 other entries.

  12. 12
    "Mutations of KRT6A are more frequent than those of KRT16 in pachyonychia congenita type 1: report of a novel and a recently reported mutation in two unrelated Chinese families."
    Bai Z.L., Feng Y.G., Tan S.S., Wang X.Y., Xiao S.X., Wang H., Jia H.Q., Wu J.W., He D.L., Kang R.H.
    Br. J. Dermatol. 159:238-240(2008) [PubMed] [Europe PMC] [Abstract]
    Annotation: PC-1 is due to mutations of the KRT16 gene or its expression partner KRT6A wheres PC-2 is caused by mutations in the KRT17 or KRT6B genes.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 8 other entries.

  13. 13
    "Novel and recurrent keratin 6A (KRT6A) mutations in Chinese patients with pachyonychia congenita type 1."
    Lv Y.M., Yang S., Zhang Z., Cui Y., Quan C., Zhou F.S., Fang Q.Y., Du W.H., Zhang F.R., Chang J.M., Tao X.P., Zhang A.L., Kang R.H., Du W.D., Zhang X.J.
    Br. J. Dermatol. 160:1327-1329(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Three novel and four recurrent keratin 6A (KRT6A) mutations were found in Chinese patients with pachyonychia congenita type 1Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 6 other entries.

  14. 14
    "Rapamycin selectively inhibits expression of an inducible keratin (K6a) in human keratinocytes and improves symptoms in pachyonychia congenita patients."
    Hickerson R.P., Leake D., Pho L.N., Leachman S.A., Kaspar R.L.
    J. Dermatol. Sci. 56:82-88(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Rapamycin selectively inhibits expression of an inducible keratin (K6a) in human keratinocytes and improves symptoms in pachyonychia congenita patients.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 7 other entries.

  15. 15
    "Prediction of local recurrence, distant metastases, and death after breast-conserving therapy in early-stage invasive breast cancer using a five-biomarker panel."
    Millar E.K., Graham P.H., O'Toole S.A., McNeil C.M., Browne L., Morey A.L., Eggleton S., Beretov J., Theocharous C., Capp A., Nasser E., Kearsley J.H., Delaney G., Papadatos G., Fox C., Sutherland R.L.
    J. Clin. Oncol. 27:4701-4708(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Studies show that the intrinsic molecular signature of five markers ER PR HER-2 CK 5/6 and EGFR demonstrated specificity of 100% and sensitivity of 75% compared with classification by gene expression profiling.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 142 other entries.

  16. 16
    "[Two mutations of the KRT6A gene in Chinese patients with pachyonychia congenita type I]."
    Bai Z.L., Feng Y.G., Tan S.S., Kang R.H., Wang X.Y., He D.L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 26:514-517(2009) [PubMed] [Europe PMC] [Abstract]
    Annotation: Mutations Y465H and N171D of the KRT16A gene were detected in the sporadic pachyonychia congenita cases.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 7 other entries.

  17. 17
    "Identification of DeltaNp63alpha protein interactions by mass spectrometry."
    Amoresano A., Di Costanzo A., Leo G., Di Cunto F., La Mantia G., Guerrini L., Calabro V.
    J. Proteome Res. 9:2042-2048(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:P48668.

    This publication is mapped to 47 other entries.

  18. 18
    "[The 521 T--> C mutation in the keratin 6A gene in a pedigree with pachyonychia congenita type I]."
    Yang L., Li M., Lai M., Ni J.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi 27:66-68(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: The mutation of 521T--> C in the K6A gene is the causing mutation in pachyonychia congenita type I.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 7 other entries.

  19. 19
    "Aberrant heterodimerization of keratin 16 with keratin 6A in HaCaT keratinocytes results in diminished cellular migration."
    Trost A., Desch P., Wally V., Haim M., Maier R.H., Reitsamer H.A., Hintner H., Bauer J.W., Onder K.
    Mech. Ageing Dev. 131:346-353(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: these data highlight the possibility of a physiological role for K6/K16 heterodimers in keratinocyte cell migration in addition to the heterodimer's known functions in cell differentiation and mechanical resilience.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 9 other entries.

  20. 20
    "[Keratin k6c mutations in focal palmoplantar keratoderma]."
    Dereure O.
    Ann Dermatol Venereol 137:423-424(2010) [PubMed] [Europe PMC] [Abstract]
    Annotation: Focal palmoplantar keratoderma is associated with mutations in keratin K6c in 3 families. 2 unrelated families have Asn172 del and the other has a deletion of AA 462-470. Review.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 7 other entries.

  21. 21
    "Network organization of the human autophagy system."
    Behrends C., Sowa M.E., Gygi S.P., Harper J.W.
    Nature 466:68-76(2010) [PubMed] [Europe PMC] [Abstract]
    Category: Interaction.
    Source: IntAct:P48668.

    This publication is cited by 6 and mapped to 1204 other entries.

  22. 22
    "Pachyonychia congenita with laryngeal obstruction."
    Haber R.M., Drummond D.
    Pediatr Dermatol 28:429-432(2011) [PubMed] [Europe PMC] [Abstract]
    Annotation: This report is the first case of pachyonychia congenita with laryngeal obstruction in which the gene mutation has been established (a deletional mutation in keratin 6a).Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 7 other entries.

  23. 23
    "Pachyonychia congenita patients with mutations in KRT6A have more extensive disease compared with patients who have mutations in KRT16."
    Spaunhurst K.M., Hogendorf A.M., Smith F.J., Lingala B., Schwartz M.E., Cywinska-Bernas A., Zeman K.J., Tang J.Y.
    Br. J. Dermatol. 166:875-878(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: Phenotypic differences exist between KRT6A and KRT16 mutations support adoption of a new classification system.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 9 other entries.

  24. 24
    "A review of the clinical phenotype of 254 patients with genetically confirmed pachyonychia congenita."
    Eliason M.J., Leachman S.A., Feng B.J., Schwartz M.E., Hansen C.D.
    J. Am. Acad. Dermatol. 67:680-686(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: We observed a higher likelihood of oral leukokeratosis in individuals harboring KRT6A mutations.Imported.
    Source: GeneRIF:3853.

    This publication is mapped to 14 other entries.

  25. 25
    "Two novel de novo mutations of KRT6A and KRT16 genes in two Chinese pachyonychia congenita pedigrees with fissured tongue or diffuse plantar keratoderma."
    Du Z.F., Xu C.M., Zhao Y., Liu W.T., Chen X.L., Chen C.Y., Fang H., Ke H.P., Zhang X.N.
    Eur. J. Dermatol. 22:476-480(2012) [PubMed] [Europe PMC] [Abstract]
    Annotation: Genotype-phenotype correlations among PC patients with codon-125 mutation in KRT16 were established while the phenotypes caused by the IVS8-2A>C mutation in KRT6A need further studies to confirm the rare feature of fissured tongueImported.
    Source: GeneRIF:3853.

    This publication is cited by 1 and mapped to 7 other entries.

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