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Hex A -- See Hexosaminidase A


A mammalian beta-hexosaminidase isoform that is a heteromeric protein comprized of both hexosaminidase alpha and hexosaminidase beta subunits. Deficiency of hexosaminidase A due to mutations in the gene encoding the hexosaminidase alpha subunit is a case of TAY-SACHS DISEASE. Deficiency of hexosaminidase A and HEXOSAMINIDASE B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE 		  1
 

HexA Deficiency -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry 		  1
Hexachlorobenzene -- Environmental aspects. : Sixty Thousand Barrels / Director: Castle, Jane  2002 1
Hexachlorobenzene -- Toxicology. : 7.30: 28/07/14  2014 1
Hexachloroethane -- Toxicology   6
HEXACO Personality Inventory : Measuring the next President's personality using an expert raters method / Beth A. Visser, Angela Book, Anthony Volk  2018 1
Hexactinellida. : Zoology. Volume XXI  1887 1
 

Hexadienoic acid -- See Sorbic acid


  1
Hexagons.   2
 

Hexahydrobenzene -- See Cyclohexane


  1
 

Hexahydrothymol -- See Menthol


  1
Hexameter.   5
 

Hexamethylene -- See Cyclohexane


  1
 

Hexamethylenebischlorophenylbiguanide -- See Chlorhexidine


  1
 

Hexamitidae -- See Also the narrower term Giardia


  1
 

Hexanaphthene -- See Cyclohexane


  1
 

Hexane -- See Also the narrower term Ketamine


  1
 

Hexane hexol -- See Mannitol


  1
 

Hexanehexol -- See Mannitol


  1
Hexapla. : Christianity and the transformation of the book : Origen, Eusebius, and the Library of Caesarea / Anthony Grafton, Megan Williams  2008 1
 

Hexapoda -- See Insects


  1
 

Hexaprotodon -- See Also the narrower term Pygmy hippopotamus


  1
 

Hexaprotodon liberiensis -- See Pygmy hippopotamus


  1
 

Hexateuch -- See Bible. Hexateuch


  1
Hexe   9
Hexe Motiv   4
Hexenglaube   19
Hexenprozess   3
Hexenverfolgung   10
Hexenverfolgung Eichstätt (Bistum) Sozialgeschichte 1590-1630 : Witchcraft, gender, and society in early modern Germany / by Jonathan B. Durrant  2007 1
Hexenverfolgung -- Geschlechterrolle -- Deutschland -- Eichstätt (Bistum) -- Geschichte -- 1590-1630. : Witchcraft, gender, and society in early modern Germany / by Jonathan B. Durrant  2007 1
Hexerei   16
Hexham National parks and reserves Australia Victoria Management : Ridge Paddock addition to the Cobra Killuc Wildlife Reserve management statement  2005 1
 

Hexiao, 1792-1871 -- See Herschel, John F. W. (John Frederick William), 1792-1871


  1
 

Hexogen -- See RDX (Cyclonite)


  1
 

Hexokinase -- See Glucokinase


  1
Hexokinase : Glucokinase and glycemic disease : from basics to novel therapeutics / volume editors, F.M. Matschinsky, M.A. Magnuson  2004 1
 

Hexokinase D -- See Glucokinase


  1
 

Hexokinase type IV -- See Glucokinase


  1
 

Hexosamines -- See Also the narrower term Glucosamine


  1
 

Hexosaminidase -- See Hexosaminidases


Enzymes that catalyze the hydrolysis of N-acylhexosamine residues in N-acylhexosamides. Hexosaminidases also act on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES 		  1
 

Hexosaminidase A -- See Also Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry 		  1
 

Hexosaminidase A Deficiency -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry 		  1
 

Hexosaminidase A Deficiency Disease -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry 		  1
 

Hexosaminidase A deficiency (Tay-Sachs) -- See Tay-Sachs disease


  1
 

Hexosaminidase alpha-Subunit Deficiency (Variant B) -- See Tay-Sachs Disease


An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry 		  1
 

Hexose phosphates -- See Also the narrower term Inositol phosphates


  1
Hexoses : Nanomaterials in glucose sensing / Krishna Burugapalli, Ning Wang, Jakub Trzebinski, Wenhui Song, Anthony Cass  2014 1
 

Hexter, Jack H., 1910-1996 -- See Hexter, J. H. (Jack H.), 1910-1996


  1
Hexter, Maurice Beck, 1891-1990. : Economic theory by Taussig, Young, and Carver at Harvard / edited by Marianne Johnson, Warren J. Samuels  2010 1
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