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Results: 1-13 |
Results: 13
A LOCUS FOR INHERITED FOCAL SEGMENTAL GLOMERULOSCLEROSIS MAPS TO CHROMOSOME 19Q13
Authors: MATHIS BJ KIM SH CALABRESE K HAAS M SEIDMAN JG SEIDMAN CE POLLAK MR
Citation: Bj. Mathis et al., A LOCUS FOR INHERITED FOCAL SEGMENTAL GLOMERULOSCLEROSIS MAPS TO CHROMOSOME 19Q13, Kidney international, 53(2), 1998, pp. 282-286
GITELMANS-SYNDROME (BARTTERS VARIANT) MAPS TO THE THIAZIDE-SENSITIVE COTRANSPORTER GENE LOCUS ON CHROMOSOME 16Q13 IN A LARGE KINDRED
Authors: POLLAK MR DELANEY VB GRAHAM RM HEBERT SC
Citation: Mr. Pollak et al., GITELMANS-SYNDROME (BARTTERS VARIANT) MAPS TO THE THIAZIDE-SENSITIVE COTRANSPORTER GENE LOCUS ON CHROMOSOME 16Q13 IN A LARGE KINDRED, Journal of the American Society of Nephrology, 7(10), 1996, pp. 2244-2248
3 INHERITED DISORDERS OF CALCIUM SENSING
Authors: POLLAK MR SEIDMAN CE BROWN EM
Citation: Mr. Pollak et al., 3 INHERITED DISORDERS OF CALCIUM SENSING, Medicine, 75(3), 1996, pp. 115-123
EXPRESSION AND CHARACTERIZATION OF INACTIVATING AND ACTIVATING MUTATIONS IN THE HUMAN CA-0(2-SENSING RECEPTOR())
Authors: BAI M QUINN S TRIVEDI S KIFOR O PEARCE SHS POLLAK MR KRAPCHO K HEBERT SC BROWN EM
Citation: M. Bai et al., EXPRESSION AND CHARACTERIZATION OF INACTIVATING AND ACTIVATING MUTATIONS IN THE HUMAN CA-0(2-SENSING RECEPTOR()), The Journal of biological chemistry, 271(32), 1996, pp. 19537-19545
A MOUSE MODEL OF HUMAN FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM
Authors: HO C CONNER DA POLLAK MR LADD DJ KIFOR O WARREN HB BROWN EM SEIDMAN JG SEIDMAN CE
Citation: C. Ho et al., A MOUSE MODEL OF HUMAN FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM, Nature genetics, 11(4), 1995, pp. 389-394
THE EXTRACELLULAR CALCIUM SENSING RECEPTOR GENE IN HUMAN PARATHYROID TUMORS
Authors: HOSOKAWA Y POLLAK MR BROWN EM ARNOLD A
Citation: Y. Hosokawa et al., THE EXTRACELLULAR CALCIUM SENSING RECEPTOR GENE IN HUMAN PARATHYROID TUMORS, Journal of bone and mineral research, 10, 1995, pp. 383-383
MUTATIONAL ANALYSIS OF THE EXTRACELLULAR CA2-SENSING RECEPTOR GENE INHUMAN PARATHYROID TUMORS()
Authors: HOSOKAWA Y POLLAK MR BROWN EM ARNOLD A
Citation: Y. Hosokawa et al., MUTATIONAL ANALYSIS OF THE EXTRACELLULAR CA2-SENSING RECEPTOR GENE INHUMAN PARATHYROID TUMORS(), The Journal of clinical endocrinology and metabolism, 80(11), 1995, pp. 3107-3110
MUTATIONS IN THE HUMAN CA2-SENSING-RECEPTOR GENE THAT CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA()
Authors: CHOU YHW POLLAK MR BRANDI ML TOSS G ARNQVIST H ATKINSON AB PAPAPOULOS SE MARX S BROWN EM SEIDMAN JG SEIDMAN CE
Citation: Yhw. Chou et al., MUTATIONS IN THE HUMAN CA2-SENSING-RECEPTOR GENE THAT CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA(), American journal of human genetics, 56(5), 1995, pp. 1075-1079
AUTOSOMAL-DOMINANT HYPOCALCEMIA CAUSED BY A CA2-SENSING RECEPTOR GENEMUTATION()
Authors: POLLAK MR BROWN EM ESTEP HL MCLAINE PN KIFOR O PARK J HEBERT SC SEIDMAN CE SEIDMAN JG
Citation: Mr. Pollak et al., AUTOSOMAL-DOMINANT HYPOCALCEMIA CAUSED BY A CA2-SENSING RECEPTOR GENEMUTATION(), Nature genetics, 8(3), 1994, pp. 303-307
MUTATIONS IN THE HUMAN CA2-SENSING RECEPTOR GENE CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA, NEONATAL SEVERE HYPERPARATHYROIDISM, AND AUTOSOMAL-DOMINANT HYPOCALCEMIA()
Authors: POLLAK MR BROWN EM CHOU YHW HEBERT SC SEIDMAN CE SEIDMAN JG
Citation: Mr. Pollak et al., MUTATIONS IN THE HUMAN CA2-SENSING RECEPTOR GENE CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA, NEONATAL SEVERE HYPERPARATHYROIDISM, AND AUTOSOMAL-DOMINANT HYPOCALCEMIA(), Journal of the American Society of Nephrology, 5(3), 1994, pp. 871-871
FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM - EFFECTS OF MUTANT-GENE DOSAGE ON PHENOTYPE
Authors: POLLAK MR CHOU YHW MARX SJ STEINMANN B COLE DEC BRANDI ML PAPAPOULOS SE MENKO FH HENDY GN BROWN EM SEIDMAN CE SEIDMAN JG
Citation: Mr. Pollak et al., FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM - EFFECTS OF MUTANT-GENE DOSAGE ON PHENOTYPE, The Journal of clinical investigation, 93(3), 1994, pp. 1108-1112
HOMOZYGOSITY MAPPING OF THE GENE FOR ALKAPTONURIA TO CHROMOSOME-3Q2
Authors: POLLAK MR CHOU YHW CERDA JJ STEINMANN B LADU BN SEIDMAN JG SEIDMAN CE
Citation: Mr. Pollak et al., HOMOZYGOSITY MAPPING OF THE GENE FOR ALKAPTONURIA TO CHROMOSOME-3Q2, Nature genetics, 5(2), 1993, pp. 201-204
MUTATIONS IN THE HUMAN CA2-SENSING RECEPTOR GENE CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM()
Authors: POLLAK MR BROWN EM CHOU YHW HEBERT SC MARX SJ STEINMANN B LEVI T SEIDMAN CE SEIDMAN JG
Citation: Mr. Pollak et al., MUTATIONS IN THE HUMAN CA2-SENSING RECEPTOR GENE CAUSE FAMILIAL HYPOCALCIURIC HYPERCALCEMIA AND NEONATAL SEVERE HYPERPARATHYROIDISM(), Cell, 75(7), 1993, pp. 1297-1303
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