Results 281 to 290 of about 4,061,678 (356)
A case of IgG-type heavy chain amyloidosis with membranous nephropathy-like changes with long-term survival. [PDF]
Kono K +14 more
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Expression Analysis of Heavy-Chain-Only Antibodies in Cloudy Catshark and Japanese Bullhead Shark. [PDF]
Uemura R +8 more
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A Mathematical Model of Myosin Heavy Chain Dynamics in the Disintegration of Golden Threadfin Bream <i>Nemipterus virgatus</i> Surimi Gel. [PDF]
Nakamizo R +3 more
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Genetic diversity of the immunoglobulin heavy chain locus in cohorts of patients affected with SARS-CoV-2. [PDF]
Malaspina P +10 more
europepmc +1 more source
Utility of binding protein fusions to immunoglobulin heavy chain constant regions from mammalian and avian species. [PDF]
Zhu N +4 more
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Smooth Muscle Myosin Heavy Chain Expression in Nodal and Extranodal Follicular Dendritic Cell Sarcoma. [PDF]
Kelley JT +5 more
europepmc +1 more source
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The Physics Teacher, 2011
While perusing various websites in search of a more challenging lab for my students, I came across a number of ideas where replacing the string in an Atwood's machine1 with a simple ball chain like the kind found in lamp pulls created an interesting system to investigate.
Paul Beeken
openaire +2 more sources
While perusing various websites in search of a more challenging lab for my students, I came across a number of ideas where replacing the string in an Atwood's machine1 with a simple ball chain like the kind found in lamp pulls created an interesting system to investigate.
Paul Beeken
openaire +2 more sources
Best Practice & Research Clinical Haematology, 2005
Heavy chain diseases (HCDs) are rare B-cell lymphoplasma-cell proliferative disorders characterized by production of truncated monoclonal immunoglobulin heavy chains without associated light chains. HCDs involving the three main immunoglobulin classes have been described; alpha-HCD is the most common and has the most uniform presentation, gamma- and mu-
Dietlind L, Wahner-Roedler +1 more
openaire +2 more sources
Heavy chain diseases (HCDs) are rare B-cell lymphoplasma-cell proliferative disorders characterized by production of truncated monoclonal immunoglobulin heavy chains without associated light chains. HCDs involving the three main immunoglobulin classes have been described; alpha-HCD is the most common and has the most uniform presentation, gamma- and mu-
Dietlind L, Wahner-Roedler +1 more
openaire +2 more sources
Hematology/Oncology Clinics of North America, 1999
This review underscores the diversity of the structural and genetic abnormalities of HCD proteins and of the clinicopathologic features of the underlying lymphoproliferative disorders. Cells producing HCD may, however, all derive from a common normal precursor, which could be a rare B cell in the process of immunoglobulin gene somatic mutation within ...
J P, Fermand, J C, Brouet
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This review underscores the diversity of the structural and genetic abnormalities of HCD proteins and of the clinicopathologic features of the underlying lymphoproliferative disorders. Cells producing HCD may, however, all derive from a common normal precursor, which could be a rare B cell in the process of immunoglobulin gene somatic mutation within ...
J P, Fermand, J C, Brouet
openaire +2 more sources
Annals of the New York Academy of Sciences, 1971
The recent elucidation of the structure of immunoglobulins, and the more precise immunologic and chemical characterization of the proteins produced by patients with proliferative disorders of plasma cells and lymphocytes have led to a clearer understanding of the biosynthetic alterations accompanying them.
E C, Franklin, B, Frangione, S, Cooper
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The recent elucidation of the structure of immunoglobulins, and the more precise immunologic and chemical characterization of the proteins produced by patients with proliferative disorders of plasma cells and lymphocytes have led to a clearer understanding of the biosynthetic alterations accompanying them.
E C, Franklin, B, Frangione, S, Cooper
openaire +2 more sources

