Packing of ganglioside-phospholipid monolayers: an x-ray diffraction and reflectivity study.

Por Majewski, J, Kuhl, T L, Kjaer, K, Smith, G S
Publicado em 2001

Phospholipid monolayers between fluid and solid states.

Por Helm, C A, Möhwald, H, Kjaer, K, Als-Nielsen, J
Publicado em 1987

Influence of surface chemistry on the structural organization of monomolecular protein layers adsorbed to functionalized aqueous interfaces.

Por Lösche, M, Piepenstock, M, Diederich, A, Grünewald, T, Kjaer, K, Vaknin, D
Publicado em 1993

Influence of chirality on the structure of phospholipid monolayers.

Por Böhm, C, Möhwald, H, Leiserowitz, L, Als-Nielsen, J, Kjaer, K
Publicado em 1993

Phases of phosphatidyl ethanolamine monolayers studied by synchrotron x-ray scattering.

Por Helm, C A, Tippmann-Krayer, P, Möhwald, H, Als-Nielsen, J, Kjaer, K
Publicado em 1991

CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations

Por Basel-Vanagaite, L., Pasmanik-Chor, M., Lurie, R., Yeheskel, A., Kjaer, K.W.
Publicado em 2011

Distinct CDH3 mutations cause ectodermal dysplasia, ectrodactyly, macular dystrophy (EEM syndrome)

Por Kjaer, K, Hansen, L, Schwabe, G, Marques-de-Faria, A, Eiberg, H, Mundlos, S, Tommerup, N, Rosenberg, T
Publicado em 2005

Cholesterol monohydrate nucleation in ultrathin films on water.

Por Rapaport, H, Kuzmenko, I, Lafont, S, Kjaer, K, Howes, P B, Als-Nielsen, J, Lahav, M, Leiserowitz, L
Publicado em 2001

A mutation in the receptor binding site of GDF5 causes Mohr‐Wriedt brachydactyly type A2

Por Kjaer, K W, Eiberg, H, Hansen, L, van der Hagen, C B, Rosendahl, K, Tommerup, N, Mundlos, S
Publicado em 2006

Bacterial S-layer protein coupling to lipids: x-ray reflectivity and grazing incidence diffraction studies.

Por Weygand, M, Wetzer, B, Pum, D, Sleytr, U B, Cuvillier, N, Kjaer, K, Howes, P B, Lösche, M
Publicado em 1999

Synchrotron X-ray study of lung surfactant-specific protein SP-B in lipid monolayers.

Por Lee, K Y, Majewski, J, Kuhl, T L, Howes, P B, Kjaer, K, Lipp, M M, Waring, A J, Zasadzinski, J A, Smith, G S
Publicado em 2001

A New Subtype of Brachydactyly Type B Caused by Point Mutations in the Bone Morphogenetic Protein Antagonist NOGGIN

Por Lehmann, K. , Seemann, P. , Silan, F. , Goecke, T. O. , Irgang, S. , Kjaer, K. W. , Kjaergaard, S. , Mahoney, M. J. , Morlot, S. , Reissner, C. , Kerr, B. , Wilkie, A. O. M. , Mundlos, S. 
Publicado em 2007

Breakpoints around the HOXD cluster result in various limb malformations

Por Dlugaszewska, B, Silahtaroglu, A, Menzel, C, Kübart, S, Cohen, M, Mundlos, S, Tümer, Z, Kjaer, K, Friedrich, U, Ropers, H‐H, Tommerup, N, Neitzel, H, Kalscheuer, V M
Publicado em 2006