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FS Collins
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Journal Articles

Molecular pathogenesis of the chromosome 16 inversion in the M4Eo subtype of acute myeloid leukemia [see comments]

PP Liu, A Hajra, C Wijmenga, FS Collins
Journal: Blood
Blood (1995) 85 (9): 2289–2302.
https://doi.org/10.1182/blood.V85.9.2289.bloodjournal8592289
Published: 1995
Journal Articles

Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesis

P Marlton, DF Claxton, P Liu, EH Estey, M Beran, M LeBeau, JR Testa, FS Collins, JD Rowley, MJ Siciliano
Journal: Blood
Blood (1995) 85 (3): 772–779.
https://doi.org/10.1182/blood.V85.3.772.bloodjournal853772
Published: 1995
Journal Articles

Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomonocytic leukemia

P Liu, DF Claxton, P Marlton, A Hajra, J Siciliano, M Freedman, SC Chandrasekharappa, K Yanagisawa, RL Stallings, FS Collins
Journal: Blood
Blood (1993) 82 (3): 716–721.
https://doi.org/10.1182/blood.V82.3.716.716
Published: 1993
Journal Articles

Interaction of Sp1 with the human gamma globin promoter: binding and transactivation of normal and mutant promoters

DL Gumucio, KL Rood, KL Blanchard-McQuate, TA Gray, A Saulino, FS Collins
Journal: Blood
Blood (1991) 78 (7): 1853–1863.
https://doi.org/10.1182/blood.V78.7.1853.1853
Published: 1991
Journal Articles

The -175T----C mutation increases promoter strength in erythroid cells: correlation with evolutionary conservation of binding sites for two trans-acting factors

DL Gumucio, WK Lockwood, JL Weber, AM Saulino, K Delgrosso, S Surrey, E Schwartz, M Goodman, FS Collins
Journal: Blood
Blood (1990) 75 (3): 756–761.
https://doi.org/10.1182/blood.V75.3.756.756
Published: 1990
Journal Articles

Sizing of the human T cell receptor alpha locus and detection of a large deletion in the Molt-4 cell line

MS Roth, FS Collins, D Ginsburg
Journal: Blood
Blood (1988) 71 (6): 1744–1747.
https://doi.org/10.1182/blood.V71.6.1744.1744
Published: 1988
Journal Articles

The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases

FS Collins, JL Cole, WK Lockwood, MC Iannuzzi
Journal: Blood
Blood (1987) 70 (6): 1797–1803.
https://doi.org/10.1182/blood.V70.6.1797.1797
Published: 1987
Journal Articles

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks

PG Waber, MA Bender, RE Gelinas, C Kattamis, A Karaklis, K Sofroniadou, G Stamatoyannopoulos, FS Collins, BG Forget, HH Jr Kazazian
Journal: Blood
Blood (1986) 67 (2): 551–554.
https://doi.org/10.1182/blood.V67.2.551.551
Published: 1986
Journal Articles

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

FS Collins, CD Boehm, PG Waber, CJ Jr Stoeckert, SM Weissman, BG Forget, HH Jr Kazazian
Journal: Blood
Blood (1984) 64 (6): 1292–1296.
https://doi.org/10.1182/blood.V64.6.1292.1292
Published: 1984