P30-HD 03110/HD/NICHD NIH HHS/United States[Grant Number] - Search Results

Year	Number of Results
1988	5
1989	2
1990	6
1991	6
1993	1
1994	4
1995	1
1997	2
1998	3
1999	1
2006	1
2007	1
2024	0

1

Suzuki K. Suzuki K. Essays Biochem. 1995;29:25-37. Essays Biochem. 1995. PMID: 9189712 Review. No abstract available.

2

Mouse models of autism spectrum disorders: the challenge for behavioral genetics.

Moy SS, Nadler JJ, Magnuson TR, Crawley JN. Moy SS, et al. Am J Med Genet C Semin Med Genet. 2006 Feb 15;142C(1):40-51. doi: 10.1002/ajmg.c.30081. Am J Med Genet C Semin Med Genet. 2006. PMID: 16419099 Review.

3

Saul R. Korey Lecture. Molecular genetics of Tay-Sachs and related disorders: a personal account.

Suzuki K. Suzuki K. J Neuropathol Exp Neurol. 1994 Jul;53(4):344-50. doi: 10.1097/00005072-199407000-00004. J Neuropathol Exp Neurol. 1994. PMID: 8021707 Review.

4

Biochemical and molecular aspects of late-onset GM2-gangliosidosis: B1 variant as a prototype.

Suzuki K, Vanier MT. Suzuki K, et al. Dev Neurosci. 1991;13(4-5):288-94. doi: 10.1159/000112175. Dev Neurosci. 1991. PMID: 1840099 Review.

5

Mutation in GM2-gangliosidosis B1 variant.

Ohno K, Suzuki K. Ohno K, et al. J Neurochem. 1988 Jan;50(1):316-8. doi: 10.1111/j.1471-4159.1988.tb13266.x. J Neurochem. 1988. PMID: 2961848

6

Bone marrow transplantation prolongs life span and ameliorates neurologic manifestations in Sandhoff disease mice.

Norflus F, Tifft CJ, McDonald MP, Goldstein G, Crawley JN, Hoffmann A, Sandhoff K, Suzuki K, Proia RL. Norflus F, et al. J Clin Invest. 1998 May 1;101(9):1881-8. doi: 10.1172/JCI2127. J Clin Invest. 1998. PMID: 9576752 Free PMC article.

7

Molecular genetics of Tay-Sachs disease in Japan.

Tanaka A, Sakazaki H, Murakami H, Isshiki G, Suzuki K. Tanaka A, et al. J Inherit Metab Dis. 1994;17(5):593-600. doi: 10.1007/BF00711597. J Inherit Metab Dis. 1994. PMID: 7837766 No abstract available.

8

A splicing defect due to an exon-intron junctional mutation results in abnormal beta-hexosaminidase alpha chain mRNAs in Ashkenazi Jewish patients with Tay-Sachs disease.

Ohno K, Suzuki K. Ohno K, et al. Biochem Biophys Res Commun. 1988 May 31;153(1):463-9. doi: 10.1016/s0006-291x(88)81247-6. Biochem Biophys Res Commun. 1988. PMID: 2837213

9

Social approach behaviors in oxytocin knockout mice: comparison of two independent lines tested in different laboratory environments.

Crawley JN, Chen T, Puri A, Washburn R, Sullivan TL, Hill JM, Young NB, Nadler JJ, Moy SS, Young LJ, Caldwell HK, Young WS. Crawley JN, et al. Neuropeptides. 2007 Jun;41(3):145-63. doi: 10.1016/j.npep.2007.02.002. Epub 2007 Apr 8. Neuropeptides. 2007. PMID: 17420046

10

Genetic cause of a juvenile form of Sandhoff disease. Abnormal splicing of beta-hexosaminidase beta chain gene transcript due to a point mutation within intron 12.

Nakano T, Suzuki K. Nakano T, et al. J Biol Chem. 1989 Mar 25;264(9):5155-8. J Biol Chem. 1989. PMID: 2522450 Free article.

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