Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Parth S. Shah"'
Publikováno v:
PRX Quantum, Vol 5, Iss 3, p 030346 (2024)
Distributing entanglement between remote sites is integral to quantum networks. Here, we demonstrate the autonomous stabilization of remote entanglement between a pair of noninteracting superconducting qubits connected by an open waveguide on a chip.
Externí odkaz:
https://doaj.org/article/01d01b0662a64e109465617f838ebf32
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 15, Iss 3, Pp GE01-GE09 (2021)
Introduction: Infertility affects about 15% of couples attempting pregnancy and in approximately 50% of these cases, male factors are responsible. Male infertility is clinically characterised by azoospermia and oligozoospermia depending on the amo
Externí odkaz:
https://doaj.org/article/bbfa0a60f10649dcb31ed91d47519fa4
Autor:
Shivaprasad H. Sathyanarayana, Sophie J. Deharvengt, Guohong Huang, Rachael E. Barney, Parth S. Shah, Joel A. Lefferts
Publikováno v:
Advances in Molecular Pathology. 5:85-108
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30a44e500ef718664ebead833437b998
https://doi.org/10.1016/j.yamp.2022.07.004
https://doi.org/10.1016/j.yamp.2022.07.004
Autor:
Sandip C Shah, Nidhi D Shah, Parth S Shah, Hari Shankar P Ray, Ketan K Vaghasia, Anil K Mehta, Bhavini S Shah, Mandava V Rao
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 8, Pp GC05-GC10 (2019)
Introduction: Among all chromosomes (46) in the human genome, particular significance has been given to chromosomes 13, 18, 21, X and Y. This is primarily because of aneuploidy in these chromosomes that result in viable pregnancies with congenital de
Externí odkaz:
https://doaj.org/article/6ad62cd54d394553bd6315391ac261be
Autor:
Nidhi P Shah, Krishna Mistry, Mudra Kansara, K Sonali, Nirali Thakkar, Parth S Shah, Sandip C Shah, Mandava V Rao
Publikováno v:
Eastern Journal of Medical Sciences. :61-65
Introduction: Male infertility (MI) in about 50% of couples is constituted due to genetic, hormonal, and epigenetic factors. Almost 10% of it is contributed to genetic anomalies. Objectives: This study was undertaken in 787 males with infertility and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1994ad8869be2e2654ba1c97da3f28b5
https://doi.org/10.32677/ejms.v6i4.3220
https://doi.org/10.32677/ejms.v6i4.3220
Publikováno v:
Lung India, Vol 33, Iss 4, Pp 404-409 (2016)
Introduction: Chronic obstructive pulmonary disease (COPD) is a global health issue with cigarette smoking being an important risk factor. COPD affects pulmonary blood vessels, right ventricle, as well as left ventricle leading to the development of
Externí odkaz:
https://doaj.org/article/9a7298216e474823b42a1ad01ac45ecf
Autor:
Parth S Shah, Nidhi D Shah, Hari Shankar P Ray, Nikunj B Khatri, Ketan K Vaghasia, Mandava V Rao, Sandip C Shah
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 12, Iss 5, Pp GC01-GC06 (2018)
Introduction: The β-thalassaemia is one of the haemoglobinopathies related to genetic disorders. It occurs due to mutation in β-gene of autosome 11. In India, it affects 1-7% of couples annually. Reports are available in few states of India about
Externí odkaz:
https://doaj.org/article/0747a224ff7d45dc892a48ae334fe426
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 11, Iss 9, Pp GD01-GD03 (2017)
The mutations in Haemoglobin Beta (HBB) gene, bring about less or no production of Hb β-chain synthesis in affected cases, leading from minor to major types depending on haematological indices. In compound heterozygotic conditions, two traits are
Externí odkaz:
https://doaj.org/article/898f384fa5e344c6973dbd8281537c3a
Publikováno v:
Eastern Journal Of Medical Sciences. 6:1-8
Background: Y chromosome microdeletions provide a pivotal role in the control of spermatogenesis. These are located on the q arm of it, specifically, the azoospermia factor (AZF) region, hence named as Yq microdeletions. The mutations in this region
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1112313d092a55b89237375f3e0267f7
https://doi.org/10.32677/ejms.2021.v06.i01.001
https://doi.org/10.32677/ejms.2021.v06.i01.001
Publikováno v:
Clinical geneticsREFERENCES. 100(6)
GOGLA2/GM130 is a Golgin protein involved in vesicle tethering, cell proliferation and autophagy. Recessive loss of function mutation in GOLGA2 has been previously reported in a single family with muscular dystrophy and microcephaly. Here we describe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c80e433606bef06cdd84ca54df50c2e
https://pubmed.ncbi.nlm.nih.gov/34424553
https://pubmed.ncbi.nlm.nih.gov/34424553