Kell antigen system (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Kell antigen system" in English language version.

refsWebsite

Global rank English rank

12doi.org

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11nih.gov

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4semanticscholar.org

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1worldcat.org

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1archive.today

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1hematologylibrary.org

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1harvard.edu

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archive.today

Lee S, Lin M, Mele A, Cao Y, Farmar J, Russo D, Redman C (August 1999). "Proteolytic processing of big endothelin-3 by the kell blood group protein". Blood. 94 (4): 1440–50. doi:10.1182/blood.V94.4.1440. PMID 10438732. Archived from the original on 2013-04-14.

doi.org

Smart, E.; Armstrong, B. (2008). "Blood group systems". ISBT Science Series. 3 (2): 68–92. doi:10.1111/j.1751-2824.2008.00188.x. ISSN 1751-2816.
Lee S, Wu X, Reid M, Zelinski T, Redman C (February 1995). "Molecular basis of the Kell (K1) phenotype". Blood. 85 (4): 912–6. doi:10.1182/blood.V85.4.912.bloodjournal854912. PMID 7849312.
Lee S, Lin M, Mele A, Cao Y, Farmar J, Russo D, Redman C (August 1999). "Proteolytic processing of big endothelin-3 by the kell blood group protein". Blood. 94 (4): 1440–50. doi:10.1182/blood.V94.4.1440. PMID 10438732. Archived from the original on 2013-04-14.
Russo DC, Lee S, Reid ME, Redman CM (Mar 2002). "Point mutations causing the McLeod phenotype". Transfusion. 42 (3): 287–93. doi:10.1046/j.1537-2995.2002.00049.x. PMID 11961232. S2CID 41663851.
Yu LC, Twu YC, Chang CY, Lin M (March 2001). "Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens". The Journal of Biological Chemistry. 276 (13): 10247–52. doi:10.1074/jbc.M009879200. PMID 11134029.
Weiner CP, Widness JA (February 1996). "Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia". American Journal of Obstetrics and Gynecology. 174 (2): 547–51. doi:10.1016/S0002-9378(96)70425-8. PMID 8623782.
Chown B, Lewis M, Kaita K (October 1957). "A new Kell blood-group phenotype". Nature. 180 (4588): 711. Bibcode:1957Natur.180..711C. doi:10.1038/180711a0. PMID 13477267. S2CID 4187507.
Allen FH, Krabbe SM, Corcoran PA (September 1961). "A new phenotype (McLeod) in the Kell blood-group system". Vox Sanguinis. 6 (5): 555–60. doi:10.1111/j.1423-0410.1961.tb03203.x. PMID 13860532. S2CID 30275809.
Stride P, Lopes Floro K (2013). "Henry VIII, McLeod syndrome and Jacquetta's curse". The Journal of the Royal College of Physicians of Edinburgh. 43 (4): 353–60. doi:10.4997/JRCPE.2013.417. PMID 24350322.
Whitley CB, Kramer K (December 2010). "A new explanation for the reproductive woes and midlife decline of Henry VIII". The Historical Journal. 53 (4): 827–848. doi:10.1017/S0018246X10000452. S2CID 159499333.
Crandall BF, Spence MA (1974). "Linkage relations of the phenylthiocarbamide locus (PTC)". Human Heredity. 24 (3): 247–52. doi:10.1159/000152657. PMID 4435792.
Conneally PM, Dumont-Driscoll M, Huntzinger RS, Nance WE, Jackson CE (1976). "Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivity". Human Heredity. 26 (4): 267–71. doi:10.1159/000152813. PMID 976995.

harvard.edu

ui.adsabs.harvard.edu

Chown B, Lewis M, Kaita K (October 1957). "A new Kell blood-group phenotype". Nature. 180 (4588): 711. Bibcode:1957Natur.180..711C. doi:10.1038/180711a0. PMID 13477267. S2CID 4187507.

hematologylibrary.org

bloodjournal.hematologylibrary.org

Lee S, Lin M, Mele A, Cao Y, Farmar J, Russo D, Redman C (August 1999). "Proteolytic processing of big endothelin-3 by the kell blood group protein". Blood. 94 (4): 1440–50. doi:10.1182/blood.V94.4.1440. PMID 10438732. Archived from the original on 2013-04-14.

nih.gov

pubmed.ncbi.nlm.nih.gov

Lee S, Wu X, Reid M, Zelinski T, Redman C (February 1995). "Molecular basis of the Kell (K1) phenotype". Blood. 85 (4): 912–6. doi:10.1182/blood.V85.4.912.bloodjournal854912. PMID 7849312.
Lee S, Lin M, Mele A, Cao Y, Farmar J, Russo D, Redman C (August 1999). "Proteolytic processing of big endothelin-3 by the kell blood group protein". Blood. 94 (4): 1440–50. doi:10.1182/blood.V94.4.1440. PMID 10438732. Archived from the original on 2013-04-14.
Russo DC, Lee S, Reid ME, Redman CM (Mar 2002). "Point mutations causing the McLeod phenotype". Transfusion. 42 (3): 287–93. doi:10.1046/j.1537-2995.2002.00049.x. PMID 11961232. S2CID 41663851.
Yu LC, Twu YC, Chang CY, Lin M (March 2001). "Molecular basis of the Kell-null phenotype: a mutation at the splice site of human KEL gene abolishes the expression of Kell blood group antigens". The Journal of Biological Chemistry. 276 (13): 10247–52. doi:10.1074/jbc.M009879200. PMID 11134029.
Weiner CP, Widness JA (February 1996). "Decreased fetal erythropoiesis and hemolysis in Kell hemolytic anemia". American Journal of Obstetrics and Gynecology. 174 (2): 547–51. doi:10.1016/S0002-9378(96)70425-8. PMID 8623782.
Chown B, Lewis M, Kaita K (October 1957). "A new Kell blood-group phenotype". Nature. 180 (4588): 711. Bibcode:1957Natur.180..711C. doi:10.1038/180711a0. PMID 13477267. S2CID 4187507.
Allen FH, Krabbe SM, Corcoran PA (September 1961). "A new phenotype (McLeod) in the Kell blood-group system". Vox Sanguinis. 6 (5): 555–60. doi:10.1111/j.1423-0410.1961.tb03203.x. PMID 13860532. S2CID 30275809.
Stride P, Lopes Floro K (2013). "Henry VIII, McLeod syndrome and Jacquetta's curse". The Journal of the Royal College of Physicians of Edinburgh. 43 (4): 353–60. doi:10.4997/JRCPE.2013.417. PMID 24350322.
Crandall BF, Spence MA (1974). "Linkage relations of the phenylthiocarbamide locus (PTC)". Human Heredity. 24 (3): 247–52. doi:10.1159/000152657. PMID 4435792.
Conneally PM, Dumont-Driscoll M, Huntzinger RS, Nance WE, Jackson CE (1976). "Linkage relations of the loci for Kell and phenylthiocarbamide taste sensitivity". Human Heredity. 26 (4): 267–71. doi:10.1159/000152813. PMID 976995.

ncbi.nlm.nih.gov

"Entrez Gene: KEL".

semanticscholar.org

api.semanticscholar.org

Russo DC, Lee S, Reid ME, Redman CM (Mar 2002). "Point mutations causing the McLeod phenotype". Transfusion. 42 (3): 287–93. doi:10.1046/j.1537-2995.2002.00049.x. PMID 11961232. S2CID 41663851.
Chown B, Lewis M, Kaita K (October 1957). "A new Kell blood-group phenotype". Nature. 180 (4588): 711. Bibcode:1957Natur.180..711C. doi:10.1038/180711a0. PMID 13477267. S2CID 4187507.
Allen FH, Krabbe SM, Corcoran PA (September 1961). "A new phenotype (McLeod) in the Kell blood-group system". Vox Sanguinis. 6 (5): 555–60. doi:10.1111/j.1423-0410.1961.tb03203.x. PMID 13860532. S2CID 30275809.
Whitley CB, Kramer K (December 2010). "A new explanation for the reproductive woes and midlife decline of Henry VIII". The Historical Journal. 53 (4): 827–848. doi:10.1017/S0018246X10000452. S2CID 159499333.

worldcat.org

search.worldcat.org

Smart, E.; Armstrong, B. (2008). "Blood group systems". ISBT Science Series. 3 (2): 68–92. doi:10.1111/j.1751-2824.2008.00188.x. ISSN 1751-2816.