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Results: 1-13 |
Results: 13
MUTATIONS IN TRANSCRIPTIONAL REGULATOR ATRX ESTABLISH THE FUNCTIONAL-SIGNIFICANCE OF A PHD-LIKE DOMAIN
Authors: GIBBONS RJ BACHOO S PICKETTS DJ AFTIMOS S ASENBAUER B BERGOFFEN J BERRY SA DAHL N FRYER A KEPPLER K KUROSAWA K LEVIN ML MASUNO M NERI G PIERPONT ME SLANEY SF HIGGS DR
Citation: Rj. Gibbons et al., MUTATIONS IN TRANSCRIPTIONAL REGULATOR ATRX ESTABLISH THE FUNCTIONAL-SIGNIFICANCE OF A PHD-LIKE DOMAIN, Nature genetics, 17(2), 1997, pp. 146-148
IDENTIFICATION OF A COMPLEX CONGENITAL HEART DEFECT SUSCEPTIBILITY LOCUS BY USING DNA POOLING AND SHARED SEGMENT ANALYSIS
Authors: SHEFFIELD VC PIERPONT ME NISHIMURA D BEEK JS BURNS TL BERG MA STONE EM PATIL SR LAUER RM
Citation: Vc. Sheffield et al., IDENTIFICATION OF A COMPLEX CONGENITAL HEART DEFECT SUSCEPTIBILITY LOCUS BY USING DNA POOLING AND SHARED SEGMENT ANALYSIS, Human molecular genetics, 6(1), 1997, pp. 117-121
A POINT MUTATION IN THE CYTB GENE OF CARDIAC MTDNA ASSOCIATED WITH COMPLEX-III DEFICIENCY IN ISCHEMIC CARDIOMYOPATHY
Authors: MARINGARCIA J IIU YP ANANTHAKRISHNAN R PIERPONT ME PIERPONT GL GOLDENTHAL MJ
Citation: J. Maringarcia et al., A POINT MUTATION IN THE CYTB GENE OF CARDIAC MTDNA ASSOCIATED WITH COMPLEX-III DEFICIENCY IN ISCHEMIC CARDIOMYOPATHY, Biochemistry and molecular biology international, 40(3), 1996, pp. 487-495
MITOCHONDRIAL DYSFUNCTION IN SPONTANEOUS INBRED TURKEY CARDIOMYOPATHY
Authors: MARINGARCIA J ANANTHAKRISHNAN R PIERPONT ME GOLDENTHAL MJ
Citation: J. Maringarcia et al., MITOCHONDRIAL DYSFUNCTION IN SPONTANEOUS INBRED TURKEY CARDIOMYOPATHY, Biochemistry and molecular biology international, 38(6), 1996, pp. 1087-1093
THE ETIOLOGY OF LEFT-VENTRICULAR DYSFUNCTION CAN EFFECT THE CATECHOLAMINE RESPONSE TO HEART-FAILURE - CATECHOLAMINES IN HEART-FAILURE
Authors: PIERPONT GL EINZIG S PIERPONT ME NOREN GR
Citation: Gl. Pierpont et al., THE ETIOLOGY OF LEFT-VENTRICULAR DYSFUNCTION CAN EFFECT THE CATECHOLAMINE RESPONSE TO HEART-FAILURE - CATECHOLAMINES IN HEART-FAILURE, ACP. Applied cardiopulmonary pathophysiology, 6(1), 1996, pp. 25-31
DOGS FED A HIGH-FAT DIET HAVE REDUCED PLASMA-CONCENTRATIONS
Authors: SANDERSON S GROSS KL OSBORNE CA LULICH J OGBUM P PIERPONT ME BIRD K KOEHLER L SWANSON L ULRICH L
Citation: S. Sanderson et al., DOGS FED A HIGH-FAT DIET HAVE REDUCED PLASMA-CONCENTRATIONS, The FASEB journal, 10(3), 1996, pp. 2919-2919
RELIABILITY OF CARNITINE CONCENTRATIONS MEASURED IN SINGLE POSTPRANDIAL URINE SAMPLES FROM DOGS
Authors: SANDERSON S OSBORNE C LULICH J PIERPONT ME GROSS K OGBURN P KOEHLER L CARVALHO M
Citation: S. Sanderson et al., RELIABILITY OF CARNITINE CONCENTRATIONS MEASURED IN SINGLE POSTPRANDIAL URINE SAMPLES FROM DOGS, American journal of veterinary research, 57(8), 1996, pp. 1185-1188
AUTOSOMAL-DOMINANT OPTIC-NERVE COLOBOMAS, VESICOURETERAL REFLUX, AND RENAL ANOMALIES
Authors: SCHIMMENTI LA PIERPONT ME CARPENTER BLM KASHTAN CE JOHNSON MR DOBYNS WB
Citation: La. Schimmenti et al., AUTOSOMAL-DOMINANT OPTIC-NERVE COLOBOMAS, VESICOURETERAL REFLUX, AND RENAL ANOMALIES, American journal of medical genetics, 59(2), 1995, pp. 204-208
HETEROTAXIA SYNDROME AND AUTOSOMAL-DOMINANT INHERITANCE
Authors: ALONSO S PIERPONT ME RADTKE W MARTINEZ J CHEN SC GRANT JW DAHNERT I TAVIAUX S ROMEY MC DEMAILLE J BOUVAGNET P
Citation: S. Alonso et al., HETEROTAXIA SYNDROME AND AUTOSOMAL-DOMINANT INHERITANCE, American journal of medical genetics, 56(1), 1995, pp. 12-15
CLINICAL PHENOTYPE ASSOCIATED WITH TERMINAL 2Q37 DELETION
Authors: CONRAD B DEWALD G CHRISTENSEN E LOPEZ M HIGGINS J PIERPONT ME
Citation: B. Conrad et al., CLINICAL PHENOTYPE ASSOCIATED WITH TERMINAL 2Q37 DELETION, Clinical genetics, 48(3), 1995, pp. 134-139
CLINICAL SEVERITY OF CONGENITAL HEART-DISEASE IN HOLT-ORAM SYNDROME
Authors: SLETTEN LJ PIERPONT ME
Citation: Lj. Sletten et Me. Pierpont, CLINICAL SEVERITY OF CONGENITAL HEART-DISEASE IN HOLT-ORAM SYNDROME, American journal of human genetics, 57(4), 1995, pp. 571-571
USING FISH TO FURTHER DESCRIBE 2 PATIENTS WITH THE CYTOGENETIC ABERRATIONS DUP(17)(P11.2-]P12) AND DEL(4)(P16.3)
Authors: HIGGINS RR MOREY MA FERTITTA A RYHN S MCCORD J PIERPONT ME BURSTEIN L BREKKEN D AHMAD J
Citation: Rr. Higgins et al., USING FISH TO FURTHER DESCRIBE 2 PATIENTS WITH THE CYTOGENETIC ABERRATIONS DUP(17)(P11.2-]P12) AND DEL(4)(P16.3), American journal of human genetics, 57(4), 1995, pp. 1796-1796
LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT ATRIOVENTRICULAR-CANAL DEFECTS- EXCLUSION OF CHROMOSOME-21
Authors: COUSINEAU AJ LAUER RM PIERPONT ME BURNS TL ARDINGER RH PATIL SR SHEFFIELD VC
Citation: Aj. Cousineau et al., LINKAGE ANALYSIS OF AUTOSOMAL-DOMINANT ATRIOVENTRICULAR-CANAL DEFECTS- EXCLUSION OF CHROMOSOME-21, Human genetics, 93(2), 1994, pp. 103-108
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