K Ray

Summary

Country: India

Publications

  1. ncbi request reprint Simple and effective strategies for detection of allele dropout in PCR-based diagnosis of Wilson disease
    Arnab Gupta
    Clin Chem 52:1611-2. 2006
  2. ncbi request reprint Gene symbol: SLC45A2
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Hum Genet 121:294. 2007
  3. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4 Raja S C Mullick Rd, Jadavpur, 700032 Kolkata, India
    Hum Genet 124:297. 2008
  4. ncbi request reprint Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients
    S Mukherjee
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Haemophilia 10:259-63. 2004
  5. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:299. 2005
  6. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:544. 2005
  7. ncbi request reprint Gene symbol: TYR. Disease: albinism, oculocutaneous 1
    K Ray
    Hum Genet 119:675. 2006
  8. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:544. 2005
  9. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:545. 2005
  10. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson's disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, West Bengal, India
    Hum Genet 118:541. 2005

Collaborators

Detail Information

Publications73

  1. ncbi request reprint Simple and effective strategies for detection of allele dropout in PCR-based diagnosis of Wilson disease
    Arnab Gupta
    Clin Chem 52:1611-2. 2006
  2. ncbi request reprint Gene symbol: SLC45A2
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Hum Genet 121:294. 2007
  3. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4 Raja S C Mullick Rd, Jadavpur, 700032 Kolkata, India
    Hum Genet 124:297. 2008
  4. ncbi request reprint Molecular pathology of haemophilia B: identification of five novel mutations including a LINE 1 insertion in Indian patients
    S Mukherjee
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Haemophilia 10:259-63. 2004
    ..Direct identification of mutations can be utilized to perform the carrier detection and prenatal diagnosis, especially in families with isolated patients...
  5. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:299. 2005
  6. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:544. 2005
  7. ncbi request reprint Gene symbol: TYR. Disease: albinism, oculocutaneous 1
    K Ray
    Hum Genet 119:675. 2006
  8. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:544. 2005
  9. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:545. 2005
  10. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson's disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, West Bengal, India
    Hum Genet 118:541. 2005
  11. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:294. 2005
  12. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:294. 2005
  13. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:295. 2005
  14. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:296. 2005
  15. ncbi request reprint Gene symbol: TYR. Disease: Albinism, oculocutaneous 1
    K Ray
    Hum Genet 116:533. 2005
  16. ncbi request reprint Gene symbol: ATP7B. Disease: Wilson disease
    K Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Kolkata 700 032, West Bengal, India
    Hum Genet 117:299. 2005
  17. ncbi request reprint Gene symbol: SLC45A2
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Hum Genet 121:295. 2007
  18. ncbi request reprint Gene symbol: SLC45A2
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Hum Genet 121:295. 2007
  19. ncbi request reprint Gene symbol: SLC45A2
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Hum Genet 121:294. 2007
  20. ncbi request reprint Tyrosinase and ocular diseases: some novel thoughts on the molecular basis of oculocutaneous albinism type 1
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Jadavpur, Kolkata 700 032, India
    Prog Retin Eye Res 26:323-58. 2007
    ....
  21. doi request reprint Comprehensive analysis of the molecular basis of oculocutaneous albinism in Indian patients lacking a mutation in the tyrosinase gene
    M Sengupta
    Division of Molecular and Human Genetics, Indian Institute of Chemical Biology a CSIR unit, 4 Raja S C Mullick Road, Jadavpur, Kolkata 700032, India
    Br J Dermatol 163:487-94. 2010
    ..There are a few reports on defects in TYR and a single report on SLC45A2 in Indians affected with OCA but no report on OCA2 (a major locus related to the disease) and TYRP1...
  22. doi request reprint A set of five microsatellite markers linked to F8 gene can detect haemophilia A carriers across India
    A Saha
    Molecular and Human Genetics Division, CSIR Indian Institute of Chemical Biology, Kolkata, India
    Haemophilia 17:e928-35. 2011
    ..In conclusion, this panel of five markers around the F8 locus can be used for carrier detection of HA with higher sensitivity across India for families affected with the disease...
  23. ncbi request reprint Chromosomal aberrations in arsenic-exposed human populations: a review with special reference to a comprehensive study in West Bengal, India
    J Mahata
    Division of Human Genetics and Genomics, Indian Institute of Chemical Biology, Jadavpur, Kolkata, India
    Cytogenet Genome Res 104:359-64. 2004
    ..01) in the frequencies of CA and SCE between the cases and control group. Presence of substantial chromosome damage in lymphocytes in the exposed population predicts an increased future carcinogenic risk by this metalloid...
  24. ncbi request reprint OCA1 in different ethnic groups of india is primarily due to founder mutations in the tyrosinase gene
    M Chaki
    Indian Institute of Chemical Biology, Kolkata, India
    Ann Hum Genet 70:623-30. 2006
    ..Direct detection of the mutations prevalent in specific ethnic groups could be used for carrier detection and genetic counselling...
  25. ncbi request reprint Subcortical white matter abnormalities related to drug resistance in Wilson disease
    D Aikath
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata 700 032, India
    Neurology 67:878-80. 2006
    ..The diagnosis was confirmed by identification of mutations in the ATP7B gene. The case demonstrates an uncommon pathology-related cerebral copper accumulation and emphasizes the importance of genetic screening in the diagnosis of WD...
  26. ncbi request reprint Microsatellite instability in squamous cell carcinoma of head and neck from the Indian patient population
    S Chakrabarti
    Department of Human Genetics, Indian Institute of Chemical Biology, Calcutta, India
    Int J Cancer 92:555-61. 2001
    ..These results suggest that the underlying mechanism generating this type of instability is different from those reported for colorectal tumors...
  27. pmc Remarkable variation in the informativeness of RFLP markers linked to hemophilia B locus in Indian population groups: implication in the strategy for carrier detection
    S Mukherjee
    Human Genetics and Genomics and Division, Indian Institute of Chemical Biology, Kolkata, India
    Dis Markers 22:327-34. 2006
    ..Thus prudent selection of the markers based on specific population groups including usage of additional markers is recommended for efficient carrier detection...
  28. doi request reprint Structural analysis of factor IX protein variants to predict functional aberration causing haemophilia B
    S Mukherjee
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Council of Scientific and Industrial Research, Kolkata, India
    Haemophilia 14:1076-81. 2008
    ..Our study truly represents an initiation of an effort that would provide a framework for first evaluation of suspected mutations by in silico approaches, which might be further validated by other experimental techniques...
  29. ncbi request reprint Molecular pathogenesis of Wilson disease: haplotype analysis, detection of prevalent mutations and genotype-phenotype correlation in Indian patients
    A Gupta
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Jadavpur, Kolkata, 700 032, India
    Hum Genet 118:49-57. 2005
    ..These findings suggest a potential role for yet unidentified modifying loci for the observed phenotypic heterogeneity among the WD patients...
  30. doi request reprint Molecular basis of albinism in India: evaluation of seven potential candidate genes and some new findings
    M Mondal
    Molecular and Human Genetics Division, CSIR Indian Institute of Chemical Biology, Kolkata 700032, India
    Gene 511:470-4. 2012
    ..This is the first report of an Indian AROA patient harboring a mutation in OCA2. Our results also reveal for the first time that mutations in SLC24A5 could contribute to extreme hypopigmentation in humans...
  31. ncbi request reprint Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4, Raja S C Mullick Road, Jadavpur, 700 032, Kolkata, India
    Hum Genet 122:556. 2007
  32. ncbi request reprint Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4, Raja S C Mullick Road, Jadavpur, 700 032, Kolkata, India
    Hum Genet 122:555. 2007
  33. ncbi request reprint SLC45A2 variations in Indian oculocutaneous albinism patients
    Mainak Sengupta
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata, West Bengal, India
    Mol Vis 13:1406-11. 2007
    ..Interestingly, in almost 31% of the cases, the second mutation has never been found. The purpose of this study was to investigate the molecular basis of OCA among Indians using SLC45A2 as the candidate gene...
  34. ncbi request reprint Novel human pathological mutations. Gene symbol: TYR. Disease: tyrosinase deficiency
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4, Raja S C Mullick Road, Jadavpur, 700 032, Kolkata, India
    Hum Genet 122:556. 2007
  35. ncbi request reprint Haplotype structure of TP53 locus in Indian population and possible association with head and neck cancer
    S Mitra
    Indian Institute of Chemical Biology, Human Genetics and Genomics Division, Kolkata 700 032, India
    Ann Hum Genet 67:26-34. 2003
    ..036) when two rare haplotypes 2-1-2 and 1-2-1 were combined. The rare haplotype 2-1-2 was found to be modestly over represented in HNSCC patients as compared to normal individuals...
  36. ncbi request reprint Analysis of haemophilia B database and strategies for identification of common point mutations in the factor IX gene
    S Mukherjee
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata 700 032, India
    Haemophilia 9:187-92. 2003
    ..Strikingly large number of mutation in codon 296 causing T to M change in catalytic domain originally proposed to be the result of the founder effect also contains largest number of haplotype suggesting recurrence of de novo mutation...
  37. ncbi request reprint Novel human pathological mutations. Gene symbol: TYR. Disease: albinism, oculocutaneous 1
    Kunal Ray
    Indian Institute of Chemical Biology, Molecular and Human Genetics Division, 4, Raja S C Mullick Road, Jadavpur, 700 032, Kolkata, India
    Hum Genet 122:555. 2007
  38. ncbi request reprint Higher prevalence of OCA1 in an ethnic group of eastern India is due to a founder mutation in the tyrosinase gene
    Moumita Chaki
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Mol Vis 11:531-4. 2005
    ..The purpose of the study was to investigate the molecular lesions causing OCA within this ethnic group for the unequivocal diagnosis of the carriers and attempt to decipher the cause for the high prevalence of OCA...
  39. ncbi request reprint Chromosomal aberrations and sister chromatid exchanges in individuals exposed to arsenic through drinking water in West Bengal, India
    J Mahata
    Division of Human Genetics and Genomics, Indian Institute of Chemical Biology, Jadavpur, Kolkata, India
    Mutat Res 534:133-43. 2003
    ..96% and 5.95, respectively). The enhanced rates of CAs and SCEs among the residents of North 24 Parganas are indicative of the cytogenetic damage due to long term exposure to arsenic through consumption of contaminated water...
  40. ncbi request reprint Gene symbol: MYOC
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Raja S C Mullick Rd, 4, Kolkata 700032, India
    Hum Genet 121:290-1. 2007
  41. ncbi request reprint Molecular pathogenesis of Wilson disease among Indians: a perspective on mutation spectrum in ATP7B gene, prevalent defects, clinical heterogeneity and implication towards diagnosis
    Arnab Gupta
    Indian Institute of Chemical Biology, Jadavpur, Kolkata, 700 032, India
    Cell Mol Neurobiol 27:1023-33. 2007
    ..We aim to identify the molecular defects in the ATP7B, the causal gene for Wilson disease (WD), in eastern Indian patients and attempt to assess the overall mutation spectrum in India for detection of mutant allele for diagnostic purposes...
  42. ncbi request reprint Gene symbol: MYOC
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4, Jadavpur, Kolkata 70032, India
    Hum Genet 121:290. 2007
  43. ncbi request reprint Gene symbol: CYP1B1
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4, Jadavpur, Kolkata 70032, India
    Hum Genet 121:292. 2007
  44. ncbi request reprint Molecular diagnosis of Wilson disease using prevalent mutations and informative single-nucleotide polymorphism markers
    Arnab Gupta
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata, India
    Clin Chem 53:1601-8. 2007
    ..We examined the use of intragenic single-nucleotide polymorphism (SNP) markers to avoid this limitation...
  45. pmc Leu432Val polymorphism in CYP1B1 as a susceptible factor towards predisposition to primary open-angle glaucoma
    Ashima Bhattacharjee
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology Council of Scientific and Industrial Research, Kolkata, India
    Mol Vis 14:841-50. 2008
    ..Since POAG is primarily a complex disease, we examined the potential of coding single nucleotide polymorphisms (cSNPs) in the gene for association with the disease...
  46. pmc Evaluation of the OPTC gene in primary open angle glaucoma: functional significance of a silent change
    Moulinath Acharya
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata, India
    BMC Mol Biol 8:21. 2007
    ....
  47. ncbi request reprint Distribution of p53 codon 72 polymorphism in Indian primary open angle glaucoma patients
    Moulinath Acharya
    Human Genetics Genomics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata, India
    Mol Vis 8:367-71. 2002
    ..The purpose of this study was to investigate whether the reported association between the p53 polymorphism and POAG is a common phenomenon irrespective of geographical location or ethnicity of the population...
  48. ncbi request reprint Primary role of CYP1B1 in Indian juvenile-onset POAG patients
    Moulinath Acharya
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Mol Vis 12:399-404. 2006
    ..Recent studies suggest a role of CYP1B1 in primary open-angle glaucoma (POAG) as a modifier locus. The purpose of the study was to further investigate the potential role of CYP1B1 in POAG patients...
  49. ncbi request reprint Determination of variants in the 3'-region of the tyrosinase gene requires locus specific amplification
    Moumita Chaki
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Hum Mutat 26:53-8. 2005
    ..We have resolved this potential problem using locus-specific amplification conditions that could be used to identify unequivocally mutations and SNPs in exon 4 and exon 5 of TYR and proximal flanking sequences...
  50. pmc Association of IL1A and IL1B loci with primary open angle glaucoma
    Suddhasil Mookherjee
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Council of Scientific and Industrial Research, Kolkata, India
    BMC Med Genet 11:99. 2010
    ..It has been reported that polymorphisms in the IL1A and IL1B genes are associated with Primary Open Angle Glaucoma (POAG). The purpose of our study was to investigate the role of these polymorphisms in eastern Indian POAG patients...
  51. pmc A novel COMMD1 mutation Thr174Met associated with elevated urinary copper and signs of enhanced apoptotic cell death in a Wilson Disease patient
    Arnab Gupta
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata, India
    Behav Brain Funct 6:33. 2010
    ..Two other changes were also identified in the gene. We have examined genotype-phenotype correlation between the detected changes and the atypical presentation of the WD patient...
  52. ncbi request reprint Mutations in MYOC gene of Indian primary open angle glaucoma patients
    Arijit Mukhopadhyay
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Mol Vis 8:442-8. 2002
    ..The purpose of this study was to investigate the molecular basis of POAG among Indians, using MYOC as the candidate gene, and broaden our understanding on the pathogenesis caused by MYOC...
  53. doi request reprint Toxicogenomics of arsenic: classical ideas and recent advances
    Pritha Ghosh
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Council of Scientific and Industrial Research, 4 Raja S C Mullick Road, Jadavpur, Kolkata 700 032, India
    Mutat Res 659:293-301. 2008
    ..Our goal in this article has been to present the current state of research on this area to help formulate strategies for future studies...
  54. ncbi request reprint SNPs in genes with copy number variation: a question of specificity
    Mainak Sengupta
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata 700 032, India
    J Genet 87:95-7. 2008
  55. ncbi request reprint Gene symbol: CYP1B1
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4, Jadavpur, Kolkata 70032, India
    Hum Genet 121:291. 2007
  56. pmc Genetic variants associated with arsenic susceptibility: study of purine nucleoside phosphorylase, arsenic (+3) methyltransferase, and glutathione S-transferase omega genes
    Sujata De Chaudhuri
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, Kolkata, India
    Environ Health Perspect 116:501-5. 2008
    ..Alteration in functions of these gene products may lead to arsenic-specific disease manifestations...
  57. ncbi request reprint Evaluation of genetic markers linked to hemophilia A locus: an Indian experience
    Atreyee Saha
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Road, Jadavpur, Kolkata, 700 032, India
    Haematologica 92:1725-6. 2007
    ....
  58. ncbi request reprint Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma
    Arijit Mukhopadhyay
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Mol Vis 11:792-7. 2005
    ..To evaluate the role of the optineurin gene (OPTN) in Indian primary open angle glaucoma (POAG) patients from different parts of the country...
  59. ncbi request reprint Upregulation of human mitochondrial NADH dehydrogenase subunit 5 in intestinal epithelial cells is modulated by Vibrio cholerae pathogenesis
    Madhubanti Sarkar
    Human Genetics and Genomics Group, Indian Institute of Chemical Biology, 4, Raja S C Mullick Road, Jadavpur, Kolkata 700 032, India
    FEBS Lett 579:3449-60. 2005
    ..This is the first report of alteration in mitochondrial gene expression upon infection of a non-invasive enteric bacterium like V. cholerae showing its modulation with adherence, motility and virulence of the organism...
  60. ncbi request reprint Genetics and bioinformatics of primary open angle glaucoma: an Indian perspective
    Kunal Ray
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata 700 032
    J Indian Med Assoc 102:708, 710, 712 passim. 2004
    ..This review is focused on the studies being conducted in India on primary open angle glaucoma to identify the molecular defects and new directions undertaken using bioinformatic approaches towards a better understanding of the disease...
  61. ncbi request reprint Bioinformatic approaches for identification and characterization of olfactomedin related genes with a potential role in pathogenesis of ocular disorders
    Arijit Mukhopadhyay
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Kolkata, India
    Mol Vis 10:304-14. 2004
    ..This endeavor would have the potential to identify new candidate genes for eye diseases in general and glaucoma in particular to be tested by wet-lab experiments...
  62. ncbi request reprint Micronuclei as biomarkers of carcinogen exposure in populations exposed to arsenic through drinking water in West Bengal, India: a comparative study in three cell types
    Anamika Basu
    Division of Human Genetics and Genomics, Indian Institute of Chemical Biology, 4, Raja S C Mullick Road, Jadavpur, Calcutta 700 032, India
    Cancer Epidemiol Biomarkers Prev 13:820-7. 2004
    ....
  63. ncbi request reprint Myocilin variants in Indian patients with open-angle glaucoma
    Ashima Bhattacharjee
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4 Raja S C Mullick Rd, Jadavpur, Kolkata 700 032, India
    Arch Ophthalmol 125:823-9. 2007
    ..To identify and evaluate MYOC variant alleles among patients with primary open-angle glaucoma (POAG) and age-matched control subjects in an Indian population...
  64. ncbi request reprint Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water
    Pritha Ghosh
    Indian Institute of Chemical Biology, Kolkata, and West Bank Hospital, Howrah, India
    Int J Cancer 118:2470-8. 2006
    ..24-2.22). These results show a protective role of GSTM1 null in arsenic toxicity. This study also indicates that asymptomatic individuals are sub clinically affected and are also significantly susceptible to arsenic-induced genotoxicity...
  65. ncbi request reprint Gene symbol: CYP1B1
    Kunal Ray
    Molecular and Human Genetics Division, Indian Institute of Chemical Biology, 4, Jadavpur, Kolkata 70032, India
    Hum Genet 121:291. 2007
  66. ncbi request reprint Comparison of health effects between individuals with and without skin lesions in the population exposed to arsenic through drinking water in West Bengal, India
    Pritha Ghosh
    Division of Molecular and Human Genetics, Indian Institute of Chemical Biology, Kolkata, India
    J Expo Sci Environ Epidemiol 17:215-23. 2007
    ....
  67. ncbi request reprint Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India
    Subhabrata Chakrabarti
    Kallam Anji Reddy Molecular Genetics Laboratory, Brien Holden Eye Research Centre, L V Prasad Eye Institute, Hyderabad, India
    Mol Vis 11:111-3. 2005
    ....
  68. ncbi request reprint Molecular pathogenesis of Parkinson's disease: identification of mutations in the Parkin gene in Indian patients
    Arindam Biswas
    S N Pradhan Centre for Neurosciences, University of Calcutta, 244B, A J C Bose Road, Kolkata 700 020, India
    Parkinsonism Relat Disord 12:420-6. 2006
    ..Clinical features of the Parkin mutants were compared. Among eastern Indian PD patients, mutation in Parkin was identified in 7.24% cases...
  69. ncbi request reprint Myocilin mutation 1109 C>T (Pro 370 Leu) is the most common gene defect causing early onset primary open angle glaucoma
    Arijit Mukhopadhyay
    Indian J Ophthalmol 51:279-81. 2003
  70. ncbi request reprint TRendys meeting report 2005
    Kunal Ray
    Indian Institute of Chemical Biology, Jadavapur, Kolkata
    Indian J Biochem Biophys 43:190-3. 2006
  71. ncbi request reprint DNA linkage based diagnosis of Wilson disease in asymptomatic siblings
    A Gupta
    Human Genetics and Genomics Division, Indian Institute of Chemical Biology, Jadavpur, Kolkata, India
    Indian J Med Res 118:208-14. 2003
    ..Hence, the present study was undertaken to identify, by a PCR-based molecular diagnostic test, presymptomatic siblings of WD affected individuals in families with multiple offspring...
  72. ncbi request reprint Wilson's disease: an update
    Shyamal K Das
    Movement Disorders Clinic, Bangur Institute of Neurology, Kolkata, India
    Nat Clin Pract Neurol 2:482-93. 2006
    ....