Brannan CI[Author] - Search Results

Year	Number of Results
1988	1
1990	1
1991	4
1992	9
1993	4
1994	3
1995	6
1996	2
1998	1
1999	2
2000	3
2001	5
2004	1
2005	1
2006	1
2007	1
2012	1
2024	0

1

Brannan CI, Bartolomei MS. Brannan CI, et al. Curr Opin Genet Dev. 1999 Apr;9(2):164-70. doi: 10.1016/S0959-437X(99)80025-2. Curr Opin Genet Dev. 1999. PMID: 10322141 Free article. Review.

2

Neurofibromin-deficient fibroblasts fail to form perineurium in vitro.

Rosenbaum T, Boissy YL, Kombrinck K, Brannan CI, Jenkins NA, Copeland NG, Ratner N. Rosenbaum T, et al. Among authors: brannan ci. Development. 1995 Nov;121(11):3583-92. doi: 10.1242/dev.121.11.3583. Development. 1995. PMID: 8582272 Free PMC article.

3

The neurofibromatosis type 1 (NF1) tumor suppressor gene and myeloid leukemia.

Largaespada DA, Brannan CI, Shaughnessy JD, Jenkins NA, Copeland NG. Largaespada DA, et al. Among authors: brannan ci. Curr Top Microbiol Immunol. 1996;211:233-9. doi: 10.1007/978-3-642-85232-9_23. Curr Top Microbiol Immunol. 1996. PMID: 8585954 Review. No abstract available.

4

Retroviral integration at the Epi1 locus cooperates with Nf1 gene loss in the progression to acute myeloid leukemia.

Blaydes SM, Kogan SC, Truong BT, Gilbert DJ, Jenkins NA, Copeland NG, Largaespada DA, Brannan CI. Blaydes SM, et al. Among authors: brannan ci. J Virol. 2001 Oct;75(19):9427-34. doi: 10.1128/JVI.75.19.9427-9434.2001. J Virol. 2001. PMID: 11533205 Free PMC article.

5

The product of the H19 gene may function as an RNA.

Brannan CI, Dees EC, Ingram RS, Tilghman SM. Brannan CI, et al. Mol Cell Biol. 1990 Jan;10(1):28-36. doi: 10.1128/mcb.10.1.28-36.1990. Mol Cell Biol. 1990. PMID: 1688465 Free PMC article.

6

A mouse model for Prader-Willi syndrome imprinting-centre mutations.

Yang T, Adamson TE, Resnick JL, Leff S, Wevrick R, Francke U, Jenkins NA, Copeland NG, Brannan CI. Yang T, et al. Among authors: brannan ci. Nat Genet. 1998 May;19(1):25-31. doi: 10.1038/ng0598-25. Nat Genet. 1998. PMID: 9590284

7

Identification of mammalian noggin and its expression in the adult nervous system.

Valenzuela DM, Economides AN, Rojas E, Lamb TM, Nuñez L, Jones P, Lp NY, Espinosa R 3rd, Brannan CI, Gilbert DJ, et al. Valenzuela DM, et al. Among authors: brannan ci. J Neurosci. 1995 Sep;15(9):6077-84. doi: 10.1523/JNEUROSCI.15-09-06077.1995. J Neurosci. 1995. PMID: 7666191 Free PMC article.

8

Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice.

Chamberlain SJ, Johnstone KA, DuBose AJ, Simon TA, Bartolomei MS, Resnick JL, Brannan CI. Chamberlain SJ, et al. Among authors: brannan ci. Hum Mol Genet. 2004 Dec 1;13(23):2971-7. doi: 10.1093/hmg/ddh314. Epub 2004 Sep 30. Hum Mol Genet. 2004. PMID: 15459179

9

Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand.

Takahashi T, Tanaka M, Brannan CI, Jenkins NA, Copeland NG, Suda T, Nagata S. Takahashi T, et al. Among authors: brannan ci. Cell. 1994 Mar 25;76(6):969-76. doi: 10.1016/0092-8674(94)90375-1. Cell. 1994. PMID: 7511063

10

A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression.

Cattanach BM, Barr JA, Evans EP, Burtenshaw M, Beechey CV, Leff SE, Brannan CI, Copeland NG, Jenkins NA, Jones J. Cattanach BM, et al. Among authors: brannan ci. Nat Genet. 1992 Dec;2(4):270-4. doi: 10.1038/ng1292-270. Nat Genet. 1992. PMID: 1303278

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