CHARACTERIZATION OF A NONCHYMOTRYPSIN-LIKE ENDOPEPTIDASE FROM ANTERIOR PITUITARY THAT HYDROLYSES LUTEINIZING HORMONE-RELEASING HORMONE AT THE TYROSYL-GLYCINE AND HISTIDYL-TRYPTOPHAN BONDSHORSTHEMKE B; BAUER K.1980; BIOCHEMISTRY; USA; DA. 1980; VOL. 19; NO 13; PP. 2867-2873; BIBL. 16 REF.Article

SUBSTRATE SPECIFICITY OF AN ADENOHYPOPHYSEAL ENDOPEPTIDASE CAPABLE OF HYDROLYZING LUTEINIZING HORMONE-RELEASING HORMONE: PREFERENTIAL CLEAVAGE OF PEPTIDE BONDS INVOLVING THE CARBOXYL TERMINUS OF HYDROPHOBIC AND BASIC AMINO ACIDSHORSTHEMKE B; BAUER K.1982; BIOCHEMISTRY (EAST.); ISSN 0006-2960; USA; DA. 1982; VOL. 21; NO 5; PP. 1033-1036; BIBL. 12 REF.Article

CHYMOTRYPTIC-LIKE HYDROLYSIS OF LULIBERIN (LH-RF) BY AN ADENOHYPOPHYSEAL ENZYME OF HIGH MOLECULAR WEIGHTHORSTHEMKE B; BAUER K.1981; BIOCHEM. BIOPHYS. RES. COMMUN.; ISSN 0006-291X; USA; DA. 1981; VOL. 103; NO 4; PP. 1322-1328; BIBL. 11 REF.Article

On the maximum entropy principle for a class of stochastic processesHORSTHEMKE, B; RÜTTERMANN, M.Stochastic processes and their applications. 1995, Vol 56, Num 1, pp 117-132, issn 0304-4149Article

No evidence for sequences structurally related to the RB1 gene in the human genomeBELKA, C; GREGER, V; ZABEL, B et al.Human genetics. 1991, Vol 86, Num 4, pp 401-403, issn 0340-6717Article

Sacl RFLPs at the D8S51 locusHORSTHEMKE, B; BURDIEK, R; LUÊDECKE, H.-J et al.Nucleic acids research. 1990, Vol 18, Num 20, issn 0305-1048, p. 6171Article

Three RFLPs at the D8S49 locusHORSTHEMKE, B; BURDIEK, R; LUÊDECKE, J et al.Nucleic acids research. 1990, Vol 18, Num 20, issn 0305-1048, p. 6172Article

Molekulargenetische Diagnostik bei Retinoblastom = Diagnostic génétique moléculaire du rétinoblastome = Molecular genetic diagnosis of retinoblastomePASSARGE, E; GREGER, V; HÖPPING, W et al.Bücherei des Augenarztes. 1988, Vol 115, pp 198-205, issn 0068-3361Article

An NciI RFLP at the D15S63 locus in the critical Prader-Willi syndrome region in 15q11-13DITTRICH, B; GROSS, S; BUITING, K et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, issn 0964-6906, p. 1509Article

Characterization of a DNA sequence family in the Prader-Willi/Angelman syndrome chromosome region in 15q11-q13DITTRICH, B; KNOBLAUCH, H; BUITING, K et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 1, pp 269-271, issn 0888-7543Article

Somatic mosaicism in a patient with bilateral retinoblastomaGREGER, V; PASSARGE, E; HORSTHEMKE, B et al.American journal of human genetics. 1990, Vol 46, Num 6, pp 1187-1193, issn 0002-9297, 7 p.Article

Degradation of substance P by neurones and glial cellsHORSTHEMKE, B; SCHULZ, M; BAUER, K et al.Biochemical and biophysical research communications (Print). 1984, Vol 125, Num 2, pp 728-733, issn 0006-291XArticle

Epimutations in human diseaseHORSTHEMKE, B.Current Topics in Microbiology and Immunology. 2006, Vol 310, pp 45-59, issn 0070-217X, 15 p.Article

Four RFLPs at the D8S42 locusHORSTHEMKE, B; BURDIEK, R; LUÊDECKE, H.-J et al.Nucleic acids research. 1990, Vol 18, Num 20, issn 0305-1048, p. 6175Article

Two RFLPs at the D8S50 locusHORSTHEMKE, B; BURDIEK, R; LUÊDECKE, H.-J et al.Nucleic acids research. 1990, Vol 18, Num 20, issn 0305-1048, p. 6172Article

Mechanism of i(6p) formation in retinoblastoma tumor cellsHORSTHEMKE, B; GREGER, V; BECHER, R et al.Cancer genetics and cytogenetics. 1989, Vol 37, Num 1, pp 95-102, issn 0165-4608Article

Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15FÄRBER, C; GROSS, S; NEESEN, J et al.Genomics (San Diego, Calif.). 2000, Vol 65, Num 2, pp 174-183, issn 0888-7543Article

The murine Ext1 gene shows a high level of sequence similarity with its human homologue and is part of a conserved linkage group on chromosome 15LOHMANN, D. R; BUITING, K; LÜDECKE, H.-J et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 3-4, pp 164-166, issn 0301-0171Article

Rapid detection of trisomy 21 by quantitative PCRVON EGGELING, F; FREYTAG, M; FAHSOLD, R et al.Human genetics. 1993, Vol 91, Num 6, pp 567-570, issn 0340-6717Article

Microdissection of banded human chromosomesSENGER, G; LUÊDECKE, H.-J; HORSTHEMKE, B et al.Human genetics. 1990, Vol 84, Num 6, pp 507-511, issn 0340-6717, 5 p.Article

Idiopathic male infertility is strongly associated with aberrant methylation of MEST and IGF2/H19 ICR1POPLINSKI, A; TÜTTELMANN, F; KANBER, D et al.International journal of andrology (Print). 2010, Vol 33, Num 4, pp 642-649, issn 0105-6263, 8 p.Article

A 5-kb imprinting center deletion in a family with Angelman syndrome reduces the shortest region of deletion overlap to 880 bpBUITING, K; LICH, C; COTTRELL, S et al.Human genetics. 1999, Vol 105, Num 6, pp 665-666, issn 0340-6717Article

Construction and characterization of band-specific DNA librariesLUÊDECKE, H.-J; SENGER, G; CLAUSSEN, U et al.Human genetics. 1990, Vol 84, Num 6, pp 512-516, issn 0340-6717, 5 p.Article

Increased prevalence of imprinting defects in patients with angelman syndrome born to subfertile couplesLUDWIG, M; KATALINIC, A; GROSS, S et al.Journal of medical genetics. 2005, Vol 42, Num 4, pp 289-291, issn 0022-2593, 3 p.Article

A DNA library from an individual Beta patellaris chromosome conferring nematode resistance obtained by microdissection of meiotic metaphase chromosomesJUNG, C; CLAUSSEN, U; HORSTHEMKE, B et al.Plant molecular biology. 1992, Vol 20, Num 3, pp 503-511, issn 0167-4412Article