Authors:
SCHULTZ RA
SWOAP SJ
MCDANIEL LD
ZHANG BQ
KOON EC
GARRY DJ
LI K
WILLIAMS RS
Citation: Ra. Schultz et al., DIFFERENTIAL EXPRESSION OF MITOCHONDRIAL-DNA REPLICATION FACTORS IN MAMMALIAN-TISSUES, The Journal of biological chemistry, 273(6), 1998, pp. 3447-3451
Authors:
MCDANIEL LD
LEGERSKI R
LEHMANN AR
FRIEDBERG EC
SCHULTZ RA
Citation: Ld. Mcdaniel et al., CONFIRMATION OF HOMOZYGOSITY FOR A SINGLE NUCLEOTIDE SUBSTITUTION MUTATION IN A COCKAYNE-SYNDROME PATIENT USING MONOALLELIC MUTATION ANALYSIS IN SOMATIC-CELL HYBRIDS, Human mutation, 10(4), 1997, pp. 317-321
Authors:
MCDANIEL LD
ZHANG BQ
KUBICZEK E
RITTER M
HUANG J
BERARD C
LEANACOX J
SCHWARTZ S
SCHULTZ RA
Citation: Ld. Mcdaniel et al., CONSTRUCTION AND SCREENING OF A COSMID LIBRARY GENERATED FROM A SOMATIC-CELL HYBRID BEARING HUMAN-CHROMOSOME-15, Genomics, 40(1), 1997, pp. 63-72
Authors:
MCDANIEL LD
PRUEITT R
PROBST L
SCHULTZ RA
Citation: Ld. Mcdaniel et al., EVALUATION OF THE ROBERTS-SYNDROME COMPLEMENTING FACTOR IN A TRANSIENT CELL-FUSION ASSAY, American journal of human genetics, 61(4), 1997, pp. 906-906
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:
SCHULTZ RA
BERARDO C
HUANGO J
KUBICZEKO E
COX L
MCDANIEL LD
RITTERO M
SCHWARTZ S
ZHANG B
Citation: Ra. Schultz et al., ISOLATION, MAPPING AND STSS FOR CLONES GENERATED FROM A CHROMOSOME-15COSMID LIBRARY, Cytogenetics and cell genetics, 67(1), 1994, pp. 19-19
Authors:
MCDANIEL LD
LEDERER WJ
KOFUJI P
SCHULZE DH
KIEVAL R
SCHULTZ RA
Citation: Ld. Mcdaniel et al., MAPPING OF THE HUMAN CARDIAC NA+ CA2+ EXCHANGER GENE (NCX1) BY FLUORESCENT INSITU HYBRIDIZATION TO CHROMOSOME REGION 2P22-]P23/, Cytogenetics and cell genetics, 63(3), 1993, pp. 192-193
Citation: Ra. Schultz et Ld. Mcdaniel, AN EVALUATION OF CANDIDATE GENES FOR BLOOM-SYNDROME, American journal of human genetics, 53(3), 1993, pp. 1356-1356