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Ubiquitin-mediated Proteolysis of a Short-lived Regulatory Protein Depends on Its Cellular Localization

The Journal of biological chemistry, 2000-12, Vol.275 (50), p.39403-39410

2000

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Welche Technologien nutzen die Kraftwerke der Zukunft?

Elektrotechnik und Informationstechnik, 2004-10, Vol.121 (10), p.391-395

Lenk, U.

2004

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A role for mammalian Ubc6 homologues in ER-associated protein degradation

Journal of cell science, 2002-07, Vol.115 (Pt 14), p.3007-3014

2002

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Entwicklungstrends in der Stromerzeugung — Perspektiven für Kraftwerke mit Gasturbinen

Elektrotechnik und Informationstechnik, 1997-10, Vol.114 (10), p.539-545

1997

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Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis

Annals of neurology, 1995-06, Vol.37 (6), p.817-819

1995

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Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

Human molecular genetics, 1993-11, Vol.2 (11), p.1877-1881

1993

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A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave

Human molecular genetics, 1996-07, Vol.5 (7), p.973-975

1996

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Predominant archaea in marine sediments degrade detrital proteins

Nature (London), 2013-04, Vol.496 (7444), p.215-218

2013

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Tuning of NiSi ∕ Si Schottky barrier heights by sulfur segregation during Ni silicidation

Applied physics letters, 2005-02, Vol.86 (6), p.062108-062108-3

2005

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Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease

The New England journal of medicine, 2012-09, Vol.367 (11), p.991-1001

2012

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Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

Haematologica (Roma), 2010-06, Vol.95 (6), p.956-962

2010

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Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Thrombosis and haemostasis, 2005-03, Vol.93 (3), p.481-487

2005

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Testosterone substitution with a new transdermal, hydroalcoholic gel applied to scrotal or non-scrotal skin: a multicentre trial

European journal of endocrinology, 2005-08, Vol.153 (2), p.317-326

2005

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Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization

Thrombosis and haemostasis, 2004-07, Vol.92 (1), p.36-41

2004

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Sildenafil response is influenced by the G protein beta 3 subunit GNB3 C825T polymorphism: a pilot study

The Journal of urology, 2003-03, Vol.169 (3), p.1048-1051

2003

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Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Haematologica (Roma), 2008-08, Vol.93 (8), p.1273-1275

2008

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Mitoxantrone: mechanism of action, antitumor activity, pharmacokinetics, efficacy in the treatment of solid tumors and lymphomas, and toxicity

Anticancer research, 1987-11, Vol.7 (6), p.1257

1987

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A phase II trial of interferon α-2b with folinic acid and 5-fluorouracil administered by 4-hour infusion in metastatic colorectal carcinoma

Seminars in oncology, 1992, Vol.19 (2), p.57-62

1992

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A phase II trial of interferon alpha-2b with folinic acid and 5-fluorouracil administered by 4-hour infusion in metastatic colorectal carcinoma

Seminars in oncology, 1992-04, Vol.19 (2 Suppl 4), p.57

1992

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Ubiquitin-mediated Proteolysis of a Short-lived Regulatory Protein Depends on Its Cellular Localization

Welche Technologien nutzen die Kraftwerke der Zukunft?

A role for mammalian Ubc6 homologues in ER-associated protein degradation

Entwicklungstrends in der Stromerzeugung — Perspektiven für Kraftwerke mit Gasturbinen

Studies of the coding region of the neuronal glutamate transporter gene in amyotrophic lateral sclerosis

Point mutations at the carboxy terminus of the human dystrophin gene: implications for an association with mental retardation in DMD patients

A Cysteine 3340 Substitution in the Dystroglycan-Binding Domain of Dystrophin Associated with Duchenne Muscular Dystrophy, Mental Retardation and Absence of the ERG b-Wave

Predominant archaea in marine sediments degrade detrital proteins

Tuning of NiSi ∕ Si Schottky barrier heights by sulfur segregation during Ni silicidation

Fractional Flow Reserve–Guided PCI versus Medical Therapy in Stable Coronary Disease

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function

Clinical phenotypes and factor VII genotype in congenital factor VII deficiency

Testosterone substitution with a new transdermal, hydroalcoholic gel applied to scrotal or non-scrotal skin: a multicentre trial

Recombinant expression of mutations causing von Willebrand disease type Normandy: characterization of a combined defect of factor VIII binding and multimerization

Sildenafil response is influenced by the G protein beta 3 subunit GNB3 C825T polymorphism: a pilot study

Variability of clinical manifestation of factor VII-deficiency in homozygous and heterozygous subjects of the European F7 gene mutation A294V

Mitoxantrone: mechanism of action, antitumor activity, pharmacokinetics, efficacy in the treatment of solid tumors and lymphomas, and toxicity

A phase II trial of interferon α-2b with folinic acid and 5-fluorouracil administered by 4-hour infusion in metastatic colorectal carcinoma

A phase II trial of interferon alpha-2b with folinic acid and 5-fluorouracil administered by 4-hour infusion in metastatic colorectal carcinoma

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