User profiles for S. Hennigs

Sven Hennig

- Verified email at vu.nl - Cited by 2668

Shannon Hennig

- Verified email at iit.it - Cited by 340

Modulators of protein–protein interactions

LG Milroy, TN Grossmann, S Hennig… - Chemical …, 2014 - ACS Publications
… Since Hedin’s characterization of trypsin and antitrypsin in 1906, (1) arguably the first … (13,
14) Furthermore, diseases common to old-age, such as cancer and Alzheimer’s are expected …

Success through diversity–how Staphylococcus epidermidis establishes as a nosocomial pathogen

…, C Lange, M Eckart, S Hennig, S Kozytska… - International Journal of …, 2010 - Elsevier
… nosocomial S. epidermidis isolates, but treatment failure is also associated with the ability of
S. … Moreover, it was demonstrated in this report that clonal diversification in S. epidermidis is …

The state of research and practice in augmentative and alternative communication for children with developmental/intellectual disabilities

KM Wilkinson, S Hennig - Mental retardation and …, 2007 - Wiley Online Library
… For instance, a search of the ComDisDome electronic database (dedicated to scholarship in
communication disorders) reveals that in the decade since Romski and Sevcik’s review, 285 …

The DNA sequence of human chromosome 21

…, H Blöcker, J Ramser, A Beck, S Klages, S Hennig… - Nature, 2000 - nature.com
Chromosome 21 is the smallest human autosome. An extra copy of chromosome 21 causes
Down syndrome, the most frequent genetic cause of significant mental retardation, which …

Cerebral ischemia detected with diffusion-weighted MR imaging after stent implantation in the carotid artery

…, R Drescher, HM Gissler, S Hennigs… - American journal …, 2002 - Am Soc Neuroradiology
… The diffusion-weighted sequence was performed with two levels of diffusion sensitization:
b = 0 and b = 1000 s/mm 2 . The higher level of diffusion sensitization was replicated in each …

The DNA sequence of the human X chromosome

…, S Hennig, J Hernandez, B Hinzmann, S Ho… - Nature, 2005 - nature.com
The human X chromosome has a unique biology that was shaped by its evolution as the sex
chromosome shared by males and females. We have determined 99.3% of the euchromatic …

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets

F Francis, S Hennig, B Korn, R Reinhardt, P De Jong… - Nature …, 1995 - nature.com
X–linked hypophosphatemic rickets (HYP) is a dominant disorder characterised by impaired
phosphate uptake in the kidney, which is likely to be caused by abnormal regulation of …

Validity and repeatability of a simple index derived from the short physical activity questionnaire used in the European Prospective Investigation into Cancer and …

…, KL Rennie, J Schuit, J Mitchell, S Hennings… - Public health …, 2003 - cambridge.org
… Finally, the repeatability of the activity index was assessed by Cohen’s weighted kappa …
11 Wareham NJ, Hennings SJ, Prentice AM, Day NE. Feasibility of heart-rate monitoring to …

[HTML][HTML] The oestrogen receptor alpha-regulated lncRNA NEAT1 is a critical modulator of prostate cancer

…, SS Nair, E Giannopoulou, R Li, S Hennig… - Nature …, 2014 - nature.com
The androgen receptor (AR) plays a central role in establishing an oncogenic cascade that
drives prostate cancer progression. Some prostate cancers escape androgen dependence …

Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left–right asymmetry

…, A Völkel, A Volz, G Sasmaz, R Reinhardt, S Hennig… - Nature …, 2002 - nature.com
Primary ciliary dyskinesia (PCD, MIM 242650) is characterized by recurrent infections of the
respiratory tract due to reduced mucociliary clearance and by sperm immobility. Half of the …