J. M. Yang

发表

A novel glutamic acid to aspartic acid mutation near the end of the 2B rod domain in the keratin 1 chain in epidermolytic hyperkeratosis.

P. Steinert, K. Wu, J. M. Yang, 1999, The Journal of investigative dermatology.

Tob is a potential marker gene for the basal layer of the epidermis and is stably expressed in human primary keratinocytes

D.Y. Lee, G. Park, E. Seo, 2006, The British journal of dermatology.

Arginine in the beginning of the 1A rod domain of the keratin 10 gene is the hot spot for the mutation in epidermolytic hyperkeratosis.

K. Park, S. Y. Jung, K. Suhr, 1999, Journal of dermatological science.

A novel H1 mutation in the keratin 1 chain in epidermolytic hyperkeratosis.

P. Steinert, K. Park, K. Moon, 1996, The Journal of investigative dermatology.

Preferential sites in keratin 10 that are mutated in epidermolytic hyperkeratosis.

S. Bale, P. Steinert, Jun-Mo Yang, 1994, American journal of human genetics.

Mutations in the H1 and 1A domains in the keratin 1 gene in epidermolytic hyperkeratosis.

S. Bale, P. Steinert, Jun-Mo Yang, 1994, The Journal of investigative dermatology.

Concurrence between the molecular overlap regions in keratin intermediate filaments and the locations of keratin mutations in genodermatoses.

S. Bale, P. Steinert, J. Compton, 1993, Biochemical and biophysical research communications.

A glutamate to lysine mutation at the end of 2B rod domain of keratin 2e gene in ichthyosis bullosa of Siemens.

K. Yoneda, P. Steinert, K. Park, 1998, Acta dermato-venereologica.

A novel threonine --> proline mutation at the end of 2B rod domain in the keratin 2e chain in ichthyosis bullosa of Siemens.

P. Steinert, S. Lee, W. Kim, 1997, The Journal of investigative dermatology.

A mutation in the V1 end domain of keratin 1 in non-epidermolytic palmar-plantar keratoderma.

S. Bale, V. Kimonis, Jun-Mo Yang, 1994, The Journal of investigative dermatology.

Trichilemmal carcinoma with a cutaneous horn

S. Y. Jung, J. Yang, E. Lee, 2000, The British journal of dermatology.

A CRX null mutation is associated with both Leber congenital amaurosis and a normal ocular phenotype.

Y. Li, I. Maumenee, O. Sundin, 2000, Investigative ophthalmology & visual science.

Comparison of diagnostic methods for onychomycosis, and proposal of a diagnostic algorithm

D.Y. Lee, K. Park, M. Jung, 2015, Clinical and experimental dermatology.

Congenital triangular alopecia in phakomatosis pigmentovascularis: report of 3 cases.

S. H. Park, K. Park, H. Kim, 2000, Acta dermato-venereologica.

Mutations in the 1A rod domain segment of the keratin 9 gene in epidermolytic palmoplantar keratoderma.

P. Steinert, K. Park, S. Lee, 1998, Acta dermato-venereologica.

The Pax-6 homeobox gene is expressed throughout the corneal and conjunctival epithelia.

O. Sundin, B. Koroma, J. M. Yang, 1997, Investigative ophthalmology & visual science.

Sequence and location of SIX3, a homeobox gene expressed in the human eye.

O. Sundin, J. M. Yang, G. Leppert, 1999, Ophthalmic genetics.

The optx2 homeobox gene is expressed in early precursors of the eye and activates retina-specific genes.

J. Toy, O. Sundin, Jun-ming Yang, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Pax-6 is first expressed in a region of ectoderm anterior to the early neural plate: implications for stepwise determination of the lens.

D. Pasko, O. Sundin, Jun-ming Yang, 1994, Developmental biology.

Coiled-coil trigger motifs in the 1B and 2B rod domain segments are required for the stability of keratin intermediate filaments.

D. Parry, P. Steinert, S. Jang, 2000, Molecular biology of the cell.

Structure and organization of the human transglutaminase 3 gene: evolutionary relationship to the transglutaminase family.

P. Steinert, Jun-Mo Yang, J. Lee, 1994, The Journal of investigative dermatology.

Novel mutations of the transglutaminase 1 gene in lamellar ichthyosis.

C. H. Lee, G. Melino, K. Yoneda, 2001, The Journal of investigative dermatology.

An alanine to proline mutation in the 1A rod domain of the keratin 10 chain in epidermolytic hyperkeratosis.

K. Yoneda, P. Steinert, Jun-Mo Yang, 1997, The Journal of investigative dermatology.