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Results by year

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

Year Number of Results
1993 1
1994 1
1995 2
1997 4
1998 10
1999 10
2000 5
2001 7
2002 13
2003 15
2004 13
2005 14
2006 18
2007 26
2008 24
2009 24
2010 26
2011 19
2012 23
2013 10
2014 1
2023 1
2024 0

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PubMed for id: 55648

250 results

Results by year

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Page 1
LMX1B mutations cause hereditary FSGS without extrarenal involvement.
Boyer O, Woerner S, Yang F, Oakeley EJ, Linghu B, Gribouval O, Tête MJ, Duca JS, Klickstein L, Damask AJ, Szustakowski JD, Heibel F, Matignon M, Baudouin V, Chantrel F, Champigneulle J, Martin L, Nitschké P, Gubler MC, Johnson KJ, Chibout SD, Antignac C. Boyer O, et al. J Am Soc Nephrol. 2013 Jul;24(8):1216-22. doi: 10.1681/ASN.2013020171. Epub 2013 May 16. J Am Soc Nephrol. 2013. PMID: 23687361 Free PMC article.
Detection of genes regulated by Lmx1b during limb dorsalization.
Feenstra JM, Kanaya K, Pira CU, Hoffman SE, Eppey RJ, Oberg KC. Feenstra JM, et al. Dev Growth Differ. 2012 May;54(4):451-62. doi: 10.1111/j.1440-169X.2012.01331.x. Epub 2012 Mar 15. Dev Growth Differ. 2012. PMID: 22417325 Free PMC article.
Association of transcription factor gene LMX1B with autism.
Thanseem I, Nakamura K, Anitha A, Suda S, Yamada K, Iwayama Y, Toyota T, Tsujii M, Iwata Y, Suzuki K, Matsuzaki H, Iwata K, Sugiyama T, Yoshikawa T, Mori N. Thanseem I, et al. PLoS One. 2011;6(8):e23738. doi: 10.1371/journal.pone.0023738. Epub 2011 Aug 25. PLoS One. 2011. PMID: 21901133 Free PMC article.
Increased symptoms of attention deficit hyperactivity disorder and major depressive disorder symptoms in Nail-patella syndrome: potential association with LMX1B loss-of-function.
López-Arvizu C, Sparrow EP, Strube MJ, Slavin C, DeOleo C, James J, Hoover-Fong J, McIntosh I, Tierney E. López-Arvizu C, et al. Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):59-66. doi: 10.1002/ajmg.b.31138. Epub 2010 Nov 2. Am J Med Genet B Neuropsychiatr Genet. 2011. PMID: 21184584 Free PMC article.
Central serotonin neurons are required for arousal to CO2.
Buchanan GF, Richerson GB. Buchanan GF, et al. Proc Natl Acad Sci U S A. 2010 Sep 14;107(37):16354-9. doi: 10.1073/pnas.1004587107. Epub 2010 Aug 30. Proc Natl Acad Sci U S A. 2010. PMID: 20805497 Free PMC article.
A spectrum of LMX1B mutations in Nail-Patella syndrome: new point mutations, deletion, and evidence of mosaicism in unaffected parents.
Marini M, Bocciardi R, Gimelli S, Di Duca M, Divizia MT, Baban A, Gaspar H, Mammi I, Garavelli L, Cerone R, Emma F, Bedeschi MF, Tenconi R, Sensi A, Salmaggi A, Bengala M, Mari F, Colussi G, Szczaluba K, Antonarakis SE, Seri M, Lerone M, Ravazzolo R. Marini M, et al. Genet Med. 2010 Jul;12(7):431-9. doi: 10.1097/GIM.0b013e3181e21afa. Genet Med. 2010. PMID: 20531206 Free article.
Nail-Patella Syndrome.
Sweeney E, Hoover-Fong JE, McIntosh I. Sweeney E, et al. 2003 May 31 [updated 2023 Dec 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 May 31 [updated 2023 Dec 14]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301311 Free Books & Documents. Review.
250 results