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Type 2 diabetes -- Molecular aspects : Molecular and cell biology of type 2 diabetes and its complications / volume editors, F. Belfiore [and others]  1998 1
Type 2 diabetes -- Molecular aspects -- Complications : Molecular and cell biology of type 2 diabetes and its complications / volume editors, F. Belfiore [and others]  1998 1
Type 2 diabetes -- Molecular aspects -- Congresses : Molecular pathogenesis of MODYs / American Diabetes Association: Symposium, Scottsdale, AZ, USA, November 6-8, 1998 ; volume editors, F.M. Matschinsky, M.A. Magnuson  2000 1
Type 2 diabetes -- Pathophysiology   2
Type 2 diabetes -- Prevention   2
Type 2 diabetes -- Treatment   2
 

Type 2 Gaucher Disease -- 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
 

Type 2 Histiocytoses -- 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
 

Type 2 Histiocytosis -- 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
 

Type 2 Spinocerebellar Ataxia -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  1
 

Type 3 Cystatins -- See Cystatins


A homologous group of endogenous CYSTEINE PROTEINASE INHIBITORS. The cystatins inhibit most CYSTEINE ENDOPEPTIDASES such as PAPAIN, and other peptidases which have a sulfhydryl group at the active site
  1
 

Type 3 Gaucher Disease -- 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
 

Type 3 Hereditary Sensory Neuropathy, Dominant -- See Dysautonomia, Familial


An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4)
  1
 

Type 3 Inositol 1,4,5-trisphosphate Receptor -- See Inositol 1,4,5-Trisphosphate Receptors


Intracellular receptors that bind to INOSITOL 1,4,5-TRISPHOSPHATE and play an important role in its intracellular signaling. Inositol 1,4,5-trisphosphate receptors are calcium channels that release CALCIUM in response to increased levels of inositol 1,4,5-trisphosphate in the CYTOPLASM
  1
 

Type 3, Neurofibromatosis -- See Neurofibromatoses


A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
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Type 4 Spinocerebellar Ataxia -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  1
 

Type 5 Spinocerebellar Ataxia -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  1
 

Type 6 Spinocerebellar Ataxia -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
  1
 

Type 7 Spinocerebellar Ataxia -- See Spinocerebellar Ataxias


A group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
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  Type A behavior -- 2 Related Subjects   2
Type A behavior.   14
Type A behavior -- Congresses. : Type A behavior pattern : research, theory, and intervention / editors, B. Kent Houston and C.R. Snyder  1988 1
Type A behavior in children -- United States. : Raising your type A child : how to help your child make the most of an achievement-oriented personality / Steven Shelov and John Kelly  1991 1
 

Type A Monoamine Oxidase -- See Monoamine Oxidase


An enzyme that catalyzes the oxidative deamination of naturally occurring monoamines. It is a flavin-containing enzyme that is localized in mitochondrial membranes, whether in nerve terminals, the liver, or other organs. Monoamine oxidase is important in regulating the metabolic degradation of catecholamines and serotonin in neural or target tissues. Hepatic monoamine oxidase has a crucial defensive role in inactivating circulating monoamines or those, such as tyramine, that originate in the gut and are absorbed into the portal circulation. (From Goodman and Gilman's, The Pharmacological Basis of Therapeutics, 8th ed, p415) EC 1.4.3.4
  1
 

Type A Personalities -- See Type A Personality


Established behavior pattern characterized by excessive drive and ambition, impatience, competitiveness, sense of time urgency, and poorly contained aggression
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Type A personality -- See Type A behavior


Here are entered works on a behavior pattern characterized by tenseness, impatience, and competitive drive, associated with a tendency to develop coronary heart disease
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Type A Personality.   3
 

Type A Potassium Channel Interacting Proteins -- See Kv Channel-Interacting Proteins


A family of neuronal calcium-sensor proteins that interact with and regulate potassium channels, type A
  1
Type and token (Linguistics)   2
  Type and type-founding -- 10 Related Subjects   10
Type and type-founding.   85
Type and type-founding -- Australia. : "Design down under"  1989 1
Type and type-founding -- Australia -- History. : A survey of Australian typefounders' specimens / by Dennis Bryans  2014 1
Type and type-founding -- Australia -- Specimens. : A survey of Australian typefounders' specimens / by Dennis Bryans  2014 1
Type and type-founding -- Awards. : Best of Graphis. Typography  1993 1
Type and type-founding -- Case studies. : TypoMag / by Laura Meseguer  2010 1
 

Type and type-founding Centaur roman -- See Centaur roman type


  1
Type and type-founding -- Design.   2
Type and type-founding -- Design -- Pictorial works.   2
Type and type-founding -- Digital techniques.   8
 

Type and type-founding Display type -- See Display type


  1
Type and type-founding -- France -- History -- 16th century : The palaeotypography of the French Renaissance : selected papers on sixteenth-century typefaces / Hendrik D.L. Vervliet  2008 1
Type and type-founding -- France -- Specimens : The palaeotypography of the French Renaissance : selected papers on sixteenth-century typefaces / Hendrik D.L. Vervliet  2008 1
 

Type and type-founding Gothic type -- See Gothic type


  1
Type and type-founding -- Great Britain -- History -- 18th century : John Baskerville : art and industry of the Enlightenment / Caroline Archer-ParrĂ© and Malcolm Dick  2017 1
Type and type-founding -- Great Britain -- History -- 19th century : The skilled compositor, 1850-1914 : an aristocrat among working men / Patrick Duffy  2017 1
Type and type-founding -- Great Britain -- History -- 20th century : The skilled compositor, 1850-1914 : an aristocrat among working men / Patrick Duffy  2017 1
Type and type-founding -- Handbooks, manuals, etc   2
Type and type-founding -- Historiography.   2
Type and type-founding -- History.   7
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