Kunkel LM - Search Results

1

Comparative sequence analysis of the mouse and human Lgn1/SMA interval.

Endrizzi M, Huang S, Scharf JM, Kelter AR, Wirth B, Kunkel LM, Miller W, Dietrich WF. Endrizzi M, et al. Among authors: kunkel lm. Genomics. 1999 Sep 1;60(2):137-51. doi: 10.1006/geno.1999.5910. Genomics. 1999. PMID: 10486205

2

The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5.

Scharf JM, Damron D, Frisella A, Bruno S, Beggs AH, Kunkel LM, Dietrich WF. Scharf JM, et al. Among authors: kunkel lm. Genomics. 1996 Dec 15;38(3):405-17. doi: 10.1006/geno.1996.0644. Genomics. 1996. PMID: 8975718

3

Identification of a candidate modifying gene for spinal muscular atrophy by comparative genomics.

Scharf JM, Endrizzi MG, Wetter A, Huang S, Thompson TG, Zerres K, Dietrich WF, Wirth B, Kunkel LM. Scharf JM, et al. Among authors: kunkel lm. Nat Genet. 1998 Sep;20(1):83-6. doi: 10.1038/1753. Nat Genet. 1998. PMID: 9731538

4

Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures.

Growney JD, Scharf JM, Kunkel LM, Dietrich WF. Growney JD, et al. Among authors: kunkel lm. Genomics. 2000 Feb 15;64(1):62-81. doi: 10.1006/geno.1999.6111. Genomics. 2000. PMID: 10708519

5

Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma.

von Deimling F, Scharf JM, Liehr T, Rothe M, Kelter AR, Albers P, Dietrich WF, Kunkel LM, Wernert N, Wirth B. von Deimling F, et al. Among authors: kunkel lm. Hum Genet. 1999 Jul-Aug;105(1-2):17-27. doi: 10.1007/s004399900067. Hum Genet. 1999. PMID: 10480350

6

Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene.

Selig S, Bruno S, Scharf JM, Wang CH, Vitale E, Gilliam TC, Kunkel LM. Selig S, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1995 Apr 25;92(9):3702-6. doi: 10.1073/pnas.92.9.3702. Proc Natl Acad Sci U S A. 1995. PMID: 7731968 Free PMC article.

7

Cloning of human microtubule-associated protein 1B and the identification of a related gene on chromosome 15.

Lien LL, Feener CA, Fischbach N, Kunkel LM. Lien LL, et al. Among authors: kunkel lm. Genomics. 1994 Jul 15;22(2):273-80. doi: 10.1006/geno.1994.1384. Genomics. 1994. PMID: 7806212

8

Identification of FLRT1, FLRT2, and FLRT3: a novel family of transmembrane leucine-rich repeat proteins.

Lacy SE, Bönnemann CG, Buzney EA, Kunkel LM. Lacy SE, et al. Among authors: kunkel lm. Genomics. 1999 Dec 15;62(3):417-26. doi: 10.1006/geno.1999.6033. Genomics. 1999. PMID: 10644439

9

A (CA)n repeat polymorphism for the human skeletal muscle alpha-actinin gene ACTN2 and its localization on the linkage map of chromosome 1.

Beggs AH, Phillips HA, Kozman H, Mulley JC, Wilton SD, Kunkel LM, Laing NG. Beggs AH, et al. Among authors: kunkel lm. Genomics. 1992 Aug;13(4):1314-5. doi: 10.1016/0888-7543(92)90054-v. Genomics. 1992. PMID: 1505962

10

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

Monaco AP, Bertelson CJ, Liechti-Gallati S, Moser H, Kunkel LM. Monaco AP, et al. Among authors: kunkel lm. Genomics. 1988 Jan;2(1):90-5. doi: 10.1016/0888-7543(88)90113-9. Genomics. 1988. PMID: 3384440

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