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...

The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa

Cell death & disease, 2014-05, Vol.5 (5), p.e1236-e1236

2014

Volltextzugriff (PDF)

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

Journal of medical genetics, 2003-08, Vol.40 (8), p.609-615

2003

Volltextzugriff (PDF)

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Human molecular genetics, 2012-08, Vol.21 (16), p.3647-3654

2012

Volltextzugriff (PDF)

Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

Molecular therapy, 2007-06, Vol.15 (6), p.1100-1105

2007

Volltextzugriff (PDF)

A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family

Eye (London), 2018-04, Vol.32 (4), p.806-812

2018

Volltextzugriff (PDF)

Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

Human molecular genetics, 2000-08, Vol.9 (13), p.1919-1926

2000

Volltextzugriff (PDF)

Minimising the risk of prion transmission by contact tonometry

British journal of ophthalmology, 2003-11, Vol.87 (11), p.1360-1362

2003

Volltextzugriff (PDF)

DnaJB6 is present in the core of Lewy bodies and is highly up-regulated in parkinsonian astrocytes

Journal of neuroscience research, 2009-01, Vol.87 (1), p.238-245

2009

Volltextzugriff (PDF)

Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

Molecular therapy, 2007-06, Vol.15 (6), p.1100

2007

Volltextzugriff (PDF)

Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system?

Biochemical Society transactions, 2004-08, Vol.32 (Pt 4), p.640-642

2004

Volltextzugriff (PDF)

Structure, Function and Evolution of DnaJ: Conservation and Adaptation of Chaperone Function

Cell stress & chaperones, 1998-03, Vol.3 (1), p.28-36

1998

Volltextzugriff (PDF)

Analysis of the levels of conservation of the J domain among the various types of DnaJ-like proteins

Cell stress & chaperones, 2000-10, Vol.5 (4), p.347-358

2000

Volltextzugriff (PDF)

Homocysteine-induced endoplasmic reticulum protein (herp) is up-regulated in parkinsonian substantia nigra and present in the core of Lewy bodies

Clinical neuropathology, 2009-09, Vol.28 (5), p.333

2009

Volltextzugriff (PDF)

Human homologues of the bacterial heat-shock protein DnaJ are preferentially expressed in neurons

Biochemical journal, 1992-06, Vol.284 (2), p.469-476

1992

Volltextzugriff (PDF)

Role of AIP and its homologue the blindness-associated protein AIPL1 in regulating client protein nuclear translocation

Biochemical Society transactions, 2004-08, Vol.32 (Pt 4), p.643-645

2004

Volltextzugriff (PDF)

Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK

The international journal of biochemistry & cell biology, 2007, Vol.39 (4), p.736-751

2007

Volltextzugriff (PDF)

Human muscle metabolism during sprint running

Journal of applied physiology (1985), 1986-07, Vol.61 (1), p.54-60

1986

Volltextzugriff (PDF)

An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene

British journal of ophthalmology, 2004-04, Vol.88 (4), p.528-532

2004

Volltextzugriff (PDF)

Unfolding retinal dystrophies: a role for molecular chaperones?

Trends in Molecular Medicine, 2001-09, Vol.7 (9), p.414-421

2001

Volltextzugriff (PDF)

Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus

Investigative ophthalmology & visual science, 2015-01, Vol.56 (1), p.578-586

2015

Volltextzugriff (PDF)

Cell stress genes and chronic neurodegenerative disorders

Neuropathology and applied neurobiology, 1995-12, Vol.21 (6), p.486-488

Cheetham, M. E.

1995

Volltextzugriff (PDF)

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

Trends in molecular medicine, 2005-04, Vol.11 (4), p.177-185

2005

Volltextzugriff (PDF)

Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Nature genetics, 2005-02, Vol.37 (2), p.166-170

2005

Volltextzugriff (PDF)

Domain Requirements of DnaJ-like (Hsp40) Molecular Chaperones in the Activation of a Steroid Hormone Receptor

The Journal of biological chemistry, 1999-11, Vol.274 (48), p.34045-34052

1999

Volltextzugriff (PDF)

Not all J domains are created equal: Implications for the specificity of Hsp40–Hsp70 interactions

Protein science, 2005-07, Vol.14 (7), p.1697-1709

2005

Volltextzugriff (PDF)

1 – 25 von 501

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(446)
Mit Volltextzugriff
(428)

Publikationsform

1 weiteren anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(322)
Life Sciences & Biomedicine
(222)
Humans
(193)
Biological And Medical Sciences
(88)
Male
(85)
Female
(84)
Physical Sciences
(75)
Animals
(66)
Adult
(63)
Medical Sciences
(59)
Physics
(51)
Biochemistry & Molecular Biology
(49)
Middle Aged
(43)
Mutation
(43)
Molecular Sequence Data
(42)
Genetics & Heredity
(37)
Ophthalmology
(37)
Astronomy & Astrophysics
(36)
Adolescent
(35)
Fundamental And Applied Biological Sciences. Psychology
(35)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

The heat-shock response co-inducer arimoclomol protects against retinal degeneration in rhodopsin retinitis pigmentosa

RPGR mutation associated with retinitis pigmentosa, impaired hearing, and sinorespiratory infections

Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)

Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

A novel missense mutation in HSF4 causes autosomal-dominant congenital lamellar cataract in a British family

Mutations in the N-terminus of the X-linked retinitis pigmentosa protein RP2 interfere with the normal targeting of the protein to the plasma membrane

Minimising the risk of prion transmission by contact tonometry

DnaJB6 is present in the core of Lewy bodies and is highly up-regulated in parkinsonian astrocytes

Hsp40 Molecules That Target to the Ubiquitin-proteasome System Decrease Inclusion Formation in Models of Polyglutamine Disease

Neuronal DnaJ proteins HSJ1a and HSJ1b: a role in linking the Hsp70 chaperone machine to the ubiquitin-proteasome system?

Structure, Function and Evolution of DnaJ: Conservation and Adaptation of Chaperone Function

Analysis of the levels of conservation of the J domain among the various types of DnaJ-like proteins

Homocysteine-induced endoplasmic reticulum protein (herp) is up-regulated in parkinsonian substantia nigra and present in the core of Lewy bodies

Human homologues of the bacterial heat-shock protein DnaJ are preferentially expressed in neurons

Role of AIP and its homologue the blindness-associated protein AIPL1 in regulating client protein nuclear translocation

Cytosolic and ER J-domains of mammalian and parasitic origin can functionally interact with DnaK

Human muscle metabolism during sprint running

An atypical phenotype of macular and peripapillary retinal atrophy caused by a mutation in the RP2 gene

Unfolding retinal dystrophies: a role for molecular chaperones?

Brittle cornea syndrome ZNF469 mutation carrier phenotype and segregation analysis of rare ZNF469 variants in familial keratoconus

Cell stress genes and chronic neurodegenerative disorders

Mechanisms of cell death in rhodopsin retinitis pigmentosa: implications for therapy

Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Domain Requirements of DnaJ-like (Hsp40) Molecular Chaperones in the Activation of a Steroid Hormone Receptor

Not all J domains are created equal: Implications for the specificity of Hsp40–Hsp70 interactions

Suchergebnisse filtern