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Attitude of employees of a university clinic to complementary and alternative medicine in oncology

Annals of oncology, 2013-10, Vol.24 (10), p.2641-2645

2013

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The gender gap in mortality: How much is explained by behavior?

Journal of health economics, 2017-07, Vol.54, p.79-90

2017

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Effects of exogenous oxytocin and estradiol on resting-state functional connectivity in women and men

Scientific reports, 2023-02, Vol.13 (1), p.3113-3113, Article 3113

2023

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Exogenous estradiol and oxytocin modulate sex differences in hippocampal reactivity during the encoding of episodic memories

NeuroImage (Orlando, Fla.), 2022-12, Vol.264, p.119689-119689, Article 119689

2022

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Anticipation of deteriorating health and information avoidance

Journal of health economics, 2023-05, Vol.89, p.102755-102755, Article 102755

2023

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MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II

The Journal of cell biology, 2011-09, Vol.194 (6), p.841-854

2011

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Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

American journal of human genetics, 2004-08, Vol.75 (2), p.261-266

2004

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Chromosome structure deficiencies in MCPH1 syndrome

Chromosoma, 2015-12, Vol.124 (4), p.491-501

2015

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Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4

European journal of human genetics : EJHG, 2013-07, Vol.21 (7), p.743-748

2013

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Evaluation of a SARS-CoV-2 test strategy in a southwestern university hospital at the beginning of the COVID-19 pandemic

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2021-03, Vol.64 (3), p.353-359

2021

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Misregulated Chromosome Condensation in MCPH1 Primary Microcephaly is Mediated by Condensin II

Cell cycle (Georgetown, Tex.), 2006-02, Vol.5 (3), p.322-326

2006

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Right Ventricular Contraction Patterns in Patients Undergoing Mitral Valve Transcatheter Edge-to-Edge Repair

JACC. Cardiovascular interventions, 2023-01, Vol.16 (2), p.242-244

2023

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A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cells

PloS one, 2012-08, Vol.7 (8), p.e40387

2012

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Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings

European journal of medical genetics, 2011-07, Vol.54 (4), p.e441-e445

2011

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Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function

PloS one, 2010-02, Vol.5 (2), p.e9242-e9242

2010

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The Effect of Distance on Long-Range Chromatin Interactions

Molecular cell, 1997-12, Vol.1 (1), p.131-139

1997

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Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA

International journal of legal medicine, 2020-01, Vol.134 (1), p.185-198

2020

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The role of EKLF in human beta-globin gene competition

Genes & development, 1996-11, Vol.10 (22), p.2894-2902

1996

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Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly

Cell cycle (Georgetown, Tex.), 2011-09, Vol.10 (17), p.2967-2977

2011

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Heterochromatin Effects on the Frequency and Duration of LCR-Mediated Gene Transcription

Cell, 1996-10, Vol.87 (1), p.105-114

1996

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MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrest

Cell cycle (Georgetown, Tex.), 2010-12, Vol.9 (24), p.4893-4899

2010

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Karyotyping of human chondrocytes in scaffold-assisted cartilage tissue engineering

Acta biomaterialia, 2012-04, Vol.8 (4), p.1519-1529

2012

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Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition

American journal of human genetics, 2002-04, Vol.70 (4), p.1015-1022

2002

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Chromatin interaction mechanism of transcriptional control in vivo

The EMBO journal, 1998-10, Vol.17 (20), p.6020-6027

1998

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Attitude of employees of a university clinic to complementary and alternative medicine in oncology

The gender gap in mortality: How much is explained by behavior?

Effects of exogenous oxytocin and estradiol on resting-state functional connectivity in women and men

Exogenous estradiol and oxytocin modulate sex differences in hippocampal reactivity during the encoding of episodic memories

Anticipation of deteriorating health and information avoidance

MCPH1 regulates chromosome condensation and shaping as a composite modulator of condensin II

Mutations in Microcephalin Cause Aberrant Regulation of Chromosome Condensation

Chromosome structure deficiencies in MCPH1 syndrome

Phenotypic variant of Brachydactyly-mental retardation syndrome in a family with an inherited interstitial 2q37.3 microdeletion including HDAC4

Evaluation of a SARS-CoV-2 test strategy in a southwestern university hospital at the beginning of the COVID-19 pandemic

Misregulated Chromosome Condensation in MCPH1 Primary Microcephaly is Mediated by Condensin II

Right Ventricular Contraction Patterns in Patients Undergoing Mitral Valve Transcatheter Edge-to-Edge Repair

A novel MCPH1 isoform complements the defective chromosome condensation of human MCPH1-deficient cells

Homozygous deletion of chromosome 15q13.3 including CHRNA7 causes severe mental retardation, seizures, muscular hypotonia, and the loss of KLF13 and TRPM1 potentially cause macrocytosis and congenital retinal dysfunction in siblings

Validation of Arxula Yeast Estrogen Screen assay for detection of estrogenic activity in water samples: Results of an international interlaboratory study

Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function

The Effect of Distance on Long-Range Chromatin Interactions

Inter-laboratory study on standardized MPS libraries: evaluation of performance, concordance, and sensitivity using mixtures and degraded DNA

The role of EKLF in human beta-globin gene competition

Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly

Heterochromatin Effects on the Frequency and Duration of LCR-Mediated Gene Transcription

MCPH1 patient cells exhibit delayed release from DNA damage-induced G2/M checkpoint arrest

Karyotyping of human chondrocytes in scaffold-assisted cartilage tissue engineering

Premature Chromosome Condensation in Humans Associated with Microcephaly and Mental Retardation: A Novel Autosomal Recessive Condition

Chromatin interaction mechanism of transcriptional control in vivo

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