Hypomagnesemia with secondary hypocalcemia (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hypomagnesemia with secondary hypocalcemia" in English language version.

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9nih.gov

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7doi.org

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2semanticscholar.org

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8^th place

1medlineplus.gov

1,581^st place

1,299^th place

1harvard.edu

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1handle.net

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doi.org

Walder R, Landau D, Meyer P, Shalev H, Tsolia M, Borochowitz Z, Boettger M, Beck G, Englehardt R, Carmi R, Sheffield V (2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nat Genet. 31 (2): 171–4. doi:10.1038/ng901. PMID 12032570. S2CID 33192419.
Schlingmann K, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth H, Konrad M (2002). "Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family". Nat Genet. 31 (2): 166–70. doi:10.1038/ng889. PMID 12032568. S2CID 40990544.
Chubanov V, Waldegger S, Mederos y Schnitzler M, Vitzthum H, Sassen M, Seyberth H, Konrad M, Gudermann T (2004). "Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia". Proc Natl Acad Sci USA. 101 (9): 2894–9. Bibcode:2004PNAS..101.2894C. doi:10.1073/pnas.0305252101. PMC 365716. PMID 14976260.
Schlingmann K, Sassen M, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble J, Cole D, Metzger D, Rahman S, Tajima T, Shu S, Waldegger S, Seyberth H, Konrad M (2005). "Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia". J Am Soc Nephrol. 16 (10): 3061–9. doi:10.1681/ASN.2004110989. PMID 16107578.
Li M, Jiang J, Yue L (2006). "Functional Characterization of Homo- and Heteromeric Channel Kinases TRPM6 and TRPM7". J Gen Physiol. 127 (5): 525–37. doi:10.1085/jgp.200609502. PMC 2151519. PMID 16636202.
Jalkanen R, Pronicka E, Tyynismaa H, Hanauer A, Walder R, Alitalo T (2006). "Genetic background of HSH in three Polish families and a patient with an X;9 translocation". Eur J Hum Genet. 14 (1): 55–62. doi:10.1038/sj.ejhg.5201515. PMID 16267500.
Voets T, Nilius B, Hoefs S, van der Kemp A, Droogmans G, Bindels R, Hoenderop J (2004). "TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption". J Biol Chem. 279 (1): 19–25. doi:10.1074/jbc.M311201200. hdl:2066/57440. PMID 14576148.

handle.net

hdl.handle.net

Voets T, Nilius B, Hoefs S, van der Kemp A, Droogmans G, Bindels R, Hoenderop J (2004). "TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption". J Biol Chem. 279 (1): 19–25. doi:10.1074/jbc.M311201200. hdl:2066/57440. PMID 14576148.

harvard.edu

ui.adsabs.harvard.edu

Chubanov V, Waldegger S, Mederos y Schnitzler M, Vitzthum H, Sassen M, Seyberth H, Konrad M, Gudermann T (2004). "Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia". Proc Natl Acad Sci USA. 101 (9): 2894–9. Bibcode:2004PNAS..101.2894C. doi:10.1073/pnas.0305252101. PMC 365716. PMID 14976260.

medlineplus.gov

"TRPM6 gene: MedlinePlus Genetics". medlineplus.gov. Retrieved 2023-07-02.

nih.gov

pubmed.ncbi.nlm.nih.gov

Walder R, Landau D, Meyer P, Shalev H, Tsolia M, Borochowitz Z, Boettger M, Beck G, Englehardt R, Carmi R, Sheffield V (2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nat Genet. 31 (2): 171–4. doi:10.1038/ng901. PMID 12032570. S2CID 33192419.
Schlingmann K, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth H, Konrad M (2002). "Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family". Nat Genet. 31 (2): 166–70. doi:10.1038/ng889. PMID 12032568. S2CID 40990544.
Chubanov V, Waldegger S, Mederos y Schnitzler M, Vitzthum H, Sassen M, Seyberth H, Konrad M, Gudermann T (2004). "Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia". Proc Natl Acad Sci USA. 101 (9): 2894–9. Bibcode:2004PNAS..101.2894C. doi:10.1073/pnas.0305252101. PMC 365716. PMID 14976260.
Schlingmann K, Sassen M, Weber S, Pechmann U, Kusch K, Pelken L, Lotan D, Syrrou M, Prebble J, Cole D, Metzger D, Rahman S, Tajima T, Shu S, Waldegger S, Seyberth H, Konrad M (2005). "Novel TRPM6 mutations in 21 families with primary hypomagnesemia and secondary hypocalcemia". J Am Soc Nephrol. 16 (10): 3061–9. doi:10.1681/ASN.2004110989. PMID 16107578.
Li M, Jiang J, Yue L (2006). "Functional Characterization of Homo- and Heteromeric Channel Kinases TRPM6 and TRPM7". J Gen Physiol. 127 (5): 525–37. doi:10.1085/jgp.200609502. PMC 2151519. PMID 16636202.
Jalkanen R, Pronicka E, Tyynismaa H, Hanauer A, Walder R, Alitalo T (2006). "Genetic background of HSH in three Polish families and a patient with an X;9 translocation". Eur J Hum Genet. 14 (1): 55–62. doi:10.1038/sj.ejhg.5201515. PMID 16267500.
Voets T, Nilius B, Hoefs S, van der Kemp A, Droogmans G, Bindels R, Hoenderop J (2004). "TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption". J Biol Chem. 279 (1): 19–25. doi:10.1074/jbc.M311201200. hdl:2066/57440. PMID 14576148.

ncbi.nlm.nih.gov

Chubanov V, Waldegger S, Mederos y Schnitzler M, Vitzthum H, Sassen M, Seyberth H, Konrad M, Gudermann T (2004). "Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia". Proc Natl Acad Sci USA. 101 (9): 2894–9. Bibcode:2004PNAS..101.2894C. doi:10.1073/pnas.0305252101. PMC 365716. PMID 14976260.
Li M, Jiang J, Yue L (2006). "Functional Characterization of Homo- and Heteromeric Channel Kinases TRPM6 and TRPM7". J Gen Physiol. 127 (5): 525–37. doi:10.1085/jgp.200609502. PMC 2151519. PMID 16636202.

semanticscholar.org

api.semanticscholar.org

Walder R, Landau D, Meyer P, Shalev H, Tsolia M, Borochowitz Z, Boettger M, Beck G, Englehardt R, Carmi R, Sheffield V (2002). "Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia". Nat Genet. 31 (2): 171–4. doi:10.1038/ng901. PMID 12032570. S2CID 33192419.
Schlingmann K, Weber S, Peters M, Niemann Nejsum L, Vitzthum H, Klingel K, Kratz M, Haddad E, Ristoff E, Dinour D, Syrrou M, Nielsen S, Sassen M, Waldegger S, Seyberth H, Konrad M (2002). "Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family". Nat Genet. 31 (2): 166–70. doi:10.1038/ng889. PMID 12032568. S2CID 40990544.