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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

Nature genetics, 1997-05, Vol.16 (1), p.64-67

1997

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Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5351), p.720-724

1998

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The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative Cases

American journal of human genetics, 1997-11, Vol.61 (5), p.1036-1043

1997

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Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

Journal of medical genetics, 1999-05, Vol.36 (5), p.360-364

1999

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Identification of PTEN mutations in five families with Bannayan-Zonana syndrome

Experimental dermatology, 1999-04, Vol.8 (2), p.134-139

1999

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Role of PTCH and p53 Genes in Early-Onset Basal Cell Carcinoma

The American journal of pathology, 2001-02, Vol.158 (2), p.381-385

2001

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Germline PTEN mutations in three families with Cowden syndrome

Experimental dermatology, 2000-04, Vol.9 (2), p.152-156

2000

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Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

Clinical cancer research, 1999-06, Vol.5 (6), p.1387-1391

1999

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PTCH Mutations in Squamous Cell Carcinoma of the Skin

Journal of investigative dermatology, 2001-04, Vol.116 (4), p.614-616

2001

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Regulation of Retinoic Acid Receptor Expression in Dermal Fibroblasts

Experimental cell research, 1994-03, Vol.211 (1), p.74-81

1994

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UV-specific p53 and PTCH mutations in sporadic basal cell carcinoma of sun-exposed skin

Journal of the American Academy of Dermatology, 2001-02, Vol.44 (2), p.293-297

2001

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Cultured Human Melanocytes Express the Intermediate Filament Vimentin

Journal of investigative dermatology, 1993-09, Vol.101 (3), p.383-386

1993

Volltextzugriff (PDF)

Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene

Human genetics, 1997-01, Vol.99 (1), p.126-129

1997

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Effect of Cellular Senescence and Retinoic Acid on the Expression of Cellular Retinoic Acid Binding Proteins in Skin Fibroblasts

Experimental cell research, 1995-07, Vol.219 (1), p.243-248

1995

Volltextzugriff (PDF)

Successful use of iv diltiazem to control perioperative refractory complex atrial tachyarrhythmias in a patient with pneumoconiosis

Canadian journal of anesthesia, 2003, Vol.50 (1), p.36-41

2003

Volltextzugriff (PDF)

The Correlation Between CVP and SVV and Intraoperative Minimal Blood Loss in Living Donor Hepatectomy

Transplantation proceedings, 2018-11, Vol.50 (9), p.2661-2663

2018

Volltextzugriff (PDF)

Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use

PloS one, 2020-06, Vol.15 (6), p.e0234549

2020

Volltextzugriff (PDF)

Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence

Journal of human genetics, 2020-04, Vol.65 (4), p.381-386

2020

Volltextzugriff (PDF)

Marchiafava-Bignami Disease with Widespread Lesions and Complete Recovery

American journal of neuroradiology : AJNR, 2010-09, Vol.31 (8), p.1506-1507

2010

Volltextzugriff (PDF)

Effects of a 12-week exercise training programme on aerobic fitness, body composition, blood lipids and C-reactive protein in adolescents with obesity

Annals of the Academy of Medicine, Singapore, 2008-04, Vol.37 (4), p.286-293

2008

Volltextzugriff (PDF)

Learning curve for endoscopic submucosal dissection of esophageal neoplasms

Diseases of the esophagus, 2016-08, Vol.29 (6), p.544-550

2016

Volltextzugriff (PDF)

Direct peroral cholangioscopy using an ultraslim endoscope and overtube balloon-assisted technique: a case series

Endoscopy, 2010-08, Vol.42 (8), p.681

2010

Volltextzugriff (PDF)

Pharmacogenomics study on cadherin 2 network with regard to HIV infection and methadone treatment outcome

PloS one, 2017-03, Vol.12 (3), p.e0174647-e0174647

2017

Volltextzugriff (PDF)

GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence

The international journal of neuropsychopharmacology, 2018-10, Vol.21 (10), p.910-917

2018

Volltextzugriff (PDF)

Glottal insufficiency with thyroid cartilage implantation: Our experience in eight patients

Clinical otolaryngology, 2012-10, Vol.37 (5), p.399-405

2012

Volltextzugriff (PDF)

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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome

Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

The Role of MMAC1 Mutations in Early-Onset Breast Cancer: Causative in Association with Cowden Syndrome and Excluded in BRCA1-Negative Cases

Phenotypic findings of Cowden syndrome and Bannayan-Zonana syndrome in a family associated with a single germline mutation in PTEN

Identification of PTEN mutations in five families with Bannayan-Zonana syndrome

Role of PTCH and p53 Genes in Early-Onset Basal Cell Carcinoma

Germline PTEN mutations in three families with Cowden syndrome

Absence of PTEN Germ-Line Mutations in Men with a Potential Inherited Predisposition to Prostate Cancer

PTCH Mutations in Squamous Cell Carcinoma of the Skin

Regulation of Retinoic Acid Receptor Expression in Dermal Fibroblasts

UV-specific p53 and PTCH mutations in sporadic basal cell carcinoma of sun-exposed skin

Cultured Human Melanocytes Express the Intermediate Filament Vimentin

Molecular basis of variegate porphyria: a de novo insertion mutation in the protoporphyrinogen oxidase gene

Effect of Cellular Senescence and Retinoic Acid on the Expression of Cellular Retinoic Acid Binding Proteins in Skin Fibroblasts

Successful use of iv diltiazem to control perioperative refractory complex atrial tachyarrhythmias in a patient with pneumoconiosis

The Correlation Between CVP and SVV and Intraoperative Minimal Blood Loss in Living Donor Hepatectomy

Genetic variants in NECTIN4 encoding an adhesion molecule are associated with continued opioid use

Genetic polymorphisms in the opioid receptor delta 1 (OPRD1) gene are associated with methadone dose in methadone maintenance treatment for heroin dependence

Marchiafava-Bignami Disease with Widespread Lesions and Complete Recovery

Effects of a 12-week exercise training programme on aerobic fitness, body composition, blood lipids and C-reactive protein in adolescents with obesity

Learning curve for endoscopic submucosal dissection of esophageal neoplasms

Direct peroral cholangioscopy using an ultraslim endoscope and overtube balloon-assisted technique: a case series

Pharmacogenomics study on cadherin 2 network with regard to HIV infection and methadone treatment outcome

GRK5 Is Associated with the Regulation of Methadone Dosage in Heroin Dependence

Glottal insufficiency with thyroid cartilage implantation: Our experience in eight patients

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