Items where Author is "Gopinath, PM"
Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Number of items: 28.

Article

Rotti, Harish and Raval, Ritu and Nair, Sreekumaran N and Gopinath, PM and Satyamoorthy, K and Valiathan, Manna (2016) Reply to ‘Lack of replication of association of THSD7A with obesity’. International Journal of Obesity, 40 (4). pp. 727-728. ISSN 0307-0565

Rotti, H and Raval, R and Nair, S and Gopinath, PM and Satyamoorthy, K (2015) A Novel Gene THSD7A is Associated with Obesity. International Journal of Obesity. pp. 1-4.

Bidchol, Abdul Mueed and Shukla, Anju and Hebbar, Shrikiran and Bhat, Ramesh Y and Matta, Divya and Shah, Hitesh and Gopinath, PM and Satyamoorthy, K and Girisha, KM (2015) Recurrent and novel GLB1 mutations in India. Gene, 40 (485). pp. 1-9. ISSN 0378-1119

Moka, Rajshekar and Sreelakshmi, K and Gopinath, PM and Satyamoorthy, K (2013) Cytogenetic evaluation of patients with clinical spectrum of turner syndrome. Journal of Human Reproductive Sciences, 6 (2). pp. 129-132.

Rajasekhar, M and Sreelakshmi, K and Gopinath, PM and Satyamoorthy, K (2013) Cytogenetic study in recurrent pregnancy loss: an experience from tertiary care centre. Genetic Counseling, 24 (3). pp. 347-349.

Muthusamy, A and Vidya, KS and Pratibha, PK and Rao, Radhakrishna M and Vidhu, SB and Guruprasad, KP and Raghavendra, U and Gopinath, PM and Satyamoorthy, K (2013) Establishment of an in vitro plantlet regeneration protocols for unique varieties of brinjal (Solanum melongena L.) var. Mattu Gulla and Perampalli Gulla. Indian Journal of Experimental Biology. ISSN 0019-5189

Kabekkodu, Shama Prasada and Bhat, Samatha and Mascarenhas, Roshan and Mallya, Sandeep and Bhat, Manoj and Pandey, Deeksha and Kushtagi, Pralhad and Gopinath, PM and Satyamoorthy, K (2013) Mitochondrial DNA Variation Analysis in Cervical Cancer. Mitochondrion.

Rajasekhar, M and Gopinath, PM and Sreelakshmi, K and Satyamoorthy, K (2013) A cytogenetic study of couples with miscarriages: An experience from manipal referral centre. International Journal of Human Genetics, 13 (2). pp. 93-97. ISSN 0972-3757

Mascarenhas, Roshan and Kabekkodu, Shama Prasada and Pai, Vijaya H and Gopinath, PM and Satyamoorthy, K (2012) Analysis of mitochondrial DNA variations in Indian patients with congenital cataract. Molecular Vision, 18. pp. 181-193.

Muthusamy, A and Pratibha, PK and Vijendra, Prabhu and Mahato, KK and Vidhu, SB and Rao, Radhakrishna M and Gopinath, PM and Satyamoorthy, K (2012) Influence of Helium-Neon Laser Irradiation on Seed Germination In Vitro and Physico-Biochemical Characters in Seedlings of Brinjal (Solanum melongena L.) var. Mattu Gulla. Photochemistry and Photobiology, 88 (5). pp. 1227-1235.

Neetha, J and Girisha, KM and Gopinath, PM and Sekhar, MR (2012) A de Novo Translocation of Chromosomes 1 and 2 in an 18 Year old boy with Syndromic Mental Retardation. GENETIC COUNSELING, 23 (4). pp. 473-476.

Vasudevan, TG and Saadi, Abdul Vahab and Girisha, KM and Gopinath, PM and Satyamoorthy, K (2011) Quantitative Fluorescent Polymerase Chain Reaction (QF-PCR) for Aneuploidy Detection. Genetic Clinics, 4 (2). pp. 1-18.

Rai, Padmalatha S and Murali, TS and Vasudevan, TG and Prasada, Shama K and Bhagavath, Ashok Kumar and Pai, Pranita and Gopinath, PM and Satyamoorthy, K (2011) Genetic variation in genes involved in folate and drug metabolism in a south indian population. Indian Journal of Human Genetics, 17 (S-1). S48-S53.

Rajasekhar, M and John, Neetha and Gopinath, PM and Satyamoorthy, K (2011) A cytogenetic study of children with developmental delay mental retardation. Int J Hum Genet, 11 (2). pp. 89-92.

Murugesan, Raju and Saadi, Abdul Vahab and Patra, Satyajit and Rao, Rekha and Rao, Jyothi and Rai, Padmalatha S and Gopinath, PM and Satyamoorthy, K (2010) Thiopurine S-methyltransferase alleles, TPMT*2, *3B and *3C, and genotype frequencies in an Indian population. Experimental and Therapeutic Medicine, 1 (1). pp. 121-127.

Girisha, KM and Rajasekhar, M and Gopinath, PM and Satyamoorthy, K (2010) Balanced Translocation in Mother Leading to Interchange Trisomy 21? Genetic Counseling, 21 (2). pp. 183-185.

Yashwanth, Radhakrishnan and Nallathambi, Chandra and Gopinath, PM (2010) Chromosomal Abnormalities among Children with Congenital Malformations. International Journal of Human Genetics, 10. pp. 57-63.

Kalavathi, V and Chandra, N and Nambiar, Renjini G and Shanker, Jayashree and Sugunashankari, P and Meena, J and Jegatheesan, T and Santhiya, ST and Ramesh, A and Gopinath, PM and Marimuthu, KM (2010) Chromosomal Abnormalities in 979 Cases of Amenorrhea: A Review. International Journal of Human Genetics, 10 (1-3). pp. 65-69.

Girisha, KM and Saadi, Abdul Vahab and Dalal, Ashwin B and Gopinath, PM and Satyamoorthy, K (2010) Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis. Ann Hematol, 89. pp. 625-626.

Rajasekhar, M and Murugesan, R and Rao, Rekha and Shetty, H and Rao, Jyothi and Gopinath, PM and Satyamoorthy, K (2010) Cytogenetic Analysis of 1400 Referral Cases: Manipal Experience. International Journal of Human Genetics, 10 (1-3). pp. 49-55.

Chandra, N and Cyril, Cyrus and Lakshminarayana, Prema and Nallasivam, P and Ramesh, A and Gopinath, PM and Marimuthu, KM (2010) Cytogenetic Evaluation of Down Syndrome : A Review of 1020 Referral Cases. International Journal of Human Genetics , 10 (1-3). pp. 87-93.

Saadi, Abdul Vahab and Kushtagi, Pralhad and Gopinath, PM and Satyamoorthy, K (2010) Quantitative Fluorescence Polymerase Chain Reaction (QF-PCR) for Prenatal Diagnosis of Chromosomal Aneuploidies. International Journal of Human Genetics, 10 ((1-3)). pp. 121-129.

Yashwanth, Radhakrishnan and Nallathambi, Chandra and Gopinath, PM (2010) Satellite Associations in Down Syndrome. International Journal of Human Genetics, 10 (1-3). pp. 101-104.

Guruprasad, KP and Mascarenhas, Roshan and Gopinath, PM and Satyamoorthy, K (2010) Studies on Brahma Rasayana in Male Swiss Albino Mice: Chromosomal Aberrations and Sperm Abnormalities. Journal of Ayurveda and Integrative Medicine, 1 (1). pp. 40-44.

Murugesan, Raju and Saadi, Abdul Vahab and Patra, Satyajit and Rao, Rekha and Rao, Jyothi and Rai, Padmalatha S and Gopinath, PM and Satyamoorthy, K (2010) Thiopurine S-methyltransferase alleles, TPMT*2, *3B and *3C, and genotype frequencies in an Indian population. experimental and therapeutic medicine, 1. pp. 121-127.

Mascarenhas, Roshan and Pai, Vijaya H and Rao, Lavanya G and Shama, Prasada K and Santhiya, ST and Graw, Jochen and Gopinath, PM and Satyamoorthy, K (2010) A novel human CRYGD mutation in a juvenile autosomal dominant cataract. Molecular Vision, 16. pp. 887-896.

Cyril, Cyrus and Rai, Padmalatha S and Chandra, N and Gopinath, PM and Satyamoorthy, K (2009) MTHFR Gene variants C677T, A1298C and association with Down syndrome: A Case-control study from South India. Indian journal of human genetics, 15 (2).

Book Section

Mascarenhas, Roshan and Prasada, Shama K and Gopinath, PM and Satyamoorthy, K (2017) Molecular Genetics of Congenital Cataract. In: Human  Genomics and Applications. Narendra Publishing House, Delhi, India, pp. 101-117.

This list was generated on Wed Jan 19 23:21:47 2022 UTC.