Nucleotide sequence of the O gene and of the origin of replication in bacteriophage lambda DNA.

Por Scherer, G
Publicado em 1978

EMBL 12, a new lambda replacement vector with sites for SalI, XbaI, BamHI, SstI and EcoRI.

Por Natt, E, Scherer, G
Publicado em 1986

Heteroduplex between an EMBL3 genomic clone and a lambda gt11 cDNA clone provides internal size standards.

Por Scherer, G, Bock, C T, Zentgraf, H
Publicado em 1990

A computer aided oligonucleotide analysis provides a model sequence for RNA polymerase-promoter recognition in E.coli.

Por Scherer, G E, Walkinshaw, M D, Arnott, S
Publicado em 1978

Anonymous DNA sequence from chromosome 21 showing a three allele insertion/deletion RFLP (HGM 9 provisional no. D21S82).

Por Xiao, G H, Grzeschik, K H, Scherer, G
Publicado em 1987

PstI RFLP identified by an anonymous single copy genomic clone localized to chromosome 14 (HGM 9 provisional no. D14S14).

Por Xiao, G H, Grzeschik, K H, Scherer, G
Publicado em 1987

A BAM HI RFLP at the human tyrosine aminotransferase (TAT) gene locus at 16q.

Por Wullich, B, Natt, E, Wienker, T F, Scherer, G
Publicado em 1989

Isolation and characterization of the human tyrosine aminotransferase gene.

Por Rettenmeier, R, Natt, E, Zentgraf, H, Scherer, G
Publicado em 1990

Isolation and characterization of the rat tyrosine aminotransferase gene.

Por Shinomiya, T, Scherer, G, Schmid, W, Zentgraf, H, Schütz, G
Publicado em 1984

The ribosome binding sites recognized by E. coli ribosomes have regions with signal character in both the leader and protein coding segments.

Por Scherer, G F, Walkinshaw, M D, Arnott, S, Morré, D J
Publicado em 1980

Point mutations in the tyrosine aminotransferase gene in tyrosinemia type II.

Por Natt, E, Kida, K, Odievre, M, Di Rocco, M, Scherer, G
Publicado em 1992

Isolation of cDNA clones coding for rat tyrosine aminotransferase.

Por Scherer, G, Schmid, W, Strange, C M, Röwekamp, W, Schütz, G
Publicado em 1982

Two novel SRY missense mutations reducing DNA binding identified in XY females and their mosaic fathers.

Por Schmitt-Ney, M, Thiele, H, Kaltwasser, P, Bardoni, B, Cisternino, M, Scherer, G
Publicado em 1995

Screening of the 1 Mb SOX9 5' control region by array CGH identifies a large deletion in a case of campomelic dysplasia with XY sex reversal

Por Pop, R, Conz, C, Lindenberg, K, Blesson, S, Schmalenberger, B, Briault, S, Pfeifer, D, Scherer, G
Publicado em 2004

Isolation and characterization of the rat tryptophan oxygenase gene.

Por Schmid, W, Scherer, G, Danesch, U, Zentgraf, H, Matthias, P, Strange, C M, Röwekamp, W, Schütz, G
Publicado em 1982

Campomelic dysplasia translocation breakpoints are scattered over 1 Mb proximal to SOX9: evidence for an extended control region.

Por Pfeifer, D, Kist, R, Dewar, K, Devon, K, Lander, E S, Birren, B, Korniszewski, L, Back, E, Scherer, G
Publicado em 1999

Determination of low level exposure to volatile aromatic hydrocarbons and genotoxic effects in workers at a styrene plant.

Por Holz, O, Scherer, G, Brodtmeier, S, Koops, F, Warncke, K, Krause, T, Austen, A, Angerer, J, Tricker, A R, Adlkofer, F
Publicado em 1995

Identification of a locus which shows no genetic recombination with the autosomal dominant polycystic kidney disease gene on chromosome 16.

Por Germino, G G, Barton, N J, Lamb, J, Higgs, D R, Harris, P, Xiao, G H, Scherer, G, Nakamura, Y, Reeders, S T
Publicado em 1990

Impaired neutral sphingomyelinase activation and cutaneous barrier repair in FAN-deficient mice.

Por Kreder, D, Krut, O, Adam-Klages, S, Wiegmann, K, Scherer, G, Plitz, T, Jensen, J M, Proksch, E, Steinmann, J, Pfeffer, K, Krönke, M
Publicado em 1999