Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4 von Ophoff, R A, Terwindt, G M, Vergouwe, M N, van Eijk, R, Oefner, P J, Hoffman, S M, Lamerdin, J E, Mohrenweiser, H W, Bulman, D E, Ferrari, M, Haan, J, Lindhout, D, van Ommen, G J, Hofker, M H, Ferrari, M D, Frants, R R

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Hex1: a new human Rad2 nuclease family member with homology to yeast exonuclease 1 von Wilson, David M., Coleman, Matthew A., Adamson, Aaron W., Christensen, Mari, Lamerdin, Jane E., Carney, James P.

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An integrated metric physical map of human chromosome 19 von Ashworth, Linda K., Batzer, Mark A., Brandriff, Brigitte, Branscomb, Elbert, de Jong, Pieter, Garcia, Emilio, Garnes, Jeffrey A., Gordon, Laurie A., Lamerdin, Jane E., Lennon, Greg, Mohrenweiser, Harvey, Olsen, Anne S., Slezak, Tom, Carrano, Anthony V.

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XRCC2 and XRCC3, New Human Rad51-Family Members, Promote Chromosome Stability and Protect against DNA Cross-Links and Other Damages von Liu, Nan, Lamerdin, Jane E, Tebbs, Robert S, Schild, David, Tucker, James D, Shen, M.Richard, Brookman, Kerry W, Siciliano, Michael J, Walter, Christi A, Fan, Wufang, Narayana, Lakshmi S, Zhou, Zi-Qiang, Adamson, Aaron W, Sorensen, Karen J, Chen, David J, Jones, Nigel J, Thompson, Larry H

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ERCC4 (XPF) encodes a human nucleotide excision repair protein with eukaryotic recombination homologs von Brookman, Kerry W., Lamerdin, Jane E., Thelen, Michael P., Hwang, Mona, Reardon, Joyce T., Sancar, Aziz, Zhou, Zi-Qiang, Walter, Christi A., Parris, Christopher N., Thompson, Larry H.

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Genomic sequence comparison of the human and mouse XRCC1 DNA repair gene regions von Lamerdin, Jane E., Montgomery, Mishelle A., Stilwagen, Stephanie A., Scheidecker, Lisa K., Tebbs, Robert S., Brookman, Kerry W., Thompson, Larry H., Carrano, Anthony V.

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Sequence analysis of the ERCC2 gene regions in human, mouse, and hamster reveals three linked genes von LAMERDIN, J. E, STILWAGEN, S. A, RAMIREZ, M. H, STUBBS, L, CARRANO, A. V

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Restoration of Nucleotide Excision Repair in a Helicase-Deficient XPD Mutant from Intragenic Suppression by a Trichothiodystrophy Mutation von George, James W., Salazar, Edmund P., Vreeswijk, Maaike P. G., Lamerdin, Jane E., Reardon, Joyce T., Zdzienicka, Malgorzata Z., Sancar, Aziz, Kadkhodayan, Saloumeh, Tebbs, Robert S., Mullenders, Leon H. F., Thompson, Larry H.

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Characterization of the Mouse Xpf DNA Repair Gene and Differential Expression during Spermatogenesis von Shannon, Mark, Lamerdin, Jane E., Richardson, Laura, McCutchen-Maloney, Sandra L., Hwang, Mona H., Handel, Mary Ann, Stubbs, Lisa, Thelen, Michael P.

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Alu fossil relics--distribution and insertion polymorphism von Arcot, S S, Adamson, A W, Lamerdin, J E, Kanagy, B, Deininger, P L, Carrano, A V, Batzer, M A

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Comparative Analysis of a Conserved Zinc Finger Gene Cluster on Human Chromosome 19q and Mouse Chromosome 7 von Shannon, Mark, Ashworth, Linda K., Mucenski, Michael L., Lamerdin, Jane E., Branscomb, Elbert, Stubbs, Lisa

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The Human XRCC9 Gene Corrects Chromosomal Instability and Mutagen Sensitivities in CHO UV40 Cells von Liu, Nan, Lamerdin, Jane E., Tucker, James D., Zi-Q. Zhou, Walter, Christi A., Albala, Joanna S., Busch, David B., Thompson, Larry H.

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Cloning and Molecular Characterization of the Chinese Hamster ERCC2 Nucleotide Excision Repair Gene von Kirchner, J.M., Salazar, E.P., Lamerdin, J.E., Montgomery, M.A., Carrano, A.V., Weber, C.A.

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Complex beta-satellite repeat structures and the expansion of the zinc finger gene cluster in 19p12 von Eichler, E E, Hoffman, S M, Adamson, A A, Gordon, L A, McCready, P, Lamerdin, J E, Mohrenweiser, H W

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The atherogenic lipoprotein phenotype is not caused by a mutation in the coding region of the low density lipoprotein receptor gene von Naggert, Jürgen K., III, Adrian Recinos, Lamerdin, Jane E., Krauss, Ronald M., Nishina, Patsy M.

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Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints von Puttagunta, R, Gordon, L A, Meyer, G E, Kapfhamer, D, Lamerdin, J E, Kantheti, P, Portman, K M, Chung, W K, Jenne, D E, Olsen, A S, Burmeister, M

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Isolation and Characterization of Mouse Xrcc-1, a DNA Repair Gene Affecting Ligation von Brookman, Kerry W., Tebbs, Robert S., Allen, Susan A., Tucker, James D., Swiger, Roy R., Lamerdin, Jane E., Carrano, Anthony V., Thompson, Larry H.

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Fanconi Anemia FANCG Protein in Mitigating Radiation- and Enzyme-Induced DNA Double-Strand Breaks by Homologous Recombination in Vertebrate Cells von Yamamoto, Kazuhiko, Ishiai, Masamichi, Matsushita, Nobuko, Arakawa, Hiroshi, Lamerdin, Jane E., Buerstedde, Jean-Marie, Tanimoto, Mitsune, Harada, Mine, Thompson, Larry H., Takata, Minoru

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High-resolution cartography of recently integrated human chromosome 19-specific Alu fossils von Arcot, S S, Adamson, A W, Risch, G W, LaFleur, J, Robichaux, M B, Lamerdin, J E, Carrano, A V, Batzer, M A

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Characterization of the hamster FancG/Xrcc9 gene and mutations in CHO UV40 and NM3 von Lamerdin, Jane E., Yamada, Nazumi A., George, James W., Souza, Brian, Christian, Allen T., Jones, Nigel J., Thompson, Larry H.

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