Citation: Bp. Chadwick et Hf. Willard, Histone H2A variants and the inactive X chromosome: identification of a second macroH2A variant, HUM MOL GEN, 10(10), 2001, pp. 1101-1113
Citation: Bp. Chadwick et al., Histone variant macroH2A contains two distinct macrochromatin domains capable of directing macroH2A to the inactive X chromosome, NUCL ACID R, 29(13), 2001, pp. 2699-2705
Citation: Bp. Chadwick et Hf. Willard, A novel chromatin protein, distantly related to histone H2A, is largely excluded from the inactive X chromosome, J CELL BIOL, 152(2), 2001, pp. 375-384
Authors:
Chadwick, BP
Leyne, M
Gill, S
Liebert, CB
Mull, J
Mezey, E
Robbins, CM
Pinkett, HW
Makalowska, I
Maayan, C
Blumenfeld, A
Axelrod, FB
Brownstein, M
Gusella, JF
Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31, MAMM GENOME, 11(1), 2000, pp. 81-83
Authors:
Hicks-Berger, CA
Chadwick, BP
Frischauf, AM
Kirley, TL
Citation: Ca. Hicks-berger et al., Expression and characterization of soluble and membrane-bound human nucleoside triphosphate diphosphohydrolase 6 (CH39L2), J BIOL CHEM, 275(44), 2000, pp. 34041-34045
Authors:
Chadwick, BP
Mull, J
Helbling, LA
Gill, S
Leyne, M
Robbins, CM
Pinkett, HW
Makalowska, I
Maayan, C
Blumenfeld, A
Axelrod, FB
Brownstein, N
Gusella, JF
Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, mapping, and expression of two novel actin genes, actin-like-7A (ACTL7A) and actin-like-7B (ACTL7B), from the familiar dysautonomia candidate region on 9q31, GENOMICS, 58(3), 1999, pp. 302-309
Authors:
Chadwick, BP
Gill, S
Leyne, M
Mull, J
Liebert, CB
Robbins, CM
Pinkett, HW
Makalowska, I
Maayan, C
Blumenfeld, A
Axelrod, FB
Brownstein, M
Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene, GENE, 240(1), 1999, pp. 67-73
Authors:
Chadwick, BP
Helbling, LA
Angrist, M
Chakravarti, A
Gusella, JF
Slaugenhaupt, SA
Citation: Bp. Chadwick et al., Assignment of persephin (PSPN), a human neurotrophic factor, to chromosome19p13.3 by radiation hybrid mapping and somatic cell hybrid PCR, CYTOG C GEN, 83(3-4), 1998, pp. 236-237