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10.1111/j.1445-5994.1981.tb03516.x http://scihub22266oqcxt.onion/10.1111/j.1445-5994.1981.tb03516.x 7030293!ä!7030293 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Aust+N+Z+J+Med 1981 ; 11 (4): 380-2 Nephropedia Template TP {{tp|p=7030293|t=1981. Glyoxalase phenotypes in patients with diabetes mellitus |pdf=|usr=}}{{7030293}} gab.com Text Glyoxalase phenotypes in patients with diabetes mellitus JO: Aust N Z J Med http://www.kidney.de/pget.php?&tw=1&pmid=7030293 #FOAvip Caucasian diabetic patients in Australian surveys showed a significant difference in the distribution of glyoxalase phenotypes. Insulin dependent diabetic patients with age of onset less than 40 years had a relative excess of glyoxalase homozygote 1-1 and a deficiency of types 2-1 and 2-2. Non-insulin dependent diabetic patients were not significantly different from non-diabetic subjects in the distribution of glyoxalase phenotypes. Insulin dependent diabetic patients without the complications of retinopathy or neuropathy also showed a significant excess of glyoxalase type 1-1 in relation to the control group. Genes controlling glyoxalase polymorphism appear to be associated with the variations of diabetes and its complications. Twit Text FOAVip Glyoxalase phenotypes in patients with diabetes mellitus ????Aust N Z J Med http://www.kidney.de/pget.php?&tw=1&pmid=7030293 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=7030293 #FOAvip English Wikipedia <ref>{{Cite pmid|7030293}}</ref> Glyoxalase phenotypes in patients with diabetes mellitus #MMPMID7030293 McCann VJ; Davis RE; Welborn TA; Constable IJ; Beale DG Aust N Z J Med 1981[Aug]; 11 (4): 380-2 PMID7030293show ga Caucasian diabetic patients in Australian surveys showed a significant difference in the distribution of glyoxalase phenotypes. Insulin dependent diabetic patients with age of onset less than 40 years had a relative excess of glyoxalase homozygote 1-1 and a deficiency of types 2-1 and 2-2. Non-insulin dependent diabetic patients were not significantly different from non-diabetic subjects in the distribution of glyoxalase phenotypes. Insulin dependent diabetic patients without the complications of retinopathy or neuropathy also showed a significant excess of glyoxalase type 1-1 in relation to the control group. Genes controlling glyoxalase polymorphism appear to be associated with the variations of diabetes and its complications. |Australia[MESH] |Diabetes Mellitus/drug therapy/*genetics[MESH] |Diabetic Neuropathies/genetics[MESH] |Diabetic Retinopathy/genetics[MESH] |Ethnicity[MESH] |HLA Antigens/genetics[MESH] |Humans[MESH] |Insulin/therapeutic use[MESH] |Lactoylglutathione Lyase/*genetics[MESH] |Lyases/*genetics[MESH] |Phenotype[MESH]Glyoxalase phenotypes in patients with diabetes mellitus (epmc).pdf DeepDyve Pubget Overpricing