Regulation of the fixA gene and fixBC operon in Bradyrhizobium japonicum.

Por Gubler, M, Hennecke, H
Publicado em 1988

Increased protein flexibility leads to promiscuous protein--DNA interactions in type IC restriction-modification systems.

Por Gubler, M, Bickle, T A
Publicado em 1991

Overexpression, purification, and characterization of UDP-N-acetylmuramyl:L-alanine ligase from Escherichia coli.

Por Gubler, M, Appoldt, Y, Keck, W
Publicado em 1996

An anticodon nuclease gene inserted into a hsd region encoding a type I DNA restriction system.

Por Linder, P, Doelz, R, Gubler, M, Bickle, T A
Publicado em 1990

Cloning of the pyruvate kinase gene (pyk) of Corynebacterium glutamicum and site-specific inactivation of pyk in a lysine-producing Corynebacterium lactofermentum strain.

Por Gubler, M, Jetten, M, Lee, S H, Sinskey, A J
Publicado em 1994

Structural and functional analysis of pyruvate kinase from Corynebacterium glutamicum.

Por Jetten, M S, Gubler, M E, Lee, S H, Sinskey, A J
Publicado em 1994

Single amino acid changes that render human IFN-alpha 2 biologically active on mouse cells.

Por Weber, H, Valenzuela, D, Lujber, G, Gubler, M, Weissmann, C
Publicado em 1987

Recombination of constant and variable modules alters DNA sequence recognition by type IC restriction-modification enzymes.

Por Gubler, M, Braguglia, D, Meyer, J, Piekarowicz, A, Bickle, T A
Publicado em 1992

Changes in thickness and anionic sites of the glomerular basement membrane after subtotal nephrectomy in the rat.

Por Dubrulle, M. P., Terzi, F., Gubler, M. C., Kleinknecht, C., Schaeverbeke, M.
Publicado em 1992

Effect of inducible thrB expression on amino acid production in Corynebacterium lactofermentum ATCC 21799.

Por Colón, G E, Jetten, M S, Nguyen, T T, Gubler, M E, Follettie, M T, Sinskey, A J, Stephanopoulos, G
Publicado em 1995

Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts

Por Sharp, A, Messiaen, L, Page, G, Antignac, C, Gubler, M, Onuchic, L, Somlo, S, Germino, G, Guay-Woodford, L
Publicado em 2005

Substitution of arginine for glycine 325 in the collagen alpha 5 (IV) chain associated with X-linked Alport syndrome: characterization of the mutation by direct sequencing of PCR-a...

Por Knebelmann, B, Deschenes, G, Gros, F, Hors, M C, Grünfeld, J P, Zhou, J, Tryggvason, K, Gubler, M C, Antignac, C
Publicado em 1992

Renin biosynthesis by human tumoral juxtaglomerular cells. Evidences for a renin precursor.

Por Galen, F X, Devaux, C, Houot, A M, Menard, J, Corvol, P, Corvol, M T, Gubler, M C, Mounier, F, Camilleri, J P
Publicado em 1984

Somatic deletion of the 5' ends of both the COL4A5 and COL4A6 genes in a sporadic leiomyoma of the esophagus.

Por Heidet, L., Boye, E., Cai, Y., Sado, Y., Zhang, X., Fléjou, J. F., Fékété, F., Ninomiya, Y., Gubler, M. C., Antignac, C.
Publicado em 1998

Determination of the genomic structure of the COL4A4 gene and of novel mutations causing autosomal recessive Alport syndrome.

Por Boye, E, Mollet, G, Forestier, L, Cohen-Solal, L, Heidet, L, Cochat, P, Grünfeld, J P, Palcoux, J B, Gubler, M C, Antignac, C
Publicado em 1998

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized muta...

Por Jeanpierre, C, Denamur, E, Henry, I, Cabanis, M O, Luce, S, Cécille, A, Elion, J, Peuchmaur, M, Loirat, C, Niaudet, P, Gubler, M C, Junien, C
Publicado em 1998

Spectrum of mutations in the COL4A5 collagen gene in X-linked Alport syndrome.

Por Knebelmann, B., Breillat, C., Forestier, L., Arrondel, C., Jacassier, D., Giatras, I., Drouot, L., Deschênes, G., Grünfeld, J. P., Broyer, M., Gubler, M. C., Antignac, C.
Publicado em 1996

A study of new NEK8 mutations in patients with severe renal cystic hypodysplasia and ciliopathy-associated defects

Por Grampa, V, Delous, M, Silbermann, F, Oyde, G, Krug, P, Filhol, E, Alessandri, JL, Sigaudy, S, Bouvier, R, Zabot, MT, Antignac, C, Gubler, M, Attié-Bitach, T, Benmerah, A, Jeanpierre, C, Saunier, S
Publicado no Cilia (2015)

Identification of human mutations in TRAF3IP1 in patients with nephronophthisis and retinal degeneration

Por Becker-Heck, A, Bizet, A, Ryan, R, Krug, P, Filhol, E, Linghu, B, Oakeley, E, Serluca, F, Legendre, F, Dörner, N, Lasbennes, MC, Duca, J, Yang, F, Damask, A, Klickstein, L, Labow, M, Schebesta, M, Bouwmeester, T, Valette, H, Pinson, L, Goubaux, B, Dubot, P, Salomon, R, Antignac, C, Gubler, M, Jeanpierre, C, Chibout, S, Bole-Feysot, C, Nitschké, P, Benmerah, A, Szustakowski, JD, Sailer, AW, Saunier, S, Saint-Mezard, P
Publicado no Cilia (2015)