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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

199 related items for PubMed ID: 24042019

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  • 7. In vivo expression of putative LMX1B targets in nail-patella syndrome kidneys.
    Heidet L, Bongers EM, Sich M, Zhang SY, Loirat C, Meyrier A, Broyer M, Landthaler G, Faller B, Sado Y, Knoers NV, Gubler MC.
    Am J Pathol; 2003 Jul; 163(1):145-55. PubMed ID: 12819019
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  • 9. A familial case of nail patella syndrome with a heterozygous in-frame indel mutation in the LIM domain of LMX1B.
    Mukai M, Fujita H, Umegaki-Arao N, Sasaki T, Yasuda-Sekiguchi F, Isojima T, Kitanaka S, Amagai M, Kubo A.
    J Dermatol Sci; 2018 Apr; 90(1):90-93. PubMed ID: 29290531
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  • 11. Steroid-resistant nephrotic syndrome as the initial presentation of nail-patella syndrome: a case of a de novo LMX1B mutation.
    Nakata T, Ishida R, Mihara Y, Fujii A, Inoue Y, Kusaba T, Isojima T, Harita Y, Kanda C, Kitanaka S, Tamagaki K.
    BMC Nephrol; 2017 Mar 23; 18(1):100. PubMed ID: 28335748
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  • 14. The LIM-homeodomain transcription factor Lmx1b plays a crucial role in podocytes.
    Rohr C, Prestel J, Heidet L, Hosser H, Kriz W, Johnson RL, Antignac C, Witzgall R.
    J Clin Invest; 2002 Apr 23; 109(8):1073-82. PubMed ID: 11956245
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  • 15. A synonymous genetic alteration of LMX1B in a family with nail-patella syndrome.
    Ham JH, Shin SJ, Joo KR, Park SM, Sung HY, Kim JS, Choi JS, Choi YJ, Song HC, Choi EJ.
    Korean J Intern Med; 2009 Sep 23; 24(3):274-8. PubMed ID: 19721866
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  • 20. A Novel Mutation in LMX1B (p.Pro219Ala) Causes Focal Segmental Glomerulosclerosis with Alport Syndrome-like Phenotype.
    Oe Y, Mishima E, Mori T, Okamoto K, Honkura Y, Nagasawa T, Yoshida M, Sato H, Suzuki J, Ikeda R, Sohara E, Uchida S, Katori Y, Miyazaki M.
    Intern Med; 2021 Sep 15; 60(18):2991-2996. PubMed ID: 33814499
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