- 同
- isolated growth hormone deficiency
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/09/27 10:26:28」(JST)
[Wiki en表示]
This article is about the human gene. For Isolated Growth Hormone Deficiency, see Growth hormone deficiency.
| IGHD |
|
| Available structures |
| PDB |
Human UniProt search: PDBe RCSB |
| List of PDB id codes |
|
1ZVO
|
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| Identifiers |
| Aliases |
IGHD |
| External IDs |
GeneCards: 3495 |
| Gene ontology |
| Molecular function |
• immunoglobulin receptor binding
• antigen binding
|
| Cellular component |
• integral component of membrane
• extracellular region
• plasma membrane
• blood microparticle
• extracellular exosome
• membrane
• external side of plasma membrane
• immunoglobulin complex, circulating
|
| Biological process |
• B cell receptor signaling pathway
• phagocytosis, recognition
• positive regulation of B cell activation
• phagocytosis, engulfment
• innate immune response
• defense response to bacterium
• immune response
• complement activation, classical pathway
|
| Sources:Amigo / QuickGO |
|
| Orthologs |
| Species |
Human |
Mouse |
| Entrez |
|
|
| Ensembl |
|
|
| UniProt |
|
|
| RefSeq (mRNA) |
|
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| RefSeq (protein) |
|
|
| Location (UCSC) |
n/a |
n/a |
| PubMed search |
[1] |
n/a |
| Wikidata |
| View/Edit Human |
|
Ig delta chain C region is a protein that in humans is encoded by the IGHD gene.[2][3]
References
- ^ "Human PubMed Reference:".
- ^ White MB, Shen AL, Word CJ, Tucker PW, Blattner FR (May 1985). "Human immunoglobulin D: genomic sequence of the delta heavy chain". Science. 228 (4700): 733–7. doi:10.1126/science.3922054. PMID 3922054.
- ^ "Entrez Gene: IGHD immunoglobulin heavy constant delta".
Further reading
- Shin SU, Wei CF, Amin AR, et al. (1992). "Structural and functional properties of mouse-human chimeric IgD.". Hum. Antibodies Hybridomas. 3 (2): 65–74. PMID 1633267.
- Roes J, Rajewsky K (1992). "Cell autonomous expression of IgD is not essential for the maturation of conventional B cells.". Int. Immunol. 3 (12): 1367–71. doi:10.1093/intimm/3.12.1367. PMID 1838007.
- Shinoda T, Takahashi N, Takayasu T, et al. (1981). "Complete amino acid sequence of the Fc region of a human delta chain". Proc. Natl. Acad. Sci. U.S.A. 78 (2): 785–9. doi:10.1073/pnas.78.2.785. PMC 319887. PMID 6785754.
- Lin LC, Putnam FW (1981). "Primary structure of the Fc region of human immunoglobulin D: implications for evolutionary origin and biological function". Proc. Natl. Acad. Sci. U.S.A. 78 (1): 504–8. doi:10.1073/pnas.78.1.504. PMC 319082. PMID 6787589.
- Putnam FW, Takahashi N, Tetaert D, et al. (1982). "Amino acid sequence of the first constant region domain and the hinge region of the delta heavy chain of human IgD". Proc. Natl. Acad. Sci. U.S.A. 78 (10): 6168–72. doi:10.1073/pnas.78.10.6168. PMC 348999. PMID 6947220.
- Takayasu T, Takahashi N, Shinoda T (1981). "Amino acid sequence and location of the three glycopeptides in the Fc region of human immunoglobulin D". Biochem. Biophys. Res. Commun. 97 (2): 635–41. doi:10.1016/0006-291X(80)90311-3. PMID 7008791.
- Takayasu T, Suzuki S, Kametani F, et al. (1982). "Amino acid sequence of galactosamine-containing glycopeptides in the hinge region of a human immunoglobulin D". Biochem. Biophys. Res. Commun. 105 (3): 1066–71. doi:10.1016/0006-291X(82)91078-6. PMID 7092891.
- Roes J, Rajewsky K (1993). "Immunoglobulin D (IgD)-deficient mice reveal an auxiliary receptor function for IgD in antigen-mediated recruitment of B cells". J. Exp. Med. 177 (1): 45–55. doi:10.1084/jem.177.1.45. PMC 2190865. PMID 8418208.
- Scott IC, Halila R, Jenkins JM, et al. (1996). "Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)". Gene. 174 (1): 135–43. doi:10.1016/0378-1119(96)00510-0. PMID 8863740.
- Zupo S, Cutrona G, Mangiola M, Ferrarini M (2002). "Role of surface IgM and IgD on survival of the cells from B-cell chronic lymphocytic leukemia". Blood. 99 (6): 2277–8. doi:10.1182/blood-2001-11-0126. PMID 11902141.
- Gala FA, Morrison SL (2002). "The role of constant region carbohydrate in the assembly and secretion of human IgD and IgA1". J. Biol. Chem. 277 (32): 29005–11. doi:10.1074/jbc.M203258200. PMID 12023968.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Schamel WW, Kuppig S, Becker B, et al. (2003). "A high-molecular-weight complex of membrane proteins BAP29/BAP31 is involved in the retention of membrane-bound IgD in the endoplasmic reticulum". Proc. Natl. Acad. Sci. U.S.A. 100 (17): 9861–6. doi:10.1073/pnas.1633363100. PMC 187866. PMID 12886015.
- Liu T, Qian WJ, Gritsenko MA, et al. (2006). "Human Plasma N-Glycoproteome Analysis by Immunoaffinity Subtraction, Hydrazide Chemistry, and Mass Spectrometry". J. Proteome Res. 4 (6): 2070–80. doi:10.1021/pr0502065. PMC 1850943. PMID 16335952.
- Lee CE, Gaëta B, Malming HR, et al. (2006). "Reconsidering the human immunoglobulin heavy-chain locus: 1. An evaluation of the expressed human IGHD gene repertoire". Immunogenetics. 57 (12): 917–25. doi:10.1007/s00251-005-0062-5. PMID 16402215.
- Lee CE, Jackson KJ, Sewell WA, Collins AM (2007). "Use of IGHJ and IGHD gene mutations in analysis of immunoglobulin sequences for the prognosis of chronic lymphocytic leukemia". Leuk. Res. 31 (9): 1247–52. doi:10.1016/j.leukres.2006.10.013. PMID 17169423.
- Samuelsson M, Hallström T, Forsgren A, Riesbeck K (2007). "Characterization of the IgD binding site of encapsulated Haemophilus influenzae serotype b". J. Immunol. 178 (10): 6316–9. doi:10.4049/jimmunol.178.10.6316. PMID 17475860.
English Journal
- Pituitary height at magnetic resonance imaging in pediatric isolated growth hormone deficiency.
- Dumrongpisutikul N1, Chuajak A2,3, Lerdlum S2.
- Pediatric radiology.Pediatr Radiol.2018 May;48(5):694-700. doi: 10.1007/s00247-018-4070-7. Epub 2018 Mar 6.
- PMID 29508041
- Prospective Follow-up of Children with Idiopathic Growth Hormone Deficiency After Termination of Gh Treatment: Is There Really Need for Treatment at Transition to Adulthood?
- Çamtosun E1, Şıklar Z1, Berberoğlu M1.
- Journal of clinical research in pediatric endocrinology.J Clin Res Pediatr Endocrinol.2018 Mar 19. doi: 10.4274/jcrpe.0010. [Epub ahead of print]
- PMID 29553045
- Effects of Therapy With Semi-occluded Vocal Tract and Choir Training on Voice in Adult Individuals With Congenital, Isolated, Untreated Growth Hormone Deficiency.
- de Andrade BMR1, Valença EHO1, Salvatori R2, Souza AHO3, Oliveira-Neto LA4, Oliveira AHA4, Oliveira MCP5, Melo EV6, Andrade MS1, Freitas CA1, Santos MP1, Custodio FA1, Monteiro GC1, de Carvalho S1, Aguiar-Oliveira MH7.
- Journal of voice : official journal of the Voice Foundation.J Voice.2018 Mar 19. pii: S0892-1997(18)30006-7. doi: 10.1016/j.jvoice.2018.02.018. [Epub ahead of print]
- PMID 29567051
Japanese Journal
- A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes
- A novel mutation in <i>HESX1</i> causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes
- 良好な成長率を維持している抗GH抗体陰性の成長ホルモン単独欠損症1A型(IGHD 1A)の1例 (内分泌クリニカル・カンファランス 51) -- (間脳・下垂体)
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