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1,633 Possible Causes for leus

  • Endocrine Dysfunction

    Diabetes mellitus carrying a mutation in the mitochondrial tRNA(Leu(UUR)) gene . Diabetologia 38 , 193–200 (1995). 24. Karaa, A. & Goldstein, A.[nature.com] Mitochondrial gene mutations in the tRNA(Leu(UUR)) region and diabetes: prevalence and clinical phenotypes in Japan . Clin. Chem. 47 , 1641–1648 (2001). 22.[nature.com] Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation . J. Med. Genet. 33 , 621–622 (1996). 62. Balestri, P. & Grosso, S.[nature.com]

  • Bacillus Anthracis

    An FtsX mutant of B. anthracis known to be resistant to the antimicrobial effects of interferon-inducible Glu-Leu-Arg (ELR)-negative CXC chemokines was not affected by the[ncbi.nlm.nih.gov]

  • Trypanosoma Brucei

    However, homozygous in situ expression of UBP1-Leu(131) in T. b. brucei did not affect the sensitivity to melarsoprol or pentamidine.[ncbi.nlm.nih.gov]

  • Tuberculid

    Immunohistologic study of the epithelioid granulomas demonstrated a predominance of Leu-1--bearing, Leu-3a--bearing, and human lymphocyte antigen-DR-expressing cells.[ncbi.nlm.nih.gov]

  • Toxoplasma Gondii

    The immunosuppression of T-cell responses was mediated by Leu 1 , Leu 2a , and Leu 3a- suppressor T cells that were induced by Toxoplasma gondii antigen and suppressed both[ncbi.nlm.nih.gov]

  • Analbuminemia

    This mutation causes the loss of the primary start codon ATG for Met1, which is replaced by a - then untranslated - triplet CTG for Leu. (p.Met1Leu).[ncbi.nlm.nih.gov] The subsequent frameshift should give rise to a putative truncated albumin variant in which the sequence Cys(538)-Thr-Leu-Ser has been changed to Cys(538)-Thr-Phe-Stop.[ncbi.nlm.nih.gov]

  • Leukostasis

    […] after granulocytopenia had reversed exhibited a dose-related, selective and irreversible refractoriness to stimulation with C5a(desarg), but their responses to n-formyl-Met-Leu-Phe[ncbi.nlm.nih.gov]

  • Blast Phase

    UR - UR - U2 - 10.1038/leu.2016.231 DO - 10.1038/leu.2016.231 M3 - Article VL - 31 SP - 585 EP - 592 JO - Leukemia T2 - Leukemia JF - Leukemia SN - 0887-6924 IS - 3 ER -[experts.illinois.edu] Hu", year "2017", month "3", day "1", doi "10.1038/leu.2016.231", language "English (US)", volume "31", pages "585--592", journal "Leukemia", issn "0887-6924", publisher "[experts.illinois.edu]

  • Renal Amyloidosis

    Direct DNA sequencing revealed a G 4993 T transversion and subsequently Arg 554 Leu mutation in the fibrinogen A alpha chain.[ncbi.nlm.nih.gov] Fibrinogen A alpha chain Leu 554: an African-American kindred with late onset renal amyloidosis. Amyloid . 1998 Sep. 5(3):188-92. [Medline] .[emedicine.medscape.com] Fibrinogen A alpha chain mutation (Arg554 Leu) associated with hereditary renal amyloidosis in a French family. Amyloid . 1998 Dec. 5(4):279-84. [Medline] .[emedicine.medscape.com]

  • Drug-induced Thrombocytopenia

    Carbimazole-dependent antibodies showed similar reactivity with platelets carrying the Leu(125) and Val(125) PECAM-1 isoforms, indicating that this polymorphic structure,[ncbi.nlm.nih.gov]

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