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Results: 1-8 |
Results: 8
OSTEOGENESIS IMPERFECTA MURINE MODELS - USE OF THE CRE LOX RECOMBINATION SYSTEM TO CREATE THE FIRST KNOCK-IN OI MOUSE/
Authors: FORLINO A PORTER FD MARINI JC
Citation: A. Forlino et al., OSTEOGENESIS IMPERFECTA MURINE MODELS - USE OF THE CRE LOX RECOMBINATION SYSTEM TO CREATE THE FIRST KNOCK-IN OI MOUSE/, European journal of human genetics, 6, 1998, pp. 803-803
USE OF THE CRE LOX RECOMBINATION SYSTEM TO CREATE THE FIRST KNOCK-IN MURINE MODEL FOR OSTEOGENESIS IMPERFECTA/
Authors: FORLINO A PORTER FD MARINI JC
Citation: A. Forlino et al., USE OF THE CRE LOX RECOMBINATION SYSTEM TO CREATE THE FIRST KNOCK-IN MURINE MODEL FOR OSTEOGENESIS IMPERFECTA/, Matrix biology, 17(2), 1998, pp. 164-164
MUTATIONS IN THE HUMAN STEROL DELTA(7)-REDUCTASE GENE AT 11Q12-13 CAUSE SMITH-LEMLI-OPITZ-SYNDROME
Authors: WASSIF CA MASLEN C KACHILELELINJEWILE S LIN D LINCK LM CONNOR WE STEINER RD PORTER FD
Citation: Ca. Wassif et al., MUTATIONS IN THE HUMAN STEROL DELTA(7)-REDUCTASE GENE AT 11Q12-13 CAUSE SMITH-LEMLI-OPITZ-SYNDROME, American journal of human genetics, 63(1), 1998, pp. 55-62
HYPOGONADISM AND OBESITY IN MICE WITH A TARGETED DELETION OF THE NHLH2 GENE
Authors: GOOD DJ PORTER FD MAHON KA PARLOW AF WESTPHAL H KIRSCH IR
Citation: Dj. Good et al., HYPOGONADISM AND OBESITY IN MICE WITH A TARGETED DELETION OF THE NHLH2 GENE, Nature genetics, 15(4), 1997, pp. 397-401
LHX2, A LIM HOMEOBOX GENE, IS REQUIRED FOR EYE, FOREBRAIN, AND DEFINITIVE ERYTHROCYTE DEVELOPMENT
Authors: PORTER FD DRAGO J XU Y CHEEMA SS WASSIF C HUANG SP LEE E GRINBERG A MASSALAS JS BODINE D ALT F WESTPHAL H
Citation: Fd. Porter et al., LHX2, A LIM HOMEOBOX GENE, IS REQUIRED FOR EYE, FOREBRAIN, AND DEFINITIVE ERYTHROCYTE DEVELOPMENT, Development, 124(15), 1997, pp. 2935-2944
DEFECTIVE PLACENTAL VASCULOGENESIS CAUSES EMBRYONIC LETHALITY IN VHL-DEFICIENT MICE
Authors: GNARRA JR WARD JM PORTER FD WAGNER JR DEVOR DE GRINBERG A EMMERTBUCK MR WESTPHAL H KLAUSNER RD LINEHAN WM
Citation: Jr. Gnarra et al., DEFECTIVE PLACENTAL VASCULOGENESIS CAUSES EMBRYONIC LETHALITY IN VHL-DEFICIENT MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9102-9107
CRE-MEDIATED SITE-SPECIFIC RECOMBINATION IN THE MURINE COL1A1 GENE - GENERATION OF A CONDITIONAL MURINE MODEL FOR OSTEOGENESIS IMPERFECTA
Authors: FORLINO A PORTER FD MARINI JC
Citation: A. Forlino et al., CRE-MEDIATED SITE-SPECIFIC RECOMBINATION IN THE MURINE COL1A1 GENE - GENERATION OF A CONDITIONAL MURINE MODEL FOR OSTEOGENESIS IMPERFECTA, American journal of human genetics, 61(4), 1997, pp. 1456-1456
KLIPPEL-TRENAUNAY-WEBER-SYNDROME ASSOCIATED WITH A 5 11 BALANCED TRANSLOCATION/
Authors: WHELAN AJ WATSON MS PORTER FD STEINER RD
Citation: Aj. Whelan et al., KLIPPEL-TRENAUNAY-WEBER-SYNDROME ASSOCIATED WITH A 5 11 BALANCED TRANSLOCATION/, American journal of medical genetics, 59(4), 1995, pp. 492-494
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