Jenkins ZA - Search Results

1

Iron homeostasis during transfusional iron overload in beta-thalassemia and sickle cell disease: changes in iron regulatory protein, hepcidin, and ferritin expression.

Jenkins ZA, Hagar W, Bowlus CL, Johansson HE, Harmatz P, Vichinsky EP, Theil EC. Jenkins ZA, et al. Pediatr Hematol Oncol. 2007 Jun;24(4):237-43. doi: 10.1080/08880010701360700. Pediatr Hematol Oncol. 2007. PMID: 17613866

2

Identification and characterization of eukaryotic initiation factor 5A-2.

Clement PM, Henderson CA, Jenkins ZA, Smit-McBride Z, Wolff EC, Hershey JW, Park MH, Johansson HE. Clement PM, et al. Among authors: jenkins za. Eur J Biochem. 2003 Nov;270(21):4254-63. doi: 10.1046/j.1432-1033.2003.03806.x. Eur J Biochem. 2003. PMID: 14622290 Free article.

3

Human eIF5A2 on chromosome 3q25-q27 is a phylogenetically conserved vertebrate variant of eukaryotic translation initiation factor 5A with tissue-specific expression.

Jenkins ZA, Hååg PG, Johansson HE. Jenkins ZA, et al. Genomics. 2001 Jan 1;71(1):101-9. doi: 10.1006/geno.2000.6418. Genomics. 2001. PMID: 11161802

4

Genetic mapping of the laminin gamma 2 gene on sheep chromosome 12.

Jenkins ZA, Montgomery GW. Jenkins ZA, et al. Mamm Genome. 1996 Nov;7(11):868-9. doi: 10.1007/s003359900257. Mamm Genome. 1996. PMID: 8875904 No abstract available.

5

Comparative linkage mapping of genes on sheep chromosome 3 provides evidence of chromosomal rearrangements in the evolution of the Bovidae.

Jenkins ZA, Henry HM, Galloway SM, Dodds KG, Montgomery GW. Jenkins ZA, et al. Cytogenet Cell Genet. 1997;78(3-4):272-4. doi: 10.1159/000134670. Cytogenet Cell Genet. 1997. PMID: 9465901

6

Genetic mapping of the ovine homologue of the mouse Hacl1 gene to sheep chromosome 1.

Jenkins ZA, Montgomery GW. Jenkins ZA, et al. Anim Genet. 1999 Feb;30(1):74. doi: 10.1046/j.1365-2052.1999.00323-12.x. Anim Genet. 1999. PMID: 10050301 No abstract available.

7

Linkage mapping of genes encoding bone morphogenetic proteins 1, 4 and 5 in sheep.

Jenkins ZA, Montgomery GW. Jenkins ZA, et al. Anim Genet. 1999 Apr;30(2):163-4. doi: 10.1046/j.1365-2052.1999.00382-4.x. Anim Genet. 1999. PMID: 10376312 No abstract available.

8

Follistatin (FST), growth hormone receptor (GHR) and prolactin receptor (PRLR) genes map to the same region of sheep chromosome 16.

Jenkins ZA, Henry HM, Sise JA, Montgomery GW. Jenkins ZA, et al. Anim Genet. 2000 Aug;31(4):280. doi: 10.1046/j.1365-2052.2000.00482.x. Anim Genet. 2000. PMID: 11086539 No abstract available.

9

Germline mutations in WTX cause a sclerosing skeletal dysplasia but do not predispose to tumorigenesis.

Jenkins ZA, van Kogelenberg M, Morgan T, Jeffs A, Fukuzawa R, Pearl E, Thaller C, Hing AV, Porteous ME, Garcia-Miñaur S, Bohring A, Lacombe D, Stewart F, Fiskerstrand T, Bindoff L, Berland S, Adès LC, Tchan M, David A, Wilson LC, Hennekam RC, Donnai D, Mansour S, Cormier-Daire V, Robertson SP. Jenkins ZA, et al. Nat Genet. 2009 Jan;41(1):95-100. doi: 10.1038/ng.270. Epub 2008 Dec 14. Nat Genet. 2009. PMID: 19079258

10

Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3.

Cameron-Christie SR, Wells CF, Simon M, Wessels M, Tang CZN, Wei W, Takei R, Aarts-Tesselaar C, Sandaradura S, Sillence DO, Cordier MP, Veenstra-Knol HE, Cassina M, Ludwig K, Trevisson E, Bahlo M, Markie DM, Jenkins ZA, Robertson SP. Cameron-Christie SR, et al. Among authors: jenkins za. Am J Hum Genet. 2018 Jun 7;102(6):1115-1125. doi: 10.1016/j.ajhg.2018.04.008. Epub 2018 May 24. Am J Hum Genet. 2018. PMID: 29805041 Free PMC article.

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