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1. Full Text Allergenic responses of red kidney bean ( Phaseolus vulgaris cv chitra) polypeptides in BALB/c mice recognized by bronchial asthma and allergic rhinitis patients
by Kumar, Sandeep and Verma, Alok Kumar and Misra, Amita and Tripathi, Anurag and Chaudhari, Bhushan P and Prasad, Rajendra and Jain, S.K and Das, Mukul and Dwivedi, Premendra D
Food Research International, ISSN 0963-9969, 2011, Volume 44, Issue 9, pp. 2868 - 2879
Allergenicity potential of red kidney beans ( ) was assessed and attempts were made to identify the responsible proteins by pepsin digestibility assay and IgE... 
Allergens | Legume allergy | Anaphylaxis | Specific IgE | FOOD ALLERGY | FOOD SCIENCE & TECHNOLOGY | SIMULATED GASTRIC FLUID | MURINE MODEL | DIGESTION | PEANUT ALLERGENS | IN-VITRO | SENSITIZATION | INFLAMMATION | PROTEINS | Proteins | Legumes | Histamine | Beans | Proteases | Analysis | Immunoglobulin G | Immunoglobulin E | Mimosaceae | Human | Cytokines | Masts | Kidney beans | Mice | Histamines | Patients
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2. Full Text Transvalvular mitral regurgitation following mitral valve replacement a diagnostic dilemma
by Dinesh Kumar, U.S and Nareppa, Umesh and Shetty, Shyam Prasad and Wali, Murugesh
Annals of Cardiac Anaesthesia, ISSN 0971-9784, 10/2015, Volume 18, Issue 4, pp. 584 - 586
After mitral valve replacement with a prosthetic valve, the valve should be competent and there should not be any residual prosthetic valve regurgitation.... 
transvalvular regurgitation | signature jets | prosthetic valve regurgitation | Chitra mechanical heart valve | Diagnosis, Differential | Echocardiography, Transesophageal | Mitral Valve - diagnostic imaging | Heart Valve Prosthesis | Humans | Adult | Male | Mitral Valve Insufficiency - diagnostic imaging | Postoperative Complications - diagnostic imaging | Case studies | Heart | Complications and side effects | Care and treatment | Surgery | Development and progression | Mitral valve insufficiency | Prostheses | Conflicts of interest | Cardiovascular disease | Physiology | Cardiology | Pulmonary hypertension | Blood clots | Heart to Heart Blog Interesting Images | Chitra mechanical heart valve; prosthetic valve regurgitation; signature jets; transvalvular regurgitation
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3. Full Text Photogrammetric reliability of frontal facial photographs with radiographs and anthropometric measurements
by Negi, Gunjan and Chitra, Prasad
Journal of Oral Biology and Craniofacial Research, ISSN 2212-4268, 2019, Volume 9, Issue 3, pp. 280 - 285
AbstractAimTo evaluate relationships between frontal cephalograms and photographic measurements of Indian population with anthropometric measurements and if... 
Otolaryngology | Frontal cephalogram | Photographs | Photogrammetry | Nemoceph
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4. Full Text CHARGE syndrome
by Blake, Kim D and Prasad, Chitra
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2006, Volume 1, Issue 1, pp. 34 - 34
CHARGE syndrome was initially defined as a non-random association of anomalies ( Coloboma, Heart defect, Atresia choanae, Retarded growth and development,... 
MEDICINE, RESEARCH & EXPERIMENTAL | CHOANAL ATRESIA | CONGENITAL HEART-DISEASE | CHD7 | MULTIPLE ANOMALIES | SPECTRUM | MUTATIONS | HALL-HITTNER-SYNDROME | ASSOCIATION | BEHAVIORS | LIMB ANOMALIES | Abnormalities, Multiple - pathology | Coloboma - pathology | Genitalia - abnormalities | Choanal Atresia - pathology | Face - abnormalities | Humans | Heart Defects, Congenital - pathology | Mutation | DNA-Binding Proteins - genetics | DNA Helicases - genetics | Abnormalities, Multiple - genetics | Syndrome
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5. Anatomical variation of the origin of the left vertebral artery from the arch of aorta
by Chitra, R and Prasad, K.S.N
Journal of the Indian Medical Association, ISSN 0019-5847, 03/2016, Volume 114, Issue 3, pp. 336 - 337
Mediastinum | Foramen transversarium | Left subclavian artery | Vertebral artery | Left common carotid artery
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6. Full Text Altered passive eruption complicating optimal orthodontic bracket placement: A case report and review of literature
by Pulgaonkar, Rohan and Chitra, Prasad
Journal of Clinical and Diagnostic Research, ISSN 2249-782X, 11/2015, Volume 9, Issue 11, pp. ZD01 - ZD03
An unusual case of altered passive eruption with gingival hyperpigmentation and a Class I malocclusion in a 12-year-old girl having no previous history of... 
Crown lengthening | Gingivectomy | Bracket positioning | Depigmentation | Dentistry Section
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7. Identification of novel anti-inflammatory agents from ayurvedic medicine for prevention of chronic diseases: "Reverse pharmacology" and "Bedside to bench" approach
by Aggarwal, Bharat B and Prasad, Sahdeo and Reuter, Simone and Kannappan, Ramaswamy and Yadav, Vivek R and Park, Byoungduck and Kim, Ji Hye and Gupta, Subash C and Phromnoi, Kanokkarn and Sundaram, Chitra and Prasad, Seema and Chaturvedi, Madan M and Sung, Bokyung
Current Drug Targets, ISSN 1389-4501, 10/2011, Volume 12, Issue 11, pp. 1595 - 1653
Inflammation, although first characterized by Cornelius Celsus, a physician in first Century Rome, it was Rudolf Virchow, a German physician in nineteenth... 
Chronic diseases | Ayurveda | Inflammation | NF-kappaB | Reverse pharmacology | reverse pharmacology | chronic diseases | MANGIFERA-INDICA L | ANTIDEPRESSANT-LIKE ACTIVITY | TUMOR-NECROSIS-FACTOR | LEUKEMIA HL-60 CELLS | SWISS ALBINO MICE | INDUCED DIABETIC-RATS | INDUCED OXIDATIVE STRESS | TRIGONELLA-FOENUM-GRAECUM | PROSTATE-CANCER CELLS | PHARMACOLOGY & PHARMACY | NF-KAPPA-B
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8. Full Text Tocotrienols, the vitamin E of the 21st century: Its potential against cancer and other chronic diseases
by Aggarwal, Bharat B and Sundaram, Chitra and Prasad, Seema and Kannappan, Ramaswamy
Biochemical Pharmacology, ISSN 0006-2952, 2010, Volume 80, Issue 11, pp. 1613 - 1631
Initially discovered in 1938 as a " fertility factor," vitamin E now refers to eight different isoforms that belong to two categories, four saturated analogues... 
Bone resorption | Neuroprotective | Atherosclerosis | Diabetes | Tocotrienols | Anticancer | Cholesterol | COLORECTAL ADENOCARCINOMA CELLS | E ALPHA-TOCOTRIENOL | SPONTANEOUSLY HYPERTENSIVE-RATS | COMPARATIVE ANTIOXIDANT ACTIVITY | RICE BRAN OIL | A REDUCTASE-ACTIVITY | LONG-CHAIN CARBOXYCHROMANOLS | GLUTAMYL-TRANSPEPTIDASE ACTIVITIES | PHARMACOLOGY & PHARMACY | GLUTATHIONE-S-TRANSFERASE | MAMMARY EPITHELIAL-CELLS | Neoplasms - metabolism | Vitamin E - pharmacokinetics | Antioxidants - chemistry | Tocotrienols - therapeutic use | Humans | Neoplasms - prevention & control | Antineoplastic Agents - therapeutic use | Tocotrienols - chemistry | Tocotrienols - pharmacology | Antioxidants - therapeutic use | Animals | Vitamin E - therapeutic use | Vitamin E - chemistry | Drug Delivery Systems - trends | Antioxidants - pharmacokinetics | Chronic Disease | Bone cancer
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9. Full Text Nephrological and urological complications of homozygous c.974G>A (p.Arg325Gln) OSGEP mutations
by Wang, Peter Zhan Tao and Prasad, Chitra and Rodriguez Cuellar, Carmen Inés and Filler, Guido
Pediatric Nephrology, ISSN 0931-041X, 11/2018, Volume 33, Issue 11, pp. 2201 - 2204
Galloway-Mowat syndrome (GAMOS) (OMIM #251300) is a severe autosomal recessive disease characterized by the combination of early-onset steroid-resistant... 
Renal tubulopathy | Urolithiasis | Neurodegeneration | tRNA N | KAE1/TCS3 (OSGEP) mutation | adenosine threonylcarbamoyltransferase defect | Galloway-Mowat syndrome | UROLOGY & NEPHROLOGY | PEDIATRICS | tRNA N-6-adenosine threonylcarbamoyltransferase defect | Case studies | Complications and side effects | Genetic disorders | Gene mutations | Child development deviations | Genetic aspects | Kidney diseases | Children | Health aspects | Developmental disabilities | Risk factors | Diseases | Creatinine | Urine | Nephrology | Epilepsy | Prophylaxis | Nephrotic syndrome | Urinary tract | Drug resistance | Fanconi syndrome | Glomerular filtration rate | Microencephaly | Hypercalciuria | Calculi | Lithiasis | Urinary tract infections | Mutation | Magnesium | Hypomagnesemia | Age | Seizures | Proteinuria
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10. Full Text Long-term evaluation of metal ion release in orthodontic patients using fluoridated oral hygiene agents: An in vivo study
by Chitra, Prasad and Prashantha, Govinakovi Shivamurthy and Rao, Arun
Journal of the World Federation of Orthodontists, ISSN 2212-4438, 09/2019, Volume 8, Issue 3, pp. 107 - 111
To investigate levels of nickel and chromium in gingival crevicular fluid from subjects undergoing orthodontic treatment with and without using fluoridated... 
Nickel release | Fluoride | Fixed appliances | Gingival crevicular fluid | Metal ion release
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11. Full Text Kidney disease and organ transplantation in methylmalonic acidaemia
by Noone, Damien and Riedl, Magdalena and Atkison, Paul and Avitzur, Yaron and Sharma, Ajay P and Filler, Guido and Siriwardena, Komudi and Prasad, Chitra
Pediatric Transplantation, ISSN 1397-3142, 06/2019, Volume 23, Issue 4, pp. e13407 - n/a
Objectives MMA is associated with chronic tubulointerstitial nephritis and a progressive decline in GFR. Optimal management of these children is uncertain. Our... 
eGFR | hyperammonemia | cystatin C | kidney disease | methylmalonic academia | Enzymes | Liver diseases | Liver | Transplantation of organs, tissues, etc | Development and progression | Kidney diseases | Carnitine | Creatinine | Cystatin | Nephritis | Nutrient deficiency | Renal function | Kidneys | Transplants & implants | Syngeneic grafts | Coenzyme Q | Vitamin B12 | Antioxidants | Allografts | Vitamin E | Cystatin C | Renal failure | Children | Low protein diet | Metabolic disorders | Liver transplantation | Kidney transplantation
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12. Full Text Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
by Braun, Daniela A and Rao, Jia and Mollet, Geraldine and Schapiro, David and Daugeron, Marie-Claire and Tan, Weizhen and Gribouval, Olivier and Boyer, Olivia and Revy, Patrick and Jobst-Schwan, Tilman and Schmidt, Johanna Magdalena and Lawson, Jennifer A and Schanze, Denny and Ashraf, Shazia and Ullmann, Jeremy F P and Hoogstraten, Charlotte A and Boddaert, Nathalie and Collinet, Bruno and Martin, Gaëlle and Liger, Dominique and Lovric, Svjetlana and Furlano, Monica and Guerrera, I Chiara and Sanchez-Ferras, Oraly and Hu, Jennifer F and Boschat, Anne-Claire and Sanquer, Sylvia and Menten, Björn and Vergult, Sarah and De Rocker, Nina and Airik, Merlin and Hermle, Tobias and Shril, Shirlee and Widmeier, Eugen and Gee, Heon Yung and Choi, Won-Il and Sadowski, Carolin E and Pabst, Werner L and Warejko, Jillian K and Daga, Ankana and Basta, Tamara and Matejas, Verena and Scharmann, Karin and Kienast, Sana D and Behnam, Babak and Beeson, Brendan and Begtrup, Amber and Bruce, Malcolm and Ch'ng, Gaik-Siew and Lin, Shuan-Pei and Chang, Jui-Hsing and Chen, Chao-Huei and Cho, Megan T and Gaffney, Patrick M and Gipson, Patrick E and Hsu, Chyong-Hsin and Kari, Jameela A and Ke, Yu-Yuan and Kiraly-Borri, Cathy and Lai, Wai-Ming and Lemyre, Emmanuelle and Littlejohn, Rebecca Okashah and Masri, Amira and Moghtaderi, Mastaneh and Nakamura, Kazuyuki and Ozaltin, Fatih and Praet, Marleen and Prasad, Chitra and Prytula, Agnieszka and Roeder, Elizabeth R and Rump, Patrick and Schnur, Rhonda E and Shiihara, Takashi and Sinha, Manish D and Soliman, Neveen A and Soulami, Kenza and Sweetser, David A and Tsai, Wen-Hui and Tsai, Jeng-Daw and Topaloglu, Rezan and Vester, Udo and Viskochil, David H and Vatanavicharn, Nithiwat and Waxler, Jessica L and Wierenga, Klaas J and Wolf, Matthias T F and Wong, Sik-Nin and Leidel, Sebastian A and Truglio, Gessica and Dedon, Peter C and Poduri, Annapurna and Mane, Shrikant and Lifton, Richard P and Bouchard, Maxime and Kannu, Peter and Chitayat, David and Magen, Daniella and Callewaert, Bert and van Tilbeurgh, Herman and Zenker, Martin and ...
Nature Genetics, ISSN 1061-4036, 2017, Volume 49, Issue 10, pp. 1529 - 1529
Galloway-Mowat syndrome (GAMOS) is an autosomal-recessive disease characterized by the combination of early-onset nephrotic syndrome (SRNS) and microcephaly... 
YEAST | UNFOLDED PROTEIN RESPONSE | TRANSFER-RNA MODIFICATION | DNA | KINASE | SECKEL-SYNDROME | GENOME MAINTENANCE | WDR73 | GALLOWAY-MOWAT SYNDROME | MASS-SPECTROMETRY | GENETICS & HEREDITY | Metalloendopeptidases - genetics | Protein-Serine-Threonine Kinases - deficiency | Microcephaly - genetics | Humans | Metalloendopeptidases - deficiency | Apoptosis - genetics | Multiprotein Complexes - genetics | Nephrotic Syndrome - genetics | DNA Repair - genetics | Telomere Homeostasis - genetics | Endoplasmic Reticulum Stress - genetics | Intracellular Signaling Peptides and Proteins - deficiency | Hernia, Hiatal - genetics | Intracellular Signaling Peptides and Proteins - genetics | Podocytes - metabolism | RNA, Transfer - metabolism | Protein-Serine-Threonine Kinases - genetics | Models, Molecular | Nephrotic Syndrome - pathology | Zebrafish | Cytoskeleton - ultrastructure | Nephrosis - genetics | Gene Knockout Techniques | Carrier Proteins - genetics | Podocytes - ultrastructure | Zebrafish Proteins - deficiency | Animals | RNA Processing, Post-Transcriptional - genetics | CRISPR-Cas Systems | Protein Conformation | Mice | Mutation | Zebrafish Proteins - genetics | Cell Movement | Genetic disorders | Gene mutations | Development and progression | Nephrotic syndrome | Genetic aspects | Microcephaly | Health aspects | Cell proliferation | Brain | CRISPR | Genes | DNA damage | Genomes | Lethality | Kinases | Proteins | Genotype & phenotype | Microencephaly | Actin | Biopsy | Cytoskeleton | Scientific imaging | Endoplasmic reticulum | Mass spectrometry | Deoxyribonucleic acid--DNA | Apoptosis | Life Sciences
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13. Full Text Bulging anterior fontanelle and dense bones in an infant
by Halgren, Camilla Raya and Lakhani, Jenna and Colaiacovo, Samantha and Prasad, Chitra
Paediatrics & Child Health, ISSN 1205-7088, 03/2019
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14. Full Text Benign reactive lymphadenopathy associated with submandibular gland enlargement during orthodontic treatment
by Pulgaonkar, Rohan and Chitra, Prasad and Moosvi, Zama
Journal of Oral and Maxillofacial Pathology, ISSN 0973-029X, 01/2017, Volume 21, Issue 1, pp. 181 - 182
Lymphadenopathy may be caused due to various reasons, most common being infections, neoplasms and immunologic disorders. Considering the frequent use of... 
Orthodontic therapy | Lymphadenopathy | Salivary gland enlargement | Delayed hypersensitivity | Antigens | Lymphatic system | Hypersensitivity (delayed) | Mucosa | Teeth | Submandibular gland | Infections | Dentistry | Dermatitis | Orthodontics | Biomaterials | Stomatitis | Cellular biology | Biopsy | Lymphomas | Differential diagnosis | Resins | Viral infections | Tumors | salivary gland enlargement | orthodontic therapy | lymphadenopathy | Case Report
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15. Full Text Heterozygous deletion of the linked genes ZIC1 and ZIC4 is involved in Dandy-Walker malformation
by Ardinger, Holly and Prasad, Chitra and Millen, Kathleen J and Grinberg, Inessa and Dobyns, William B and Northrup, Hope
Nature Genetics, ISSN 1061-4036, 10/2004, Volume 36, Issue 10, pp. 1053 - 1055
Dandy-Walker malformation (DWM; OMIM #220200) is a common but poorly understood congenital cerebellar malformation in humans. Through physical mapping of 3q2... 
CEREBELLAR DEVELOPMENT | CLASSIFICATION | GENETICS & HEREDITY | Chromosome Deletion | Physical Chromosome Mapping | Humans | Dandy-Walker Syndrome - genetics | Molecular Sequence Data | Transcription Factors - genetics | Cerebellum - abnormalities | Nerve Tissue Proteins - genetics | Dandy-Walker Syndrome - pathology | Magnetic Resonance Imaging | Phenotype | Animals | Mice, Mutant Strains | Heterozygote | Zinc Fingers - genetics | Mice | Child | Chromosomes, Human, Pair 3 - genetics | Disease Models, Animal | Genetic Linkage | Complications and side effects | Hydrocephalus | Gene mutations | Genetic aspects | Diagnosis | Research | Gene expression | Health aspects | Risk factors
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