Kunkel LM - Search Results

1

Rapid detection of CA polymorphisms in cloned DNA: application to the 5' region of the dystrophin gene.

Feener CA, Boyce FM, Kunkel LM. Feener CA, et al. Among authors: kunkel lm. Am J Hum Genet. 1991 Mar;48(3):621-7. Am J Hum Genet. 1991. PMID: 1998344 Free PMC article.

2

Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13.

Lien LL, Boyce FM, Kleyn P, Brzustowicz LM, Menninger J, Ward DC, Gilliam TC, Kunkel LM. Lien LL, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7873-6. doi: 10.1073/pnas.88.17.7873. Proc Natl Acad Sci U S A. 1991. PMID: 1881920 Free PMC article.

3

Dystrophin is transcribed in brain from a distant upstream promoter.

Boyce FM, Beggs AH, Feener C, Kunkel LM. Boyce FM, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1991 Feb 15;88(4):1276-80. doi: 10.1073/pnas.88.4.1276. Proc Natl Acad Sci U S A. 1991. PMID: 1996328 Free PMC article.

4

Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.

Beggs AH, Koenig M, Boyce FM, Kunkel LM. Beggs AH, et al. Among authors: kunkel lm. Hum Genet. 1990 Nov;86(1):45-8. doi: 10.1007/BF00205170. Hum Genet. 1990. PMID: 2253937

5

Molecular studies of progressive muscular dystrophy (Duchenne).

Kunkel LM, Monaco AP, Hoffman E, Koenig M, Feener C, Bertelson C. Kunkel LM, et al. Enzyme. 1987;38(1-4):72-5. doi: 10.1159/000469192. Enzyme. 1987. PMID: 3440453

6

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

7

Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24.

Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM. Ahn AH, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 1994 May 10;91(10):4446-50. doi: 10.1073/pnas.91.10.4446. Proc Natl Acad Sci U S A. 1994. PMID: 8183929 Free PMC article.

8

A mutation in the alpha 3 chain of type IX collagen causes autosomal dominant multiple epiphyseal dysplasia with mild myopathy.

Bönnemann CG, Cox GF, Shapiro F, Wu JJ, Feener CA, Thompson TG, Anthony DC, Eyre DR, Darras BT, Kunkel LM. Bönnemann CG, et al. Among authors: kunkel lm. Proc Natl Acad Sci U S A. 2000 Feb 1;97(3):1212-7. doi: 10.1073/pnas.97.3.1212. Proc Natl Acad Sci U S A. 2000. PMID: 10655510 Free PMC article.

9

The genomic organization of human dystrobrevin.

Sadoulet-Puccio HM, Feener CA, Schaid DJ, Thibodeau SN, Michels VV, Kunkel LM. Sadoulet-Puccio HM, et al. Among authors: kunkel lm. Neurogenetics. 1997 May;1(1):37-42. doi: 10.1007/s100480050006. Neurogenetics. 1997. PMID: 10735273

10

Primary gamma-sarcoglycanopathy (LGMD 2C): broadening of the mutational spectrum guided by the immunohistochemical profile.

Bönnemann CG, Wong J, Jones KJ, Lidov HG, Feener CA, Shapiro F, Darras BT, Kunkel LM, North KN. Bönnemann CG, et al. Among authors: kunkel lm. Neuromuscul Disord. 2002 Mar;12(3):273-80. doi: 10.1016/s0960-8966(01)00276-0. Neuromuscul Disord. 2002. PMID: 11801399

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