Create issue ticket

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]

  • Atypical Phenylketonuria

    The abscissa value of 1 denotes including Phe/Sum, Phe, Tyr, Leu.[clinchem.aaccjnls.org] The method separates 6 amino acids, Val, Met, Ile, Leu, Tyr, and Phe in 35 min.[clinchem.aaccjnls.org] Ranges for the ratios were Phe/Tyr 0.41–1.14, Phe/Leu 0.46–0.86, and Phe/Sum 0.12–0.23.[clinchem.aaccjnls.org]

  • 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]

  • Cyanosis

    This novel variant was named Hb F-Circleville [GγE7(63)His Leu].[bloodjournal.org] It is rare for methemoglobinemia to occur as result of hemoglobinopathies other than hemoglobin M, but hemoglobinChile (b28 Leu Met) is such a hemoglobin.[medtextfree.wordpress.com] Sequencing of the PCR amplified Gγ gene revealed heterozygosity for a CAT CTT mutation (His Leu) at codon 63. (GenBank Acession # AY662983 ).[bloodjournal.org]

  • 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]

  • Nocturnal Hypoglycemia

    Seite 5 - CYS 8 GLY 9 SER 10 HIS 11 LEU 12 VAL 13 GLU 14 ALA 15 LEU 16 TYR 17 LEU 18 VAL 19... ‎[books.google.com]

  • Olfactory Neuroblastoma

    Immunohistochemical reactions for NSE, synaptophysin, chromogranin A, HNK-1/Leu-7 and S-100 revealed a characteristic immunophenotype.[ncbi.nlm.nih.gov]

  • Sympathetic Ophthalmia

    Very few natural killer (NK) cells (Leu 7 ) were identified throughout the choroid.[ncbi.nlm.nih.gov] The data demonstrated that the predominant cells within the choroidal infiltrate were T-lymphocytes (Leu 1 ).[ncbi.nlm.nih.gov] A smaller proportion of the T cells demonstrated the specific determinants of the suppressor subtype (Leu 2a ).[ncbi.nlm.nih.gov]

  • Pelizaeus-Merzbacher Disease

    This results in a Leu-to-Pro change in a carrier mother and in her two affected sons.[ncbi.nlm.nih.gov] Here we report a PMD patient with a very mild phenotype carrying a novel mutation (485G-- T) in exon 4 of the PLP1 gene that causes a Trp(162)Leu substitution in the protein[ncbi.nlm.nih.gov] Here, we found that expression of the PLP1-A243V mutant, which causes severe disease, depletes some ER chaperones with a KDEL (Lys-Asp-Glu-Leu) motif, in HeLa cells, MO3.13[ncbi.nlm.nih.gov]

  • Schistosomiasis Japonica

    When Leu-2a T lymphocytes were depleted from low responder T lymphocytes, a vigorous response by the Leu-2a-depleted T lymphocytes (Leu-2a-3a ) to the schistosomal adult worm[jimmunol.org] The suppressor T lymphocytes were mitomycin C resistant and were positive for Leu-2a, but were negative for Leu-3a.[jimmunol.org] By adding back the Leu-2a T lymphocytes into autologous T lymphocyte subpopulations, the specific response to the adult worm antigen was completely suppressed.[jimmunol.org]

Further symptoms