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Histamine -- Physiological effect.   2
Histamine -- physiology.   2
Histamine -- Physiopathologie. : Histamine in inflammation / edited by Robin L. Thurmond  2010 1
Histamine -- Receptors. : The third histamine receptor : selective ligands as potential therapeutic agents in CNS disorders / editor, Divya Vohora  2009 1
 

Hister beetles -- See Histeridae


  1
Histèria col·lectiva. : Koro : clinical and historical developments of the culturally defined genital retraction disorder / Arabinda Narayan Chowdhury  2021 1
Histeridae -- Canada. : Coleoptera histeridae of Canada / Yves Bousquet, Serge Laplante  2005 1
 

Histerone -- See Testosterone


A potent androgenic steroid and major product secreted by the LEYDIG CELLS of the TESTIS. Its production is stimulated by LUTEINIZING HORMONE from the PITUITARY GLAND. In turn, testosterone exerts feedback control of the pituitary LH and FSH secretion. Depending on the tissues, testosterone can be further converted to DIHYDROTESTOSTERONE or ESTRADIOL
  1
 

Histers -- See Histeridae


  1
 

Histiocytes -- See Macrophages


  1
 

Histiocytic Disorder, Malignant -- See Histiocytic Disorders, Malignant


Distinctive neoplastic disorders of histiocytes. Included are malignant neoplasms of MACROPHAGES and DENDRITIC CELLS
  1
Histiocytic Disorders, Malignant : Histiocytic disorders / Oussama Abla, Gritta Janka, editors  2018 1
 

Histiocytic Lymphoma -- See Lymphoma, Large B-Cell, Diffuse


Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation
  1
 

Histiocytic Lymphoma, Diffuse -- See Lymphoma, Large B-Cell, Diffuse


Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation
  1
 

Histiocytic Lymphoma, Nodular -- See Lymphoma, Follicular


Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES
  1
 

Histiocytic Lymphomas -- See Lymphoma, Large B-Cell, Diffuse


Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation
  1
 

Histiocytic Lymphomas, Diffuse -- See Lymphoma, Large B-Cell, Diffuse


Malignant lymphoma composed of large B lymphoid cells whose nuclear size can exceed normal macrophage nuclei, or more than twice the size of a normal lymphocyte. The pattern is predominantly diffuse. Most of these lymphomas represent the malignant counterpart of B-lymphocytes at midstage in the process of differentiation
  1
 

Histiocytic Lymphomas, Nodular -- See Lymphoma, Follicular


Malignant lymphoma in which the lymphomatous cells are clustered into identifiable nodules within the LYMPH NODES. The nodules resemble to some extent the GERMINAL CENTER of lymph node follicles and most likely represent neoplastic proliferation of lymph node-derived follicular center B-LYMPHOCYTES
  1
 

Histiocytic Reticuloses, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive
  1
 

Histiocytic Reticulosis, Familial -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive
  1
 

Histiocytoid Hemangioma -- See Hemangioma


A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000)
  1
 

Histiocytoid Hemangiomas -- See Hemangioma


A vascular anomaly due to proliferation of BLOOD VESSELS that forms a tumor-like mass. The common types involve CAPILLARIES and VEINS. It can occur anywhere in the body but is most frequently noticed in the SKIN and SUBCUTANEOUS TISSUE. (from Stedman, 27th ed, 2000)
  1
 

Histiocytoses, Familial Hemophagocytic -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive
  1
 

Histiocytoses, Generalized -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytoses, Kerasin -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Histiocytoses, Langerhans Cell -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytoses, Lipoid (Kerasin Type) -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Histiocytoses, Type 2 -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytosis, Familial Hemophagocytic -- See Lymphohistiocytosis, Hemophagocytic


A group of related disorders characterized by LYMPHOCYTOSIS; HISTIOCYTOSIS; and hemophagocytosis. The two major forms are familial and reactive
  1
 

Histiocytosis, Generalized -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytosis, Kerasin -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
Histiocytosis, Langerhans-Cell : Histiocytic disorders / Oussama Abla, Gritta Janka, editors  2018 1
 

Histiocytosis, Lipoid (Kerasin Type) -- See Gaucher Disease


An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
  1
 

Histiocytosis, Type 2 -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytosis-X -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
 

Histiocytosis X, Pulmonary -- See Histiocytosis, Langerhans-Cell


A group of disorders resulting from the abnormal proliferation of and tissue infiltration by LANGERHANS CELLS which can be detected by their characteristic Birbeck granules (X bodies), or by monoclonal antibody staining for their surface CD1 ANTIGENS. Langerhans-cell granulomatosis can involve a single organ, or can be a systemic disorder
  1
Dance -- Histiography : Dance history : a methodology for study / edited by Janet Adshead and June Layson  1983 1
Histochemical techniques : Histochemical techniques / J. D. Bancroft ; introductory chapter by A. Stevens ; with a foreword by A. G. E. Pearse  1975 1
Histochemie : Genome visualization by classic methods in light microscopy / Jean-Marie Exbrayat  2001 1
  Histochemistry -- 2 Related Subjects   2
Histochemistry.   11
Brain -- Histochemistry. : Chemoarchitectonic atlas of the developing mouse brain / David M. Jacobowitz, Louise C. Abbott  1998 1
Brain -- Histochemistry -- Atlases : Chemoarchitectonic atlas of the developing mouse brain / David M. Jacobowitz, Louise C. Abbott  1998 1
Histochemistry -- Congresses. : Trends in enzyme histochemistry and cytochemistry  1980 1
Fruit trees -- Histochemistry : Handbook of cytology, histology, and histochemistry of fruit tree diseases / editor, Alan R. Biggs  2019 1
Histochemistry -- Laboratory manuals   4
Histochemistry -- Periodicals   13
Salivary glands -- Histochemistry : HISTOCHEMISTRY OF THE SALIVARY GLANDS  2019 1
Histochemistry -- Technique.   7
Histochimie. : Genome visualization by classic methods in light microscopy / Jean-Marie Exbrayat  2001 1
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