Prins JB - Search Results

1

Familial isolated hyperparathyroidism is linked to a 1.7 Mb region on chromosome 2p13.3-14.

Warner JV, Nyholt DR, Busfield F, Epstein M, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Teh BT, Prins JB, Cardinal JW. Warner JV, et al. Among authors: prins jb. J Med Genet. 2006 Mar;43(3):e12. doi: 10.1136/jmg.2005.035766. J Med Genet. 2006. PMID: 16525030 Free PMC article.

2

Genetic testing in familial isolated hyperparathyroidism: unexpected results and their implications.

Warner J, Epstein M, Sweet A, Singh D, Burgess J, Stranks S, Hill P, Perry-Keene D, Learoyd D, Robinson B, Birdsey P, Mackenzie E, Teh BT, Prins JB, Cardinal J. Warner J, et al. Among authors: prins jb. J Med Genet. 2004 Mar;41(3):155-60. doi: 10.1136/jmg.2003.016725. J Med Genet. 2004. PMID: 14985373 Free PMC article.

3

A report of a national mutation testing service for the MEN1 gene: clinical presentations and implications for mutation testing.

Cardinal JW, Bergman L, Hayward N, Sweet A, Warner J, Marks L, Learoyd D, Dwight T, Robinson B, Epstein M, Smith M, Teh BT, Cameron DP, Prins JB. Cardinal JW, et al. Among authors: prins jb. J Med Genet. 2005 Jan;42(1):69-74. doi: 10.1136/jmg.2003.017319. J Med Genet. 2005. PMID: 15635078 Free PMC article.

4

Autosomal dominant hypocalcemia: a novel activating mutation (E604K) in the cysteine-rich domain of the calcium-sensing receptor.

Tan YM, Cardinal J, Franks AH, Mun HC, Lewis N, Harris LB, Prins JB, Conigrave AD. Tan YM, et al. Among authors: prins jb. J Clin Endocrinol Metab. 2003 Feb;88(2):605-10. doi: 10.1210/jc.2002-020081. J Clin Endocrinol Metab. 2003. PMID: 12574188

5

Mouse chromosome 3.

Prins JB, Meisler MH, Seldin MF. Prins JB, et al. Mamm Genome. 1994;5 Spec No:S40-50. Mamm Genome. 1994. PMID: 7719016 No abstract available.

6

Type 1 diabetes in mice is linked to the interleukin-1 receptor and Lsh/Ity/Bcg genes on chromosome 1.

Cornall RJ, Prins JB, Todd JA, Pressey A, DeLarato NH, Wicker LS, Peterson LB. Cornall RJ, et al. Among authors: prins jb. Nature. 1991 Sep 19;353(6341):262-5. doi: 10.1038/353262a0. Nature. 1991. PMID: 1832743

7

Polygenic control of autoimmune diabetes in nonobese diabetic mice.

Ghosh S, Palmer SM, Rodrigues NR, Cordell HJ, Hearne CM, Cornall RJ, Prins JB, McShane P, Lathrop GM, Peterson LB, et al. Ghosh S, et al. Among authors: prins jb. Nat Genet. 1993 Aug;4(4):404-9. doi: 10.1038/ng0893-404. Nat Genet. 1993. PMID: 8401590

8

Mapping the diabetes polygene Idd3 on mouse chromosome 3 by use of novel congenic strains.

Lord CJ, Bohlander SK, Hopes EA, Montague CT, Hill NJ, Prins JB, Renjilian RJ, Peterson LB, Wicker LS, Todd JA, et al. Lord CJ, et al. Among authors: prins jb. Mamm Genome. 1995 Sep;6(9):563-70. doi: 10.1007/BF00352359. Mamm Genome. 1995. PMID: 8535060

9

Pancreatic beta-cell IL-22 receptor deficiency induces age-dependent dysregulation of insulin biosynthesis and systemic glucose homeostasis.

Sajiir H, Wong KY, Müller A, Keshvari S, Burr L, Aiello E, Mezza T, Giaccari A, Sebastiani G, Dotta F, Ramm GA, Macdonald GA, McGuckin MA, Prins JB, Hasnain SZ. Sajiir H, et al. Among authors: prins jb. Nat Commun. 2024 May 29;15(1):4527. doi: 10.1038/s41467-024-48320-2. Nat Commun. 2024. PMID: 38811550 Free PMC article.

10

Liver and pancreatic-targeted interleukin-22 as a therapeutic for metabolic dysfunction-associated steatohepatitis.

Sajiir H, Keshvari S, Wong KY, Borg DJ, Steyn FJ, Fercher C, Taylor K, Taylor B, Barnard RT, Müller A, Moniruzzaman M, Miller G, Wang R, Fotheringham A, Schreiber V, Sheng YH, Hancock JL, Loo D, Burr L, Huynh T, Lockett J, Ramm GA, Macdonald GA, Prins JB, McGuckin MA, Hasnain SZ. Sajiir H, et al. Among authors: prins jb. Nat Commun. 2024 May 29;15(1):4528. doi: 10.1038/s41467-024-48317-x. Nat Commun. 2024. PMID: 38811532 Free PMC article.

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