Searchable abstracts of presentations at key conferences in endocrinology

ea0005oc17 | Obesity and Diabetes | BES2003

Autocrine FGF-2 is essential for human preadipocyte differentiation

Patel N , Kumar S , Eggo M

Preadipocytes differentiate into mature adipocytes when treated with insulin, T3, isobutylmethylxanthine and dexamethasone but the role of their autocrine factors in their survival and function has only recently been appreciated. We have examined the expression and role of autocrine FGF-2 during preadipocyte differentiation. Using human preadipocytes isolated from subcutaneous fat, we induced differentiation in differentiation medium with and without the insulin-sensitising dr...

ea0029p759 | Endocrine Disruptors | ICEECE2012

Bisphenol-A exposure from electronic gadgets: A risk assessment

Kumar N. , Khan R. , Kumar P. , Sharma V.

We are living in the electronic era and day to day exposed by estrogenic disruptors such as Bisphenol-A (BPA). Electronic gadgets such as cellular phones, CDs, DVDs, RFIDs even baby feeding bottles are made with composition of BPA and their huge application are matter of debate in present. The chronic exposures of BPA have become a major health concern. In this study we assessed the neurobehavioral alterations caused by BPA in the rats. We examined the neurobehavioral changes ...

ea0090p343 | Diabetes, Obesity, Metabolism and Nutrition | ECE2023

Prevalence of mutations in cublin-megalin receptor genes in Diabetis Mellitus: Subset analysis of an Indian NGS (Next Generation Sequencing) study

Bangaraiahgari Ramesh , Bhargav Panchangam Ramakanth , Kumar N Udaya , Bangaraiahgari Rajesh , Mayilvaganan Sabaretnam , Bangaraiahgari Chakrapani

Background: Diabetes mellitus (DM) is the commonest endocrinopathy, Worldwide. Amongst the protean complex genetic variations, cubulin gene and megalin gene mutations in diabetes are important in dictating genotype-phenotypic correlations and natural clinical course of diabetes. The genetic studies in this area are especially very sparse from Indian sub-continent. In this context, we analyzed the prevalence of cubulin (CBN) and megalin (LRP2) gene mutations, as part of NGS (Ne...

ea0090p765 | Thyroid | ECE2023

An Fifty Six Gene panel Next Generation Sequencing Study of Follicular differentiated Thyroid Cancer: An Indian Study

Bangaraiahgari Ramesh , Bhargav Panchangam Ramakanth , Mayilvaganan Sabaretnam , Bangaraiahgari Rajesh , Kumar N Udaya , Bangaraiahgari Chakrapani

Background: Follicular differentiated thyroid cancer (FDTC) is the most common endocrine cancer, globally. Next-generation sequencing (NGS) in thyroid cancer allows for high-throughput genetic sequencing in short time. This analysis offers useful information on tumor biology. NGS Studies on follicular differentiated thyroid cancer are scanty from South East Asia. In this context, we set out study the pattern of a genetic panel wide somatic mutations in thyroid cancer.<p cl...

ea0029p266 | Calcium &amp; Vitamin D metabolism | ICEECE2012

Primary hypoparathyroidism presenting as adult onset seizure: a report of two cases

Varma T. , Panchani R. , Saini A. , Tripathi S. , Gupta N. , Kumar S\.

Introduction: Primary Hypoparathyroidism presents most commonly in childhood to early adolescence. Disease may be familial or sporadic.Most commonly hypoparathyroidism is secondary to neck operations especially Thyroid surgeries. Primary can be congenital eg- Digeorge syndrome or inherited by AD, AR or X linked mediated.We report 2 cases of late onset seizure due to Digeorge syndrome and Autosomal Dominant Hypoparathyroidism in a elderly lady.Case Report...

ea0090ep912 | Reproductive and Developmental Endocrinology | ECE2023

Quantification of miRNAs (miR4743-5p, miR149-5p, and miR331-5p) in the placenta of south Indian pregnant women with Early and Late onset of Preeclampsia

Bangaraiahgari Ramesh , Bangaraiahgari Bangaraiahgari Rajesh , Bhargav Panchangam Panchangam Ramakanth , Kumar N Nelagiri Udaya , Vudathala Srinivas , Vijayan Vinaya , Reddy Banala Rajkiran , Bangaraiahgari Chakrapani

Background: Preeclampsia (PE) is a multifactorial and multisystem disorder, with unknown pathophysiology, but factors such as defective trophoblast invasion and narrowing of spiral arteries may be contributing to the onset of PE and affecting mother and foetus development. Early prediction of PE may improve the surveillance and prognosis of hypertension in pregnant women in preventing associated complications. Therefore, it is essential to find markers for the detection of PE ...

ea0038p311 | Pituitary | SFEBES2015

The burden of AIP mutations in pituitary adenoma patients from the UK

Caimari F , Dang M N , Gabrovska P , Hernandez-Ramirez L C , Stals K , Bussell A M , Cranston T , Karavitaki N , Kumar A V , Hunter S , Kearney T , Trainer P J , Izatt I , Bevan J , Quinton R , Grieve J , Baldeweg S E , Grossman A B , Morrison P , Korbonits M

Introduction: Familial isolated pituitary adenoma (FIPA) and young-onset sporadic pituitary adenoma patients are suggested to be screened for mutations in AIP, a gene described in 2006 and amenable to UK testing since 2008.Methods: affected subjects have been tested in Exeter and Oxford genetic laboratories. Data were collected from 120 FIPA-families and 193 sporadic cases with young-onset disease (<30y) from 49 centres in the UK. The Mann&#...