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DNAI1
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<h2 id="external-links">External links</h2> <ul><li><a href="https://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gene&part=pcd">GeneReviews/NIH/NCBI/UW entry on Primary Ciliary Dyskinesia</a></li></ul> <h2 id="further-reading">Further reading</h2> <ul><li>Guichard C, Harricane MC, Lafitte JJ, et al. (2001). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1275621">"Axonemal dynein intermediate-chain gene (DNAI1) mutations result in situs inversus and primary ciliary dyskinesia (Kartagener syndrome)"</a>. <i>American Journal of Human Genetics</i>. 68 (4): 1030–1035. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1086%2F319511">10.1086/319511</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1275621">1275621</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11231901">11231901</a>.</li> <li>Zariwala M, Noone PG, Sannuti A, et al. (2002). "Germline mutations in an intermediate chain dynein cause primary ciliary dyskinesia". <i>American Journal of Respiratory Cell and Molecular Biology</i>. 25 (5): 577–583. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1165%2Fajrcmb.25.5.4619">10.1165/ajrcmb.25.5.4619</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11713099">11713099</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:38096706">38096706</a>.</li> <li>Tai CY, Dujardin DL, Faulkner NE, Vallee RB (2002). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173479">"Role of dynein, dynactin, and CLIP-170 interactions in LIS1 kinetochore function"</a>. <i>Journal of Cell Biology</i>. 156 (6): 959–968. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1083%2Fjcb.200109046">10.1083/jcb.200109046</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2173479">2173479</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11889140">11889140</a>.</li> <li>Noone PG, Zariwala M, Sannuti A, et al. (2002). "Mutations in DNAI1 (IC78) cause primary ciliary dyskinesia". <i>Chest</i>. 121 (3 Suppl): 97S. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1378%2Fchest.121.3_suppl.97S">10.1378/chest.121.3_suppl.97S</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11893720">11893720</a>.</li> <li>Strausberg RL, Feingold EA, Grouse LH, et al. (2003). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139241">"Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"</a>. <i>Proceedings of the National Academy of Sciences of the United States of America</i>. 99 (26): 16899–16903. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2002PNAS...9916899M">2002PNAS...9916899M</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1073%2Fpnas.242603899">10.1073/pnas.242603899</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139241">139241</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12477932">12477932</a>.</li> <li>Ficarro S, Chertihin O, Westbrook VA, et al. (2003). <a href="https://doi.org/10.1074%2Fjbc.M202325200">"Phosphoproteome analysis of capacitated human sperm — Evidence of tyrosine phosphorylation of a kinase-anchoring protein 3 and valosin-containing protein/p97 during capacitation"</a>. <i>Journal of Biological Chemistry</i>. 278 (13): 11579–89. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1074%2Fjbc.M202325200">10.1074/jbc.M202325200</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12509440">12509440</a>.</li> <li>Ota T, Suzuki Y, Nishikawa T, et al. (2004). <a href="https://doi.org/10.1038%2Fng1285">"Complete sequencing and characterization of 21,243 full-length human cDNAs"</a>. <i>Nature Genetics</i>. 36 (1): 40–45. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fng1285">10.1038/ng1285</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/14702039">14702039</a>.</li> <li>Humphray SJ, Oliver K, Hunt AR, et al. (2004). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734081">"DNA sequence and analysis of human chromosome 9"</a>. <i>Nature</i>. 429 (6990): 369–374. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2004Natur.429..369H">2004Natur.429..369H</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fnature02465">10.1038/nature02465</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734081">2734081</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/15164053">15164053</a>.</li> <li>Gerhard DS, Wagner L, Feingold EA, et al. (2004). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC528928">"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)"</a>. <i>Genome Research</i>. 14 (10B): 2121–2127. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1101%2Fgr.2596504">10.1101/gr.2596504</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC528928">528928</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/15489334">15489334</a>.</li> <li>Zariwala MA, Leigh MW, Ceppa F, et al. (2006). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648054">"Mutations of DNAI1 in primary ciliary dyskinesia: evidence of founder effect in a common mutation"</a>. <i>American Journal of Respiratory and Critical Care Medicine</i>. 174 (8): 858–866. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1164%2Frccm.200603-370OC">10.1164/rccm.200603-370OC</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648054">2648054</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/16858015">16858015</a>.</li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Pennarun G, Escudier E, Chapelin C, Bridoux AM, Cacheux V, Roger G, Clement A, Goossens M, Amselem S, Duriez B (Jan 2000). "Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesia". American Journal of Human Genetics. 65 (6): 1508–19. doi:10.1086/302683. PMC 1288361. PMID 10577904. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288361" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1288361</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>"Entrez Gene: DNAI1 dynein, axonemal, intermediate chain 1". <a href="https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=27019" target="_blank">https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=27019</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>"Entrez Gene: DNAI1 dynein, axonemal, intermediate chain 1". <a href="https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=27019" target="_blank">https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=27019</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> </ol>