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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 6
2007 18
2008 35
2009 25
2010 36
2011 27
2012 29
2013 33
2014 38
2015 44
2016 38
2017 37
2018 34
2019 34
2020 43
2021 42
2022 55
2023 32
2024 4

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PubMed for id: 1648427

500 results

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Page 1
DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort.
Aiello V, Ciurli F, Conti A, Cristalli CP, Lerario S, Montanari F, Sciascia N, Vischini G, Fabbrizio B, Di Costanzo R, Olivucci G, Pietra A, Lopez A, Zambianchi L, La Manna G, Capelli I. Aiello V, et al. Genes (Basel). 2023 Dec 19;15(1):3. doi: 10.3390/genes15010003. Genes (Basel). 2023. PMID: 38275584 Free PMC article.
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies.
Martino J, Liu Q, Vukojevic K, Ke J, Lim TY, Khan A, Gupta Y, Perez A, Yan Z, Milo Rasouly H, Vena N, Lippa N, Giordano JL, Saraga M, Saraga-Babic M, Westland R, Bodria M, Piaggio G, Bendapudi PK, Iglesias AD, Wapner RJ, Tasic V, Wang F, Ionita-Laza I, Ghiggeri GM, Kiryluk K, Sampogna RV, Mendelsohn CL, D'Agati VD, Gharavi AG, Sanna-Cherchi S. Martino J, et al. Genet Med. 2023 Dec;25(12):100983. doi: 10.1016/j.gim.2023.100983. Epub 2023 Sep 21. Genet Med. 2023. PMID: 37746849
X-linked Alport Syndrome with Type IV Collagen α5 Chain Staining Revealing Normal Expression in the Glomerular Basement Membrane and Negative on Bowman's Capsule and Distal Tubular Basement Membrane: A Case Report.
Okamoto T, Shima H, Doi T, Nozu K, Inoue T, Tashiro M, Wariishi S, Bando H, Azuma H, Iwasaka N, Ohara T, Okada K, Minakuchi J. Okamoto T, et al. Tohoku J Exp Med. 2023 Sep 20;261(1):69-73. doi: 10.1620/tjem.2023.J060. Epub 2023 Jul 27. Tohoku J Exp Med. 2023. PMID: 37495524 Free article.
500 results