Apoorva Joshi

ORCID: 0000-0003-4867-0057
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Research Areas
  • Birth, Development, and Health
  • Pregnancy and preeclampsia studies
  • Gestational Diabetes Research and Management
  • Helicobacter pylori-related gastroenterology studies
  • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
  • Neuroendocrine Tumor Research Advances
  • Gastrointestinal motility and disorders
  • Digestive system and related health
  • Pharmaceutical Practices and Patient Outcomes
  • COVID-19 and Mental Health
  • Facial Trauma and Fracture Management
  • Bioactive Compounds and Antitumor Agents
  • Infant Nutrition and Health
  • MicroRNA in disease regulation
  • Long-Term Effects of COVID-19
  • Effects and risks of endocrine disrupting chemicals
  • NF-κB Signaling Pathways
  • Per- and polyfluoroalkyl substances research
  • COVID-19 and healthcare impacts
  • Pharmaceutical Economics and Policy
  • Medication Adherence and Compliance
  • Amino Acid Enzymes and Metabolism
  • Pharmacogenetics and Drug Metabolism
  • Dietary Effects on Health
  • Biopolymer Synthesis and Applications

All India Institute of Medical Sciences, Nagpur
2024

All India Institute of Medical Sciences Raipur
2021-2024

Ruxmaniben Deepchand Gardi Medical College
2024

Children's Hospital of Philadelphia
2019-2021

Bombay Hospital
2020

University of Sioux Falls
2019

Baruch S. Blumberg Institute
2014-2018

Philadelphia University
2018

Fox Chase Cancer Center
2017

AIMTo evaluate the effect of orally administered plecanatide on colorectal dysplasia in Apc +/Min-FCCC mice with dextran sodium sulfate (DSS)-induced inflammation. METHODS Inflammation driven carcinogenesis was induced Apc+/Min-FCCC by administering DSS their drinking water.Mice were fed a diet supplemented (0-20 ppm) and its multiplicity histopathologically confirmed polypoid, Plecanatide-mediated activation guanylate cyclase-C suppresses

10.4292/wjgpt.v8.i1.47 article EN World Journal of Gastrointestinal Pharmacology and Therapeutics 2017-01-01

Our results indicate that plecanatide and dolcanatide, guanylate cyclase-C receptor agonists designed to replicate the activity of human intestinal peptide uroguanylin, maintain barrier function exhibit potent anti-nociceptive in animal models visceral hypersensitivity, suggesting a novel mechanism, beyond well described secretory function, for these treatment functional constipation disorders inflammatory bowel disease.

10.3748/wjg.v24.i17.1888 article EN cc-by-nc World Journal of Gastroenterology 2018-05-06

Abstract Context Gestational diabetes (GDM) has profound effects on the intrauterine metabolic milieu and is linked to obesity in offspring, but mechanisms driving these remain largely unknown. Alterations DNA methylation gene expression amniocytes exposed GDM utero represent a potential mechanism leading dysfunction later life. Objective To profile changes genome-wide human GDM. Design A nested case-control study (n = 14 pairs) was performed matched for offspring sex, maternal...

10.1210/clinem/dgaa466 article EN The Journal of Clinical Endocrinology & Metabolism 2020-07-20

Prenatal exposure to bisphenol A (BPA) is linked obesity and diabetes but the molecular mechanisms driving these phenomena are not known. Alterations in deoxyribonucleic acid (DNA) methylation amniocytes exposed BPA utero represent a potential mechanism leading metabolic dysfunction later life.To profile changes genome-wide DNA expression second trimester human utero.A nested case-control study was performed matched for offspring sex, maternal race/ethnicity, age, gestational age at...

10.1210/clinem/dgz037 article EN The Journal of Clinical Endocrinology & Metabolism 2019-09-19

Background Most elderly patients suffer from multiple diseases and are on drugs for treatment. Polypharmacy in the elderly, physiological changes with old age, pharmacokinetics pharmacodynamic effects of many drugs, newer drug prescription trends like diabetes cardiovascular disease make prescribing more difficult. There chances drug-drug interactions easily available over-the-counter (OTC) medications. To prevent irrational use there is a need analysis studies. Prescription studies will...

10.7759/cureus.52770 article EN Cureus 2024-01-23

Maxillomandibular fractures can be described as a complete or incomplete break causing discontinuity of the bone tissues in maxillary mandibular structures resulting from application an excessive force.The intimate relationship between maxillofacial with oral cavity, nasal orbits, and adjacent cranial make it functionally cosmetically important structure.Most etiological causes these are: road accidents, contact sport injuries, assaults, falls other industrial accidents.Several...

10.4172/2161-1122.1000467 article EN Dentistry 2017-01-01

Introduction: Uroguanylin (UG) is an endogenous natriuretic peptide that binds and activates GC-C receptors located on the luminal side of GI tract to stimulate cGMP synthesis, a second messenger regulates electrolytes fluid transport, maintains epithelial cell homeostasis facilitates barrier function in tract. The biologically active UG (16 amino acid) assumes several distinct topological isomers aqueous solution only one those are active. Based thermal bond energy calculations, 3-D...

10.14309/00000434-201410002-01819 article EN The American Journal of Gastroenterology 2014-10-01

Introduction: Irritable bowel syndrome (IBS) is a gastrointestinal (GI) disorder with symptoms comprised of abdominal pain and alterations in habits. The key mechanism its pathophysiology considered to be visceral hypersensitivity, which could due loss barrier function gut permeability. GI inflammation might also contributory factor. Population-based studies have shown ˜10 fold higher risk inflammatory diseases IBS patients as compared those no prior history (Porter CK et al. BMC...

10.14309/00000434-201410002-01799 article EN The American Journal of Gastroenterology 2014-10-01

Background: Pregnancies complicated by gestational diabetes (GDM) or maternal obesity (MOB) induce abnormal fetal development that can lead to and later in life with sex specific manifestations. Alterations miRNA expression GDM MOB exposed offspring effects on have not been fully described. Hypothesis: Exposure an aberrant intrauterine milieu leads changes target gene human liver. Methods: Candidate was measured second trimester AF from women diagnosed via multiplex assay (Firefly Bioworks,...

10.2337/db18-163-lb article EN Diabetes 2018-06-22

The COVID-19 pandemic had imposed a city-level quarantine, local lockdown, and border closures for patient-level isolation to control virus spread. There is lack of studies on the health-related quality life (HRQoL) in elderly countries like India during COVID-19. After obtaining written informed consent from patients, data was recorded case record form-cum-questionnaire. assessed with help Centers disease prevention (CDC) HRQoL-14 measures, which are based general health improvement,...

10.21926/obm.geriatr.2204216 article EN OBM Geriatrics 2022-12-11

Earlier identifying drug interactions may help in risk reduction elderly patients.Drug prescription data of 212 patients tertiary health care center had been analyzed for possible with investigational drugs COVID-19 treatment. Drug interaction checked from Stockley's Interaction 2019 and Martindale the Complete Reference 2017 standard reference books Pharmacology.Different types prescribed were 260 out which 68 (26.36%) category fixed-dose combinations. Around 150 (70.75%) having one or more...

10.4103/jrpp.jrpp_20_107 article EN DOAJ (DOAJ: Directory of Open Access Journals) 2021-04-30

Genetic factors contribute to 15% of all causes male infertility. Y chromosome microdeletion is the second most common genetic cause Screening important for Yq as defect can be transferred offspring. Aim our study detect frequency in idiopathic infertile men using both EAA and non markers central region India. Forty from infertility clinic, seeking treatment were recruited cases. Thirty normal fertile same origin controls. Semen analysis was done cytogenetic included study. Simplex multiplex...

10.18231/j.ijogr.2021.066 article EN cc-by-nc-sa Indian Journal of Obstetrics and Gynecology Research 2021-08-15

Background MIRAGE syndrome is a rare multisystem disorder characterized by myelodysplasia, infection, growth restriction, adrenal hypoplasia, genital phenotypes, and enteropathy. The associated with mutations in Sterile Alpha Motif Domain Containing 9 (SAMD9) gene, encoding an endosome fusion facilitator protein additional function factor signaling. To date, there are no reported cases of severe insulin resistance infancy. Clinical Case patient was premature female infant born at 30 6/7...

10.1210/js.2019-sun-268 article EN cc-by-nc-nd Journal of the Endocrine Society 2019-04-01

Background: Gestational diabetes (GDM) has profound effects on the intrauterine metabolic milieu, induces marked abnormalities in fetal glucose and insulin secretion is linked to obesity offspring, but mechanisms remain largely unknown. Objective: To measure changes gene expression genome wide DNA methylation human amniocytes, a stem cell, exposed GDM utero. Methods: EdgeR identified differentially expressed genes from RNASeq via fold change, p-values, q-values calculated after Bonferoni...

10.2337/db19-184-or article EN Diabetes 2019-06-01

Abstract Introduction MENIN and RET mutations in MEN1 families, are rare, and, when they co-exist either mutation may predominate the clinical picture. We report a family, with both mutations, suspect that not be an innocent bystander. Clinical Cases GM (36M): 2009: Presented skin lesions lactotroph adenoma causing chiasmal compression. Treatment: Hypophysectomy Cabergoline. This resulted restoration of sexual function fertility. 2013: Developed hyperparathyroidism [Calcium 10.6mg%...

10.1210/jendso/bvaa046.1622 article EN cc-by-nc-nd Journal of the Endocrine Society 2020-04-01

Abstract Introduction The MEN 1 syndrome is an enigmatic disorder, manifesting a wide spectrum of disorders, in members family, harbouring the same gene mutation. We present one such with MENIN mutation marked diversity clinical presentation Clinical cases 1992: RB (Age: 13) presented accelerated puberty, galactorrhoea and lactotroph adenoma. Treated Bromocriptine, followed by hypophysectomy radiotherapy. He was on hormone replacement for hypopituitarism. 1996: gained 21 kg weight had...

10.1210/jendso/bvaa046.1711 article EN cc-by-nc-nd Journal of the Endocrine Society 2020-04-01

Abstract Background Perfluorooctanoic acid (PFOA), is a persistent fluorinated compound with oil and water repelling properties found in cookware, food packaging municipal systems. Adult animals exposed to PFOA develop hepatomegaly, fatty liver, peroxisome proliferation, immunotoxicity. Rodents utero have altered hepatic lipid metabolism, increased de novo lipogenesis susceptibility non-alcoholic liver disease (NAFLD), but underlying molecular mechanisms remain unknown. With increasing rates...

10.1210/jendso/bvac150.933 article EN cc-by-nc-nd Journal of the Endocrine Society 2022-11-01

Abstract Background: Perfluorooctanoic acid (PFOA), is a persistent fluorinated compound with oil and water repelling properties found in cookware, food packaging municipal systems. Adult animals exposed to PFOA develop hepatomegaly, fatty liver, peroxisome proliferation, immunotoxicity. Rodents PFCs utero have altered hepatic lipid metabolism, increased de novo lipogenesis susceptibility non-alcoholic liver disease (NAFLD), but underlying molecular mechanisms remain unknown. With increasing...

10.1210/jendso/bvab048.1003 article EN cc-by-nc-nd Journal of the Endocrine Society 2021-05-01

Abstract Background: Gestational diabetes (GDM) has profound effects on the intrauterine metabolic milieu, induces marked abnormalities in fetal glucose and insulin secretion is linked to obesity offspring, but mechanisms remain largely unknown. Epigenetic modifications stems cells may be one mechanism by which an utero exposure can lead development of later life. Objective: To identify novel pathways contributing offspring exposed GDM integrating data generated from transcriptome methylome...

10.1210/jendso/bvab048.1339 article EN cc-by-nc-nd Journal of the Endocrine Society 2021-05-01

<i>Background: </i>In the work up of male infertility, Y chromosome microdeletion screening is crucial. PCR a very sensitive technique to screen microdeletion. In current study, was detected by based technique. To best our knowledge, no such study has been reported from Chhattishgarh state India so far. <i>Material and methods:</i> A total seventy-three subjects were enrolled for during period one year. Out which forty-seven cases (infertile men with oligozoospermia azoospermia) twenty-five...

10.11648/j.ijgg.20210902.12 article EN International Journal of Genetics and Genomics 2021-01-01
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