Du YZ - Search Results

1

Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.

Roessler E, Du YZ, Mullor JL, Casas E, Allen WP, Gillessen-Kaesbach G, Roeder ER, Ming JE, Ruiz i Altaba A, Muenke M. Roessler E, et al. Among authors: du yz. Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13424-9. doi: 10.1073/pnas.2235734100. Epub 2003 Oct 27. Proc Natl Acad Sci U S A. 2003. PMID: 14581620 Free PMC article.

2

The genomic structure, chromosome location, and analysis of the human DKK1 head inducer gene as a candidate for holoprosencephaly.

Roessler E, Du Y, Glinka A, Dutra A, Niehrs C, Muenke M. Roessler E, et al. Cytogenet Cell Genet. 2000;89(3-4):220-4. doi: 10.1159/000015618. Cytogenet Cell Genet. 2000. PMID: 10965128

3

Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1).

Roessler E, Mittaz L, Du Y, Scott HS, Chang J, Rossier C, Guipponi M, Matsuda SP, Muenke M, Antonarakis SE. Roessler E, et al. Hum Genet. 1999 Nov;105(5):489-95. doi: 10.1007/s004390051135. Hum Genet. 1999. PMID: 10598817

4

SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.

Nanni L, Ming JE, Du Y, Hall RK, Aldred M, Bankier A, Muenke M. Nanni L, et al. Am J Med Genet. 2001 Jul 22;102(1):1-10. doi: 10.1002/1096-8628(20010722)102:1<1::aid-ajmg1336>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471164 Review.

5

Localization in rats of genetic loci regulating susceptibility to experimental erosive arthritis and related autoimmune diseases.

Wilder RL, Griffiths MM, Remmers EF, Cannon GW, Caspi RR, Kawahito Y, Gulko PS, Longman RE, Dracheva SV, Du Y, Sun SH, Wang J, Shepard JS, Joe B, Ge L, Chen S, Chang L, Hoffman J, Silver PB, Reese VR. Wilder RL, et al. Transplant Proc. 1999 May;31(3):1585-8. doi: 10.1016/s0041-1345(99)00047-0. Transplant Proc. 1999. PMID: 10331011 No abstract available.

6

Genomic cloning and genetic mapping of the rat Nramp1 (Bcg) gene on chromosome 9.

Ge L, Remmers EF, Du Y, Wilder RL. Ge L, et al. Mamm Genome. 1996 Nov;7(11):856-7. doi: 10.1007/s003359900251. Mamm Genome. 1996. PMID: 8875897 No abstract available.

7

A genetic map of microsatellite markers on rat chromosome 7.

Du Y, Remmers EF, Zha H, Goldmuntz EA, Szpirer J, Szpirer C, Wilder RL. Du Y, et al. Mamm Genome. 1995 Apr;6(4):295-8. doi: 10.1007/BF00352420. Mamm Genome. 1995. PMID: 7613038

8

Four polymorphic markers on rat chromosome 12 form a single linkage group.

Mathern P, Goldmuntz EA, Zha H, Du Y, Crofford LJ, Wilder RL, Remmers EF. Mathern P, et al. Biochem Genet. 1993 Oct;31(9-10):441-8. doi: 10.1007/BF02396228. Biochem Genet. 1993. PMID: 8122998

9

Localization of the gene responsible for the op (osteopetrotic) defect in rats on chromosome 10.

Remmers EF, Du Y, Ding YP, Kotake S, Ge L, Zha H, Goldmuntz EA, Hansen C, Wilder RL. Remmers EF, et al. J Bone Miner Res. 1996 Dec;11(12):1856-61. doi: 10.1002/jbmr.5650111205. J Bone Miner Res. 1996. PMID: 8970886

10

Linkage maps of rat chromosomes 15, 16, 17, 19, and X.

Du Y, Remmers EF, Goldmuntz EA, Zha H, Mathern P, Ding YP, Kotake S, Szpirer J, Szpirer C, Wilder RL. Du Y, et al. Genomics. 1996 Feb 15;32(1):113-6. doi: 10.1006/geno.1996.0083. Genomics. 1996. PMID: 8786096

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