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ABCG8

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

    cassette sub-family G member 8 is a protein that in humans is encoded by the ABCG8 gene. The protein encoded by this gene is a member of the superfamily of

    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

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

    arrayed on chromosome 2, in a head-to-head orientation with family member ABCG8. Mutations in this gene may contribute to sterol accumulation and atherosclerosis

    ABCG5

    ABCG5

    ABCG5

  • Sitosterolemia
  • Genetically-inherited lipid metabolic disorder

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

    Sitosterolemia

    Sitosterolemia

    Sitosterolemia

  • Chromosome 2
  • Human chromosome

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

    Chromosome 2

    Chromosome 2

    Chromosome_2

  • Stanol ester
  • Class of chemical compounds

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

    Stanol ester

    Stanol ester

    Stanol_ester

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

    Reverse cholesterol transport

    Reverse_cholesterol_transport

  • Familial hypercholesterolemia
  • Genetic disorder characterized by high cholesterol levels

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

    Familial hypercholesterolemia

    Familial hypercholesterolemia

    Familial_hypercholesterolemia

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

    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

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

    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 GF, Kim

    ATP-binding domain of ABC transporters

    ATP-binding domain of ABC transporters

    ATP-binding_domain_of_ABC_transporters

  • Hereditary stomatocytosis
  • Medical condition

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

    Hereditary stomatocytosis

    Hereditary stomatocytosis

    Hereditary_stomatocytosis

  • List of human protein-coding genes 1
  • HGNC:74; Q9UNQ0 73 ABCG4 HGNC:13884; Q9H172 74 ABCG5 HGNC:13886; Q9H222 75 ABCG8 HGNC:13887; Q9H221 76 ABHD1 HGNC:17553; Q96SE0 77 ABHD2 HGNC:18717; P08910

    List of human protein-coding genes 1

    List_of_human_protein-coding_genes_1

  • Andre Franke
  • German geneticist

    association analysis in an ethnically different population, rs11887534 (ABCG8-D19H) was identified as a disease-relevant factor. In 2020, during the first

    Andre Franke

    Andre Franke

    Andre_Franke

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

    ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8". J. Hum. Genet. 47 (6): 285–310. doi:10.1007/s100380200041. PMID 12111378

    ABCD4

    ABCD4

    ABCD4

  • 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 2007;39:995-999

    Study of Health in Pomerania

    Study_of_Health_in_Pomerania

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

    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
  • CTSA Gallbladder disease 1; 600803; ABCB4 Gallbladder disease 4; 611465; ABCG8 GAMT deficiency; 612736; GAMT Gastric cancer, familial diffuse; 137215;

    List of OMIM disorder codes

    List_of_OMIM_disorder_codes

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Online names & meanings

  • Keerath
  • Boy/Male

    Indian

    Keerath

    Sing gods praise or glory, Lord Shiva

  • Eha
  • Girl/Female

    Indian

    Eha

    Desirous

  • Madan
  • Girl/Female

    Indian, Punjabi, Sikh, Telugu

    Madan

    Battlefield; Lord Shri Krishna

  • Poorvi | பூர்வீ
  • Girl/Female

    Tamil

    Poorvi | பூர்வீ

    A classical melody, From the east

  • Durgesh
  • Girl/Female

    Gujarati, Hindu, Indian, Mythological, Rajasthani, Tamil

    Durgesh

    Goddess Durga

  • Hindson
  • Surname or Lastname

    English

    Hindson

    English : patronymic from Hind.

  • Kelvy
  • Girl/Female

    Hindu

    Kelvy

    Education

  • Eyanosa
  • Boy/Male

    Native American

    Eyanosa

    big both ways.

  • Devasena
  • Boy/Male

    Indian, Sanskrit

    Devasena

    With an Army of the Gods

  • Jyothiranjan
  • Boy/Male

    Hindu

    Jyothiranjan

    Happy, Joyous, Flame

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ABCG8

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