Larsson C - Search Results

1

Assignment of the human FAU gene to a subregion of chromosome 11q13.

Kas K, Schoenmakers E, van de Ven W, Weber G, Nordenskjöld M, Michiels L, Merregaert J, Larsson C. Kas K, et al. Among authors: larsson c. Genomics. 1993 Aug;17(2):387-92. doi: 10.1006/geno.1993.1337. Genomics. 1993. PMID: 8406491

2

Exclusion of FAU as the multiple endocrine neoplasia type 1 (MEN1) gene.

Kas K, Weber G, Merregaert J, Michiels L, Sandelin K, Skogseid B, Thompson N, Nordenskjöld M, Larsson C, Friedman E. Kas K, et al. Among authors: larsson c. Hum Mol Genet. 1993 Apr;2(4):349-53. doi: 10.1093/hmg/2.4.349. Hum Mol Genet. 1993. PMID: 8099302

3

Isolation and characterization of a novel gene close to the human phosphoinositide-specific phospholipase C beta 3 gene on chromosomal region 11q13.

Lagercrantz J, Carson E, Larsson C, Nordenskjöld M, Weber G. Lagercrantz J, et al. Among authors: larsson c. Genomics. 1996 Feb 1;31(3):380-4. doi: 10.1006/geno.1996.0063. Genomics. 1996. PMID: 8838322

4

A putative human zinc-finger gene (ZFPL1) on 11q13, highly conserved in the mouse and expressed in exocrine pancreas. The European Consortium on MEN 1.

Höppener JW, De Wit MJ, Simarro-Doorten AY, Roijers JF, van Herrewaarden HM, Lips CJ, Parente F, Quincey D, Gaudray P, Khodaei S, Weber G, Teh B, Farnebo F, Larsson C, Zhang CX, Calender A, Pannett AA, Forbes SA, Bassett JH, Thakker RV, Lemmens I, Van de Ven WJ, Kas K. Höppener JW, et al. Among authors: larsson c. Genomics. 1998 Jun 1;50(2):251-9. doi: 10.1006/geno.1998.5307. Genomics. 1998. PMID: 9653652

5

Sublocalization of the multiple endocrine neoplasia type 1 gene.

Larsson C, Weber G, Janson M. Larsson C, et al. Henry Ford Hosp Med J. 1992;40(3-4):159-61. Henry Ford Hosp Med J. 1992. PMID: 1362396 Free article.

6

Molecular characterization of human and murine C11orf5, a new member of the FAUNA gene cluster.

Lemmens IH, Farnebo F, Piehl F, Merregaert J, Van de Ven WJ, Larsson C, Kas K. Lemmens IH, et al. Among authors: larsson c. Mamm Genome. 2000 Jan;11(1):78-80. doi: 10.1007/s003350010016. Mamm Genome. 2000. PMID: 10602999 No abstract available.

7

Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus.

Larsson C, Weber G, Kvanta E, Lewis K, Janson M, Jones C, Glaser T, Evans G, Nordenskjöld M. Larsson C, et al. Hum Genet. 1992 May;89(2):187-93. doi: 10.1007/BF00217121. Hum Genet. 1992. PMID: 1350263

8

Mapping of the gene for multiple endocrine neoplasia type I to chromosome 11q13.

Nordenskjöld M, Larsson C, Oberg K, Nakamura Y. Nordenskjöld M, et al. Among authors: larsson c. Pathol Biol (Paris). 1989 Nov;37(9):951. Pathol Biol (Paris). 1989. PMID: 2575240 No abstract available.

9

Genomic organization and complete cDNA sequence of the human phosphoinositide-specific phospholipase C beta 3 gene (PLCB3).

Lagercrantz J, Carson E, Phelan C, Grimmond S, Rosén A, Daré E, Nordenskjöld M, Hayward NK, Larsson C, Weber G. Lagercrantz J, et al. Among authors: larsson c. Genomics. 1995 Apr 10;26(3):467-72. doi: 10.1016/0888-7543(95)80164-h. Genomics. 1995. PMID: 7607669

10

Family screening in multiple endocrine neoplasia type 1 (MEN 1).

Larsson C, Nordenskjöld M. Larsson C, et al. Ann Med. 1994 Jun;26(3):191-8. doi: 10.3109/07853899409147889. Ann Med. 1994. PMID: 7915525 Free article.

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