نتائج البحث

Investigating Major Recurring Campylobacter jejuni Lineages in Luxembourg Using Four Core or Whole Genome Sequencing Typing Schemes

• Authors : NENNIG, Morgane; LLARENA, Ann-Katrin; HEROLD, Malte ...

Subjects: whole genome sequencing; Campylobacter jejuni; typing schemes

• Source: Frontiers in Cellular and Infection Microbiology, 10 (2021-01-08)

تفاصيل العنوان

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into the complex genetic architecture

• Authors : Chia, Ruth; Sabir, Marya S.; Bandres-Ciga, Sara

Subjects: Lewy body dementia; whole-genome sequencing; GBA

تفاصيل العنوان

IDENTIFICATION AND FUNCTIONAL CHARACTERIZATION OF VPS41 AS A POTENTIAL GENETIC MODIFIER OF PENETRANCE IN P.G2019S LRRK2-ASSOCIATED PARKINSON’S DISEASE

• Authors : Ohnmacht, Jochen; Bobbili, Dheeraj; Meyrath, Max ...

Subjects: Parkinson’s disease; VPS41; LRRK2

• Source: Precision Medicine in Parkinson’s Disease, Esch-sur-Alzette, Luxembourg [LU], 26/01/2023 - 27/01/2023

تفاصيل العنوان

Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

• Authors : Yaldiz, Burcu; Kucuk, Erdi; Hampstead, Juliet ...

Subjects: Life sciences; Genetics & genetic processes; Human health sciences

• Source: Human Genomics, 17 (1), 39 (2023-05-03)

تفاصيل العنوان

Nanopore Single-Molecule Sequencing for Mitochondrial DNA Methylation Analysis: Investigating Parkin-Associated Parkinsonism as a Proof of Concept

• Authors : Lüth, Theresa; WASNER, Kobi; Klein, Christine

Subjects: mitochondrial DNA; methylation; Nanopore

• Source: Frontiers in Aging Neuroscience (2021-09-28)

تفاصيل العنوان

Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype study

• Authors : Amanat, Sana; Gallego-Martinez, Alvaro; Sollini, Joseph ...

Subjects: Tinnitus; Extreme phenotype; Axon initial segment

• Source: EBioMedicine, 66 (103309) (2021-04)

تفاصيل العنوان

Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research.

• Authors : Rajan, Roopa; Divya, K. P.; Kandadai, Rukmini Mridula

Subjects: Parkinson's disease; biobank; common genetic variation

• Source: Frontiers in Neurology, 11, 524 (2020-06-18)

تفاصيل العنوان

Blood contains circulating cell-free respiratory competent mitochondria.

• Authors : Al Amir Dache, Zahra; Otandault, Amaëlle; Tanos, Rita

Subjects: Blotting; Western; Cell Line

• Source: FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34 (3), 3616-3630 (2020)

تفاصيل العنوان

Discordant Monozygotic Parkinson Disease Twins: Role of Mitochondrial Integrity

• Authors : Dulovic-Mahlow, Marija; König, Inke R.; Trinh, Joanne

Subjects: Life sciences; Biochemistry; biophysics & molecular biology

• Source: Annals of Neurology (2020-10-23)

تفاصيل العنوان

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses

• Authors : Van Bergen, Nicole; Guo, Yiran; Rankin, Julia ...

Subjects: metabolite repair; mitochondria; febrile illness

• Source: Brain: a Journal of Neurology, 142 (1), 50-58 (2019-01-01)

تفاصيل العنوان