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Results: 1-8 |
Results: 8
SUBSTRATE-SPECIFICITY OF AND PRODUCT FORMATION BY MUCONATE CYCLOISOMERASES - AN ANALYSIS OF WILD-TYPE ENZYMES AND ENGINEERED VARIANTS
Authors: VOLLMER MD HOIER H HECHT HJ SCHELL U GRONING J GOLDMAN A SCHLOMANN M
Citation: Md. Vollmer et al., SUBSTRATE-SPECIFICITY OF AND PRODUCT FORMATION BY MUCONATE CYCLOISOMERASES - AN ANALYSIS OF WILD-TYPE ENZYMES AND ENGINEERED VARIANTS, Applied and environmental microbiology, 64(9), 1998, pp. 3290-3299
MOLECULAR CHARACTERIZATION OF BREAKPOINTS IN PATIENTS WITH HOLOPROSENCEPHALY AND DEFINITION OF THE HPE2 CRITICAL REGION 2P21
Authors: SCHELL U WIENBERG J KOHLER A BRAYWARD P WARD DE WILSON WG ALLEN WP LEBEL RR SAWYER JR CAMPBELL PL AUGHTON DJ PUNNETT HH LAMMER EJ KAO FT WARD DC MUENKE M
Citation: U. Schell et al., MOLECULAR CHARACTERIZATION OF BREAKPOINTS IN PATIENTS WITH HOLOPROSENCEPHALY AND DEFINITION OF THE HPE2 CRITICAL REGION 2P21, Human molecular genetics, 5(2), 1996, pp. 223-229
MUTATIONS IN FGFRI AND FGFR2 CAUSE FAMILIAL AND SPORADIC PFEIFFER SYNDROME
Authors: SCHELL U HEHR A FELDMAN GJ ROBIN NH ZACKAI EH DEDIESMULDERS C VISKOCHIL DH STEWART JM WOLFF G OHASHI H PRICE RA COHEN MM MUENKE M
Citation: U. Schell et al., MUTATIONS IN FGFRI AND FGFR2 CAUSE FAMILIAL AND SPORADIC PFEIFFER SYNDROME, Human molecular genetics, 4(3), 1995, pp. 323-328
FIBROBLAST-GROWTH-FACTOR RECEPTOR MUTATIONS IN HUMAN SKELETAL DISORDERS
Authors: MUENKE M SCHELL U
Citation: M. Muenke et U. Schell, FIBROBLAST-GROWTH-FACTOR RECEPTOR MUTATIONS IN HUMAN SKELETAL DISORDERS, Trends in genetics, 11(8), 1995, pp. 308-313
TRANSLOCATION T(2-3)(P21-22-Q26) AND MYELOID DISORDERS - FISH ANALYSIS AND MOLECULAR STUDY
Authors: RAYNAUD SD PARGANAS E SCHELL U GROSGEORGE J NUCIFORA G BARIN C TAILLAN B MUENKE M IHLE J AYRAUD N
Citation: Sd. Raynaud et al., TRANSLOCATION T(2-3)(P21-22-Q26) AND MYELOID DISORDERS - FISH ANALYSIS AND MOLECULAR STUDY, Blood, 86(10), 1995, pp. 2946-2946
ISOLATION OF CANDIDATE GENES FROM THE HOLOPROSENCEPHALY MINIMAL CRITICAL REGION ON CHROMOSOME-2
Authors: SCHELL U ROMMENS J AUGHTON D PUNNETT H LAMMER E MUENKE M
Citation: U. Schell et al., ISOLATION OF CANDIDATE GENES FROM THE HOLOPROSENCEPHALY MINIMAL CRITICAL REGION ON CHROMOSOME-2, American journal of human genetics, 57(4), 1995, pp. 59-59
A COMMON MUTATION IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-1 GENE IN PFEIFFER-SYNDROME
Authors: MUENKE M SCHELL U HEHR A ROBIN NH LOSKEN HW SCHINZEL A PULLEYN LJ RUTLAND P REARDON W MALCOLM S WINTER RM
Citation: M. Muenke et al., A COMMON MUTATION IN THE FIBROBLAST GROWTH-FACTOR RECEPTOR-1 GENE IN PFEIFFER-SYNDROME, Nature genetics, 8(3), 1994, pp. 269-274
PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY MINIMAL CRITICAL REGION IN 2P21
Authors: MUENKE M SCHELL U WIENBERG J BRAYWARD P HEHR A KAO FT WARD DC
Citation: M. Muenke et al., PHYSICAL MAPPING OF THE HOLOPROSENCEPHALY MINIMAL CRITICAL REGION IN 2P21, Cytogenetics and cell genetics, 67(4), 1994, pp. 242-243
Risultati: 1-8 |