Výsledky vyhledávání - "Selma D'Silva"

Human leukocyte antigen (HLA) alleles as predictive factors for benefit from lenalidomide in acute myeloid leukemia (AML)

Autor: Sachin, Punatar, Anant, Gokarn, Lingaraj, Nayak, Avinash, Bonda, Sumeet, Mirgh, Akanksha, Chichra, Meenakshi, Singh, Selma, D'silva, Navin, Khattry

Publikováno v: Am J Blood Res

Objectives: Lenalidomide is an active agent in acute myeloid leukemia (AML); response rates are about 15-30%. There are no well-defined predictive factors for benefit from lenalidomide in AML. One of the mechanisms of lenalidomide is natural killer (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0098423be0385f963aafcbb224912ac8
https://pubmed.ncbi.nlm.nih.gov/34824888

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Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults

Autor: Malay B. Mukherjee, Kanjaksha Ghosh, Roshan B. Colah, Selma D'Silva, Ashish Chiddarwar

Publikováno v: Annals of Human Genetics. 81:11-19

Summary Objective: The present study was undertaken to investigate the genotype and allele frequencies of the variants in the four bilirubin metabolism genes (UGT1A1, OATP2, HMOX1, and BLVRA) and their association with hyperbilirubinemia. Material an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ba3dfa46dbcd8f242f44863f3283175d
https://doi.org/10.1111/ahg.12179

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Genetic lesions in the UGT1A1 genes among Gilbert's syndrome patients from India

Autor: Ashish Chiddarwar, Malay B. Mukherjee, Kanjaksha Ghosh, Roshan B. Colah, Selma D'Silva

Publikováno v: Molecular biology reports. 45(6)

The present study was undertaken to investigate genetic variations present in the coding regions of the UGT1A1 gene among the Gilbert’s syndrome patients. Analysis of genetic variations was performed by direct DNA sequencing among the patients that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61bb5e3cf0ef229b8106db9035f1f64c
https://pubmed.ncbi.nlm.nih.gov/30105552

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Killer immunoglobulin like receptor gene profiling in Western Indian population

Autor: Selma D'Silva, Sandeep Kumar Dhanda, Meenakshi Singh

Publikováno v: Human Immunology. 80:427-428

One hundred and sixty one healthy unrelated hematopoietic stem cell transplant donors from Western Indian were enrolled in this study. The study was initiated to observe the genotypic diversity of 16 killer immunoglobulin like receptor (KIR) genes in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9983951938e39921dfc30d85a1581fc
https://doi.org/10.1016/j.humimm.2019.03.010

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Killer Immunoglobulin like Receptor and Hematopoetic Stem Cell Transplantation: A Brief Review

Autor: Meenakshi Singh, Selma D'Silva

Publikováno v: Journal of Blood & Lymph.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f15333aac6d2f4caee3f4c11ea6faf2
https://doi.org/10.4172/2165-7831.1000218

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Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates

Autor: Malay B. Mukherjee, Roshan B. Colah, Selma D'Silva, Kanjaksha Ghosh

Publikováno v: Gene. 547:18-22

Genetic association studies have linked a number of single nucleotide polymorphisms (SNPs) with unconjugated hyperbilirubinemia. The present study was undertaken to validate the association of SNPs with development of hyperbilirubinemia in Indian neo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf78cae843b4b9064325ecb60e7b090
https://doi.org/10.1016/j.gene.2014.05.047

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Association of (GT)n Repeats Promoter Polymorphism of Heme Oxygenase-1 Gene with Serum Bilirubin Levels in Healthy Indian Adults

Autor: Selma D'Silva, Kanjaksha Ghosh, Malay B. Mukherjee, Vikrant Borse, Roshan B. Colah

Publikováno v: Genetic Testing and Molecular Biomarkers. 15:215-218

Aim: The present study was undertaken to investigate a length polymorphism of (GT)n repeats of the heme oxygenase-1 (HMOX-1) gene and its association with serum bilirubin levels in apparently healthy adults. Methods: A total of 211 individuals (norma

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2f697cd490c7cb4aea2232435f01092
https://doi.org/10.1089/gtmb.2010.0132

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Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?

Autor: Rati Devendra, Kanjaksha Ghosh, Selma D'Silva, Prabhakar Kedar, Malay B. Mukherjee, Roshan B. Colah, Prashant Warang, Ashish Chiddarwar

Publikováno v: Annals of hematology. 94(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56c59934574adecf632aa7031cc6bd23
https://pubmed.ncbi.nlm.nih.gov/24947795

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G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India

Autor: Kanjaksha Ghosh, Selma D'Silva, Malay B. Mukherjee, Roshan B. Colah

Publikováno v: The Journal of Maternal-Fetal & Neonatal Medicine. 25:1833-1834

We read with interest the report entitled “Neonatal hyperbilirubinemia and G71R mutation of the UGT1A1 gene in Turkish patients” by Narter et al. [1]. We have also been studying the genetic risk fa...

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2291c773a8149bf702c2b32027bde5aa
https://doi.org/10.3109/14767058.2011.644362

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