UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson’s disease

Scientific reports, 2017-07, Vol.7 (1), p.6306-10, Article 6306

2017

Volltextzugriff (PDF)

Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5

Movement disorders, 2023-12, Vol.38 (12), p.2217-2229

2023

Volltextzugriff (PDF)

Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene

Stem cell research, 2022-08, Vol.63, p.102856-102856, Article 102856

2022

Volltextzugriff (PDF)

Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population

Neurobiology of aging, 2014-05, Vol.35 (5), p.1212.e11-1212.e13

2014

Volltextzugriff (PDF)

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort

Neurobiology of aging, 2017-02, Vol.50, p.169.e3-169.e4

2017

Volltextzugriff (PDF)

Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene

Stem cell research, 2019-05, Vol.37, p.101432-101432, Article 101432

2019

Volltextzugriff (PDF)

Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation

Stem cell research, 2019-05, Vol.37, p.101447-101447, Article 101447

2019

Volltextzugriff (PDF)

Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant

Stem cell research, 2018-04, Vol.28, p.1-5

2018

Volltextzugriff (PDF)

A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

BMC neurology, 2017-01, Vol.17 (1), p.2-2, Article 2

2017

Volltextzugriff (PDF)

Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation

Stem cell research, 2017-12, Vol.25 (C), p.123-127

2017

Volltextzugriff (PDF)

Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family

Parkinsonism & related disorders, 2019-05, Vol.62, p.236-238

2019

Volltextzugriff (PDF)

Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia

Parkinsonism & related disorders, 2023-02, Vol.107, p.105294-105294, Article 105294

2023

Volltextzugriff (PDF)

A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration

Parkinsonism & related disorders, 2023-04, Vol.109, p.105353-105353, Article 105353

2023

Volltextzugriff (PDF)

Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity

Human molecular genetics, 2016-05, Vol.25 (10), p.1965-1978

2016

Volltextzugriff (PDF)

PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population

Neurobiology of aging, 2018-11, Vol.71, p.265.e15-265.e16

2018

Volltextzugriff (PDF)

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Neurology, 2014-01, Vol.82 (3), p.283-283

2014

Volltextzugriff (PDF)

Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease

Parkinsonism & related disorders, 2018-05, Vol.50, p.48-53

2018

Volltextzugriff (PDF)

Simulated lunar microgravity transiently arrests growth and induces osteocyte-chondrocyte lineage differentiation in human Wharton’s jelly stem cells

NPJ microgravity, 2024-05, Vol.10 (1), p.51-51, Article 51

2024

Volltextzugriff (PDF)

Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson’s Disease in a Taiwanese Population: An 11-Year Follow-Up Study

Journal of movement disorders, 2023-05, Vol.16 (2), p.168-179

2023

Volltextzugriff (PDF)

Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders

Frontiers in neurology, 2014-01, Vol.5, p.59-59

2014

Volltextzugriff (PDF)

Balance matters more: Research on the effect of corporate social responsibility equilibrium on stock price crash risk

PloS one, 2024-10, Vol.19 (10), p.e0306879

2024

Volltextzugriff (PDF)

Do political connections facilitate or inhibit firms' digital transformation? Evidence from China's A-share private listed companies

PloS one, 2024-05, Vol.19 (5), p.e0302586-e0302586

2024

Volltextzugriff (PDF)

Prognostic value of sarcopenia in patients with liver cirrhosis: A systematic review and meta-analysis

PloS one, 2017-10, Vol.12 (10), p.e0186990-e0186990

2017

Volltextzugriff (PDF)

Comprehensive intellectual property ability and firm productivity: A quasi-natural experiment based on national intellectual property demonstration advantage firm policy in China

PloS one, 2024-04, Vol.19 (4), p.e0302693-e0302693

2024

Volltextzugriff (PDF)

How does the integration of cultural and tourism industries impact the value added to tourism value chain: Evidences from Jiangsu Province of China

PloS one, 2023-06, Vol.18 (6), p.e0287610-e0287610

2023

Volltextzugriff (PDF)

1 – 25 von 3.623

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.299)
Mit Volltextzugriff
(3.424)

Publikationsform

Artikel
(1.604)
Buchkapitel
(1.095)
Tagungsberichte
(891)
Bücher
(31)
Berichte
(2)

Sprache

Englisch
(3.432)
Koreanisch
(181)
Chinesisch
(18)
Japanisch
(3)
Deutsch
(1)
Schwedisch
(1)

1 weiteren anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.326)
Technology
(1.533)
Engineering
(764)
Computer Science
(726)
Materials Science
(659)
Materials Science, Multidisciplinary
(631)
Life Sciences & Biomedicine
(627)
Humans
(547)
Computer Science, Artificial Intelligence
(386)
Engineering, Electrical & Electronic
(377)
Computer Science, Theory & Methods
(354)
Female
(345)
Male
(337)
Engineering, Manufacturing
(281)
Computer Science, Information Systems
(245)
Middle Aged
(236)
Computer Science, Hardware & Architecture
(224)
Adult
(213)
Computer Science, Software Engineering
(210)
Data Mining
(201)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson’s disease

Phenotypic Heterogeneity in Patients with Mutations in the Mitochondrial Complex I Assembly Gene NDUFAF5

Generation of a human induced pluripotent stem cell line NTUHi002-A from a patient with aceruloplasminemia harboring a homozygous splicing mutation c.607+1 delG in CP gene

Vitamin D receptor genetic variants and Parkinson's disease in a Taiwanese population

Lack of RAB39B mutations in early-onset and familial Parkinson's disease in a Taiwanese cohort

Reprogramming of a human induced pluripotent stem cell (iPSC) line (IBMSi012-A) from an early-onset Parkinson's disease patient harboring a homozygous p.D331Y mutation in the PLA2G6 gene

Generation of induced pluripotent stem cells (IBMSi011-A) from a patient with Parkinson's disease carrying LRRK2 p.I1371V mutation

Generation of 2 induced pluripotent stem cell lines derived from patients with Parkinson's disease carrying LRRK2 G2385R variant

A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review

Generation of induced pluripotent stem cells from a patient with Parkinson's disease carrying LRRK2 p.I2012T mutation

Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family

Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia

A novel C19orf12 frameshift mutation in a MPAN pedigree impairs mitochondrial function and connectivity leading to neurodegeneration

Lovastatin protects neurite degeneration in LRRK2-G2019S parkinsonism through activating the Akt/Nrf pathway and inhibiting GSK3β activity

PDE8B mutation is not associated with Parkinson's disease in a Taiwanese population

The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease

Catechol-O-methyltransferase (COMT) genetic variants are associated with cognitive decline in patients with Parkinson's disease

Simulated lunar microgravity transiently arrests growth and induces osteocyte-chondrocyte lineage differentiation in human Wharton’s jelly stem cells

Clinical Characteristics, Genetic Features, and Long-Term Outcome of Wilson’s Disease in a Taiwanese Population: An 11-Year Follow-Up Study

Lack of c9orf72 repeat expansion in taiwanese patients with mixed neurodegenerative disorders

Balance matters more: Research on the effect of corporate social responsibility equilibrium on stock price crash risk

Do political connections facilitate or inhibit firms' digital transformation? Evidence from China's A-share private listed companies

Prognostic value of sarcopenia in patients with liver cirrhosis: A systematic review and meta-analysis

Comprehensive intellectual property ability and firm productivity: A quasi-natural experiment based on national intellectual property demonstration advantage firm policy in China

How does the integration of cultural and tourism industries impact the value added to tourism value chain: Evidences from Jiangsu Province of China

Suchergebnisse filtern