Search Results - "Shastri, Shivaram S"

Influence of MDR1 and CYP3A5 genetic polymorphisms on trough levels and therapeutic response of imatinib in newly diagnosed patients with chronic myeloid leukemia by Harivenkatesh, Natarajan, Kumar, Lalit, Bakhshi, Sameer, Sharma, Atul, Kabra, Madhulika, Velpandian, Thirumurthy, Gogia, Ajay, Shastri, Shivaram S., Biswas, Nihar Ranjan, Gupta, Yogendra Kumar

“…[Display omitted] Polymorphisms in genes coding for imatinib transporters and metabolizing enzymes may affect imatinib pharmacokinetics and clinical response…”
Get full text

Association of SPINK1 Gene Mutation and CFTR Gene Polymorphisms in Patients With Pancreas Divisum Presenting With Idiopathic Pancreatitis by Garg, Pramod Kumar, Khajuria, Rajni, Kabra, Madhulika, Shastri, Shivaram S

“…BACKGROUNDPancreas divisum has been associated with idiopathic pancreatitis. However, the causal association remains controversial. OBJECTIVETo study the gene…”
Get full text

Spectrum of GJB2 gene variants in Indian children with non-syndromic hearing loss by Singh, Pawan, Sharma, Shipra, Ghosh, Manju, Shastri, Shivaram, Gupta, Neerja, Kabra, Madhulika

“…Post hoc sample size was calculated (http://clincalc.com/stats/power.aspx) based on the frequency of GJB2 mutations (10%) in north India[3] with allowable…”
Get full text

Do polymorphisms in MDR1 and CYP3A5 genes influence the risk of cytogenetic relapse in patients with chronic myeloid leukemia on imatinib therapy? by Harivenkatesh, Natarajan, Kumar, Lalit, Bakhshi, Sameer, Sharma, Atul, Kabra, Madhulika, Velpandian, Thirumurthy, Gogia, Ajay, Shastri, Shivaram S., Gupta, Yogendra Kumar

“…Influence of polymorphisms in the genes coding for imatinib transporters and metabolizing enzymes on cytogenetic relapse in patients with chronic myeloid…”
Get full text

Association of Angiotensin-Converting Enzyme Insertion(I)/Deletion (D) Genotype in Alzheimer's Disease Patients of North Indian Population by Nirmal, Sonali, Tripathi, Manjari, Shastri, Shivaram S., Sagar, Rajesh, S., Vivekanandhan

“…ABSTRACT Several lines of evidence support for the role of angiotensin-converting enzyme (ACE) in Alzheimer's disease (AD) patients. Most human genetic studies…”
Get full text

Characterisation of mutations and genotype–phenotype correlation in cystic fibrosis: Experience from India by Shastri, Shivaram S, Kabra, Madhulika, Kabra, Sushil Kumar, Pandey, Ravindra M, Menon, P.S.N

“…Abstract Background Very little is known about the genetics of cystic fibrosis (CF) from the Indian subcontinent. The aims of the study were to identify the…”
Get full text

Carrier frequency of F508del mutation of cystic fibrosis in Indian population by Kapoor, Vishal, Shastri, Shivaram S., Kabra, Madhulika, Kabra, Sushil Kumar, Ramachandran, Vijaya, Arora, Sadhna, Balakrishnan, Prahlad, Deorari, Ashok Kumar, Paul, Vinod Kumar

“…Background: Cystic fibrosis (CF) is considered to be very rare in Indian subcontinent. Based on reports of CF in migrants from Indian subcontinent to United…”
Get full text

TMC1 may be a common gene for nonsyndromic hereditary hearing loss in Indian population by Singh, Pawan Kumar, Sharma, Shipra, Ghosh, Manju, Shastri, Shivaram S, Gupta, Neerja, Roy Chowdhury, Madhumita, Kabra, Madhulika

“…Background: Hearing impairment is very heterogeneous and most common sensory disorder. The prevalence of prelingual hearing loss is 1:500, with both…”
Get full text

Prenatal diagnosis of Duchenne muscular dystrophy by Maheshwari, M, Vijaya, R, Kabra, M, Arora, S, Shastri, S S, Deka, D, Kriplani, A, Menon, P S

“…Duchenne muscular dystrophy (DMD) is one of the most common X-linked genetic disorders seen in children. Mutations in the DMD gene coding for the protein…”
Get more information