Berry GT - Search Results

1

The structural organization of the human Na+/myo-inositol cotransporter (SLC5A3) gene and characterization of the promoter.

Mallee JJ, Atta MG, Lorica V, Rim JS, Kwon HM, Lucente AD, Wang Y, Berry GT. Mallee JJ, et al. Among authors: berry gt. Genomics. 1997 Dec 15;46(3):459-65. doi: 10.1006/geno.1997.5055. Genomics. 1997. PMID: 9441750 Free article.

2

The human osmoregulatory Na+/myo-inositol cotransporter gene (SLC5A3): molecular cloning and localization to chromosome 21.

Berry GT, Mallee JJ, Kwon HM, Rim JS, Mulla WR, Muenke M, Spinner NB. Berry GT, et al. Genomics. 1995 Jan 20;25(2):507-13. doi: 10.1016/0888-7543(95)80052-n. Genomics. 1995. PMID: 7789985 Free article.

3

The 21q22.1 STS marker, VN02 (EST00541 cDNA), is part of the 3' sequence of the human Na+/myo-inositol cotransporter (SLC5A3) gene.

Berry GT, Mallee JJ, Blouin JL, Antonarakis SE. Berry GT, et al. Cytogenet Cell Genet. 1996;73(1-2):77-8. doi: 10.1159/000134311. Cytogenet Cell Genet. 1996. PMID: 8646889

4

Multiple comparison of primary structure of the osmoregulatory Na+/myo-inositol cotransporter from bovine, human, and canine species.

Mallee JJ, Parella T, Kwon HM, Berry GT. Mallee JJ, et al. Among authors: berry gt. Mamm Genome. 1996 Mar;7(3):252. doi: 10.1007/s003359900076. Mamm Genome. 1996. PMID: 8833264 No abstract available.

5

Murine chromosome 16 telomeric region, homologous with human chromosome 21q22, contains the osmoregulatory Na(+)/myo-inositol cotransporter (SLC5A3) gene.

McVeigh KE, Mallee JJ, Lucente A, Barnoski BL, Wu S, Berry GT. McVeigh KE, et al. Among authors: berry gt. Cytogenet Cell Genet. 2000;88(1-2):153-8. doi: 10.1159/000015509. Cytogenet Cell Genet. 2000. PMID: 10773690

6

Transcription of the sodium/myo-inositol cotransporter gene is regulated by multiple tonicity-responsive enhancers spread over 50 kilobase pairs in the 5'-flanking region.

Rim JS, Atta MG, Dahl SC, Berry GT, Handler JS, Kwon HM. Rim JS, et al. Among authors: berry gt. J Biol Chem. 1998 Aug 7;273(32):20615-21. doi: 10.1074/jbc.273.32.20615. J Biol Chem. 1998. PMID: 9685419 Free PMC article.

7

Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations.

Fukao T, Mitchell GA, Song XQ, Nakamura H, Kassovska-Bratinova S, Orii KE, Wraith JE, Besley G, Wanders RJ, Niezen-Koning KE, Berry GT, Palmieri M, Kondo N. Fukao T, et al. Among authors: berry gt. Genomics. 2000 Sep 1;68(2):144-51. doi: 10.1006/geno.2000.6282. Genomics. 2000. PMID: 10964512

8

Mosaicism for an intragenic deletion in a boy with mild ornithine transcarbamylase deficiency.

Maddalena A, Sosnoski DM, Berry GT, Nussbaum RL. Maddalena A, et al. Among authors: berry gt. N Engl J Med. 1988 Oct 13;319(15):999-1003. doi: 10.1056/NEJM198810133191507. N Engl J Med. 1988. PMID: 2843770 No abstract available.

9

Hyperammonia Possibly due to Corticosteroids.

Berry GT, Kaplan PB, Lichtenstein GR. Berry GT, et al. Arch Neurol. 2000 Jul;57(7):1085-10856. Arch Neurol. 2000. PMID: 10891999 No abstract available.

10

Diabetes-like renal glomerular disease in Fanconi-Bickel syndrome.

Berry GT, Baker L, Kaplan FS, Witzleben CL. Berry GT, et al. Pediatr Nephrol. 1995 Jun;9(3):287-91. doi: 10.1007/BF02254185. Pediatr Nephrol. 1995. PMID: 7632512

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