Create issue ticket

10 Possible Causes for 3, A,, alpha like, meprin

Show results in: Română

  • Meprobamate

    MSDS: D213000.pdf Product Rating Keywords: Buy 1471-56-3 Purchase 1471-56-3 Order 1471-56-3 1471-56-3 supplier 1471-56-3 manufacturer 1471-56-3 distributor 1471-56-3 cost[trc-canada.com] Gene Name GABRA2 Uniprot ID P47869 Uniprot Name Gamma-aminobutyric acid receptor subunit alpha-2 Molecular Weight 51325.85 Da References Rho JM, Donevan SD, Rogawski MA: Barbiturate-like[drugbank.ca] Kessobamate; Klort; Larten; Lepenil; Lepetown; Letyl; Libiolan; Madiol; Mar-Bate; Margonil; Mendel; Mepamtin; Mepantin; Mepavlon; Mepiosine; Meposed; Mepranil; Mepriam; Meprin[druglib.com] Diron; Ecuanil; Equanil; Equinil; Fas-Cile 200; Gadexyl; Harmonin; Hartol; Holbamate; Kesso-Bamate; Klort; Larten; Lepetown; Libiolan; Mar-Bate; Mepantin; Mepavlon; Meposed; Meprin[webbook.nist.gov]

    Missing: A
  • Sulindac

    […] and (3) sulindac/inulin/VSL#3 was performed on 17 patients with FAP in a single center intervention study.[ncbi.nlm.nih.gov] Product description What it looks like Aclin - orange-yellow tablet marked "SD/100" on one side and a Greek alpha symbol on the reverse.[news-medical.net] Preferential binding and internalization of these drugs into colon cancer cells was obtained using a targeting strategy against the protein meprin A, which we demonstrate[ncbi.nlm.nih.gov] Epub 2017 Mar 3.[ncbi.nlm.nih.gov]

    Missing: A
  • Mulibrey Nanism Syndrome

    Discussion 3-M dwarfism is a clinical entity which is not often recognized in childhood. Here, we describe a patient with 3-M syndrome associated with GHD.[ijponline.biomedcentral.com] […] growth factor I, resistance to; 270450; IGF1R Interleukin 1 receptor antagonist deficiency; 612852; IL1RN Interleukin-2 receptor, alpha chain, deficiency of; 606367; IL2RA[howlingpixel.com] This entry represents the MATH (meprin and TRAF homology) domain found in TRIM37, which is a member of the tripartite motif (RING, B-Box, and coiled-coil domains) family and[ebi.ac.uk] Retrieved 2009-05-07 . 1 2 3 OMIM (1966-2009). Mulibrey nanism. NCBI (Johns Hopkins University).[ipfs.io]

    Missing: A
  • Chromosome 6 Ring Syndrome

    Of 100 peripheral lymphocyte metaphases analyzed, chromosome 6 was replaced in 73% by a monocentric ring chromosome, in 10% by a dicentric, in 1% by a tricentric, and 3% by[ncbi.nlm.nih.gov] like 6q22.31 gap junction protein alpha 1 6q15-q16 gap junction protein, alpha 10, 62kDa 6p21.3-p21.1 glyoxalase I 6p21.3-p21.1 glyoxalase I 6p21.2 glucagon like peptide[okdb.appliedbioinfo.net] Her course was one of extreme marasmus, with death at 3 months of age. She presented the classical features of the syndrome and chromosome mosaicism 46, XX/47, XX, r(?).[unboundmedicine.com] Chromosome analysis was performed by GTG banding of peripheral blood and the karyotype was 46,XX,r(13)(p13q34)[97]/46,XX,dic r(13;13)(p13q34;p13q34) [3].[sciencedomain.org]

    Missing: A
  • Glucomannan

    ENZYME class: 3 Release of 16-Jan-19 Hydrolases All UniProtKB/Swiss-Prot entries corresponding to class 3.-.-.- .[enzyme.expasy.org] We suggest that this metabolic alteration may derive from a primary decrease of alpha-lipoprotein, most likely because of an inadequate water intake.[ncbi.nlm.nih.gov] Karting Toll-like receptors as key mediators in innate antifungal immunity Med Mycol, 42 (2004), pp. 485-498 [55] S. Roy, R. Dickerson, S. Khanna, E. Collard, U.[elsevier.es] NaNO 3 with 200 ppm aq. NaN 3 .[academic.oup.com]

    Missing: A
  • Immunodeficiency due to Ficolin 3 Deficiency

    Symptoms of Immunodeficiency due to ficolin 3 deficiency Clinical features : Imported from Human Phenotype Ontology (HPO) Abnormality of the immune system Immunodeficiency[familydiagnosis.com] Fibrinogen-like, C-terminal Gene Ontology ( GO ) Pathways (from Reactome ) Phenotype (from MGI , Zfin or HPO ) HP:0000007 Autosomal recessive inheritance "A mode of inheritance[manteia.igbmc.fr] .; MBio. 2 , e00276-11 (2011), Abstract ; Enhanced activity of meprin-О , a pro-migratory and pro-angiogenic protease, in colorectal cancer : D.[enzolifesciences.com] Ficolin-3, also known as H-ficolin, can activate the lectin pathway of the complement system; deficiency may thus lead to defects in the complement system (summary by {3:Munthe-Fog[diseaseinfosearch.org]

    Missing: A
  • Ring Chromosome 18

    The peripheral blood lymphocytes revealed a karyotype of 46,XY,r(18)[81]/45,XY,-18[3]/46,XY,idic r(18)[3]/46,XY[13].[ncbi.nlm.nih.gov] […] protein 4 (H-l(3)mbt-like protein 4) (L(3)mbt-like protein 4) (L3mbt-like 4) LAMA1 18p11.3 P25391 LAMA1_HUMAN 150320 Laminin subunit alpha-1 precursor (Laminin A chain) ([uniprot.org] Yao H 1 , Yang C 2 , Huang X 1 , Yang L 1 , Zhao W 3, 2 , Yin D 3, 2 , Qin Y 1 , Mu F 3, 2 , Liu L 3, 2 , Tian P 1 , Liu Z 1 , Yang Y 4, 5, 6 .[ncbi.nlm.nih.gov] In 3 patients, additional duplications in 18p (of 1.4 Mb, 2 Mb, and 5.8 Mb) were detected.[ncbi.nlm.nih.gov]

    Missing: A
  • Adenocarcinoma of the Ovary

    To clarify the significance of glypican-3 expression in ovarian clear cell adenocarcinoma, we evaluated glypican-3 expression by immunohistochemistry in nonneoplastic and[ncbi.nlm.nih.gov] However, like sex cord tumors, they can cause ovarian torsion or hemorrhage and, in children, isosexual precocious puberty.[en.wikipedia.org] Low meprin alpha expression differentiates primary ovarian mucinous carcinoma from gastrointestinal cancers that commonly metastasise to the ovaries .[nature.com] 2-3 weeks.[ncbi.nlm.nih.gov]

    Missing: A
  • Fatal Infantile Cytochrome C Oxidase Deficiency

    K18189] FASTKD2; FAST kinase domain-containing protein 2 [kegg:K18190] COX1; cytochrome c oxidase subunit 1 [EC:1.9.3.1] [kegg:K02256] COX3; cytochrome c oxidase subunit 3[bio2rdf.org] […] stemming from quiescence of the disease, at which time lactate is likely not present. 6 Cerebral dysgenesis can be seen, especially in PDH deficiency, with E1 alpha subunit[dovepress.com] […] mitochondriell); MEKK1 (MAP/ERK Kinase Kinase 1); MEKK3 (MAP/ERK Kinase Kinase 3); MEMO1 (Methylierungs-Modifizierer für Klasse I HLA); MEN1 (Multiple endokrine Neoplasie I); MEP1A (Meprin[google.com] Gather your clinical history that helps us during interpretation 3 Post results counseling Ounce your test results are released you will have a free session with our expert[dnalabsuae.com]

    Missing: A
  • X-Linked Partial Corpus callosum Dysgenesis

    RINNOVABILE DOPO 5 ANNI) LYME, MALATTIA DI RA0030 CODICE MALATTIA WHIPPLE, MALATTIA DI RA0020 CODICE MALATTIA RA0010 HANSEN, MALATTIA DI ESEMPI DI MALATTIE AFFERENTI AL GRUPPO 3.[dochero.tips] Qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan Qualitative or quantitative defects of sarcoglycan Qualitative or quantitative[se-atlas.de] […] mitochondriell); MEKK1 (MAP/ERK Kinase Kinase 1); MEKK3 (MAP/ERK Kinase Kinase 3); MEMO1 (Methylierungs-Modifizierer für Klasse I HLA); MEN1 (Multiple endokrine Neoplasie I); MEP1A (Meprin[google.com] Neurodev Disord 2011; 3: 3-27. In article CrossRef PubMed [2] Shenoy C. “Shapiro syndrome". QJM. 2008; 101 (1): 61-2.[pubs.sciepub.com]

    Missing: A