B B Webber - JoVE Visualize

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Hemoglobin|December 1, 1993

Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatographyD D Pobedimskaya, T P Molchanova, R Amernick, et al.

International Journal of Oral and Maxillofacial Surgery|October 6, 2014

Low-level laser therapy improves peri-implant bone formation: resonance frequency, electron microscopy, and stereology findings in a rabbit modelF V Gomes, L Mayer, F P Massotti, et al.

Hemoglobin|January 1, 1991

Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----GlnJ B Wilson, M Ramachandran, B B Webber, et al.

Hemoglobin|January 1, 1990

Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantitiesM Harkness, D R Harkness, F Kutlar, et al.

Hemoglobin|January 1, 1989

Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.

Hemoglobin|January 1, 1986

HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black familyJ E Bowman, R Bloom, S S Chen, et al.

Biochimica Et Biophysica Acta|November 10, 1988

Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140V B Jogessar, K Westermeyer, B B Webber, et al.

Biochimica Et Biophysica Acta|June 5, 1986

Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identificationT H Huisman, J B Wilson, A Kutlar, et al.

Hemoglobin|January 1, 1989

Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemiaJ B Wilson, B B Webber, A Kutlar, et al.

Hemoglobin|January 1, 1988

Hb Duan [alpha 75(EF4)Asp----Ala], Hb Westmead [alpha 122(H5)His----Gln], and alpha-thalassemia-2 (-4.2 Kb deletion) in a Chinese familyS Liang, Z Tang, C Su, et al.

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Showing results (21-30 of 36) with videos related to

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Pageof 4

Hemoglobin|December 1, 1993

Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatographyD D Pobedimskaya, T P Molchanova, R Amernick, et al.

International Journal of Oral and Maxillofacial Surgery|October 6, 2014

Low-level laser therapy improves peri-implant bone formation: resonance frequency, electron microscopy, and stereology findings in a rabbit modelF V Gomes, L Mayer, F P Massotti, et al.

Hemoglobin|January 1, 1991

Hb Cleveland or alpha 2 beta 2(93)(F9)Cys----Arg;121(GH4)Glu----GlnJ B Wilson, M Ramachandran, B B Webber, et al.

Hemoglobin|January 1, 1990

Hb Sun Prairie or alpha(2)130(H13)Ala----Pro beta 2, a new unstable variant occurring in low quantitiesM Harkness, D R Harkness, F Kutlar, et al.

Hemoglobin|January 1, 1989

Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb SJ F Codrington, F A Codrington, J H Wisse, et al.

Hemoglobin|January 1, 1986

HB Chicago or alpha (2)136 (H19) Leu----Met beta 2 and a -G gamma-G gamma-globin gene arrangement in a black familyJ E Bowman, R Bloom, S S Chen, et al.

Biochimica Et Biophysica Acta|November 10, 1988

Hb natal or alpha 2(minus Tyr-Arg) beta 2: a high oxygen affinity alpha chain variant with a deleted carboxy-terminus resulting from a TAC----TAA (Tyr----terminating codon) mutation in codon alpha 140V B Jogessar, K Westermeyer, B B Webber, et al.

Biochimica Et Biophysica Acta|June 5, 1986

Hb J-Antakya or alpha 2 beta (2)65(E9)Lys----Met in a Turkish family and Hb complutense or alpha 2 beta (2)127(H5)Gln----Glu in a Spanish family; correction of a previously published identificationT H Huisman, J B Wilson, A Kutlar, et al.

Hemoglobin|January 1, 1989

Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemiaJ B Wilson, B B Webber, A Kutlar, et al.

Hemoglobin|January 1, 1988

Hb Duan [alpha 75(EF4)Asp----Ala], Hb Westmead [alpha 122(H5)His----Gln], and alpha-thalassemia-2 (-4.2 Kb deletion) in a Chinese familyS Liang, Z Tang, C Su, et al.

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