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Analysis of polymorphisms in the dopamine beta hydroxylase gene: association with attention deficit hyperactivity disorder in Indian children.
Bhaduri N, Sinha S, Chattopadhyay A, Gangopadhyay PK, Singh M, Mukhopadhyay KK. Bhaduri N, et al. Indian Pediatr. 2005 Feb;42(2):123-9. Indian Pediatr. 2005. PMID: 15767706
METHODS: Genomic DNA was amplified for exon 2 *444g/a and intron 5 (Taq I) polymorphism in the DBH gene followed by restriction fragment length polymorphism (RFLP) analysis. ...RESULTS: In the limited number of samples analyzed, a slight increase in transmission of …
METHODS: Genomic DNA was amplified for exon 2 *444g/a and intron 5 (Taq I) polymorphism in the DBH gene followed by restriction fragm …
Screening of rural children in West Bengal for fragile-X syndrome.
Dutta S, Das M, Bhowmik AD, Sinha S, Chattopadhyay A, Mukhopadhyay K. Dutta S, et al. Indian J Med Res. 2009 Dec;130(6):714-9. Indian J Med Res. 2009. PMID: 20090132
Based on the records of scholastic backwardness, 179 children were short-listed and examined by a team of experts comprising of child psychiatrist, clinical psychologist, paediatrician and special educator. ...Down syndrome also had a lower frequency (0.15/1000 chil …
Based on the records of scholastic backwardness, 179 children were short-listed and examined by a team of experts comprising of child …
Study on DBH genetic polymorphisms and plasma activity in attention deficit hyperactivity disorder patients from Eastern India.
Bhaduri N, Sarkar K, Sinha S, Chattopadhyay A, Mukhopadhyay K. Bhaduri N, et al. Cell Mol Neurobiol. 2010 Mar;30(2):265-74. doi: 10.1007/s10571-009-9448-5. Epub 2009 Sep 16. Cell Mol Neurobiol. 2010. PMID: 19757024
Dysfunctions in the norepinephric pathway have been speculated in the etiology of attention deficit hyperactivity disorder (ADHD), a common problem for children. ...Plasma DbetaH activity was measured using a photometric assay and its correlation with the genetic po …
Dysfunctions in the norepinephric pathway have been speculated in the etiology of attention deficit hyperactivity disorder (ADHD), a
Correlation between cystathionine beta synthase gene polymorphisms, plasma homocysteine and idiopathic mental retardation in Indian individuals from Kolkata.
Dutta S, Chatterjee A, Sinha S, Chattopadhyay A, Mukhopadhyay K. Dutta S, et al. Neurosci Lett. 2009 Apr 10;453(3):214-8. doi: 10.1016/j.neulet.2009.02.040. Epub 2009 Feb 21. Neurosci Lett. 2009. PMID: 19429038
A significant difference was also noticed in genotype frequencies of male IMR cases (P=0.005). Four other sites, G919A, C1105T, G1316A and G1330A, were not polymorphic in the studied population. ...The data presented here is probably indicative of a higher risk of I
A significant difference was also noticed in genotype frequencies of male IMR cases (P=0.005). Four other sites, G919A, C1105T, G1316
Screening for methylenetetrahydrofolate reductase C677T and A1298C polymorphisms in Indian patients with idiopathic mental retardation.
Dutta S, Das Bhowmik A, Sinha S, Chattopadhyay A, Mukhopadhyay K. Dutta S, et al. Nutr Neurosci. 2008 Feb;11(1):18-24. doi: 10.1179/147683008X301351. Nutr Neurosci. 2008. PMID: 18510799
TDT analysis revealed preferential transmission of C677 allele to a small group of mild IMR probands (chi(2) = 5.545; P = 0.018). ...
TDT analysis revealed preferential transmission of C677 allele to a small group of mild IMR probands (chi(2) = 5.545; P = 0.018). ...
Lack of association between down syndrome and polymorphisms in dopamine receptor D4 and serotonin transporter genes.
Das Bhowmik A, Dutta S, Sinha S, Chattopadhyay A, Mukhopadhyay K. Das Bhowmik A, et al. Neurochem Res. 2008 Jul;33(7):1286-91. doi: 10.1007/s11064-007-9581-9. Epub 2008 Feb 13. Neurochem Res. 2008. PMID: 18270821
A variable number of tandem repeat (VNTR) in the exon 3 of DRD4 and an insertion/deletion polymorphism in the promoter region of 5HT transporter (5HTTLPR) have been found to be associated with different neurobehavioral disorders; however, association of these polymorphisms
A variable number of tandem repeat (VNTR) in the exon 3 of DRD4 and an insertion/deletion polymorphism in the promoter region of 5HT
MAOA promoter polymorphism and attention deficit hyperactivity disorder (ADHD) in indian children.
Das M, Bhowmik AD, Sinha S, Chattopadhyay A, Chaudhuri K, Singh M, Mukhopadhyay K. Das M, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):637-42. doi: 10.1002/ajmg.b.30385. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16856146
Attention deficit hyperactivity disorder (ADHD) is a highly disabling, early onset childhood neurobehavioral disorder with a higher occurrence in boys as compared to girls. ...We have analyzed the MAOA promoter polymorphism in a group of ADHD probands, their …
Attention deficit hyperactivity disorder (ADHD) is a highly disabling, early onset childhood neurobehavioral disorder with a h …
Cystathionine beta-synthase T833C/844INS68 polymorphism: a family-based study on mentally retarded children.
Dutta S, Sinha S, Chattopadhyay A, Gangopadhyay PK, Mukhopadhyay J, Singh M, Mukhopadhyay K. Dutta S, et al. Behav Brain Funct. 2005 Dec 26;1:25. doi: 10.1186/1744-9081-1-25. Behav Brain Funct. 2005. PMID: 16375773 Free PMC article.
A large number of polymorphisms have been reported in the CBS gene, some of which impair its activity and among these, a T833C polymorphism in cis with a 68 bp insertion at 844 in the exon 8 is found to be associated with mild hyperhomocysteinemia in differen
A large number of polymorphisms have been reported in the CBS gene, some of which impair its activity and among these, a T833C
Association of dopamine D4 receptor (DRD4) polymorphisms with attention deficit hyperactivity disorder in Indian population.
Bhaduri N, Das M, Sinha S, Chattopadhyay A, Gangopadhyay PK, Chaudhuri K, Singh M, Mukhopadhyay K. Bhaduri N, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Jan 5;141B(1):61-6. doi: 10.1002/ajmg.b.30225. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16331654
Attention deficit hyperactivity disorder (ADHD) is a childhood onset neurobehavioral disorder. Several studies worldwide have implicated a possible association between ADHD and transmission of different polymorphisms of the dopamine D4 receptor gene (DRD4) in differ …
Attention deficit hyperactivity disorder (ADHD) is a childhood onset neurobehavioral disorder. Several studies worldwide have implica …
Looking at the lobule-importance of ears and years in rheumatology.
Sharma A, Chattopadhyay A, Narang T, Naidu G, Dogra S. Sharma A, et al. Among authors: chattopadhyay a. Rheumatology (Oxford). 2020 Aug 13:keaa426. doi: 10.1093/rheumatology/keaa426. Online ahead of print. Rheumatology (Oxford). 2020. PMID: 32793976 No abstract available.
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