Mitochondrial DNA in Human Diversity and Health: From the Golden Age to the Omics Era

CL Hernández - Genes, 2023 - mdpi.com
Mitochondrial DNA (mtDNA) is a small fraction of our hereditary material. However, this
molecule has had an overwhelming presence in scientific research for decades until the …

Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel

C Faccinetto, D Sabbatini, P Serventi, M Rigato… - International Journal of …, 2021 - Springer
With the recent advances in next-generation sequencing (NGS), mitochondrial whole-
genome sequencing has begun to be applied to the field of the forensic biology as an …

Ion torrent high throughput mitochondrial genome sequencing (HTMGS)

NR Harvey, CL Albury, S Stuart, MC Benton, DA Eccles… - Plos one, 2019 - journals.plos.org
The implementation and popularity of next generation sequencing (NGS) has led to the
development of various rapid whole mitochondrial genome sequencing techniques. We …

Three reportedly unrelated families with Liddle syndrome inherited from a common ancestor

L Pagani, Y Diekmann, M Sazzini, S De Fanti… - …, 2018 - Am Heart Assoc
Liddle syndrome is considered a rare Mendelian hypertension. We have previously
described 3 reportedly unrelated families, native of an Italian area around the Strait of …

Mitochondrial DNA in Human Diversity and Health: From the Golden Age to the Omics Era

CL Hernández De La Fuente - 2023 - docta.ucm.es
Mitochondrial DNA (mtDNA) is a small fraction of our hereditary material. However, this
molecule has had an overwhelming presence in scientific research for decades until the …

[PDF][PDF] Introduction to NGS platforms and their role in plant genetic modification

M Shariat, S Neysi - 2022 - sid.ir
Background: DNA sequencing is one of the most important techniques in the field of
molecular biology, according to which the order of nucleotides can be determined in a piece …

[PDF][PDF] Three reportedly unrelated families with Liddle's syndrome inherited from a common ancestor Short title: Genotyping families with Liddle syndrome

L Pagani, Y Diekmann, M Sazzini, S De Fanti… - academia.edu
Liddle's Syndrome (LS) is considered a rare Mendelian hypertension. We have previously
described three reportedly unrelated families, native of an Italian area around the Strait of …

[PDF][PDF] Nobody is unrelated: An evolutionary approach to assess the prevalence of Liddle syndrome in Sicily

L Pagani, Y Diekmann, M Sazzin, S De Fanti… - researchgate.net
Liddle Syndrome is a rare dominant Mendelian disease characterized by salt-sensitive
hypertension and increased incidence of premature cardio-and cerebro-vascular events …