PubMed for id: 934719

Save citations to file

Email citations

Subject: PubMed for id: 934719 - PubMed

To:

From:

Selection:

Format:

MeSH and other data

Add to Collections

Add to My Bibliography

Your saved search

Name of saved search:

Search terms:

38844942,38840068,38833260,38816375,38811176,38811173,38796585,38790272,38790217,38783254,38754567,38735540,38721948,38703433,38701954,38701081,38691531,38674450,38674423,38659011,38640279,38627775,38602877,38594301,38587568,38578409,38563166,38556082,38553020,38552739,38544690,38534090,38528140,38518394,38518393,38515174,38494888,38491289,38477756,38472515,38465704,38459354,38457558,38454288,38437842,38431907,38413848,38413761,38412189,38408254,38407562,38397478,38397168,38382588,38378725,38378678,38378613,38374469,38359484,38355682,38355238,38352994,38351344,38348997,38347443,38342426,38334784,38321214,38311059,38310242,38297851,38297848,38297847,38297846,38297845,38297844,38297842,38296632,38296324,38295749,38291196,38289678,38282009,38280389,38278860,38278051,38274408,38267829,38267463,38266052,38254937,38254107,38253033,38243601,38242899,38231444,38221796,38218275,38218018,38197511,38194445,38194286,38191017,38189974,38189623,38186349,38186093,38184995,38182057,38172427,38172182,38167558,38167320,38167128,38157301,38149346,38141656,38139438,38135239,38134852,38131025,38129970,38126281,38111038,38110744,38110175,38108361,38104646,38103727,38103445,38102706,38097651,38093297,38086867,38084023,38070832,38069401,38069086,38066485,38062644,38061908,38057991,38056576,38056549,38056117,38054405,38043973,38043112,38042490,38037722,38037112,38029595,38016437,38014592,38011198,38002950,37996878,37990933,37988592,37981655,37977818,37977051,37976835,37974252,37968200,37962101,37952154,37952086,37943620,37935454,37932750,37931151,37930162,37929431,37927186,37924449,37919361,37917582,37916923,37915172,37906143,37905486,37903775,37902276,37895288,37894867,37892203,37891192,37887549,37871882,37864512,37864333,37864300,37859980,37858736,37844444,37837560,37814107,37813209,37801830,37789630,37789629,37786244,37778667,37770806,37759745,37755702,37752530,37738562,37731249,37730229,37715942,37712597,37708136,37697831,37691516,37690683,37686337,37683890,37681746,37679651,37678008,37668839,37660570,37659026,37654703,37646720,37643960,37643955,37642267,37640998,37640596,37640054,37638031,37633739,37628652,37628590,37628577,37625567,37611564,37600721,37597120,37596645,37586294,37584462,37582836,37573175,37563198,37561809,37561579,37561388,37561279,37559350,37558483,37543941,37537240,37537203,37532514,37530213,37528592,37510362,37510254,37506976,37495753,37492931,37479820,37477685,37473993,37468331,37466950,37466410,37463106,37462885,37459161,37450052,37440664,37440024,37438890,37438083,37433570,37422204,37419036,37417821,37401273,37399495,37399346,37399203,37393735,37390746,37386251,37386014,37373495,37373150,37369584,37368868,37368386,37368382,37341837,37337429,37336020,37331337,37328946,37325812,37322474,37315234,37312453,37287646,37279265,37278357,37278166,37277527,37277488,37276687,37273125,37272646,37272645,37271870,37244253,37243350,37240244,37239446,37239361,37237007,37234800,37232061,37231428,37227124,37225965,37225480,37222941,37217689,37211999,37211996,37207672,37199681,37199218,37198144,37189200,37188450,37178259,37173518,37173411,37170787,37167444,37165931,37163979,37160697,37149131,37127645,37126974,37125626,37121229,37121227,37114731,37114263,37108761,37108562,37108470,37107686,37107638,37107589,37107585,37106574,37102300,37101210,37100771,37099947,37099934,37093292,37092661,37088824,37088079,37086676,37086329,37075593,37072551,37071854,37070846,37068843,37068190,37066759,37062854,37062750,37062025,37055579,37052590,37041640,37031186,37027908,37027300,37023310,37022747,37009795,37009772,37002809,36995380,36989619,36984609,36982769,36980924,36980899,36980833,36965335,36964137,36958120,36951427,36948373,36942482,36934406,36933359,36929150,36928321,36927636,36927560,36917610,36914558,36912880,36911992,36882306,36882007,36876911,36871673,36863132,36848084,36843515,36843332,36837553,36835101,36833385,36833263,36825706,36823092,36811727,36810733,36807241,36804529,36803022,36799720,36797591,36795064,36794641,36791536,36785559,36781206,36774923,36764706,36764464,36764426,36764396,36756824,36755494,36755103,36753545,36751702,36750736,36750499,36748654,36748152,36746137,36746056,36745553,36743950,36740137,36736132,36723965,36719978,36719116,36717082,36715725,36708132,36707947,36703504,36702373,36696506,36674868,36672845,36672810,36671423,36656851,36653756,36648576,36646238,36645345,36644884,36635047,36633841,36630074,36617157,36613674,36611846,36598134,36597364,36597107,36593740,36592224,36587182,36576366,36574989,27729144,27644946[uid]

Test search terms

Would you like email updates of new search results?

Email: (change)

Frequency:

Which day?

Report format:

Send at most:

Send even when there aren't any new results

Optional text in email:

Your RSS Feed

Results by year

Year	Number of Results
2016	2
2017	1
2021	1
2022	12
2023	373
2024	167

500 results

Page of 50

Results by year

Page 1

Deciphering potential causative factors for undiagnosed Waardenburg syndrome through multi-data integration.

Sun F, Xiao M, Ji D, Zheng F, Shi T. Sun F, et al. Orphanet J Rare Dis. 2024 Jun 6;19(1):226. doi: 10.1186/s13023-024-03220-y. Orphanet J Rare Dis. 2024. PMID: 38844942 Free PMC article.

Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITT.

Miura H, Nakamura A, Kurosaki A, Kotani A, Motojima M, Tanaka K, Kakuta S, Ogiwara S, Ohmi Y, Komaba H, Schilit SLP, Morton CC, Gurumurthy CB, Ohtsuka M. Miura H, et al. BMC Genomics. 2024 Jun 5;25(1):568. doi: 10.1186/s12864-024-10250-0. BMC Genomics. 2024. PMID: 38840068 Free PMC article.

Self-Reported Functional Vision in USH2A-Associated Retinal Degeneration as Measured by the Michigan Retinal Degeneration Questionnaire.

Parekh B, Duncan JL, Samarakoon L, Melia M, Abalem MF, Andrews CA, Audo I, Ayala AR, Bradley C, Cheetham JK, Dagnelie G, Durham TA, Huckfeldt RM, Lacy GD, Malbin B, Michaelides M, Musch DC, Peck-Dimit N, Stingl K, Weng CY, Zmejkoski AZ, Jayasundera KT; Foundation Fighting Blindness Clinical Consortium Investigator Group. Parekh B, et al. Invest Ophthalmol Vis Sci. 2024 Jun 3;65(6):5. doi: 10.1167/iovs.65.6.5. Invest Ophthalmol Vis Sci. 2024. PMID: 38833260 Free PMC article.

Gene expression signatures in blood from a West African sepsis cohort define host response phenotypes.

Chenoweth JG, Colantuoni C, Striegel DA, Genzor P, Brandsma J, Blair PW, Krishnan S, Chiyka E, Fazli M, Mehta R, Considine M, Cope L, Knight AC, Elayadi A, Fox A, Hertzano R, Letizia AG, Owusu-Ofori A, Boakye I, Aduboffour AA, Ansong D, Biney E, Oduro G, Schully KL, Clark DV. Chenoweth JG, et al. Nat Commun. 2024 May 30;15(1):4606. doi: 10.1038/s41467-024-48821-0. Nat Commun. 2024. PMID: 38816375 Free PMC article.

[The updates of the ACMG variant interpretation guidelines affect the pathogenicity determination of OTOF gene variations in patients with auditory neuropathy].

Wu KL, Li J, Wang HY, Wang QJ. Wu KL, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 May 7;59(5):455-463. doi: 10.3760/cma.j.cn115330-20231129-00254. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024. PMID: 38811176 Chinese.

[Evaluation of the outcomes of cochlear implant in children with auditory neuropathy].

Ren CC, Lin Y, Fan XQ, Liang PF, Zhang XY, Gao ZJ, Zha DJ. Ren CC, et al. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024 May 7;59(5):432-438. doi: 10.3760/cma.j.cn115330-20230913-00089. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2024. PMID: 38811173 Chinese.

A novel homozygous missense variant identified in the myosin VIIA motor domain of a Moroccan patient with usher syndrome.

Ouarhache M, Kettani O, Fizazi KE, Bouguenouch L, Ouldim K. Ouarhache M, et al. Mol Biol Rep. 2024 May 25;51(1):683. doi: 10.1007/s11033-024-09603-5. Mol Biol Rep. 2024. PMID: 38796585

CHD7 Disorder-Not CHARGE Syndrome-Presenting as Isolated Cochleovestibular Dysfunction.

Driesen J, Van Hoecke H, Maes L, Janssens S, Acke F, De Leenheer E. Driesen J, et al. Genes (Basel). 2024 May 19;15(5):643. doi: 10.3390/genes15050643. Genes (Basel). 2024. PMID: 38790272 Free PMC article.

The Segregation of p.Arg68Ter-CLDN14 Mutation in a Syrian Deaf Family, Phenotypic Variations, and Comparative Analysis with the GJB2 Gene.

Tlili A, Mutery AA, Chouchen J. Tlili A, et al. Genes (Basel). 2024 May 6;15(5):588. doi: 10.3390/genes15050588. Genes (Basel). 2024. PMID: 38790217 Free PMC article.

Genetic heterogeneity in epilepsy and comorbidities: insights from Pakistani families.

Yasin M, Licchetta L, Khan N, Ullah I, Jan Z, Dawood M, Ahmed AN, Azeem A, Minardi R, Carelli V, Saleha S. Yasin M, et al. BMC Neurol. 2024 May 23;24(1):172. doi: 10.1186/s12883-024-03671-7. BMC Neurol. 2024. PMID: 38783254 Free PMC article.

500 results

Page of 50

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

500 results

Results by year