Crossref journal-article
Springer Science and Business Media LLC
Nature Genetics (297)
Bibliography

Guris, D. L., Fantes, J., Tara, D., Druker, B. J., & Imamoto, A. (2001). Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome. Nature Genetics, 27(3), 293–298.

Authors 5
  1. Deborah L. Guris (first)
  2. Judith Fantes (additional)
  3. David Tara (additional)
  4. Brian J. Druker (additional)
  5. Akira Imamoto (additional)
References 30 Referenced 243
  1. Emanuel, B.S., Burdarf, M.L. & Scambler, P.J. in Heart Development (eds. Harvey, R.P. & Rosenthal, N.) 463–478 (Academic, San Diego, 1999). (10.1016/B978-012329860-7/50028-3) / Heart Development by BS Emanuel (1999)
  2. Dunham, I. et al. The DNA sequence of human chromosome 22. Nature 402, 489–495 (1999). (10.1038/990031) / Nature by I Dunham (1999)
  3. ten Hoeve, J., Morris, C., Heisterkamp, N. & Groffen, J. Isolation and chromosomal localization of CRKL, a human crk-like gene. Oncogene 8, 2469–2474 (1993). / Oncogene by J ten Hoeve (1993)
  4. La Bonne, C. & Bronner-Fraser, M. Induction and patterning of the neural crest, a stem cell-like precursor population. J. Neurobiol. 36, 175–189 (1998). (10.1002/(SICI)1097-4695(199808)36:2<175::AID-NEU6>3.0.CO;2-Z) / J. Neurobiol. by C La Bonne (1998)
  5. Feller, S.M. et al. Physiological signals and oncogenesis mediated through Crk family adapter proteins. J. Cell. Physiol. 177, 535–552 (1998). (10.1002/(SICI)1097-4652(199812)177:4<535::AID-JCP5>3.0.CO;2-E) / J. Cell. Physiol. by SM Feller (1998)
  6. Sattler, M. & Salgia, R. Role of the adapter protein CRKL in signal transduction of normal hematopoietic and BCR/ABL-transformed cells. Leukemia 12, 637–644 (1998). (10.1038/sj.leu.2401010) / Leukemia by M Sattler (1998)
  7. D'Amico-Martel, A. & Noden, D.M. Contributions of placodal and neural crest cells to avian cranial peripheral ganglia. Am. J. Anat. 166, 445–468 (1983). (10.1002/aja.1001660406) / Am. J. Anat. by A D'Amico-Martel (1983)
  8. Le Douarin, N.M. & Smith, J. Development of the peripheral nervous system from the neural crest. Annu. Rev. Cell Dev. Biol. 4, 375–404 (1988). (10.1146/annurev.cb.04.110188.002111) / Annu. Rev. Cell Dev. Biol. by NM Le Douarin (1988)
  9. Shah, N.M., Marchionni, M.A., Isaacs, I., Stroobant, P. & Anderson, D.J. Glial growth factor restricts mammalian neural crest stem cells to a glial fate. Cell 77, 349–360 (1994). (10.1016/0092-8674(94)90150-3) / Cell by NM Shah (1994)
  10. Dong, Z. et al. Neu differentiation factor is a neuron-glia signal and regulates survival, proliferation, and maturation of rat Schwann cell precursors. Neuron 15, 585–596 (1995). (10.1016/0896-6273(95)90147-7) / Neuron by Z Dong (1995)
  11. Stemple, D.L. & Anderson, D.J. Isolation of a stem cell for neurons and glia from the mammalian neural crest. Cell 71, 973–985 (1992). (10.1016/0092-8674(92)90393-Q) / Cell by DL Stemple (1992)
  12. Waldo, K.L., Kumiski, D. & Kirby, M.L. Cardiac neural crest is essential for the persistence rather than the formation of an arch artery. Dev. Dyn. 205, 281–292 (1996). (10.1002/(SICI)1097-0177(199603)205:3<281::AID-AJA8>3.0.CO;2-E) / Dev. Dyn. by KL Waldo (1996)
  13. Kirby, M.L. in Heart Development (eds. Harvey, R.P. & Rosenthal, N.) 179–193 (Academic, San Diego, 1999). (10.1016/B978-012329860-7/50013-1) / Heart Development by ML Kirby (1999)
  14. Conway, S.J., Henderson, D.J. & Copp, A.J. Pax3 is required for cardiac neural crest migration in the mouse: evidence from the splotch (Sp2H) mutant. Development 124, 505–514 (1997). (10.1242/dev.124.2.505) / Development by SJ Conway (1997)
  15. Edelmann, L. et al. A common molecular basis for rearrangement disorders on chromosome 22q11. Hum. Mol. Genet. 8, 1157–1167 (1999). (10.1093/hmg/8.7.1157) / Hum. Mol. Genet. by L Edelmann (1999)
  16. Shaikh, T.H. et al. Chromosome 22-specific low copy repeats and the 22q11.2 deletion syndrome: genomic organization and deletion endpoint analysis. Hum. Mol. Genet. 9, 489–501 (2000). (10.1093/hmg/9.4.489) / Hum. Mol. Genet. by TH Shaikh (2000)
  17. McDonald-McGinn, D.M. et al. Detection of a 22q11.2 deletion in cardiac patients suggests a risk for velopharyngeal incompetence. Pediatrics 99, E9 (1997). (10.1542/peds.99.5.e9) / Pediatrics by DM McDonald-McGinn (1997)
  18. Eicher, P.S. et al. Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow. J. Pediatr. 137, 158–164 (2000). (10.1067/mpd.2000.105356) / J. Pediatr. by PS Eicher (2000)
  19. Kimber, W.L. et al. Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse. Hum. Mol. Genet. 8, 2229–2237 (1999). (10.1093/hmg/8.12.2229) / Hum. Mol. Genet. by WL Kimber (1999)
  20. Lindsay, E.A. et al. Congenital heart disease in mice deficient for the DiGeorge syndrome region. Nature 401, 379–383 (1999). / Nature by EA Lindsay (1999)
  21. Gripp, K.W., Zackai, E.H. & Stolle, C.A. Mutations in the human TWIST gene. Hum. Mutat. 15, 150–155 (2000). (10.1002/(SICI)1098-1004(200002)15:2<150::AID-HUMU3>3.0.CO;2-D) / Hum. Mutat. by KW Gripp (2000)
  22. Chen, Z.F. & Behringer, R.R. twist is required in head mesenchyme for cranial neural tube morphogenesis. Genes Dev. 9, 686–699 (1995). (10.1101/gad.9.6.686) / Genes Dev. by ZF Chen (1995)
  23. Van Esch, H. et al. GATA3 haplo-insufficiency causes human HDR syndrome. Nature 406, 419–422 (2000). (10.1038/35019088) / Nature by H Van Esch (2000)
  24. Kurahashi, H. et al. Another critical region for deletion of 22q11: a study of 100 patients. Am. J. Med. Genet. 72, 180–185 (1997). (10.1002/(SICI)1096-8628(19971017)72:2<180::AID-AJMG10>3.0.CO;2-J) / Am. J. Med. Genet. by H Kurahashi (1997)
  25. Amati, F. et al. Atypical deletions suggest five 22q11.2 critical regions related to the DiGeorge/velo-cardio-facial syndrome. Eur. J. Hum. Genet. 7, 903–909 (1999). (10.1038/sj.ejhg.5200399) / Eur. J. Hum. Genet. by F Amati (1999)
  26. Mark, M. et al. Two rhombomeres are altered in Hoxa-1 mutant mice. Development 119, 319–338 (1993). (10.1242/dev.119.2.319) / Development by M Mark (1993)
  27. Chong, S.S. et al. A revision of the lissencephaly and Miller–Dieker syndrome critical regions in chromosome 17p13.3. Hum. Mol. Genet. 6, 147–155 (1997). (10.1093/hmg/6.2.147) / Hum. Mol. Genet. by SS Chong (1997)
  28. Begbie, J., Brunet, J.F., Rubenstein, J.L. & Graham, A. Induction of the epibranchial placodes. Development 126, 895–902 (1999). (10.1242/dev.126.5.895) / Development by J Begbie (1999)
  29. Farrell, M., Waldo, K., Li, Y.X. & Kirby, M.L. A novel role for cardiac neural crest in heart development. Trends Cardiovasc. Med. 9, 214–220 (1999). (10.1016/S1050-1738(00)00023-2) / Trends Cardiovasc. Med. by M Farrell (1999)
  30. Conway, S.J., Henderson, D.J., Kirby, M.L., Anderson, R.H. & Copp, A.J. Development of a lethal congenital heart defect in the splotch (Pax3) mutant mouse. Cardiovasc. Res. 36, 163–173 (1997). (10.1016/S0008-6363(97)00172-7) / Cardiovasc. Res. by SJ Conway (1997)
Dates
Type When
Created 23 years, 1 month ago (July 26, 2002, 4:48 a.m.)
Deposited 2 years, 3 months ago (May 18, 2023, 4:23 p.m.)
Indexed 2 weeks, 2 days ago (Aug. 12, 2025, 5:39 p.m.)
Issued 24 years, 5 months ago (March 1, 2001)
Published 24 years, 5 months ago (March 1, 2001)
Published Print 24 years, 5 months ago (March 1, 2001)
Funders 0

None

@article{Guris_2001, title={Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome}, volume={27}, ISSN={1546-1718}, url={http://dx.doi.org/10.1038/85855}, DOI={10.1038/85855}, number={3}, journal={Nature Genetics}, publisher={Springer Science and Business Media LLC}, author={Guris, Deborah L. and Fantes, Judith and Tara, David and Druker, Brian J. and Imamoto, Akira}, year={2001}, month=mar, pages={293–298} }