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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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J Arnemann

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Prenatal Diagnosis|October 20, 2000

Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.

Genomics|January 25, 2000

Clustered cadherin genes: a sequence-ready contig for the desmosomal cadherin locus on human chromosome 18D M Hunt, V K Sahota, K Taylor, et al.

Scandinavian Journal of Immunology|December 19, 2000

Genomic organization and regulation of the human interleukin-18 geneU Kalina, K Ballas, N Koyama, et al.

Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 1, 1995

Comparative mapping of YRRM- and TSPY-related cosmids in man and hominoid apesW Schempp, A Binkele, J Arnemann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutationsS Saitoh, K Buiting, P K Rogan, et al.

The Journal of Biological Chemistry|June 5, 1991

Desmosomal glycoproteins II and III. Cadherin-like junctional molecules generated by alternative splicingA E Parker, G N Wheeler, J Arnemann, et al.

The Biochemical Journal|February 14, 1998

Characterization of the regulatory regions in the human desmoglein genes encoding the pemphigus foliaceous and pemphigus vulgaris antigensM J Adams, M B Reichel, I A King, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 1, 1991

Desmosomal glycoprotein DGI, a component of intercellular desmosome junctions, is related to the cadherin family of cell adhesion moleculesG N Wheeler, A E Parker, C L Thomas, et al.

Human Molecular Genetics|May 20, 1999

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.

Pageof 4

Search research articles

Showing results (31-40 of 40) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 40 results.

Prenatal Diagnosis|October 20, 2000

Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.

Genomics|January 25, 2000

Clustered cadherin genes: a sequence-ready contig for the desmosomal cadherin locus on human chromosome 18D M Hunt, V K Sahota, K Taylor, et al.

Scandinavian Journal of Immunology|December 19, 2000

Genomic organization and regulation of the human interleukin-18 geneU Kalina, K Ballas, N Koyama, et al.

Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|June 1, 1995

Comparative mapping of YRRM- and TSPY-related cosmids in man and hominoid apesW Schempp, A Binkele, J Arnemann, et al.

Proceedings of the National Academy of Sciences of the United States of America|July 23, 1996

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutationsS Saitoh, K Buiting, P K Rogan, et al.

The Journal of Biological Chemistry|June 5, 1991

Desmosomal glycoproteins II and III. Cadherin-like junctional molecules generated by alternative splicingA E Parker, G N Wheeler, J Arnemann, et al.

The Biochemical Journal|February 14, 1998

Characterization of the regulatory regions in the human desmoglein genes encoding the pemphigus foliaceous and pemphigus vulgaris antigensM J Adams, M B Reichel, I A King, et al.

Proceedings of the National Academy of Sciences of the United States of America|June 1, 1991

Desmosomal glycoprotein DGI, a component of intercellular desmosome junctions, is related to the cadherin family of cell adhesion moleculesG N Wheeler, A E Parker, C L Thomas, et al.

Human Molecular Genetics|May 20, 1999

N-terminal deletion in a desmosomal cadherin causes the autosomal dominant skin disease striate palmoplantar keratodermaL Rickman, D Simrak, H P Stevens, et al.

European Journal of Human Genetics : EJHG|April 21, 2001

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratodermaD M Hunt, L Rickman, N V Whittock, et al.

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