Wildin RS - Search Results

1

Developmental regulation of lck gene expression in T lymphocytes.

Wildin RS, Garvin AM, Pawar S, Lewis DB, Abraham KM, Forbush KA, Ziegler SF, Allen JM, Perlmutter RM. Wildin RS, et al. J Exp Med. 1991 Feb 1;173(2):383-93. doi: 10.1084/jem.173.2.383. J Exp Med. 1991. PMID: 1988541 Free PMC article.

2

Functional dissection of the murine lck distal promoter.

Wildin RS, Wang HU, Forbush KA, Perlmutter RM. Wildin RS, et al. J Immunol. 1995 Aug 1;155(3):1286-95. J Immunol. 1995. PMID: 7636195

3

Regulation of Src-family protein tyrosine kinase transcription during lymphocyte ontogeny.

Longo NS, Wang X, Wildin RS, Abraham KM. Longo NS, et al. Among authors: wildin rs. Mol Immunol. 1999 Oct-Nov;36(15-16):979-92. doi: 10.1016/s0161-5890(99)00134-0. Mol Immunol. 1999. PMID: 10698302

4

Rescue of the autoimmune scurfy mouse by partial bone marrow transplantation or by injection with T-enriched splenocytes.

Smyk-Pearson SK, Bakke AC, Held PK, Wildin RS. Smyk-Pearson SK, et al. Among authors: wildin rs. Clin Exp Immunol. 2003 Aug;133(2):193-9. doi: 10.1046/j.1365-2249.2003.02217.x. Clin Exp Immunol. 2003. PMID: 12869024 Free PMC article.

5

Heterogeneous AVPR2 gene mutations in congenital nephrogenic diabetes insipidus.

Wildin RS, Antush MJ, Bennett RL, Schoof JM, Scott CR. Wildin RS, et al. Am J Hum Genet. 1994 Aug;55(2):266-77. Am J Hum Genet. 1994. PMID: 7913579 Free PMC article.

6

Identification of novel candidate disease genes from de novo exonic copy number variants.

Gambin T, Yuan B, Bi W, Liu P, Rosenfeld JA, Coban-Akdemir Z, Pursley AN, Nagamani SCS, Marom R, Golla S, Dengle L, Petrie HG, Matalon R, Emrick L, Proud MB, Treadwell-Deering D, Chao HT, Koillinen H, Brown C, Urraca N, Mostafavi R, Bernes S, Roeder ER, Nugent KM, Bader PI, Bellus G, Cummings M, Northrup H, Ashfaq M, Westman R, Wildin R, Beck AE, Immken L, Elton L, Varghese S, Buchanan E, Faivre L, Lefebvre M, Schaaf CP, Walkiewicz M, Yang Y, Kang SL, Lalani SR, Bacino CA, Beaudet AL, Breman AM, Smith JL, Cheung SW, Lupski JR, Patel A, Shaw CA, Stankiewicz P. Gambin T, et al. Genome Med. 2017 Sep 21;9(1):83. doi: 10.1186/s13073-017-0472-7. Genome Med. 2017. PMID: 28934986 Free PMC article.

7

Clinical and molecular features of the immunodysregulation, polyendocrinopathy, enteropathy, X linked (IPEX) syndrome.

Wildin RS, Smyk-Pearson S, Filipovich AH. Wildin RS, et al. J Med Genet. 2002 Aug;39(8):537-45. doi: 10.1136/jmg.39.8.537. J Med Genet. 2002. PMID: 12161590 Free PMC article. Review.

8

Prospective immunological profiling in a case of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX).

Bakke AC, Purtzer MZ, Wildin RS. Bakke AC, et al. Among authors: wildin rs. Clin Exp Immunol. 2004 Aug;137(2):373-8. doi: 10.1111/j.1365-2249.2004.02537.x. Clin Exp Immunol. 2004. PMID: 15270855 Free PMC article.

9

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.

Wildin RS, Ramsdell F, Peake J, Faravelli F, Casanova JL, Buist N, Levy-Lahad E, Mazzella M, Goulet O, Perroni L, Bricarelli FD, Byrne G, McEuen M, Proll S, Appleby M, Brunkow ME. Wildin RS, et al. Nat Genet. 2001 Jan;27(1):18-20. doi: 10.1038/83707. Nat Genet. 2001. PMID: 11137992

10

Clinical utility of direct mutation testing for congenital nephrogenic diabetes insipidus in families.

Wildin RS, Cogdell DE. Wildin RS, et al. Pediatrics. 1999 Mar;103(3):632-9. doi: 10.1542/peds.103.3.632. Pediatrics. 1999. PMID: 10049968

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