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ABCG5

  • ABCG5
  • Protein-coding gene in the species Homo sapiens

    cassette sub-family G member 5 is a protein that in humans is encoded by the ABCG5 gene. The protein encoded by this gene is a member of the superfamily of

    ABCG5

    ABCG5

    ABCG5

  • ABCG8
  • Protein-coding gene in the species Homo sapiens

    arrayed on chromosome 2, in a head-to-head orientation with family member ABCG5. Mutations in this gene may contribute to sterol accumulation and atherosclerosis

    ABCG8

    ABCG8

    ABCG8

  • Sterolin
  • Family of protein complexes

    ABCG5 and ABCG8 genes encode for two proteins sterolin-1 and -2, respectively. Sterolin-1 and –2 are two ‘half’ adenosine triphosphate binding (ATP) cassette

    Sterolin

    Sterolin

  • Chromosome 2
  • Human chromosome

    family member 3 AFTPH: encoding protein Aftiphilin ALMS1: Alstrom syndrome 1 ABCG5 and ABCG8: ATP-binding cassette, subfamily A, members 5 and 8 ASXL2: Additional

    Chromosome 2

    Chromosome 2

    Chromosome_2

  • Sitosterolemia
  • Genetically-inherited lipid metabolic disorder

    cholesterol, so most plant sterols remain in the cell. In a healthy subject, the ABCG5/ABCG8 sterol efflux transporter pumps any unesterified sterols back into

    Sitosterolemia

    Sitosterolemia

    Sitosterolemia

  • Phytosterol
  • Class of steroids derived from plants

    diffusively, and because they are poorly assimilated, they are excreted by ABCG5/G8 and/or back-diffused, repeating this shuttle between the lumen and the

    Phytosterol

    Phytosterol

    Phytosterol

  • Reverse cholesterol transport
  • non-ABCA1-mediated CEC. Fibrates activate PPAR-α, which as a result upregulates ABCA1, ABCG5, and ABCG8. Not all of them have shown expected improvements when combined

    Reverse cholesterol transport

    Reverse_cholesterol_transport

  • Stanol ester
  • Class of chemical compounds

    independent risk factor for coronary heart disease (CHD). Two ABC transporters (ABCG5 and ABCG8) play an important role in the regulating the intestinal absorption

    Stanol ester

    Stanol ester

    Stanol_ester

  • Study of Health in Pomerania
  • Population based epidemiological study

    genome-wide association scan identifies the hepatic cholesterol transporter ABCG5/ABCG8 as a susceptibility factor for human gallstone disease. Nat Genetics

    Study of Health in Pomerania

    Study_of_Health_in_Pomerania

  • Familial hypercholesterolemia
  • Genetic disorder characterized by high cholesterol levels

    with FH and also features cholesterol accumulation in tissues, is due to ABCG5 and ABCG8 mutations. The LDL receptor gene is located on the short arm of

    Familial hypercholesterolemia

    Familial hypercholesterolemia

    Familial_hypercholesterolemia

  • ABCA8
  • Protein-coding gene in the species Homo sapiens

    ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8". Journal of Human Genetics. 47 (6): 285–310. doi:10.1007/s100380200041

    ABCA8

    ABCA8

    ABCA8

  • Hereditary stomatocytosis
  • Medical condition

    stomatocytosis, a disorder of lipid metabolism associated with mutations in ABCG5 and/or ABCG8, which encode sterol transporters. The resulting abnormal sterol

    Hereditary stomatocytosis

    Hereditary stomatocytosis

    Hereditary_stomatocytosis

  • ATP-binding domain of ABC transporters
  • Water-soluble domain of transmembrane ABC transporters

    ABCD1; ABCD2; ABCD3; ABCD4; ABCE1; ABCF1; ABCF2; ABCF3; ABCG1; ABCG2; ABCG4; ABCG5; ABCG8; CFTR; TAP1; TAP2; TAPL; Hung LW, Wang IX, Nikaido K, Liu PQ, Ames

    ATP-binding domain of ABC transporters

    ATP-binding domain of ABC transporters

    ATP-binding_domain_of_ABC_transporters

  • List of human protein-coding genes 1
  • HGNC:73; P45844 72 ABCG2 HGNC:74; Q9UNQ0 73 ABCG4 HGNC:13884; Q9H172 74 ABCG5 HGNC:13886; Q9H222 75 ABCG8 HGNC:13887; Q9H221 76 ABHD1 HGNC:17553; Q96SE0

    List of human protein-coding genes 1

    List_of_human_protein-coding_genes_1

  • Andre Franke
  • German geneticist

    of the likely causative variant for cholesterol gallstone disease at the ABCG5/8 lithogenic locus". Hepatology. 57 (6): 2407–2417. doi:10.1002/hep.26009

    Andre Franke

    Andre Franke

    Andre_Franke

  • ABCD4
  • Protein-coding gene in the species Homo sapiens

    ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8". J. Hum. Genet. 47 (6): 285–310. doi:10.1007/s100380200041.

    ABCD4

    ABCD4

    ABCD4

  • ABCA7
  • Protein-coding gene in the species Homo sapiens

    ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8". Journal of Human Genetics. 47 (6): 285–310. doi:10.1007/s100380200041

    ABCA7

    ABCA7

    ABCA7

  • List of OMIM disorder codes
  • Simpson-Golabi-Behmel syndrome, type 2; 300209; OFD1 Sitosterolemia; 210250; ABCG5 Sitosterolemia; 210250; ABCG8 Sjögren–Larsson syndrome; 270200; ALDH3A2

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

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ABCG5

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Online names & meanings

  • Feilding
  • Boy/Male

    British, English

    Feilding

    From the Field

  • Azar
  • Girl/Female

    Indian

    Azar

    Fire, th month of iranian calendar

  • CHIENG
  • Male

    African

    CHIENG

    God of day; God of the sun.

  • Becher
  • Boy/Male

    Hebrew

    Becher

    First born.

  • Gilles
  • Boy/Male

    Australian, Dutch, French, German, Greek, Irish, Latin, Netherlands, Swiss

    Gilles

    Shield Bearer; Kid; Young Goat; Small Goat; Servant of Jesus

  • Rajendar | ராஜேந்தர 
  • Boy/Male

    Tamil

    Rajendar | ராஜேந்தர 

    Lord of kings, Emperor

  • Himnish | ஹிமநிஷ 
  • Boy/Male

    Tamil

    Himnish | ஹிமநிஷ 

    Lord Shiva

  • Saheed
  • Boy/Male

    Arabic, Muslim

    Saheed

    Lucky; Blissful

  • Laurynn
  • Girl/Female

    British, English, Latin

    Laurynn

    Variant Form of Laura; Laurel

  • Bahhas |
  • Boy/Male

    Muslim

    Bahhas |

    Examiner

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ABCG5

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