Leafhopper Transmission of Corn Stunt

Por Kunkel, L. O.
Publicado em 1946

Improved diagnosis of Duchenne/Becker muscular dystrophy.

Por Beggs, A H, Kunkel, L M
Publicado em 1990

An RFLP detecting single copy X-chromosome fragment, dic56, from Xp22-Xpter [HGM8 assignment no. DXS 143].

Por Middlesworth, W, Bertelson, C, Kunkel, L M
Publicado em 1985

Accurate and superaccurate gene mapping.

Por Lange, K, Kunkel, L, Aldridge, J, Latt, S A
Publicado em 1985

Mutational analysis of the PEX gene in patients with X-linked hypophosphatemic rickets.

Por Holm, I A, Huang, X, Kunkel, L M
Publicado em 1997

Regional localization on the human X of DNA segments cloned from flow sorted chromosomes.

Por Kunkel, L M, Tantravahi, U, Eisenhard, M, Latt, S A
Publicado em 1982

Loss of FilaminC (FLNc) Results in Severe Defects in Myogenesis and Myotube Structure

Por Dalkilic, I., Schienda, J., Thompson, T. G., Kunkel, L. M.
Publicado em 2006

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

Por Feener, C A, Boyce, F M, Kunkel, L M
Publicado em 1991

Dystrophin is transcribed in brain from a distant upstream promoter.

Por Boyce, F M, Beggs, A H, Feener, C, Kunkel, L M
Publicado em 1991

Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

Por Kwan, S P, Kunkel, L, Bruns, G, Wedgwood, R J, Latt, S, Rosen, F S
Publicado em 1986

Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.

Por McNally, E M, Yoshida, M, Mizuno, Y, Ozawa, E, Kunkel, L M
Publicado em 1994

Two RFLPs identified by a human chromosome #2 clone at 2p15-2p16 (HGM8 assignment no. D2S5).

Por Shiloh, Y, Kanda, N, Kunkel, L M, Bruns, G, Sakai, K, Latt, S A
Publicado em 1985

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion.

Por Kunkel, L M, Monaco, A P, Middlesworth, W, Ochs, H D, Latt, S A
Publicado em 1985

Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrier.

Por Hurko, O, Hoffman, E P, McKee, L, Johns, D R, Kunkel, L M
Publicado em 1989

Expression and cytokine regulation of glucocorticoid receptors in Kaposi's sarcoma.

Por Guo, W. X., Antakly, T., Cadotte, M., Kachra, Z., Kunkel, L., Masood, R., Gill, P.
Publicado em 1996

Haplotype structure enables prioritization of common markers and candidate genes in autism spectrum disorder

Por Vardarajan, B N, Eran, A, Jung, J-Y, Kunkel, L M, Wall, D P
Publicado em 2013

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

Por Selig, S, Bruno, S, Scharf, J M, Wang, C H, Vitale, E, Gilliam, T C, Kunkel, L M
Publicado em 1995

Identification and isolation of transcribed human X chromosome DNA sequences.

Por Kunkel, L M, Tantravahi, U, Kurnit, D M, Eisenhard, M, Bruns, G P, Latt, S A
Publicado em 1983

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

Por Beggs, A H, Neumann, P E, Arahata, K, Arikawa, E, Nonaka, I, Anderson, M S, Kunkel, L M
Publicado em 1992

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.

Por Bertelson, C J, Bartley, J A, Monaco, A P, Colletti-Feener, C, Fischbeck, K, Kunkel, L M
Publicado em 1986