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Results: 1-17 |
Results: 17
DNA-DAMAGE INDUCED VIA INDEPENDENT GENERATION OF THE RADICAL RESULTING FROM FORMAL HYDROGEN-ATOM ABSTRACTION FROM THE C1'-POSITION OF A NUCLEOTIDE
Authors: TRONCHE C GOODMAN BK GREENBERG MM
Citation: C. Tronche et al., DNA-DAMAGE INDUCED VIA INDEPENDENT GENERATION OF THE RADICAL RESULTING FROM FORMAL HYDROGEN-ATOM ABSTRACTION FROM THE C1'-POSITION OF A NUCLEOTIDE, Chemistry & biology, 5(5), 1998, pp. 263-271
NEW CYTOGENETIC TECHNOLOGY AND ITS APPLICATION IN MATERNAL-FETAL MEDICINE
Authors: STETTEN G GOODMAN BK FOX HE
Citation: G. Stetten et al., NEW CYTOGENETIC TECHNOLOGY AND ITS APPLICATION IN MATERNAL-FETAL MEDICINE, Journal of maternal-fetal investigation, 7(4), 1997, pp. 155-162
C1' ACYLATED DERIVATIVES OF 2'-DEOXYURIDINE - PHOTOLABILE PRECURSORS OF 2'-DEOXYURIDIN-1'-YL
Authors: GREENBERG MM YOO DJ GOODMAN BK
Citation: Mm. Greenberg et al., C1' ACYLATED DERIVATIVES OF 2'-DEOXYURIDINE - PHOTOLABILE PRECURSORS OF 2'-DEOXYURIDIN-1'-YL, Nucleosides & nucleotides, 16(1-2), 1997, pp. 33-40
FAMILIAL TANDEM DUPLICATION OF BANDS Q31.1 TO Q32.3 ON CHROMOSOME-4 WITH MILD PHENOTYPIC EFFECT
Authors: GOODMAN BK CAPONE GT HENNESSEY J THOMAS GH
Citation: Bk. Goodman et al., FAMILIAL TANDEM DUPLICATION OF BANDS Q31.1 TO Q32.3 ON CHROMOSOME-4 WITH MILD PHENOTYPIC EFFECT, American journal of medical genetics, 73(2), 1997, pp. 119-124
DELETION OF PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE
Authors: ARCH EM GOODMAN BK VANWESEP RA LIAW D CLARKE K PARSONS R MCKUSICK VA GERAGHTY MT
Citation: Em. Arch et al., DELETION OF PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE, American journal of medical genetics, 71(4), 1997, pp. 489-493
MIDAS SYNDROME IN A 46,XX NEWBORN WITH AMBIGUOUS GENITALIA AND A CRYPTIC, DE-NOVO X-Y TRANSLOCATION
Authors: CAMACHO JA GOODMAN BK HAMOSH A HURKO O THOMAS GH
Citation: Ja. Camacho et al., MIDAS SYNDROME IN A 46,XX NEWBORN WITH AMBIGUOUS GENITALIA AND A CRYPTIC, DE-NOVO X-Y TRANSLOCATION, American journal of human genetics, 61(4), 1997, pp. 515-515
DELETION OF 10Q23.2-Q24.1 INCLUDING PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE
Authors: ARCH EM GOODMAN BK LIAW D PARSONS R VANWESEP RA CLARKE K MCKUSICK VA GERAGHTY MT
Citation: Em. Arch et al., DELETION OF 10Q23.2-Q24.1 INCLUDING PTEN IN A PATIENT WITH BANNAYAN-RILEY-RUVALCABA-SYNDROME SUGGESTS ALLELISM WITH COWDEN-DISEASE, American journal of human genetics, 61(4), 1997, pp. 663-663
DUPLICATION XQ27-QTER AT XP22.3 IN A SEVERELY AFFECTED CHILD AND HIS PHENOTYPICALLY NORMAL MOTHER
Authors: GOODMAN BK LEPPERT M HARUM K RUTBERG J THOMAS GH GERAGHTY MT
Citation: Bk. Goodman et al., DUPLICATION XQ27-QTER AT XP22.3 IN A SEVERELY AFFECTED CHILD AND HIS PHENOTYPICALLY NORMAL MOTHER, American journal of human genetics, 61(4), 1997, pp. 717-717
DNA-DAMAGE INDUCED VIA 5,6-DIHYDROTHYMID-5-YL IN SINGLE-STRANDED OLIGONUCLEOTIDES
Authors: GREENBERG MM BARVIAN MR COOK GP GOODMAN BK MATRAY TJ TRONCHE C VENKATESAN H
Citation: Mm. Greenberg et al., DNA-DAMAGE INDUCED VIA 5,6-DIHYDROTHYMID-5-YL IN SINGLE-STRANDED OLIGONUCLEOTIDES, Journal of the American Chemical Society, 119(8), 1997, pp. 1828-1839
LOSS OF FUNCTION MUTATIONS IN CONSERVED REGIONS OF THE HUMAN ARGINASE-I GENE
Authors: VOCKLEY JG GOODMAN BK TABOR DE KERN RM JENKINSON CP GRODY WW CEDERBAUM SD
Citation: Jg. Vockley et al., LOSS OF FUNCTION MUTATIONS IN CONSERVED REGIONS OF THE HUMAN ARGINASE-I GENE, Biochemical and molecular medicine, 59(1), 1996, pp. 44-51
DELIVERY OF CYTOSOLIC LIVER ARGINASE INTO THE MITOCHONDRIAL MATRIX SPACE - A POSSIBLE NOVEL SITE FOR GENE REPLACEMENT THERAPY
Authors: WISSMANN PB GOODMAN BK VOCKLEY JG KERN RM CEDERBAUM SD GRODY WW
Citation: Pb. Wissmann et al., DELIVERY OF CYTOSOLIC LIVER ARGINASE INTO THE MITOCHONDRIAL MATRIX SPACE - A POSSIBLE NOVEL SITE FOR GENE REPLACEMENT THERAPY, Somatic cell and molecular genetics, 22(6), 1996, pp. 489-498
INDEPENDENT GENERATION AND REACTIVITY OF 2'-DEOXYURID-1'-YL
Authors: GOODMAN BK GREENBERG MM
Citation: Bk. Goodman et Mm. Greenberg, INDEPENDENT GENERATION AND REACTIVITY OF 2'-DEOXYURID-1'-YL, Journal of organic chemistry, 61(1), 1996, pp. 2-3
MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 7P ANOMALIES AND CLINICAL CORRELATION WITH SAETHRE-CHOTZEN SYNDROME
Authors: GOODMAN BK GREEN ED LEWANDA AF ROSENGREN S JABS EW
Citation: Bk. Goodman et al., MOLECULAR CYTOGENETIC ANALYSIS OF CHROMOSOME 7P ANOMALIES AND CLINICAL CORRELATION WITH SAETHRE-CHOTZEN SYNDROME, American journal of human genetics, 57(4), 1995, pp. 636-636
IDENTIFICATION OF MUTATIONS (D128G, H141L) IN THE LIVER ARGINASE GENEOF PATIENTS WITH HYPERARGININEMIA
Authors: VOCKLEY JG TABOR DE KERN RM GOODMAN BK WISSMANN PB KANG DS GRODY WW CEDERBAUM SD
Citation: Jg. Vockley et al., IDENTIFICATION OF MUTATIONS (D128G, H141L) IN THE LIVER ARGINASE GENEOF PATIENTS WITH HYPERARGININEMIA, Human mutation, 4(2), 1994, pp. 150-154
FUNCTIONAL AND MOLECULAR ANALYSIS OF LIVER ARGINASE PROMOTER SEQUENCES FROM MAN AND MACACA-FASCICULARIS
Authors: GOODMAN BK KLEIN D TABOR DE VOCKLEY JG CEDERBAUM SD GRODY WW
Citation: Bk. Goodman et al., FUNCTIONAL AND MOLECULAR ANALYSIS OF LIVER ARGINASE PROMOTER SEQUENCES FROM MAN AND MACACA-FASCICULARIS, Somatic cell and molecular genetics, 20(4), 1994, pp. 313-325
FUNCTIONAL-ANALYSIS OF THE LIVER ARGINASE PROMOTER
Authors: GOODMAN BK KLEIN D TABOR DE KERN RM VOCKLEY JG CEDERBAUM SD GRODY WW
Citation: Bk. Goodman et al., FUNCTIONAL-ANALYSIS OF THE LIVER ARGINASE PROMOTER, American journal of human genetics, 53(3), 1993, pp. 688-688
PCR-SSCP MUTATION DETECTION ANALYSIS OF HUMAN LIVER-ARGINASE - IDENTIFICATION OF A POINT MUTATION IN 2 UNRELATED ASKRENAZI JEWISH FAMILIES
Authors: TABOR DE VOCKLEY JG KERN RM GOODMAN BK WISSMAN PW GRODY WW CEDERBAUM SD
Citation: De. Tabor et al., PCR-SSCP MUTATION DETECTION ANALYSIS OF HUMAN LIVER-ARGINASE - IDENTIFICATION OF A POINT MUTATION IN 2 UNRELATED ASKRENAZI JEWISH FAMILIES, American journal of human genetics, 53(3), 1993, pp. 1235-1235
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