H. Witt

Details der Publikationsliste

Zeitraum

1994 - 2008

Anzahl

25

Co-Autoren

Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts (2008)

Annese, V, Barclay, M. L, Bingham, S. A, Brand, S, Buening, C, ...

Background: DLG5 p. R30Q has been reported to be associated with Crohn disease ( CD), but this association has not been replicated in most studies. A recent analysis of gender-stratified data from...

Evaluation of the-26G > A CC16 polymorphism in acute respiratory distress syndrome (2005)

Frerking, I, Sengler, C, Gunther, A, Walmrath, HD, Stevens, P, Witt, H, ...

Objective: Different risk factors are presumably involved in the pathogenesis of acute respiratory distress syndrome (ARDS) including genetic factors. Clara cell protein 16 (CC16) is a potential...

Hydrogen bonding to P700: Site-directed mutagenesis of threonine A739 of photosystem I in Chlamydomonas reinhardtii (2002)

Witt, H., Schlodder, E., Teutloff, C., Niklas, J., Bordignon, E., Carbonera, D., ...

The primary electron donor P700 of photosystem I is a dimer comprised of chlorophyll a (P-B) and chlorophyll a' (P-A). P-A is involved in a hydrogen bond network with several surrounding amino acid...

Die spektralen und räumlichen Eigenschaften von Fernerkundungssensoren bei der Ableitung von Landoberflächenparametern (1998)

Witt, H.

Die Arbeit befaßt sich mit der Ableitung von Landoberflächenparametern aus multispektralen Fernerkundungsdaten im sichtbaren und nahen infraroten Bereich und untersucht die Bedeutung der spektralen...

Genomic expression profiling of human inflammatory cardiomyopathy (DCMi) suggests novel therapeutic targets

Wittchen, F., Suckau, L., Witt, H., Skurk, C., Lassner, D., Fechner, H., ...

The clinical phenotype of human dilated cardiomyopathy (DCM) encompasses a broad spectrum of etiologically distinct disorders. As targeting of etiology-related pathogenic pathways may be more...

Chronic pancreatitis and cystic fibrosis

Witt, H

Recent discoveries of trypsinogen and trypsin inhibitor mutations in patients with chronic pancreatitis (CP) support the hypothesis that an inappropriate activation of pancreatic zymogens to active...

HFE gene mutation and transferrin saturation in very low birthweight infants

Maier, R., Witt, H., Buhrer, C., Monch, E., Kottgen, E.

AIM—To determine if there is an association between high transferrin saturation and the C282Y HFE gene mutation in very low birthweight (VLBW) infants.
METHODS—One hundred and forty three VLBW...

Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases

Verlaan, M, Drenth, J, Truninger, K, Koudova, M, Schulz, H, Bargetzi, M, ...

Background: Xenobiotic mediated cellular injury is thought to play a major role in the pathogenesis of pancreatic diseases. Genetic variations that reduce the expression or activity of detoxifying...