Citation: Ka. Henning et al., HUMANIZING THE YEAST TELOMERASE TEMPLATE, Proceedings of the National Academy of Sciences of the United Statesof America, 95(10), 1998, pp. 5667-5671
Authors:
MOGAYZEL PJ
HENNING KA
BITTNER ML
NOVOTNY EA
SCHWIEBERT EM
GUGGINO WB
JIANG Y
ROSENFELD MA
Citation: Pj. Mogayzel et al., FUNCTIONAL HUMAN CFTR PRODUCED BY STABLE CHINESE-HAMSTER OVARY CELL-LINES DERIVED USING YEAST ARTIFICIAL CHROMOSOMES, Human molecular genetics, 6(1), 1997, pp. 59-68
Authors:
HENNING KA
NOVOTNY EA
COMPTON ST
STATHAM V
LIU PP
ROSENFELD MA
Citation: Ka. Henning et al., PRODUCTION OF FUNCTIONAL HUMAN ARTIFICIAL CHROMOSOMES BY THE MODIFICATION OF YACS CONTAINING HUMAN CENTROMERIC DNA, American journal of human genetics, 61(4), 1997, pp. 2082-2082
Authors:
BREGMAN DB
HALABAN R
HENNING KA
FRIEDBERG EC
WARREN SL
Citation: Db. Bregman et al., UV-INDUCED UBIQUITINATION OF RNA-POLYMERASE-II IS DEFICIENT IN COCKAYNES-SYNDROME CELLS, The FASEB journal, 10(6), 1996, pp. 1658-1658
Authors:
BREGMAN DB
HALABAN R
VANGOOL AJ
HENNING KA
FRIEDBERG EC
WARREN SL
Citation: Db. Bregman et al., UV-INDUCED UBIQUITINATION OF RNA-POLYMERASE-II - A NOVEL MODIFICATIONDEFICIENT IN COCKAYNE-SYNDROME CELLS, Proceedings of the National Academy of Sciences of the United Statesof America, 93(21), 1996, pp. 11586-11590
Authors:
HENNING KA
LI L
IYER N
MCDANIEL LD
REAGAN MS
LEGERSKI R
SCHULTZ RA
STEFANINI M
LEHMANN AR
MAYNE LV
FRIEDBERG EC
Citation: Ka. Henning et al., THE COCKAYNE-SYNDROME GROUP-A GENE ENCODES A WD REPEAT PROTEIN THAT INTERACTS WITH CSB PROTEIN AND A SUBUNIT OF RNA-POLYMERASE-II TFIIH, Cell, 82(4), 1995, pp. 555-564
Authors:
HENNING KA
PETERSON C
LEGERSKI R
FRIEDBERG EC
Citation: Ka. Henning et al., CLONING THE DROSOPHILA HOMOLOG OF THE XERODERMA-PIGMENTOSUM COMPLEMENTATION GROUP-C GENE REVEALS HOMOLOGY BETWEEN THE PREDICTED HUMAN AND DROSOPHILA POLYPEPTIDES AND THAT ENCODED BY THE YEAST RAD4 GENE, Nucleic acids research, 22(3), 1994, pp. 257-261
Citation: Ec. Friedberg et Ka. Henning, THE CONUNDRUM OF XERODERMA-PIGMENTOSUM - A RARE DISEASE WITH FREQUENTCOMPLEXITIES, MUTATION RESEARCH, 289(1), 1993, pp. 47-53