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Results: 1-25 | 26-42 |
Results: 26-42/42
EVIDENCE THAT 2 PHENOTYPICALLY DISTINCT MOUSE PKD MUTATIONS, BPK AND JCPK, ARE ALLELIC
Authors: GUAYWOODFORD LM BRYDA EC CHRISTINE B LINDSEY JR COLLIER WR AVNER ED DEUSTACHIO P FLAHERTY L
Citation: Lm. Guaywoodford et al., EVIDENCE THAT 2 PHENOTYPICALLY DISTINCT MOUSE PKD MUTATIONS, BPK AND JCPK, ARE ALLELIC, Kidney international, 50(4), 1996, pp. 1158-1165
THE MOUSE BPK MUTATION, A MODEL OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE (ARPKD) AND JCPK, A PHENOTYPICALLY DISTINCT PKD MUTATION, ARE ALLELIC
Authors: GUAYWOODFORD LM BRYDA EC LINDSAY JR AVNER ED FLAHERTY L
Citation: Lm. Guaywoodford et al., THE MOUSE BPK MUTATION, A MODEL OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE (ARPKD) AND JCPK, A PHENOTYPICALLY DISTINCT PKD MUTATION, ARE ALLELIC, Pediatric research, 39(4), 1996, pp. 2151-2151
A NEW MOUSE MODEL FOR POLYCYSTIC KIDNEY-DISEASE (PKD)
Authors: GUAYWOODFORD LM ROBERT B STJOHN PL ABRAHAMSON DR
Citation: Lm. Guaywoodford et al., A NEW MOUSE MODEL FOR POLYCYSTIC KIDNEY-DISEASE (PKD), Molecular biology of the cell, 6, 1995, pp. 1883-1883
THE MOUSE BPK MUTATION, A NEW MODEL OF AUTOSOMAL RECESSIVE POLYCYSTICKIDNEY-DISEASE (ARPKD) IS GENETICALLY DISTINCT
Authors: GUAYWOODFORD LM CHRISTINE BS AVNER ED
Citation: Lm. Guaywoodford et al., THE MOUSE BPK MUTATION, A NEW MODEL OF AUTOSOMAL RECESSIVE POLYCYSTICKIDNEY-DISEASE (ARPKD) IS GENETICALLY DISTINCT, Journal of the American Society of Nephrology, 6(3), 1995, pp. 696-696
HIGH-RESOLUTION GENETIC-MAPPING OF THE MOUSE CPK MUTATION
Authors: GUAYWOODFORD LM DEUSTACHIO P
Citation: Lm. Guaywoodford et P. Deustachio, HIGH-RESOLUTION GENETIC-MAPPING OF THE MOUSE CPK MUTATION, Journal of the American Society of Nephrology, 6(3), 1995, pp. 696-696
DOMINANTLY-TRANSMITTED GLOMERULOCYSTIC DISEASE (GCD) - A DISTINCT GENETIC ENTITY
Authors: SHARP CK BERGMAN SM ROBBIN M GUAYWOODFORD LM
Citation: Ck. Sharp et al., DOMINANTLY-TRANSMITTED GLOMERULOCYSTIC DISEASE (GCD) - A DISTINCT GENETIC ENTITY, Journal of the American Society of Nephrology, 6(3), 1995, pp. 727-727
SEQUENCE-ANALYSIS OF THE HUMAN HTG737 GENE AND ITS POLYMORPHIC SITES IN PATIENTS WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE
Authors: ONUCHIC LF SCHRICK JJ MA J HUDSON T GUAYWOODFORD LM ZERRES K WOYCHIK RP REEDERS ST
Citation: Lf. Onuchic et al., SEQUENCE-ANALYSIS OF THE HUMAN HTG737 GENE AND ITS POLYMORPHIC SITES IN PATIENTS WITH AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE, Mammalian genome, 6(11), 1995, pp. 805-808
FAMILIAL GLOMERULOCYSTIC DISEASE (GCD) TRANSMITTED AS A DOMINANT TRAIT WITH EVIDENCE FOR ANTICIPATION - A NEW ENTITY
Authors: SHARPE C BERGMAN SM GUAYWOODFORD LM
Citation: C. Sharpe et al., FAMILIAL GLOMERULOCYSTIC DISEASE (GCD) TRANSMITTED AS A DOMINANT TRAIT WITH EVIDENCE FOR ANTICIPATION - A NEW ENTITY, Pediatric research, 37(4), 1995, pp. 369-369
THE SEVERE PERINATAL FORM OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE MAPS TO CHROMOSOME 6P21.1-P12 - IMPLICATIONS FOR GENETIC-COUNSELING
Authors: GUAYWOODFORD LM MUECHER G HOPKINS SD AVNER ED GERMINO GG GUILLOT AP HERRIN J HOLLEMAN R IRONS DA PRIMACK W THOMSON PD WALDO FB LUNT PW ZERRES K
Citation: Lm. Guaywoodford et al., THE SEVERE PERINATAL FORM OF AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE MAPS TO CHROMOSOME 6P21.1-P12 - IMPLICATIONS FOR GENETIC-COUNSELING, American journal of human genetics, 56(5), 1995, pp. 1101-1107
THE SEVERE PERINATAL PHENOTYPE OF ARPKD (AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE) MAPS TO CHROMOSOME 6P21-CEN
Authors: GUAYWOODFORD LM HOPKINS SD MUECHER G ZERRES K
Citation: Lm. Guaywoodford et al., THE SEVERE PERINATAL PHENOTYPE OF ARPKD (AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY-DISEASE) MAPS TO CHROMOSOME 6P21-CEN, Journal of the American Society of Nephrology, 5(3), 1994, pp. 624-624
IDENTIFICATION OF A SIMPLE SEQUENCE POLYMORPHISM WITHIN THE MOUSE LOCUS D12NYU2
Authors: GUAYWOODFORD LM BRUNS GAP DEUSTACHIO P
Citation: Lm. Guaywoodford et al., IDENTIFICATION OF A SIMPLE SEQUENCE POLYMORPHISM WITHIN THE MOUSE LOCUS D12NYU2, Mammalian genome, 5(4), 1994, pp. 251-252
IDENTIFICATION OF A SIMPLE SEQUENCE POLYMORPHISM WITHIN THE MOUSE LOCUS D12NYU2 (VOL 5, PG 251, 1994)
Authors: GUAYWOODFORD LM BRUNS GAP DEUSTACHIO P
Citation: Lm. Guaywoodford et al., IDENTIFICATION OF A SIMPLE SEQUENCE POLYMORPHISM WITHIN THE MOUSE LOCUS D12NYU2 (VOL 5, PG 251, 1994), Mammalian genome, 5(10), 1994, pp. 658-658
THE MOUSE CONGENITAL POLYCYSTIC KIDNEY (CPK) LOCUS MAPS WITHIN 1.3 CMOF THE CHROMOSOME-12 MARKER D12NYU2
Authors: SIMON EA COOK S DAVISSON MT DEUSTACHIO P GUAYWOODFORD LM
Citation: Ea. Simon et al., THE MOUSE CONGENITAL POLYCYSTIC KIDNEY (CPK) LOCUS MAPS WITHIN 1.3 CMOF THE CHROMOSOME-12 MARKER D12NYU2, Genomics, 21(2), 1994, pp. 415-418
COMBINED CYSTIC-DISEASE OF THE LIVER AND KIDNEY
Authors: DAGATA IDA JONAS MM PEREZATAYDE AR GUAYWOODFORD LM
Citation: Ida. Dagata et al., COMBINED CYSTIC-DISEASE OF THE LIVER AND KIDNEY, Seminars in liver disease, 14(3), 1994, pp. 215-228
IDENTIFICATION AND CHARACTERIZATION OF NOVEL GENES EXPRESSED DURING EARLY METANEPHRIC INDUCTION
Authors: ROSENBLUM ND GUAYWOODFORD LM YAGER TD
Citation: Nd. Rosenblum et al., IDENTIFICATION AND CHARACTERIZATION OF NOVEL GENES EXPRESSED DURING EARLY METANEPHRIC INDUCTION, Pediatric research, 35(4), 1994, pp. 10000372-10000372
A MOLECULAR DEFECT IN THE VASOPRESSIN V2-RECEPTOR GENE CAUSING NEPHROGENIC DIABETES-INSIPIDUS
Authors: HOLTZMAN EJ HARRIS HW KOLAKOWSKI LF GUAYWOODFORD LM BOTELHO B AUSIELLO DA
Citation: Ej. Holtzman et al., A MOLECULAR DEFECT IN THE VASOPRESSIN V2-RECEPTOR GENE CAUSING NEPHROGENIC DIABETES-INSIPIDUS, The New England journal of medicine, 328(21), 1993, pp. 1534-1537
REVERSIBLE FANCONI SYNDROME-ASSOCIATED WITH VALPROATE THERAPY
Authors: LANDE MB KIM MS BARTLETT C GUAYWOODFORD LM
Citation: Mb. Lande et al., REVERSIBLE FANCONI SYNDROME-ASSOCIATED WITH VALPROATE THERAPY, The Journal of pediatrics, 123(2), 1993, pp. 320-322
Risultati: 1-25 | 26-42 |