Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Pawan K. Jain"'
Autor:
Sagar Mothkuri, Honey Gupta, Pawan K. Jain, Tata Narsinga Rao, Gade Padmanabham, Supriya Chakrabarti
Publikováno v:
Micromachines, Vol 12, Iss 2, p 213 (2021)
Functionalized carbon nanotube (FCNT) and Manganese Oxide (MnO2) nanoflower hybrid material was synthesized using hydrothermal technique as a promising electrode material for supercapacitor applications. The morphological investigation revealed the f
Externí odkaz:
https://doaj.org/article/5759f48c4c0e423286de810b7d36c276
Publikováno v:
Indian Journal of Anaesthesia, Vol 58, Iss 2, Pp 210-213 (2014)
Externí odkaz:
https://doaj.org/article/041cc0fafe264816b3c608d1d7d7c946
Publikováno v:
Advanced Nanomaterials ISBN: 9783031119958
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eee026daf2c5db355297181bd00b0b37
https://doi.org/10.1007/978-3-031-11996-5_7
https://doi.org/10.1007/978-3-031-11996-5_7
Autor:
Sharon A. Ross, Asad Umar, Barbara K. Dunn, Mukesh Verma, Pawan K. Jain, Richard B. Hayes, Wendy Wang
Publikováno v:
Annals of the New York Academy of Sciences. 983:298-319
Recent advances in molecular biology that have provided a greater understanding of multistage carcinogenesis include the use of biomarkers of early detection and risk assessment. Prominent among such biomarkers are epigenetic changes. The field of ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd4d4ef9e8bb229eb77e7735c49fc5f1
https://doi.org/10.1111/j.1749-6632.2003.tb05984.x
https://doi.org/10.1111/j.1749-6632.2003.tb05984.x
Autor:
Pawan K. Jain
Publikováno v:
Annals of the New York Academy of Sciences. 983:71-83
Epigenetics is the study of mitotically heritable changes in gene expression without any changes in the primary DNA sequence. The major step in epigenetic gene regulation is gene inactivation by hypermethylation of CpG islands located in the promoter
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbb4bf25598e99eb82972fed60d12315
https://doi.org/10.1111/j.1749-6632.2003.tb05963.x
https://doi.org/10.1111/j.1749-6632.2003.tb05963.x
Autor:
Ross I. S. Zbar, Dilip Deshmukh, Kunihiro Fukushima, Hana Skarka, Elizabeth A. Thomas, Anil K. Lalwani, Arabandi Ramesh, Ishwar C. Verma, Edward R. Wilcox, Subrinder Kumar, C. R. Srikumari Srisailapathy, Richard J.H. Smith, Pawan K. Jain, Sigrid Wayne, Barbara Ploplis
Publikováno v:
Human Molecular Genetics. 4:2391-2394
A locus for recessive neurosensory nonsyndromic hearing impairment maps to chromosome 9q13-q21 in two regionally separate consanguineous families from India. Each family demonstrates a LOD score greater than 4.5 to this region. D9S15, tightly linked
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e6eb5bdfe2b48a14309e09cf30fd94
https://doi.org/10.1093/hmg/4.12.2391
https://doi.org/10.1093/hmg/4.12.2391
Publikováno v:
Radiology. 223(3)
A 47-year-old woman presented with a 5-year history of intermittent episodes of excruciating back pain confined to the sacral area. There was no radiation of pain, but the right leg occasionally “gave way.” The back pain usually resolved spontane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e91463311d567b93c47a05cd8c6c1348
https://pubmed.ncbi.nlm.nih.gov/12034948
https://pubmed.ncbi.nlm.nih.gov/12034948
Autor:
Pawan K. Jain, Roger E. Kelley
Publikováno v:
Journal of neuroimaging : official journal of the American Society of Neuroimaging. 10(1)
Three patients with hemichorea/hemiballismus/hemidystonia caused by discrete contralateral infarction of the corpus striatum are presented. The infarcts were all small on CT or MRI brain scan and were lacunar in type. Small discrete infarction of bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c48dd4cd084a56e269939cea28a3ac91
https://pubmed.ncbi.nlm.nih.gov/10666978
https://pubmed.ncbi.nlm.nih.gov/10666978
Publikováno v:
Human genetics. 100(1)
We have characterized the mutations in 1050 carriers of the beta-thalassemia gene and analyzed their regional distribution in India. The majority of beta-thalassemia carriers were migrants from Pakistan and their pattern of mutations differed from th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7dbfc2494bb9a982ad9f49e585ab76ac
https://pubmed.ncbi.nlm.nih.gov/9225979
https://pubmed.ncbi.nlm.nih.gov/9225979
Autor:
Marketa Wills, Barbara Plopils, Kunihiro Fukushima, Marci M. Lesperance, Richard J.H. Smith, Fred H. Bess, Pawan K. Jain, Theresa B. San Agustin, James W. Hail, Hana Skarka, Edward R. Wilcox
Publikováno v:
Human molecular genetics. 4(10)
Mapping genes for nonsyndromic hereditary hearing impairment may lead to identification of genes that are essential for the development and preservation of hearing. We studied a family with autosomal dominant, progressive, low frequency sensorineural
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9661d47a1b521919e5590795808695
https://pubmed.ncbi.nlm.nih.gov/8595423
https://pubmed.ncbi.nlm.nih.gov/8595423