QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice
We reported earlier that the endocochlear potential (EP) differs between C57BL/6J (B6) and BALB/cJ (BALB) mice, being lower in BALBs by about 10 mV (Ohlemiller et al. Hear Res 220: 10–26, 2006). This difference corresponds to strain differences with respect to the density of marginal cells in cochle...
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description | We reported earlier that the endocochlear potential (EP) differs between C57BL/6J (B6) and BALB/cJ (BALB) mice, being lower in BALBs by about 10 mV (Ohlemiller et al. Hear Res 220: 10–26, 2006). This difference corresponds to strain differences with respect to the density of marginal cells in cochlear stria vascularis. After about 1 year of age, BALB mice also tend toward EP reduction that correlates with further marginal cell loss. We therefore suggested that early
sub-clinical
features of the BALB stria vascularis may predispose these mice to a condition modeling Schuknecht’s strial presbycusis. We further reported (Ohlemiller et al. J Assoc Res Otolaryngol 12: 45–58, 2011) that the acute effects of a 2-h 110 dB SPL noise exposure differ between B6 and BALB mice, such that the EP remains unchanged in B6 mice, but is reduced by 40–50 mV in BALBs. In about 25 % of BALBs, the EP does not completely recover, so that permanent EP reduction may contribute to noise-induced permanent threshold shifts in BALBs. To identify genes and alleles that may promote
natural EP variation
as well as noise-related EP reduction in BALB mice, we have mapped related quantitative trait loci (QTLs) using 12 recombinant inbred (RI) strains formed from B6 and BALB (CxB1–CxB12). EP and strial marginal cell density were measured in B6 mice, BALB mice, their F1 hybrids, and RI mice without noise exposure, and 1–3 h after broadband noise (4–45 kHz, 110 dB SPL, 2 h). For unexposed mice, the strain distribution patterns for EP and marginal cell density were used to generate preliminary QTL maps for both EP and marginal cell density. Six QTL regions were at least statistically suggestive, including a significant QTL for marginal cell density on chromosome 12 that overlapped a weak QTL for EP variation. This region, termed
Maced
(Marginal cell density QTL) supports the notion of marginal cell density as a genetically influenced contributor to natural EP variation. Candidate genes for
Maced
notably include
Foxg1, Foxa1, Akap6, Nkx2-1,
and
Pax9
. Noise exposure produced significant EP reductions in two RI strains as well as significant EP increases in two RI strains. QTL mapping of the EP in noise-exposed RI mice yielded four suggestive regions. Two of these overlapped with QTL regions we previously identified for noise-related EP reduction in CBA/J mice (Ohlemiller et al. Hear Res 260: 47–53, 2010) on chromosomes 5 and 18 (
Nirep
). The present map may narrow the
Nirep
interval to a ~10-Mb |
doi_str_mv | 10.1007/s10162-016-0558-8 |
format | Article |
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sub-clinical
features of the BALB stria vascularis may predispose these mice to a condition modeling Schuknecht’s strial presbycusis. We further reported (Ohlemiller et al. J Assoc Res Otolaryngol 12: 45–58, 2011) that the acute effects of a 2-h 110 dB SPL noise exposure differ between B6 and BALB mice, such that the EP remains unchanged in B6 mice, but is reduced by 40–50 mV in BALBs. In about 25 % of BALBs, the EP does not completely recover, so that permanent EP reduction may contribute to noise-induced permanent threshold shifts in BALBs. To identify genes and alleles that may promote
natural EP variation
as well as noise-related EP reduction in BALB mice, we have mapped related quantitative trait loci (QTLs) using 12 recombinant inbred (RI) strains formed from B6 and BALB (CxB1–CxB12). EP and strial marginal cell density were measured in B6 mice, BALB mice, their F1 hybrids, and RI mice without noise exposure, and 1–3 h after broadband noise (4–45 kHz, 110 dB SPL, 2 h). For unexposed mice, the strain distribution patterns for EP and marginal cell density were used to generate preliminary QTL maps for both EP and marginal cell density. Six QTL regions were at least statistically suggestive, including a significant QTL for marginal cell density on chromosome 12 that overlapped a weak QTL for EP variation. This region, termed
Maced
(Marginal cell density QTL) supports the notion of marginal cell density as a genetically influenced contributor to natural EP variation. Candidate genes for
Maced
notably include
Foxg1, Foxa1, Akap6, Nkx2-1,
and
Pax9
. Noise exposure produced significant EP reductions in two RI strains as well as significant EP increases in two RI strains. QTL mapping of the EP in noise-exposed RI mice yielded four suggestive regions. Two of these overlapped with QTL regions we previously identified for noise-related EP reduction in CBA/J mice (Ohlemiller et al. Hear Res 260: 47–53, 2010) on chromosomes 5 and 18 (
Nirep
). The present map may narrow the
Nirep
interval to a ~10-Mb region of proximal Chr. 18 that includes
Zeb1
,
Arhgap12
,
Mpp7
, and
Gjd4
. This study marks the first exploration of natural gene variants that modulate the EP. Their orthologs may underlie some human hearing loss that originates in the lateral wall.</description><identifier>ISSN: 1525-3961</identifier><identifier>EISSN: 1438-7573</identifier><identifier>DOI: 10.1007/s10162-016-0558-8</identifier><identifier>PMID: 26980469</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Action Potentials ; Animals ; Auditory Threshold ; Cell Count ; Cochlea - physiology ; Medicine ; Medicine & Public Health ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Neurobiology ; Neurosciences ; Noise ; Otorhinolaryngology ; Quantitative Trait Loci ; Research Article ; Species Specificity</subject><ispartof>Journal of the Association for Research in Otolaryngology, 2016-06, Vol.17 (3), p.173-194</ispartof><rights>Association for Research in Otolaryngology 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-58f68eefc99f3b80cf5c51af46a37e92b2fd37a88df967b463cbebbe3d1cc7fd3</citedby><cites>FETCH-LOGICAL-c536t-58f68eefc99f3b80cf5c51af46a37e92b2fd37a88df967b463cbebbe3d1cc7fd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854825/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4854825/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,41464,42533,51294,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26980469$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ohlemiller, Kevin K.</creatorcontrib><creatorcontrib>Kiener, Anna L.</creatorcontrib><creatorcontrib>Gagnon, Patricia M.</creatorcontrib><title>QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice</title><title>Journal of the Association for Research in Otolaryngology</title><addtitle>JARO</addtitle><addtitle>J Assoc Res Otolaryngol</addtitle><description>We reported earlier that the endocochlear potential (EP) differs between C57BL/6J (B6) and BALB/cJ (BALB) mice, being lower in BALBs by about 10 mV (Ohlemiller et al. Hear Res 220: 10–26, 2006). This difference corresponds to strain differences with respect to the density of marginal cells in cochlear stria vascularis. After about 1 year of age, BALB mice also tend toward EP reduction that correlates with further marginal cell loss. We therefore suggested that early
sub-clinical
features of the BALB stria vascularis may predispose these mice to a condition modeling Schuknecht’s strial presbycusis. We further reported (Ohlemiller et al. J Assoc Res Otolaryngol 12: 45–58, 2011) that the acute effects of a 2-h 110 dB SPL noise exposure differ between B6 and BALB mice, such that the EP remains unchanged in B6 mice, but is reduced by 40–50 mV in BALBs. In about 25 % of BALBs, the EP does not completely recover, so that permanent EP reduction may contribute to noise-induced permanent threshold shifts in BALBs. To identify genes and alleles that may promote
natural EP variation
as well as noise-related EP reduction in BALB mice, we have mapped related quantitative trait loci (QTLs) using 12 recombinant inbred (RI) strains formed from B6 and BALB (CxB1–CxB12). EP and strial marginal cell density were measured in B6 mice, BALB mice, their F1 hybrids, and RI mice without noise exposure, and 1–3 h after broadband noise (4–45 kHz, 110 dB SPL, 2 h). For unexposed mice, the strain distribution patterns for EP and marginal cell density were used to generate preliminary QTL maps for both EP and marginal cell density. Six QTL regions were at least statistically suggestive, including a significant QTL for marginal cell density on chromosome 12 that overlapped a weak QTL for EP variation. This region, termed
Maced
(Marginal cell density QTL) supports the notion of marginal cell density as a genetically influenced contributor to natural EP variation. Candidate genes for
Maced
notably include
Foxg1, Foxa1, Akap6, Nkx2-1,
and
Pax9
. Noise exposure produced significant EP reductions in two RI strains as well as significant EP increases in two RI strains. QTL mapping of the EP in noise-exposed RI mice yielded four suggestive regions. Two of these overlapped with QTL regions we previously identified for noise-related EP reduction in CBA/J mice (Ohlemiller et al. Hear Res 260: 47–53, 2010) on chromosomes 5 and 18 (
Nirep
). The present map may narrow the
Nirep
interval to a ~10-Mb region of proximal Chr. 18 that includes
Zeb1
,
Arhgap12
,
Mpp7
, and
Gjd4
. This study marks the first exploration of natural gene variants that modulate the EP. Their orthologs may underlie some human hearing loss that originates in the lateral wall.</description><subject>Action Potentials</subject><subject>Animals</subject><subject>Auditory Threshold</subject><subject>Cell Count</subject><subject>Cochlea - physiology</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred C57BL</subject><subject>Neurobiology</subject><subject>Neurosciences</subject><subject>Noise</subject><subject>Otorhinolaryngology</subject><subject>Quantitative Trait Loci</subject><subject>Research Article</subject><subject>Species Specificity</subject><issn>1525-3961</issn><issn>1438-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kUlvFDEQhS0EIgv8AC7IEhcuzXhpbxekzBCWqBEgwtlyu8uTjnrsid0Dyr_HowlRQOJSLul99Vylh9ALSt5QQtSiUEIla2ppiBC60Y_QMW25bpRQ_HHtBRMNN5IeoZNSrgmhSkjzFB0xaTRppTlG379ddviz227HuMYp4PM4JJ_81QQu469phjiPbsLvxhAgQ_RQcA_zL4CIV0Itu4W8wC4OeHnWLRf-Am9GD8_Qk-CmAs_v3lP04_355epj03358Gl11jVecDk3QgepAYI3JvBeEx-EF9SFVjquwLCehYErp_UQjFR9K7nvoe-BD9R7VbVT9Pbgu931Gxh83TW7yW7zuHH51iY32r-VOF7ZdfppWy1azUQ1eH1nkNPNDspsN2PxME0uQtoVS5VWRCtmdEVf_YNep12O9bw9JVtBNWGVogfK51RKhnC_DCV2H5k9RGZrsfvI7N755cMr7if-ZFQBdgBKleIa8oOv_-v6G3oUoP8</recordid><startdate>20160601</startdate><enddate>20160601</enddate><creator>Ohlemiller, Kevin K.</creator><creator>Kiener, Anna L.</creator><creator>Gagnon, Patricia M.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20160601</creationdate><title>QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice</title><author>Ohlemiller, Kevin K. ; Kiener, Anna L. ; Gagnon, Patricia M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-58f68eefc99f3b80cf5c51af46a37e92b2fd37a88df967b463cbebbe3d1cc7fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Action Potentials</topic><topic>Animals</topic><topic>Auditory Threshold</topic><topic>Cell Count</topic><topic>Cochlea - physiology</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred C57BL</topic><topic>Neurobiology</topic><topic>Neurosciences</topic><topic>Noise</topic><topic>Otorhinolaryngology</topic><topic>Quantitative Trait Loci</topic><topic>Research Article</topic><topic>Species Specificity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ohlemiller, Kevin K.</creatorcontrib><creatorcontrib>Kiener, Anna L.</creatorcontrib><creatorcontrib>Gagnon, Patricia M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of the Association for Research in Otolaryngology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ohlemiller, Kevin K.</au><au>Kiener, Anna L.</au><au>Gagnon, Patricia M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice</atitle><jtitle>Journal of the Association for Research in Otolaryngology</jtitle><stitle>JARO</stitle><addtitle>J Assoc Res Otolaryngol</addtitle><date>2016-06-01</date><risdate>2016</risdate><volume>17</volume><issue>3</issue><spage>173</spage><epage>194</epage><pages>173-194</pages><issn>1525-3961</issn><eissn>1438-7573</eissn><abstract>We reported earlier that the endocochlear potential (EP) differs between C57BL/6J (B6) and BALB/cJ (BALB) mice, being lower in BALBs by about 10 mV (Ohlemiller et al. Hear Res 220: 10–26, 2006). This difference corresponds to strain differences with respect to the density of marginal cells in cochlear stria vascularis. After about 1 year of age, BALB mice also tend toward EP reduction that correlates with further marginal cell loss. We therefore suggested that early
sub-clinical
features of the BALB stria vascularis may predispose these mice to a condition modeling Schuknecht’s strial presbycusis. We further reported (Ohlemiller et al. J Assoc Res Otolaryngol 12: 45–58, 2011) that the acute effects of a 2-h 110 dB SPL noise exposure differ between B6 and BALB mice, such that the EP remains unchanged in B6 mice, but is reduced by 40–50 mV in BALBs. In about 25 % of BALBs, the EP does not completely recover, so that permanent EP reduction may contribute to noise-induced permanent threshold shifts in BALBs. To identify genes and alleles that may promote
natural EP variation
as well as noise-related EP reduction in BALB mice, we have mapped related quantitative trait loci (QTLs) using 12 recombinant inbred (RI) strains formed from B6 and BALB (CxB1–CxB12). EP and strial marginal cell density were measured in B6 mice, BALB mice, their F1 hybrids, and RI mice without noise exposure, and 1–3 h after broadband noise (4–45 kHz, 110 dB SPL, 2 h). For unexposed mice, the strain distribution patterns for EP and marginal cell density were used to generate preliminary QTL maps for both EP and marginal cell density. Six QTL regions were at least statistically suggestive, including a significant QTL for marginal cell density on chromosome 12 that overlapped a weak QTL for EP variation. This region, termed
Maced
(Marginal cell density QTL) supports the notion of marginal cell density as a genetically influenced contributor to natural EP variation. Candidate genes for
Maced
notably include
Foxg1, Foxa1, Akap6, Nkx2-1,
and
Pax9
. Noise exposure produced significant EP reductions in two RI strains as well as significant EP increases in two RI strains. QTL mapping of the EP in noise-exposed RI mice yielded four suggestive regions. Two of these overlapped with QTL regions we previously identified for noise-related EP reduction in CBA/J mice (Ohlemiller et al. Hear Res 260: 47–53, 2010) on chromosomes 5 and 18 (
Nirep
). The present map may narrow the
Nirep
interval to a ~10-Mb region of proximal Chr. 18 that includes
Zeb1
,
Arhgap12
,
Mpp7
, and
Gjd4
. This study marks the first exploration of natural gene variants that modulate the EP. Their orthologs may underlie some human hearing loss that originates in the lateral wall.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>26980469</pmid><doi>10.1007/s10162-016-0558-8</doi><tpages>22</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central; SpringerLink Journals - AutoHoldings |
subjects | Action Potentials Animals Auditory Threshold Cell Count Cochlea - physiology Medicine Medicine & Public Health Mice Mice, Inbred BALB C Mice, Inbred C57BL Neurobiology Neurosciences Noise Otorhinolaryngology Quantitative Trait Loci Research Article Species Specificity |
title | QTL Mapping of Endocochlear Potential Differences between C57BL/6J and BALB/cJ mice |
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