Dedicator of cytokinesis protein 8 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Dedicator of cytokinesis protein 8" in English language version.

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11nih.gov

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6doi.org

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2ensembl.org

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2semanticscholar.org

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1harvard.edu

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1web.archive.org

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doi.org

Ruusala A, Aspenström P (August 2004). "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology". FEBS Lett. 572 (1–3): 159–66. Bibcode:2004FEBSL.572..159R. doi:10.1016/j.febslet.2004.06.095. PMID 15304341. S2CID 9107914.
Lu M, Ravichandran KS (2006). "Dock180–ELMO Cooperation in Rac Activation". Regulators and Effectors of Small GTPases: Rho Family. Methods in Enzymology. Vol. 406. pp. 388–402. doi:10.1016/S0076-6879(06)06028-9. ISBN 9780121828110. PMID 16472672.
Takahashi K, Kohno T, Ajima R, Sasaki H, Minna JD, Fujiwara T, Tanaka N, Yokota J (February 2006). "Homozygous deletion and reduced expression of the DOCK8 gene in human lung cancer". Int. J. Oncol. 28 (2): 321–8. doi:10.3892/ijo.28.2.321. PMID 16391785.
Idbaih A, Carvalho Silva R, Crinière E, Marie Y, Carpentier C, Boisselier B, Taillibert S, Rousseau A, Mokhtari K, Ducray F, Thillet J, Sanson M, Hoang-Xuan K, Delattre JY (July 2008). "Genomic changes in progression of low-grade gliomas". J. Neurooncol. 90 (2): 133–40. doi:10.1007/s11060-008-9644-z. PMID 18618226. S2CID 20747824.
Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, Bergmann M, Davis J, Belohradsky BH, Grimbacher B (2004). "Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity". J. Pediatr. 144 (1): 93–9. doi:10.1016/S0022-3476(03)00449-9. PMID 14722525.
Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined immunodeficiency associated with DOCK8 mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401.
- "Scientists Identify Genetic Cause of Previously Undefined Primary Immune Deficiency Disease". National Institutes of Health (Press release). September 24, 2009. Archived from the original on 2009-09-26.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000107099 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000052085 – Ensembl, May 2017

harvard.edu

ui.adsabs.harvard.edu

Ruusala A, Aspenström P (August 2004). "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology". FEBS Lett. 572 (1–3): 159–66. Bibcode:2004FEBSL.572..159R. doi:10.1016/j.febslet.2004.06.095. PMID 15304341. S2CID 9107914.

nih.gov

pubmed.ncbi.nlm.nih.gov

Ruusala A, Aspenström P (August 2004). "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology". FEBS Lett. 572 (1–3): 159–66. Bibcode:2004FEBSL.572..159R. doi:10.1016/j.febslet.2004.06.095. PMID 15304341. S2CID 9107914.
Lu M, Ravichandran KS (2006). "Dock180–ELMO Cooperation in Rac Activation". Regulators and Effectors of Small GTPases: Rho Family. Methods in Enzymology. Vol. 406. pp. 388–402. doi:10.1016/S0076-6879(06)06028-9. ISBN 9780121828110. PMID 16472672.
Takahashi K, Kohno T, Ajima R, Sasaki H, Minna JD, Fujiwara T, Tanaka N, Yokota J (February 2006). "Homozygous deletion and reduced expression of the DOCK8 gene in human lung cancer". Int. J. Oncol. 28 (2): 321–8. doi:10.3892/ijo.28.2.321. PMID 16391785.
Idbaih A, Carvalho Silva R, Crinière E, Marie Y, Carpentier C, Boisselier B, Taillibert S, Rousseau A, Mokhtari K, Ducray F, Thillet J, Sanson M, Hoang-Xuan K, Delattre JY (July 2008). "Genomic changes in progression of low-grade gliomas". J. Neurooncol. 90 (2): 133–40. doi:10.1007/s11060-008-9644-z. PMID 18618226. S2CID 20747824.
Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, Bergmann M, Davis J, Belohradsky BH, Grimbacher B (2004). "Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity". J. Pediatr. 144 (1): 93–9. doi:10.1016/S0022-3476(03)00449-9. PMID 14722525.
Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined immunodeficiency associated with DOCK8 mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401.
- "Scientists Identify Genetic Cause of Previously Undefined Primary Immune Deficiency Disease". National Institutes of Health (Press release). September 24, 2009. Archived from the original on 2009-09-26.
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.
- "Entrez Gene: DOCK8 dedicator of cytokinesis 8".
- Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined immunodeficiency associated with DOCK8 mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401.
  - "Scientists Identify Genetic Cause of Previously Undefined Primary Immune Deficiency Disease". National Institutes of Health (Press release). September 24, 2009. Archived from the original on 2009-09-26.
  nih.gov
  - Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined immunodeficiency associated with DOCK8 mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401.
    - "Scientists Identify Genetic Cause of Previously Undefined Primary Immune Deficiency Disease". National Institutes of Health (Press release). September 24, 2009. Archived from the original on 2009-09-26.

semanticscholar.org

api.semanticscholar.org

Ruusala A, Aspenström P (August 2004). "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology". FEBS Lett. 572 (1–3): 159–66. Bibcode:2004FEBSL.572..159R. doi:10.1016/j.febslet.2004.06.095. PMID 15304341. S2CID 9107914.
Idbaih A, Carvalho Silva R, Crinière E, Marie Y, Carpentier C, Boisselier B, Taillibert S, Rousseau A, Mokhtari K, Ducray F, Thillet J, Sanson M, Hoang-Xuan K, Delattre JY (July 2008). "Genomic changes in progression of low-grade gliomas". J. Neurooncol. 90 (2): 133–40. doi:10.1007/s11060-008-9644-z. PMID 18618226. S2CID 20747824.

web.archive.org

Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined immunodeficiency associated with DOCK8 mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401.
- "Scientists Identify Genetic Cause of Previously Undefined Primary Immune Deficiency Disease". National Institutes of Health (Press release). September 24, 2009. Archived from the original on 2009-09-26.