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

Year Number of Results
1976 1
1987 3
1988 2
1989 5
1990 2
1991 3
1992 3
1993 5
1994 3
1995 6
1996 3
1997 10
1998 9
1999 6
2000 10
2001 15
2002 11
2003 9
2004 6
2005 4
2006 12
2007 14
2008 8
2009 10
2010 9
2011 6
2012 7
2013 11
2014 7
2015 10
2016 5
2017 6
2018 9
2019 12
2020 9
2021 8
2022 3
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233 results
Results by year
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Page 1
Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney.
Eales JM, Jiang X, Xu X, Saluja S, Akbarov A, Cano-Gamez E, McNulty MT, Finan C, Guo H, Wystrychowski W, Szulinska M, Thomas HB, Pramanik S, Chopade S, Prestes PR, Wise I, Evangelou E, Salehi M, Shakanti Y, Ekholm M, Denniff M, Nazgiewicz A, Eichinger F, Godfrey B, Antczak A, Glyda M, Król R, Eyre S, Brown J, Berzuini C, Bowes J, Caulfield M, Zukowska-Szczechowska E, Zywiec J, Bogdanski P, Kretzler M, Woolf AS, Talavera D, Keavney B, Maffia P, Guzik TJ, O'Keefe RT, Trynka G, Samani NJ, Hingorani A, Sampson MG, Morris AP, Charchar FJ, Tomaszewski M. Eales JM, et al. Among authors: woolf as. Nat Genet. 2021 May;53(5):630-637. doi: 10.1038/s41588-021-00835-w. Epub 2021 May 6. Nat Genet. 2021. PMID: 33958779
ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.
Cuvertino S, Stuart HM, Chandler KE, Roberts NA, Armstrong R, Bernardini L, Bhaskar S, Callewaert B, Clayton-Smith J, Davalillo CH, Deshpande C, Devriendt K, Digilio MC, Dixit A, Edwards M, Friedman JM, Gonzalez-Meneses A, Joss S, Kerr B, Lampe AK, Langlois S, Lennon R, Loget P, Ma DYT, McGowan R, Des Medt M, O'Sullivan J, Odent S, Parker MJ, Pebrel-Richard C, Petit F, Stark Z, Stockler-Ipsiroglu S, Tinschert S, Vasudevan P, Villa O, White SM, Zahir FR; DDD Study, Woolf AS, Banka S. Cuvertino S, et al. Among authors: woolf as. Am J Hum Genet. 2017 Dec 7;101(6):1021-1033. doi: 10.1016/j.ajhg.2017.11.006. Am J Hum Genet. 2017. PMID: 29220674 Free PMC article.
Urofacial Syndrome.
Newman WG, Woolf AS. Newman WG, et al. Among authors: woolf as. 2013 Aug 22 [updated 2018 Jun 7]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2013 Aug 22 [updated 2018 Jun 7]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 23967498 Free Books & Documents. Review.
Growing a new human kidney.
Woolf AS. Woolf AS. Kidney Int. 2019 Oct;96(4):871-882. doi: 10.1016/j.kint.2019.04.040. Epub 2019 May 25. Kidney Int. 2019. PMID: 31399199 Free PMC article. Review.
Perinatal renal disease.
Chitty LS, Woolf AS. Chitty LS, et al. Among authors: woolf as. Semin Fetal Neonatal Med. 2008 Jun;13(3):117. doi: 10.1016/j.siny.2007.10.004. Epub 2007 Dec 21. Semin Fetal Neonatal Med. 2008. PMID: 18160356 No abstract available.
Genetically engineered kidneys.
Woolf AS, Fine LG. Woolf AS, et al. Pediatr Nephrol. 1993 Oct;7(5):605-8. doi: 10.1007/BF00852565. Pediatr Nephrol. 1993. PMID: 8251332 Review.
Cell biology of ureter development.
Woolf AS, Davies JA. Woolf AS, et al. J Am Soc Nephrol. 2013 Jan;24(1):19-25. doi: 10.1681/ASN.2012020127. Epub 2012 Nov 2. J Am Soc Nephrol. 2013. PMID: 23123402 Free article. Review.
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects.
Sanchez-Martin I, Magalhães P, Ranjzad P, Fatmi A, Richard F, Manh TPV, Saurin AJ, Feuillet G, Denis C, Woolf AS, Schanstra JP, Zürbig P, Caubit X, Fasano L. Sanchez-Martin I, et al. Among authors: woolf as. Hum Mol Genet. 2021 Dec 17:ddab362. doi: 10.1093/hmg/ddab362. Online ahead of print. Hum Mol Genet. 2021. PMID: 34919690
233 results