DLX5 (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "DLX5" in English language version.

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Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K (Mar 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proceedings of the National Academy of Sciences of the United States of America. 91 (6): 2250–4. Bibcode:1994PNAS...91.2250S. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.
Shamseldin HE, Faden MA, Alashram W, Alkuraya FS (Jan 2012). "Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation". Journal of Medical Genetics. 49 (1): 16–20. doi:10.1136/jmedgenet-2011-100556. PMID 22121204. S2CID 25692622.
Robledo RF, Rajan L, Li X, Lufkin T (May 2002). "The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development". Genes & Development. 16 (9): 1089–101. doi:10.1101/gad.988402. PMC 186247. PMID 12000792.
Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen MM, Abate-Shen C (May 1997). "Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism". Molecular and Cellular Biology. 17 (5): 2920–32. doi:10.1128/mcb.17.5.2920. PMC 232144. PMID 9111364.

Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K (Mar 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proceedings of the National Academy of Sciences of the United States of America. 91 (6): 2250–4. Bibcode:1994PNAS...91.2250S. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K (Mar 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proceedings of the National Academy of Sciences of the United States of America. 91 (6): 2250–4. Bibcode:1994PNAS...91.2250S. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.
"Entrez Gene: DLX5 distal-less homeobox 5".
Robledo RF, Rajan L, Li X, Lufkin T (May 2002). "The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development". Genes & Development. 16 (9): 1089–101. doi:10.1101/gad.988402. PMC 186247. PMID 12000792.
Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen MM, Abate-Shen C (May 1997). "Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism". Molecular and Cellular Biology. 17 (5): 2920–32. doi:10.1128/mcb.17.5.2920. PMC 232144. PMID 9111364.

Simeone A, Acampora D, Pannese M, D'Esposito M, Stornaiuolo A, Gulisano M, Mallamaci A, Kastury K, Druck T, Huebner K (Mar 1994). "Cloning and characterization of two members of the vertebrate Dlx gene family". Proceedings of the National Academy of Sciences of the United States of America. 91 (6): 2250–4. Bibcode:1994PNAS...91.2250S. doi:10.1073/pnas.91.6.2250. PMC 43348. PMID 7907794.
Shamseldin HE, Faden MA, Alashram W, Alkuraya FS (Jan 2012). "Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation". Journal of Medical Genetics. 49 (1): 16–20. doi:10.1136/jmedgenet-2011-100556. PMID 22121204. S2CID 25692622.
Robledo RF, Rajan L, Li X, Lufkin T (May 2002). "The Dlx5 and Dlx6 homeobox genes are essential for craniofacial, axial, and appendicular skeletal development". Genes & Development. 16 (9): 1089–101. doi:10.1101/gad.988402. PMC 186247. PMID 12000792.
Zhang H, Hu G, Wang H, Sciavolino P, Iler N, Shen MM, Abate-Shen C (May 1997). "Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism". Molecular and Cellular Biology. 17 (5): 2920–32. doi:10.1128/mcb.17.5.2920. PMC 232144. PMID 9111364.

Shamseldin HE, Faden MA, Alashram W, Alkuraya FS (Jan 2012). "Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation". Journal of Medical Genetics. 49 (1): 16–20. doi:10.1136/jmedgenet-2011-100556. PMID 22121204. S2CID 25692622.