Mumm S - Search Results

1

Identification of a U7snRNA homologue mapping to the human Xq27.1 region, between the DXS1232 and DXS119 loci.

Mostardini M, Appierto V, Pergolizzi R, Zucchi I, Mumm S, DeBellis G, Milanesi L, Rogozin IB, Biunno I. Mostardini M, et al. Among authors: mumm s. Gene. 1997 Mar 18;187(2):221-4. doi: 10.1016/s0378-1119(96)00754-8. Gene. 1997. PMID: 9099884

2

Sequence and gene content in 35 kb genomic clone mapping in the human Xq27.1 region.

Biunno I, Rogozin IB, Appierto V, Milanesi L, Mostardini M, Mumm S, Pergolizzi R, Zucchi I, De Bellis G. Biunno I, et al. Among authors: mumm s. DNA Seq. 1997;8(1-2):1-15. doi: 10.3109/10425179709020880. DNA Seq. 1997. PMID: 9522116

3

Identification of CXorf1, a novel intronless gene in Xq27.3, expressed in human hippocampus.

Redolfi E, Montagna C, Mumm S, Affer M, Susani L, Reinbold R, Hol F, Vezzoni P, Cimino M, Zucchi I. Redolfi E, et al. Among authors: mumm s. DNA Cell Biol. 1998 Dec;17(12):1009-16. doi: 10.1089/dna.1998.17.1009. DNA Cell Biol. 1998. PMID: 9881668

4

Mapping of the MYCL2 processed gene to Xq22-23 and identification of an additional L MYC-related sequence in Xq27.2.

Redolfi E, Pizzuti A, Di Bacco A, Susani L, Labella T, Affer M, Montagna C, Reinbold R, Mumm S, Vezzoni P, Zucchi I. Redolfi E, et al. Among authors: mumm s. FEBS Lett. 1999 Mar 12;446(2-3):273-7. doi: 10.1016/s0014-5793(99)00243-4. FEBS Lett. 1999. PMID: 10100857 Free article.

5

Transcription map of Xq27: candidates for several X-linked diseases.

Zucchi I, Jones J, Affer M, Montagna C, Redolfi E, Susani L, Vezzoni P, Parvari R, Schlessinger D, Whyte MP, Mumm S. Zucchi I, et al. Among authors: mumm s. Genomics. 1999 Apr 15;57(2):209-18. doi: 10.1006/geno.1999.5768. Genomics. 1999. PMID: 10198160

6

SOX3 gene maps near DXS984 in Xq27.1, within candidate regions for several X-linked disorders.

Mumm S, Zucchi I, Pilia G. Mumm S, et al. Am J Med Genet. 1997 Oct 31;72(3):376-8. Am J Med Genet. 1997. PMID: 9332676 No abstract available.

7

YAC/STS map across 12 Mb of Xq27 at 25-kb resolution, merging Xq26-qter.

Zucchi I, Mumm S, Pilia G, Macmillan S, Reinbold R, Susani L, Weissenbach J, Schlessinger D. Zucchi I, et al. Among authors: mumm s. Genomics. 1996 May 15;34(1):42-54. doi: 10.1006/geno.1996.0239. Genomics. 1996. PMID: 8661022

8

Physical and transcript map of the hereditary prostate cancer region at xq27.

Stephan DA, Howell GR, Teslovich TM, Coffey AJ, Smith L, Bailey-Wilson JE, Malechek L, Gildea D, Smith JR, Gillanders EM, Schleutker J, Hu P, Steingruber HE, Dhami P, Robbins CM, Makalowska I, Carpten JD, Sood R, Mumm S, Reinbold R, Bonner TI, Baffoe-Bonnie A, Bubendorf L, Heiskanen M, Kallioneimi OP, Baxevanis AD, Joseph SS, Zucchi I, Burk RD, Isaacs W, Ross MT, Trent JM. Stephan DA, et al. Among authors: mumm s. Genomics. 2002 Jan;79(1):41-50. doi: 10.1006/geno.2001.6681. Genomics. 2002. PMID: 11827456

9

4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndrome.

Porta G, MacMillan S, Nagaraja R, Mumm S, Zucchi I, Pilia G, Maio S, Featherstone T, Schlessinger D. Porta G, et al. Among authors: mumm s. Genome Res. 1997 Jan;7(1):27-36. doi: 10.1101/gr.7.1.27. Genome Res. 1997. PMID: 9037599 Free article.

10

22-Mb integrated physical and genetic map based on YAC/STS content spanning the interval DXS1125-DXS95 in human Xq12-q21.31.

Mumm S, Jermak C, Waeltz P, Schmatz M, Terrell J, McCauley B, Shoemaker M, Srivastava A, Kere J, Nagaraja R. Mumm S, et al. Gene. 1998 Feb 27;208(2):147-56. doi: 10.1016/s0378-1119(97)00665-3. Gene. 1998. PMID: 9524253

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