The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Mutation analysis and molecular genetics of epidermolysis bullosa
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Citations
Cites
The CpG dinucleotide and human genetic disease
Cooper, D. N., & Youssoufian, H. (1988) · Human Genetics · doi:10.1007/bf00278187 · Cited by 931
Epiligrin, a new cell adhesion ligand for integrin α3β1 in epithelial basement membranes
Carter, W. G., Ryan, M. C., & Gahr, P. J. (1991) · Cell · doi:10.1016/0092-8674(91)90092-d · Cited by 759
A new nomenclature for the laminins
Burgeson, R. E., Chiquet, M., Deutzmann, R., Ekblom, P., Engel, J., Kleinman, H., Martin, G. R., Meneguzzi, G., Paulsson, M., Sanes, J., et al. (1994) · Matrix Biology · doi:10.1016/0945-053x(94)90184-8 · Cited by 743
Ganguly, A., Rock, M. J., & Prockop, D. J. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.21.10325 · Cited by 674
Cloning and Primary Structural Analysis of the Bullous Pemphigoid Autoantigen BP180
Giudice, G. J., Emery, D. J., & Diaz, L. A. (1992) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12616580 · Cited by 568
Mutations in collagen genes: causes of rare and some common diseases in humans
Kuivaniemi, H., Tromp, G., & Prockop, D. J. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.7.2010058 · Cited by 479
Guo, L., Degenstein, L., Dowling, J., Yu, Q.-C., Wollmann, R., Perman, B., & Fuchs, E. (1995) · Cell · doi:10.1016/0092-8674(95)90333-x · Cited by 442
Connective tissue and its heritable disorders : molecular, genetic, and medical aspects
Royce, P. M., & Steinmann, B. U. (1993) · Cited by 440
Type VII collagen forms an extended network of anchoring fibrils.
Keene, D. R., Sakai, L. Y., Lunstrum, G. P., Morris, N. P., & Burgeson, R. E. (1987) · The Journal of cell biology · doi:10.1083/jcb.104.3.611 · Cited by 390
Plectin deficiency results in muscular dystrophy with epidermolysis bullosa
Smith, F. J. D., Eady, R. A. J., Leigh, I. M., McMillan, J. R., Rugg, E. L., Kelsell, D. P., Bryant, S. P., Spurr, N. K., Geddes, J. F., Kirtschig, G., et al. (1996) · Nature Genetics · doi:10.1038/ng0896-450 · Cited by 388
Self-citation
Cited by
Hynes (2002) · doi:10.1016/s0092-8674(02)00971-6 · Cited by 8,606
LAMININ FUNCTIONS IN TISSUE MORPHOGENESIS
Miner, J. H., & Yurchenco, P. D. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.094555 · Cited by 757
Collagens and collagen-related diseases
Myllyharju, J., & Kivirikko, K. I. (2001) · Annals of Medicine · doi:10.3109/07853890109002055 · Cited by 756
Functional Diversity of Laminins
Domogatskaya, A., Rodin, S., & Tryggvason, K. (2012) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-101011-155750 · Cited by 393
Bone Marrow Transplantation for Recessive Dystrophic Epidermolysis Bullosa
Wagner, J. E., Ishida-Yamamoto, A., McGrath, J. A., Hordinsky, M., Keene, D. R., Woodley, D. T., Chen, M., Riddle, M. J., Osborn, M. J., Lund, T., et al. (2010) · New England Journal of Medicine · doi:10.1056/nejmoa0910501 · Cited by 374
Metadata
- Authors
- Pulkkinen, L., & Uitto, J.
- Venue
- Matrix Biology
- Publisher
- Elsevier BV
- Published
- 1999-02
- Volume
- 18
- Issue
- 1
- Pages
- 29-42
- ISSN
- 0945-053X (ISSN-L)
- OpenAlex
- W2000327471
- Cited by
- 291
- References
- 51
- FWCI
- 7.12
- Type
- journal article
- Language
- en
- Open access
- closed
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- CoChat. (2026). Citation check: Mutation analysis and molecular genetics of epidermolysis bullosa. https://app.cochat.ai/papers/10.1016/s0945-053x(98)00005-5
- The paper
- Pulkkinen, L., & Uitto, J. (1999). Mutation analysis and molecular genetics of epidermolysis bullosa. Matrix Biology. https://doi.org/10.1016/s0945-053x(98)00005-5
Data sources
Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.