Lia M - Search Results

1

Postgastrulation Smad2-deficient embryos show defects in embryo turning and anterior morphogenesis.

Heyer J, Escalante-Alcalde D, Lia M, Boettinger E, Edelmann W, Stewart CL, Kucherlapati R. Heyer J, et al. Among authors: lia m. Proc Natl Acad Sci U S A. 1999 Oct 26;96(22):12595-600. doi: 10.1073/pnas.96.22.12595. Proc Natl Acad Sci U S A. 1999. PMID: 10535967 Free PMC article.

2

Haploinsufficiency of Flap endonuclease (Fen1) leads to rapid tumor progression.

Kucherlapati M, Yang K, Kuraguchi M, Zhao J, Lia M, Heyer J, Kane MF, Fan K, Russell R, Brown AM, Kneitz B, Edelmann W, Kolodner RD, Lipkin M, Kucherlapati R. Kucherlapati M, et al. Among authors: lia m. Proc Natl Acad Sci U S A. 2002 Jul 23;99(15):9924-9. doi: 10.1073/pnas.152321699. Epub 2002 Jul 15. Proc Natl Acad Sci U S A. 2002. PMID: 12119409 Free PMC article.

3

The DNA mismatch repair genes Msh3 and Msh6 cooperate in intestinal tumor suppression.

Edelmann W, Umar A, Yang K, Heyer J, Kucherlapati M, Lia M, Kneitz B, Avdievich E, Fan K, Wong E, Crouse G, Kunkel T, Lipkin M, Kolodner RD, Kucherlapati R. Edelmann W, et al. Among authors: lia m. Cancer Res. 2000 Feb 15;60(4):803-7. Cancer Res. 2000. PMID: 10706084

4

Mammalian MutS homologue 5 is required for chromosome pairing in meiosis.

Edelmann W, Cohen PE, Kneitz B, Winand N, Lia M, Heyer J, Kolodner R, Pollard JW, Kucherlapati R. Edelmann W, et al. Among authors: lia m. Nat Genet. 1999 Jan;21(1):123-7. doi: 10.1038/5075. Nat Genet. 1999. PMID: 9916805

5

Tumorigenesis in Mlh1 and Mlh1/Apc1638N mutant mice.

Edelmann W, Yang K, Kuraguchi M, Heyer J, Lia M, Kneitz B, Fan K, Brown AM, Lipkin M, Kucherlapati R. Edelmann W, et al. Among authors: lia m. Cancer Res. 1999 Mar 15;59(6):1301-7. Cancer Res. 1999. PMID: 10096563

6

TBX1 is responsible for cardiovascular defects in velo-cardio-facial/DiGeorge syndrome.

Merscher S, Funke B, Epstein JA, Heyer J, Puech A, Lu MM, Xavier RJ, Demay MB, Russell RG, Factor S, Tokooya K, Jore BS, Lopez M, Pandita RK, Lia M, Carrion D, Xu H, Schorle H, Kobler JB, Scambler P, Wynshaw-Boris A, Skoultchi AI, Morrow BE, Kucherlapati R. Merscher S, et al. Among authors: lia m. Cell. 2001 Feb 23;104(4):619-29. doi: 10.1016/s0092-8674(01)00247-1. Cell. 2001. PMID: 11239417 Free article.

7

Chromosomal deletions around the albino locus in the mouse cause loss of hormone-inducible expression of the unlinked structural gene encoding cytosolic aspartate aminotransferase.

Lia M, Barouki R, Waelsch SG. Lia M, et al. Proc Natl Acad Sci U S A. 1995 Jan 31;92(3):788-90. doi: 10.1073/pnas.92.3.788. Proc Natl Acad Sci U S A. 1995. PMID: 7846052 Free PMC article.

8

Regulatory genes linked to the albino locus in the mouse confer competence for inducible expression on the structural gene encoding serine dehydratase.

Lia M, Bali D, Gluecksohn-Waelsch S. Lia M, et al. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2453-5. doi: 10.1073/pnas.89.6.2453. Proc Natl Acad Sci U S A. 1992. PMID: 1312724 Free PMC article.

9

Selective loss of a DNase I hypersensitive site upstream of the tyrosine aminotransferase gene in mice homozygous for lethal albino deletions.

Zaret KS, Milos P, Lia M, Bali D, Gluecksohn-Waelsch S. Zaret KS, et al. Among authors: lia m. Proc Natl Acad Sci U S A. 1992 Jul 15;89(14):6540-4. doi: 10.1073/pnas.89.14.6540. Proc Natl Acad Sci U S A. 1992. PMID: 1378630 Free PMC article.

10

The interplay of body mass index, gestational weight gain, and birthweight over 3800 g in vaginal breech birth: A retrospective study.

Tautenhahn H, Dathan-Stumpf A, Kabbani N, Stepan H, Lia M. Tautenhahn H, et al. Among authors: lia m. Acta Obstet Gynecol Scand. 2024 Nov 9. doi: 10.1111/aogs.15002. Online ahead of print. Acta Obstet Gynecol Scand. 2024. PMID: 39520214

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