AAAAAA

   
Results: 1-10 |
Results: 10
T235 VARIANT OF THE ANGIOTENSINOGEN GENE AND BLOOD-PRESSURE IN THE CHILEAN POPULATION
Authors: FARDELLA CE CLAVERIE X VIGNOLO P MONTERO J VILLARROEL L
Citation: Ce. Fardella et al., T235 VARIANT OF THE ANGIOTENSINOGEN GENE AND BLOOD-PRESSURE IN THE CHILEAN POPULATION, Journal of hypertension, 16(6), 1998, pp. 829-833
SALT-WASTING CONGENITAL ADRENAL-HYPERPLASIA - DETECTION OF MUTATIONS IN CYP21B GENE IN A CHILEAN POPULATION
Authors: FARDELLA CE POGGI H PINEDA P SOTO J TORREALBA I CATTANI A OESTREICHER E FORADORI A
Citation: Ce. Fardella et al., SALT-WASTING CONGENITAL ADRENAL-HYPERPLASIA - DETECTION OF MUTATIONS IN CYP21B GENE IN A CHILEAN POPULATION, The Journal of clinical endocrinology and metabolism, 83(9), 1998, pp. 3357-3360
MOLECULAR-BIOLOGY OF MINERALOCORTICOID METABOLISM
Authors: FARDELLA CE MILLER WL
Citation: Ce. Fardella et Wl. Miller, MOLECULAR-BIOLOGY OF MINERALOCORTICOID METABOLISM, Annual review of nutrition, 16, 1996, pp. 443-470
GENETIC-VARIATION IN P450C11AS IN CHILEAN PATIENTS WITH LOW RENIN HYPERTENSION
Authors: FARDELLA CE RODRIGUEZ H MONTERO J ZHANG GR VIGNOLO P ROJAS A VILLARROEL L MILLER WL
Citation: Ce. Fardella et al., GENETIC-VARIATION IN P450C11AS IN CHILEAN PATIENTS WITH LOW RENIN HYPERTENSION, The Journal of clinical endocrinology and metabolism, 81(12), 1996, pp. 4347-4351
GENE CONVERSION IN THE CYP11B2 GENE ENCODING P450C11AS IS ASSOCIATED WITH, BUT DOES NOT CAUSE, THE SYNDROME OF CORTICOSTERONE METHYLOXIDASE-II DEFICIENCY
Authors: FARDELLA CE HUM DW RODRIGUEZ H ZHANG GR BARRY FL ILICKI A BLOCH CA MILLER WL
Citation: Ce. Fardella et al., GENE CONVERSION IN THE CYP11B2 GENE ENCODING P450C11AS IS ASSOCIATED WITH, BUT DOES NOT CAUSE, THE SYNDROME OF CORTICOSTERONE METHYLOXIDASE-II DEFICIENCY, The Journal of clinical endocrinology and metabolism, 81(1), 1996, pp. 321-326
ARTIFICIAL MUTATIONS IN P450C11AS (ALDOSTERONE SYNTHASE) CAN INCREASEENZYMATIC-ACTIVITY - A MODEL FOR LOW-RENIN HYPERTENSION
Authors: FARDELLA CE RODRIGUEZ H HUM DW MELLON SH MILLER WL
Citation: Ce. Fardella et al., ARTIFICIAL MUTATIONS IN P450C11AS (ALDOSTERONE SYNTHASE) CAN INCREASEENZYMATIC-ACTIVITY - A MODEL FOR LOW-RENIN HYPERTENSION, The Journal of clinical endocrinology and metabolism, 80(3), 1995, pp. 1040-1043
MUTATION T318M IN THE CYPIIB2 GENE ENCODING P450CIIAS (ALDOSTERONE SYNTHASE) CAUSES CORTICOSTERONE METHYL OXIDASE-II DEFICIENCY
Authors: ZHANG GG RODRIGUEZ H FARDELLA CE HARRIS DA MILLER WL
Citation: Gg. Zhang et al., MUTATION T318M IN THE CYPIIB2 GENE ENCODING P450CIIAS (ALDOSTERONE SYNTHASE) CAUSES CORTICOSTERONE METHYL OXIDASE-II DEFICIENCY, American journal of human genetics, 57(5), 1995, pp. 1037-1043
POINT MUTATION ARG-440-]HIS IN P450C17 CAUSES COMPLETE 17-ALPHA-HYDROXYLASE DEFICIENCY
Authors: FARDELLA CE HUM DW HOMOKI J MILLER WL
Citation: Ce. Fardella et al., POINT MUTATION ARG-440-]HIS IN P450C17 CAUSES COMPLETE 17-ALPHA-HYDROXYLASE DEFICIENCY, Pediatric research, 35(4), 1994, pp. 10000098-10000098
POINT MUTATION OF ARG440 TO HIS IN CYTOCHROME P450C17 CAUSES SEVERE 17-ALPHA-HYDROXYLASE DEFICIENCY
Authors: FARDELLA CE HUM DW HOMOKI J MILLER WL
Citation: Ce. Fardella et al., POINT MUTATION OF ARG440 TO HIS IN CYTOCHROME P450C17 CAUSES SEVERE 17-ALPHA-HYDROXYLASE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 79(1), 1994, pp. 160-164
DELETION OF AMINO-ACIDS ASP (487)-SER(488)-PHE(489) IN HUMAN CYTOCHROME P450C17 CAUSES SEVERE 17-ALPHA-HYDROXYLASE DEFICIENCY
Authors: FARDELLA CE ZHANG LH MAHACHOKLERTWATTANA P LIN D MILLER WL
Citation: Ce. Fardella et al., DELETION OF AMINO-ACIDS ASP (487)-SER(488)-PHE(489) IN HUMAN CYTOCHROME P450C17 CAUSES SEVERE 17-ALPHA-HYDROXYLASE DEFICIENCY, The Journal of clinical endocrinology and metabolism, 77(2), 1993, pp. 489-493
Risultati: 1-10 |