BIOMAT Database Logo BIOMAT Database Logo

Mutations in HFE, the hemochromatosis candidate gene, in patients with NIDDM. 1998

D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit

UI MeSH Term Description Entries
D008285 Major Histocompatibility Complex The genetic region which contains the loci of genes which determine the structure of the serologically defined (SD) and lymphocyte-defined (LD) TRANSPLANTATION ANTIGENS, genes which control the structure of the IMMUNE RESPONSE-ASSOCIATED ANTIGENS, HUMAN; the IMMUNE RESPONSE GENES which control the ability of an animal to respond immunologically to antigenic stimuli, and genes which determine the structure and/or level of the first four components of complement. Histocompatibility Complex,Complex, Histocompatibility,Complex, Major Histocompatibility,Complices, Histocompatibility,Complices, Major Histocompatibility,Histocompatibility Complex, Major,Histocompatibility Complices,Histocompatibility Complices, Major,Major Histocompatibility Complices
D008565 Membrane Proteins Proteins which are found in membranes including cellular and intracellular membranes. They consist of two types, peripheral and integral proteins. They include most membrane-associated enzymes, antigenic proteins, transport proteins, and drug, hormone, and lectin receptors. Cell Membrane Protein,Cell Membrane Proteins,Cell Surface Protein,Cell Surface Proteins,Integral Membrane Proteins,Membrane-Associated Protein,Surface Protein,Surface Proteins,Integral Membrane Protein,Membrane Protein,Membrane-Associated Proteins,Membrane Associated Protein,Membrane Associated Proteins,Membrane Protein, Cell,Membrane Protein, Integral,Membrane Proteins, Integral,Protein, Cell Membrane,Protein, Cell Surface,Protein, Integral Membrane,Protein, Membrane,Protein, Membrane-Associated,Protein, Surface,Proteins, Cell Membrane,Proteins, Cell Surface,Proteins, Integral Membrane,Proteins, Membrane,Proteins, Membrane-Associated,Proteins, Surface,Surface Protein, Cell
D012016 Reference Values The range or frequency distribution of a measurement in a population (of organisms, organs or things) that has not been selected for the presence of disease or abnormality. Normal Range,Normal Values,Reference Ranges,Normal Ranges,Normal Value,Range, Normal,Range, Reference,Ranges, Normal,Ranges, Reference,Reference Range,Reference Value,Value, Normal,Value, Reference,Values, Normal,Values, Reference
D003545 Cysteine A thiol-containing non-essential amino acid that is oxidized to form CYSTINE. Cysteine Hydrochloride,Half-Cystine,L-Cysteine,Zinc Cysteinate,Half Cystine,L Cysteine
D003924 Diabetes Mellitus, Type 2 A subclass of DIABETES MELLITUS that is not INSULIN-responsive or dependent (NIDDM). It is characterized initially by INSULIN RESISTANCE and HYPERINSULINEMIA; and eventually by GLUCOSE INTOLERANCE; HYPERGLYCEMIA; and overt diabetes. Type II diabetes mellitus is no longer considered a disease exclusively found in adults. Patients seldom develop KETOSIS but often exhibit OBESITY. Diabetes Mellitus, Adult-Onset,Diabetes Mellitus, Ketosis-Resistant,Diabetes Mellitus, Maturity-Onset,Diabetes Mellitus, Non-Insulin-Dependent,Diabetes Mellitus, Slow-Onset,Diabetes Mellitus, Stable,MODY,Maturity-Onset Diabetes Mellitus,NIDDM,Diabetes Mellitus, Non Insulin Dependent,Diabetes Mellitus, Noninsulin Dependent,Diabetes Mellitus, Noninsulin-Dependent,Diabetes Mellitus, Type II,Maturity-Onset Diabetes,Noninsulin-Dependent Diabetes Mellitus,Type 2 Diabetes,Type 2 Diabetes Mellitus,Adult-Onset Diabetes Mellitus,Diabetes Mellitus, Adult Onset,Diabetes Mellitus, Ketosis Resistant,Diabetes Mellitus, Maturity Onset,Diabetes Mellitus, Slow Onset,Diabetes, Maturity-Onset,Diabetes, Type 2,Ketosis-Resistant Diabetes Mellitus,Maturity Onset Diabetes,Maturity Onset Diabetes Mellitus,Non-Insulin-Dependent Diabetes Mellitus,Noninsulin Dependent Diabetes Mellitus,Slow-Onset Diabetes Mellitus,Stable Diabetes Mellitus
D006432 Hemochromatosis A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed) Diabetes, Bronze,Bronze Diabetes,Bronzed Cirrhosis,Familial Hemochromatosis,Genetic Hemochromatosis,Haemochromatosis,Hemochromatoses,Iron Storage Disorder,Pigmentary Cirrhosis,Primary Hemochromatosis,Troisier-Hanot-Chauffard Syndrome,Von Recklenhausen-Applebaum Disease,Bronzed Cirrhoses,Cirrhoses, Bronzed,Cirrhoses, Pigmentary,Cirrhosis, Bronzed,Cirrhosis, Pigmentary,Disease, Von Recklenhausen-Applebaum,Diseases, Von Recklenhausen-Applebaum,Disorder, Iron Storage,Disorders, Iron Storage,Familial Hemochromatoses,Genetic Hemochromatoses,Haemochromatoses,Hemochromatose,Hemochromatoses, Familial,Hemochromatoses, Genetic,Hemochromatosis, Familial,Hemochromatosis, Genetic,Iron Storage Disorders,Pigmentary Cirrhoses,Recklenhausen-Applebaum Disease, Von,Recklenhausen-Applebaum Diseases, Von,Storage Disorder, Iron,Storage Disorders, Iron,Syndrome, Troisier-Hanot-Chauffard,Syndromes, Troisier-Hanot-Chauffard,Troisier Hanot Chauffard Syndrome,Troisier-Hanot-Chauffard Syndromes,Von Recklenhausen Applebaum Disease,Von Recklenhausen-Applebaum Diseases
D006639 Histidine An essential amino acid that is required for the production of HISTAMINE. Histidine, L-isomer,L-Histidine,Histidine, L isomer,L-isomer Histidine
D006680 HLA Antigens Antigens determined by leukocyte loci found on chromosome 6, the major histocompatibility loci in humans. They are polypeptides or glycoproteins found on most nucleated cells and platelets, determine tissue types for transplantation, and are associated with certain diseases. Human Leukocyte Antigen,Human Leukocyte Antigens,Leukocyte Antigens,HL-A Antigens,Antigen, Human Leukocyte,Antigens, HL-A,Antigens, HLA,Antigens, Human Leukocyte,Antigens, Leukocyte,HL A Antigens,Leukocyte Antigen, Human,Leukocyte Antigens, Human
D006720 Homozygote An individual in which both alleles at a given locus are identical. Homozygotes
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis.
January 2009, Clinics (Sao Paulo, Brazil),
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Hemochromatosis (HFE) gene mutations in Brazilian chronic hemodialysis patients.
September 2005, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Distribution of HFE gene mutations in Slovenian patients with hereditary hemochromatosis.
August 2008, Annals of hematology,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Prevalence of HFE (hemochromatosis) gene mutations in patients with cluster headache.
October 2005, Headache,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Mutations in the hemochromatosis gene (HFE) and stroke.
October 2002, Stroke,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Mutations of the HFE gene among Turkish hereditary hemochromatosis patients.
October 2005, Annals of hematology,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Iron related hemochromatosis (HFE) gene mutations in Friedreich Ataxia patients.
January 2017, Parkinsonism & related disorders,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Multicentric origin of hemochromatosis gene (HFE) mutations.
April 1999, American journal of human genetics,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Prevalence of hemochromatosis gene (HFE) mutations in Greek patients with myelodysplastic syndromes.
January 2003, Acta haematologica,
D Dubois-Laforgue, and S Caillat-Zucman, and I Djilali-Saiah, and E Larger, and A Mercadier, and C Boitard, and J F Bach, and J Timsit
Prevalence of hemochromatosis gene (HFE) mutations in Greece.
January 2003, Acta haematologica,
Copied contents to your clipboard!