Type2 Diabetes mellitus is a chronic and most common form of diabetes characterized by hyperglycemia arising from problems with the utilization or production insulin. Various agents related to an increased risk developing T2DM include pro-inflammatory cytokines that are critically associated progressive resistance insulin pathogenesis newly diagnosed T2DM. The study aimed possible association T...

BACKGROUND There is a heteromorphic alternative life in the brown seaweed, Saccharina japonica (Aresch.) C. E. Lane, C. Mayes et G. W. Saunders ( = Laminaria japonica Aresch.), with macroscopic monoecious sporophytes and microscopic diecious gametophytes. Female gametophytes are genetically different from males. It is very difficult to identify the parent of a sporophyte using only routine cyto...

an enzyme-linked immunosorbent assay for neopterin using penicillinase as marker enzyme is reported here by polyclonal antibodies against neopterin conjugated to bovine serum albumin which were raised in rabbits. immunoglobulin fractions were purified and coated on wells of microtiter plates. a chain heterology was introduced in neopterin derivative and conjugated to penicillinase. the assay is...

Coincidence. . . . . . . . . . . . .............................. 54 Non-disjunction . . . . . . . . .............................. 55 Gynandromorphs. . . . . . . ............................... 55 Absence of gynandromorp s hybrids.. .................... 60 Somatic mutations, . . . . . ................................... 61 SUMVARY.. ................................................................

rprue anophthalmos is a rare clinical *entity, and the diagnosis can only be made by histologie examination of the orbital contents. Cases with pathologic substantiation of both the intraorbital and the intracranial com¬ ponents of the visual system are still rare.13 We present herein the radiologic and postmortem follow-up in a case of an X-linked recessive form of anophthalmos originally repo...

A family is reported in which three boys, two full brothers and a half brother, presented with marked delay in motor milestones, severe limb and truncal ataxia, nystagmus, speech delay and moderate global retardation. Autosomal recessive and sex linked recessive forms of cerebellar hypoplasia are reviewed and it is suggested that this family may have a rare, if not unique, form of sex-linked ce...

Sex linked recessive deafness is a rare cause of male genetic deafness, estimated to account for 6.2% of male genetic deafness in 1966. A male excess was found in the deaf population of Ireland in 1851. Reevaluation of this survey of 1851 confirms sex linked deafness as a factor in the disproportionate number of deaf males and suggests that 5% of congenital male deafness was the result of sex l...