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  2. GLUT1 deficiency - Wikipedia

    en.wikipedia.org/wiki/GLUT1_deficiency

    GLUT1 deficiency syndrome, also known as GLUT1-DS, De Vivo disease or Glucose transporter type 1 deficiency syndrome, is an autosomal dominant genetic metabolic disorder associated with a deficiency of GLUT1, the protein that transports glucose across the blood brain barrier. [1] Glucose Transporter Type 1 Deficiency Syndrome has an estimated ...

  3. Glutaric aciduria type 1 - Wikipedia

    en.wikipedia.org/wiki/Glutaric_aciduria_type_1

    Glutaric acidemia type 1 (GA1) is an inherited disorder in which the body is unable to completely break down the amino acids lysine, hydroxylysine and tryptophan.Excessive levels of their intermediate breakdown products (glutaric acid, glutaryl-CoA, 3-hydroxyglutaric acid, glutaconic acid) can accumulate and cause damage to the brain (and also other organs [1]), but particularly the basal ...

  4. GLUT1 - Wikipedia

    en.wikipedia.org/wiki/GLUT1

    n/a Ensembl n/a n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) n/a n/a PubMed search n/a n/a Wikidata View/Edit Human Glucose transporter 1 (or GLUT1), also known as solute carrier family 2, facilitated glucose transporter member 1 (SLC2A1), is a uniporter protein that in humans is encoded by the SLC2A1 gene. GLUT1 facilitates the transport of glucose across ...

  5. As US life expectancy lags, nutritional deficiency is often ...

    www.aol.com/us-life-expectancy-lags-nutritional...

    Nutritional deficiency is far from a leading cause of death in the United States, but the mortality rate has grown significantly enough in recent years to impact life expectancy.

  6. Glucose transporter - Wikipedia

    en.wikipedia.org/wiki/Glucose_transporter

    Because glucose is a vital source of energy for all life, ... Km = 6.2 [1] intermediate-affinity glucose transporter [3] Hxt5: Km = 10 mM [4] ... GLUT1 deficiency ...

  7. Congenital disorder of glycosylation - Wikipedia

    en.wikipedia.org/wiki/Congenital_disorder_of...

    mannosyltransferase VIII deficiency causes ALG12-CDG (CDG-Ig) [21] glucosyltransferase I deficiency causes ALG6-CDG (CDG-Ic) [22] glucosyltransferase II deficiency causes ALG8-CDG (CDG-Ih). [23] Glc3Man9GlcNAc2-PP-Dol A protein with hitherto unknown activity, MPDU-1, is required for the efficient presentation of Dol-P-Man and Dol-P-Glc.

  8. Hurler syndrome - Wikipedia

    en.wikipedia.org/wiki/Hurler_syndrome

    A British study from 2008 found a median estimated life expectancy of 8.7 years for patients with Hurler syndrome. In comparison, the median life expectancy for all forms of MPS type I was 11.6 years. Patients who received successful bone marrow transplants had a 2-year survival rate of 68% and a 10-year survival rate of 64%. Patients who did ...

  9. Global wine glut compounds headaches for struggling ... - AOL

    www.aol.com/news/global-wine-glut-compounds...

    Global wine glut compounds headaches for struggling California vineyards. Louis Sahagún. April 1, 2024 at 3:00 AM.