Pheromone-Regulated Expression of Sex Pheromone Plasmid pAD1-Encoded Aggregation Substance Depends on at Least Six Upstream Genes and a cis-Acting, Orientation-Dependent Factor

Por Muscholl-Silberhorn, Albrecht B.
Publicado em 2000

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)

Por ALBRECHT, B., MERGENTHALER, S., EGGERMANN, K., ZERRES, K., PASSARGE, E., EGGERMANN, T.
Publicado em 2001

Quantum state-controlled directional spontaneous emission of photons into a nanophotonic waveguide

Por Mitsch, R., Sayrin, C., Albrecht, B., Schneeweiss, P., Rauschenbeutel, A.
Publicado no Nat Commun (2014)

Discussion Addendum for: 4-Methoxy-4'-nitrophenyl. Recent Advances in the Stille Biaryl Coupling Reaction and Applications in Complex Natural Products Synthesis

Por Williams, Robert M., Stille, J., Echavarren, A., Hendrix, J., Albrecht, B., Williams, R.
Publicado em 2011

Partial hexasomy 15pter→15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report

Por Nietzel, A, Albrecht, B, Starke, H, Heller, A, Gillessen-Kaesbac..., G, Claussen, U, Liehr, T
Publicado em 2003

Unexpected high frequency of de novo unbalanced translocations in patients with Wolf-Hirschhorn syndrome (WHS)

Por WIECZOREK, D., KRAUSE, M., MAJEWSKI, F., ALBRECHT, B., MEINECKE, P., RIESS, O., GILLESSEN-KAESBAC..., G.
Publicado em 2000

Voluntary motor drive: possible reduction in Tourette syndrome

Por Heise, C. A., Wanschura, V., Albrecht, B., Uebel, H., Roessner, V., Himpel, S., Paulus, W., Rothenberger, A., Tergau, F.
Publicado em 2008

Two Missense Mutations in the Primary Autosomal Recessive Microcephaly Gene MCPH1 Disrupt the Function of the Highly Conserved N-Terminal BRCT Domain of Microcephalin

Por Ghani-Kakhki, M., Robinson, P.N., Morlot, S., Mitter, D., Trimborn, M., Albrecht, B., Varon, R., Sperling, K., Neitzel, H.
Publicado em 2012

Incidence of Virulence Factors and Antibiotic Resistance among Enterococci Isolated from Food

Por Franz, Charles M. A. P., Muscholl-Silberhorn, Albrecht B., Yousif, Nuha M. K., Vancanneyt, Marc, Swings, Jean, Holzapfel, Wilhelm H.
Publicado em 2001

Hallermann-Streiff Syndrome: No Evidence for a Link to Laminopathies

Por Kortüm, F., Chyrek, M., Fuchs, S., Albrecht, B., Gillessen-Kaesbach, G., Mütze, U., Seemanova, E., Tinschert, S., Wieczorek, D., Rosenberger, G., Kutsche, K.
Publicado em 2011

Human Ring Chromosomes – New Insights for their Clinical Significance

Por Guilherme, RS, Klein, E, Hamid, AB, Bhatt, S, Volleth, M, Polityko, A, Kulpanovich, A, Dufke, A, Albrecht, B, Morlot, S, Brecevic, L, Petersen, MB, Manolakos, E, Kosyakova, N, Liehr, T
Publicado em 201

Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome

Por Seifert, W, Holder‐Espinasse, M, Spranger, S, Hoeltzenbein, M, Rossier, E, Dollfus, H, Lacombe, D, Verloes, A, Chrzanowska, K H, Maegawa, G H B, Chitayat, D, Kotzot, D, Huhle, D, Meinecke, P, Albrecht, B, Mathijssen, I, Leheup, B, Raile, K, Hennies, H C, Horn, D
Publicado em 2006

The relationship between ADHD and key cognitive phenotypes is not mediated by shared familial effects with IQ

Por Wood, A. C., Rijsdijk, F., Johnson, K. A., Andreou, P., Albrecht, B., Arias-Vasquez, A., Buitelaar, J. K., McLoughlin, G., Rommelse, N. N. J., Sergeant, J. A., Sonuga-Barke, E. J. S., Uebel, H., van der Meere, J. J., Banaschewski, T., Gill, M., Manor, I., Miranda, A., Mulas, F., Oades, R. D., Roeyers, H., Rothenberger, A., Steinhausen, H. C., Faraone, S. V., Asherson, P., Kuntsi, J.
Publicado em 2010

Separation of cognitive impairments in attention deficit hyperactivity disorder into two familial factors

Por Kuntsi, J., Wood, A.C., Rijsdijk, F., Johnson, K.A., Andreou, P., Albrecht, B., Arias-Vasquez, A., Buitelaar, J.K., Mcloughlin, G., Rommelse, N.N.J., Sergeant, J.A., Sonuga-Barke, E.J.S., Uebel, H., van der Meere, J.J., Banaschewski, T., Gill, M., Manor, I., Miranda, A., Mulas, F., Oades, R.D., Roeyers, H., Rothenberger, A., Steinhausen, H.C., Faraone, S.V., Asherson, P.
Publicado em 2010

Genotypic and Phenotypic Spectrum in Tricho-Rhino-Phalangeal Syndrome Types I and III

Por Lüdecke, H.-J., Schaper, J., Meinecke, P., Momeni, P., Groß, S., von Holtum, D., Hirche, H., Abramowicz, M. J., Albrecht, B., Apacik, C., Christen, H.-J., Claussen, U., Devriendt, K., Fastnacht, E., Forderer, A., Friedrich, U., Goodship, T. H. J., Greiwe, M., Hamm, H., Hennekam, R. C. M., Hinkel, G. K., Hoeltzenbein, M., Kayserili, H., Majewski, F., Mathieu, M., McLeod, R., Midro, A. T., Moog, U., Nagai, T., Niikawa, N., Ørstavik, K. H., Plöchl, E., Seitz, C., Schmidtke, J., Tranebjærg, L., Tsukahara, M., Wittwer, B., Zabel, B., Gillessen-Kaesbach, G., Horsthemke, B.
Publicado em 2001