Estimation of synthetic accessibility score of drug-like molecules based on molecular complexity and fragment contributions

Por Ertl, Peter, Schuffenhauer, Ansgar
Publicado em 2009

Natural product-likeness score and its applications in the drug discovery process

Por Ertl, Peter, Roggo, S, Schuffenhauer, A
Publicado no Chem Cent J (2008)

An HDR (hypoparathyroidism, deafness, renal dysplasia) syndrome locus maps distal to the DiGeorge syndrome region on 10p13/14

Por Lichtner, P., Konig, R., Hasegawa, T., Van Esch, H., Meitinger, T., Schuffenhauer, S.
Publicado em 2000

Mosaicism for a dup(12)(q22q13) in a patient with hypomelanosis of Ito and asymmetry

Por SCHMIDT, H., UHRIG, S., LEDERER, G., MURKEN, J., SPEICHER, M., SCHUFFENHAUER, S.
Publicado em 2000

De novo deletion (14)(q11.2q13) including PAX9: clinical and molecular findings

Por Schuffenhauer, S., Leifheit, H., Lichtner, P., Peters, H., Murken, J., Emmerich, P
Publicado em 1999

BIOS: Similarity-based design of natural product derived compound collections

Por Wetzel, S, Renner, S, Nören-Müller, A, Schuffenhauer, A, Ertl, P, Waldmann, Herbert
Publicado no Chem Cent J (2008)

Phenotypic expression of the fibroblast growth factor receptor 3 (FGFR3) mutation P250R in a large craniosynostosis family.

Por Golla, A, Lichmer, P, von Gernet, S, Winterpacht, A, Fairley, J, Murken, J, Schuffenhauer, S
Publicado em 1997

Charting biologically relevant chemical space: A structural classification of natural products (SCONP)

Por Koch, Marcus A., Schuffenhauer, Ansgar, Scheck, Michael, Wetzel, Stefan, Casaulta, Marco, Odermatt, Alex, Ertl, Peter, Waldmann, Herbert
Publicado em 2005

An optimized probe set for the detection of small interchromosomal aberrations by use of 24-color FISH.

Por Azofeifa, J, Fauth, C, Kraus, J, Maierhofer, C, Langer, S, Bolzer, A, Reichman, J, Schuffenhauer, S, Speicher, M R
Publicado em 2000

Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

Por Meindl, A, Hosenfeld, D, Brückl, W, Schuffenhauer, S, Jenderny, J, Bacskulin, A, Oppermann, H C, Swensson, O, Bouloux, P, Meitinger, T
Publicado em 1993

High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.

Por Callen, D F, Eyre, H, Lane, S, Shen, Y, Hansmann, I, Spinner, N, Zackai, E, McDonald-McGinn, D, Schuffenhauer, S, Wauters, J
Publicado em 1993

Multiplex-FISH for pre- and postnatal diagnostic applications.

Por Uhrig, S, Schuffenhauer, S, Fauth, C, Wirtz, A, Daumer-Haas, C, Apacik, C, Cohen, M, Müller-Navia, J, Cremer, T, Murken, J, Speicher, M R
Publicado em 1999

A Multi-Pumping Flow System for In Situ Measurements of Dissolved Manganese in Aquatic Systems

Por Meyer, David, Prien, Ralf D., Dellwig, Olaf, Waniek, Joanna J., Schuffenhauer, Ingo, Donath, Jan, Krüger, Siegfried, Pallentin, Malte, Schulz-Bull, Detlef E.
Publicado no Sensors (Basel) (2016)

Parental origin and mechanisms of formation of cytogenetically recognisable de novo direct and inverted duplications

Por Kotzot, D., Martinez, M., Bagci, G., Basaran, S., Baumer, A., Binkert, F., Brecevic, L., Castellan, C., Chrzanowska, K., Dutly, F., Gutkowska, A., Karauzum, S. B., Krajewska-Walasek, M., Luleci, G., Miny, P., Riegel, M., Schuffenhauer, S., Seidel, H., Schinzel, A.
Publicado em 2000

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Por Ryan, A K, Goodship, J A, Wilson, D I, Philip, N, Levy, A, Seidel, H, Schuffenhauer, S, Oechsler, H, Belohradsky, B, Prieur, M, Aurias, A, Raymond, F L, Clayton-Smith, J, Hatchwell, E, McKeown, C, Beemer, F A, Dallapiccola, B, Novelli, G, Hurst, J A, Ignatius, J, Green, A J, Winter, R M, Brueton, L, Brøndum-Nielsen, K, Scambler, P J
Publicado em 1997