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ALX4 (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "ALX4" in Arabic language version.

refsWebsite
Global rank Arabic rank
12nih.gov
4th place
6th place
5doi.org
2nd place
5th place
2web.archive.org
1st place
1st place
1biologists.org
3,870th place
4,192nd place

biologists.org

dev.biologists.org

doi.org

  • Forsthoefel PF (نوفمبر 1963). "The embryological development of the effects of Strong's luxoid gene in the mouse". Journal of Morphology. ج. 113 ع. 3: 427–51. DOI:10.1002/jmor.1051130307. PMID:14079603.
  • Kuijper S، Feitsma H، Sheth R، Korving J، Reijnen M، Meijlink F (سبتمبر 2005). "Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh". Developmental Biology. ج. 285 ع. 2: 533–44. DOI:10.1016/j.ydbio.2005.06.017. PMID:16039644.
  • Panman L، Drenth T، Tewelscher P، Zuniga A، Zeller R (1 يوليو 2004). "Genetic interaction of Gli3 and Alx4 during limb development". The International Journal of Developmental Biology. ج. 49 ع. 4: 443–8. DOI:10.1387/ijdb.051984lp. PMID:15968591.
  • Kayserili H، Uz E، Niessen C، Vargel I، Alanay Y، Tuncbilek G، Yigit G، Uyguner O، Candan S، Okur H، Kaygin S، Balci S، Mavili E، Alikasifoglu M، Haase I، Wollnik B، Akarsu NA (نوفمبر 2009). "ALX4 dysfunction disrupts craniofacial and epidermal development". Human Molecular Genetics. ج. 18 ع. 22: 4357–66. DOI:10.1093/hmg/ddp391. PMID:19692347.
  • Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Forsthoefel PF (نوفمبر 1963). "The embryological development of the effects of Strong's luxoid gene in the mouse". Journal of Morphology. ج. 113 ع. 3: 427–51. DOI:10.1002/jmor.1051130307. PMID:14079603.
  • Kuijper S، Feitsma H، Sheth R، Korving J، Reijnen M، Meijlink F (سبتمبر 2005). "Function and regulation of Alx4 in limb development: complex genetic interactions with Gli3 and Shh". Developmental Biology. ج. 285 ع. 2: 533–44. DOI:10.1016/j.ydbio.2005.06.017. PMID:16039644.
  • Niswander L (2002). "Interplay between the molecular signals that control vertebrate limb development". The International Journal of Developmental Biology. ج. 46 ع. 7: 877–81. PMID:12455624.
  • Panman L، Drenth T، Tewelscher P، Zuniga A، Zeller R (1 يوليو 2004). "Genetic interaction of Gli3 and Alx4 during limb development". The International Journal of Developmental Biology. ج. 49 ع. 4: 443–8. DOI:10.1387/ijdb.051984lp. PMID:15968591.
  • Takahashi M، Tamura K، Büscher D، Masuya H، Yonei-Tamura S، Matsumoto K، Naitoh-Matsuo M، Takeuchi J، Ogura K، Shiroishi T، Ogura T، Izpisúa Belmonte JC (نوفمبر 1998). "The role of Alx-4 in the establishment of anteroposterior polarity during vertebrate limb development". Development. ج. 125 ع. 22: 4417–25. PMID:9778501. مؤرشف من الأصل في 2018-06-17.
  • Meijlink F، Beverdam A، Brouwer A، Oosterveen TC، Berge DT (1999). "Vertebrate aristaless-related genes". The International Journal of Developmental Biology. ج. 43 ع. 7: 651–63. PMID:10668975.
  • Kayserili H، Uz E، Niessen C، Vargel I، Alanay Y، Tuncbilek G، Yigit G، Uyguner O، Candan S، Okur H، Kaygin S، Balci S، Mavili E، Alikasifoglu M، Haase I، Wollnik B، Akarsu NA (نوفمبر 2009). "ALX4 dysfunction disrupts craniofacial and epidermal development". Human Molecular Genetics. ج. 18 ع. 22: 4357–66. DOI:10.1093/hmg/ddp391. PMID:19692347.
  • Wu YQ، Badano JL، McCaskill C، Vogel H، Potocki L، Shaffer LG (نوفمبر 2000). "Haploinsufficiency of ALX4 as a potential cause of parietal foramina in the 11p11.2 contiguous gene-deletion syndrome". American Journal of Human Genetics. ج. 67 ع. 5: 1327–32. DOI:10.1016/S0002-9297(07)62963-2. PMC:1288575. PMID:11017806.
  • Bartsch O، Wuyts W، Van Hul W، Hecht JT، Meinecke P، Hogue D، Werner W، Zabel B، Hinkel GK، Powell CM، Shaffer LG، Willems PJ (أبريل 1996). "Delineation of a contiguous gene syndrome with multiple exostoses, enlarged parietal foramina, craniofacial dysostosis, and mental retardation, caused by deletions in the short arm of chromosome 11". American Journal of Human Genetics. ج. 58 ع. 4: 734–42. PMC:1914683. PMID:8644736.

ncbi.nlm.nih.gov

web.archive.org