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W F Moo-Penn

Showing results (21-30 of 35) with videos related to

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Biochimica Et Biophysica Acta|February 22, 1977
Hemoglobin Tarrant: alpha126(H9) Asp leads to Asn. A new hemoglobin variant in the alpha1beta1 contact region showing high oxygen affinity and reduced cooperativityW F Moo-Penn, D L Jue, M H Johnson, et al.
Biochimica Et Biophysica Acta|May 29, 1980
Hemoglobin Tampa:beta 79 (EF3) aspartic acid replaced by tyrosineM H Johnson, D L Jue, L C Patchen, et al.
Sangre|June 1, 1990
[Hemoglobin Setif (alpha 94 (G1) Asp----Tyr) in a Spanish family]J M de Pablos, M A de las Nieves, A Romero, et al.
Biochimica Et Biophysica Acta|September 14, 1983
Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2W F Moo-Penn, R M Baine, D L Jue, et al.
American Journal of Clinical Pathology|August 1, 1976
Hemoglobin Jackson, alpha 127 (H10) Lys replaced by AsnW F Moo-Penn, K C Bechtel, M H Johnson, et al.
Blood|August 1, 1980
Hemoglobin Ohio (beta 142 Ala replaced by): a new abnormal hemoglobin with high oxygen affinity and erythrocytosisW F Moo-Penn, R G Schneider, T Shih, et al.
Pediatric Research|June 1, 1983
Hemoglobin Cheverly: an unstable hemoglobin associated with chronic mild anemiaA M Yeager, W H Zinkham, D L Jue, et al.
Biochimica Et Biophysica Acta|December 22, 1976
Hemoglobin Fannin-Lubbock [alpha2 beta 2 119 (GH2) Gly replaced by Asp]. A new hemoglobin variant at the alpha1 beta 1 contactW F Moo-Penn, K C Bechtel, M H Johnson, et al.
Biochemistry|January 9, 1990
Structural, functional, and subunit assembly properties of hemoglobin Attleboro [alpha 138 (H21) Ser----Pro], a variant possessing a site maturation at a critical C-terminal residueM J McDonald, L A Michalski, S M Turci, et al.
Journal of Clinical Microbiology|April 1, 1990
Purification and characterization of a pilin specific for Brazilian purpuric fever-associated Haemophilus influenzae biogroup aegyptius (H. aegyptius) strainsR S Weyant, W F Bibb, D S Stephens, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

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Pageof 4
Biochimica Et Biophysica Acta|February 22, 1977
Hemoglobin Tarrant: alpha126(H9) Asp leads to Asn. A new hemoglobin variant in the alpha1beta1 contact region showing high oxygen affinity and reduced cooperativityW F Moo-Penn, D L Jue, M H Johnson, et al.
Biochimica Et Biophysica Acta|May 29, 1980
Hemoglobin Tampa:beta 79 (EF3) aspartic acid replaced by tyrosineM H Johnson, D L Jue, L C Patchen, et al.
Sangre|June 1, 1990
[Hemoglobin Setif (alpha 94 (G1) Asp----Tyr) in a Spanish family]J M de Pablos, M A de las Nieves, A Romero, et al.
Biochimica Et Biophysica Acta|September 14, 1983
Hemoglobin Evanston: alpha 14(A12) Trp leads to Arg. A variant hemoglobin associated with alpha-thalassemia-2W F Moo-Penn, R M Baine, D L Jue, et al.
American Journal of Clinical Pathology|August 1, 1976
Hemoglobin Jackson, alpha 127 (H10) Lys replaced by AsnW F Moo-Penn, K C Bechtel, M H Johnson, et al.
Blood|August 1, 1980
Hemoglobin Ohio (beta 142 Ala replaced by): a new abnormal hemoglobin with high oxygen affinity and erythrocytosisW F Moo-Penn, R G Schneider, T Shih, et al.
Pediatric Research|June 1, 1983
Hemoglobin Cheverly: an unstable hemoglobin associated with chronic mild anemiaA M Yeager, W H Zinkham, D L Jue, et al.
Biochimica Et Biophysica Acta|December 22, 1976
Hemoglobin Fannin-Lubbock [alpha2 beta 2 119 (GH2) Gly replaced by Asp]. A new hemoglobin variant at the alpha1 beta 1 contactW F Moo-Penn, K C Bechtel, M H Johnson, et al.
Biochemistry|January 9, 1990
Structural, functional, and subunit assembly properties of hemoglobin Attleboro [alpha 138 (H21) Ser----Pro], a variant possessing a site maturation at a critical C-terminal residueM J McDonald, L A Michalski, S M Turci, et al.
Journal of Clinical Microbiology|April 1, 1990
Purification and characterization of a pilin specific for Brazilian purpuric fever-associated Haemophilus influenzae biogroup aegyptius (H. aegyptius) strainsR S Weyant, W F Bibb, D S Stephens, et al.
Pageof 4