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1.
Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signaling.
Hum Mol Genet
; 28(3): 351-371, 2019 02 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30239736
2.
Validation of a Host Response Assay, SeptiCyte LAB, for Discriminating Sepsis from Systemic Inflammatory Response Syndrome in the ICU.
Am J Respir Crit Care Med
; 198(7): 903-913, 2018 10 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29624409
3.
Adherence of Observational Studies Published in Indian Journals to STRO BE Statement.
J Assoc Physicians India
; 66(12): 39-42, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-31315323
4.
DDOST mutations identified by whole-exome sequencing are implicated in congenital disorders of glycosylation.
Am J Hum Genet
; 90(2): 363-8, 2012 Feb 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-22305527
5.
Mutations in the glycosylphosphatidylinositol gene PIGL cause CHIME syndrome.
Am J Hum Genet
; 90(4): 685-8, 2012 Apr 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-22444671
6.
Aberrant firing of replication origins potentially explains intragenic nonrecurrent rearrangements within genes, including the human DMD gene.
Genome Res
; 22(1): 25-34, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22090376
7.
Adverse Drug Reactions and Prescription Patterns of Antiretroviral Drugs: A Longitudinal Observational Study From a Tertiary Care Hospital in Western India.
Cureus
; 16(3): e56424, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38638708
8.
Assessment of risk of bias in randomized controlled trials published in Indian journals pertaining to pharmacology.
Perspect Clin Res
; 14(1): 16-19, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-36909217
9.
Human solid tumors and clinical relevance of the enhanced permeation and retention effect: a 'golden gate' for nanomedicine in preclinical studies?
Nanomedicine (Lond)
; 18(2): 169-190, 2023 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-37042320
10.
Investigator knowledge, awareness, and registrations of academic clinical trials with the Clinical Trial Registry of India: An observational study.
Perspect Clin Res
; 14(4): 187-193, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38025286
11.
Targeted polymerase chain reaction-based enrichment and next generation sequencing for diagnostic testing of congenital disorders of glycosylation.
Genet Med
; 13(11): 921-32, 2011 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-21811164
12.
The skin microbiome of elasmobranchs follows phylosymbiosis, but in teleost fishes, the microbiomes converge.
Microbiome
; 8(1): 93, 2020 06 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-32534596
13.
Increasing autophagy and blocking Nrf2 suppress laminopathy-induced age-dependent cardiac dysfunction and shortened lifespan.
Aging Cell
; 17(3): e12747, 2018 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-29575479
14.
TRiC/CCT chaperonins are essential for maintaining myofibril organization, cardiac physiological rhythm, and lifespan.
FEBS Lett
; 591(21): 3447-3458, 2017 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-28963798
15.
Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels.
PLoS One
; 12(2): e0170843, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28152038
16.
An audit of the approval letters issued by Drugs Controller General of India to Ethics Committees in India.
Perspect Clin Res
; 7(4): 165-167, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27843791
17.
An Audit of Protocol Deviations Submitted to an Institutional Ethics Committee of a Tertiary Care Hospital.
PLoS One
; 11(1): e0146334, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26735850
18.
Impact of recent regulatory notifications on an institutional ethics committee.
Indian J Med Ethics
; 1(4): 210-214, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-27473067
19.
Comprehensive mutation analysis for congenital muscular dystrophy: a clinical PCR-based enrichment and next-generation sequencing panel.
PLoS One
; 8(1): e53083, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-23326386
20.
Assessment of target enrichment platforms using massively parallel sequencing for the mutation detection for congenital muscular dystrophy.
J Mol Diagn
; 14(3): 233-46, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22426012