MMADHC (Catalan Wikipedia)

Analysis of information sources in references of the Wikipedia article "MMADHC" in Catalan language version.

refsWebsite

Global rank Catalan rank

14nih.gov

4^th place

7^th place

13doi.org

2^nd place

6^th place

8worldcat.org

5^th place

3uzh.ch

3,633^rd place

6,235^th place

2ensembl.org

1,626^th place

8,169^th place

1wikidata.org

43^rd place

170^th place

1sciencedirect.com

149^th place

111^th place

1nejm.org

2,374^th place

2,440^th place

1orpha.net

3,537^th place

4,222^nd place

1ivami.com

low place

doi.org (Global: 2^nd place; Catalan: 6^th place)

dx.doi.org

Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene identification for the cblD defect of vitamin B12 metabolism». The New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 1533-4406. PMID: 18385497.
Yamada, Kazuhiro; Gherasim, Carmen; Banerjee, Ruma; Koutmos, Markos «Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases». The Journal of Biological Chemistry, 290, 49, 12-2015, pàg. 29155–29166. DOI: 10.1074/jbc.M115.682435. ISSN: 0021-9258. PMC: 4705922. PMID: 26364851.
Mah, Wayne; Deme, Justin C.; Watkins, David; Fung, Stephen; Janer, Alexandre «Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B12 metabolism». Molecular Genetics and Metabolism, 108, 2, 2-2013, pàg. 112–118. DOI: 10.1016/j.ymgme.2012.11.284. ISSN: 1096-7192.
Deme, Justin C.; Miousse, Isabelle R.; Plesa, Maria; Kim, Jaeseung C.; Hancock, Mark A. «Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism». Molecular Genetics and Metabolism, 107, 3, 11-2012, pàg. 352–362. DOI: 10.1016/j.ymgme.2012.07.001. ISSN: 1096-7206. PMID: 22832074.
Kazuhiro Yamada, Carmen Gherasim, Ruma Banerjee, and Markos Koutmos «Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases». The Journal of biological chemistry, 2015, pàg. 2. DOI: 10.1074/jbc.M115.682435. PMID: 26364851.
Institut national de la santé et de la recherche médicale «Methylmalonic acidemia with homocystinuria, type cblD». Orphanet. Qeios, 2-2020.
Jusufi, Jehona ; Suormala, Terttu ; Burda, Patricie ; Fowler, Brian ; Froese, D Sean ; Baumgartner, Matthias R «Characterization of functional domains of the cblD (MMADHC) gene product». Journal of inherited metabolic disease, 2014, pàg. 1. DOI: 10.1007/s10545-014-9709-4. PMID: 24722857.
Fettelschoss, Victoria; Burda, Patricie; Sagné, Corinne; Coelho, David; De Laet, Corinne «Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1». The Journal of Biological Chemistry, 292, 28, 14-07-2017, pàg. 11980–11991. DOI: 10.1074/jbc.M117.784819. ISSN: 0021-9258. PMC: 5512089. PMID: 28572511.
McCorvie, Thomas J ; Ferreira, Douglas ; Yue, Wyatt W ; Froese, D Sean «The complex machinery of human cobalamin metabolism». Journal of inherited metabolic disease, 2023, pàg. 4 - 6. DOI: 10.1002/jimd.12593. PMID: 36680553.
Li, Zhu; Gouda, Harsha; Pillay, Shubhadra; Yaw, Madeline; Ruetz, Markus «The human B12 trafficking chaperones: CblA, ATR, CblC and CblD». Methods in Enzymology, 668, 2022, pàg. 137–156. DOI: 10.1016/bs.mie.2021.12.009. ISSN: 1557-7988. PMC: 9418966. PMID: 35589192.
Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene Identification for the cblD Defect of Vitamin B 12 Metabolism» (en anglès). New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 0028-4793.
Baumgartner, Matthias R.; Hörster, Friederike; Dionisi-Vici, Carlo; Haliloglu, Goknur; Karall, Daniela «Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia». Orphanet Journal of Rare Diseases, 9, 1, 9-2014, pàg. 130. DOI: 10.1186/s13023-014-0130-8. ISSN: 1750-1172. PMC: PMC4180313. PMID: 25205257.

doi.org

Baumgartner, Matthias R.; Hörster, Friederike; Dionisi-Vici, Carlo; Haliloglu, Goknur; Karall, Daniela «Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia». Orphanet Journal of Rare Diseases, 9, 1, 9-2014, pàg. 130. DOI: 10.1186/s13023-014-0130-8. ISSN: 1750-1172. PMC: PMC4180313. PMID: 25205257.

ensembl.org (Global: 1,626^th place; Catalan: 8,169^th place)

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000168288 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000026766 – Ensembl, May 2017

ivami.com (Global: low place; Catalan: low place)

«Pruebas genéticas - Acidemia metilmalónica (Methylmalonic acidemia) – Genes MUT, MMAA, MMAB, MMADHC y MCEE. - IVAMI». [Consulta: 25 octubre 2023].

nejm.org (Global: 2,374^th place; Catalan: 2,440^th place)

Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene Identification for the cblD Defect of Vitamin B 12 Metabolism» (en anglès). New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 0028-4793.

nih.gov (Global: 4^th place; Catalan: 7^th place)

ncbi.nlm.nih.gov

«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.
Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene identification for the cblD defect of vitamin B12 metabolism». The New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 1533-4406. PMID: 18385497.
Yamada, Kazuhiro; Gherasim, Carmen; Banerjee, Ruma; Koutmos, Markos «Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases». The Journal of Biological Chemistry, 290, 49, 12-2015, pàg. 29155–29166. DOI: 10.1074/jbc.M115.682435. ISSN: 0021-9258. PMC: 4705922. PMID: 26364851.
Deme, Justin C.; Miousse, Isabelle R.; Plesa, Maria; Kim, Jaeseung C.; Hancock, Mark A. «Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism». Molecular Genetics and Metabolism, 107, 3, 11-2012, pàg. 352–362. DOI: 10.1016/j.ymgme.2012.07.001. ISSN: 1096-7206. PMID: 22832074.
Kazuhiro Yamada, Carmen Gherasim, Ruma Banerjee, and Markos Koutmos «Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases». The Journal of biological chemistry, 2015, pàg. 2. DOI: 10.1074/jbc.M115.682435. PMID: 26364851.
Jusufi, Jehona ; Suormala, Terttu ; Burda, Patricie ; Fowler, Brian ; Froese, D Sean ; Baumgartner, Matthias R «Characterization of functional domains of the cblD (MMADHC) gene product». Journal of inherited metabolic disease, 2014, pàg. 1. DOI: 10.1007/s10545-014-9709-4. PMID: 24722857.
Fettelschoss, Victoria; Burda, Patricie; Sagné, Corinne; Coelho, David; De Laet, Corinne «Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1». The Journal of Biological Chemistry, 292, 28, 14-07-2017, pàg. 11980–11991. DOI: 10.1074/jbc.M117.784819. ISSN: 0021-9258. PMC: 5512089. PMID: 28572511.
McCorvie, Thomas J ; Ferreira, Douglas ; Yue, Wyatt W ; Froese, D Sean «The complex machinery of human cobalamin metabolism». Journal of inherited metabolic disease, 2023, pàg. 4 - 6. DOI: 10.1002/jimd.12593. PMID: 36680553.
Li, Zhu; Gouda, Harsha; Pillay, Shubhadra; Yaw, Madeline; Ruetz, Markus «The human B12 trafficking chaperones: CblA, ATR, CblC and CblD». Methods in Enzymology, 668, 2022, pàg. 137–156. DOI: 10.1016/bs.mie.2021.12.009. ISSN: 1557-7988. PMC: 9418966. PMID: 35589192.
Baumgartner, Matthias R.; Hörster, Friederike; Dionisi-Vici, Carlo; Haliloglu, Goknur; Karall, Daniela «Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia». Orphanet Journal of Rare Diseases, 9, 1, 9-2014, pàg. 130. DOI: 10.1186/s13023-014-0130-8. ISSN: 1750-1172. PMC: PMC4180313. PMID: 25205257.

pubmed.ncbi.nlm.nih.gov

Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene identification for the cblD defect of vitamin B12 metabolism». The New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 1533-4406. PMID: 18385497.
Deme, Justin C.; Miousse, Isabelle R.; Plesa, Maria; Kim, Jaeseung C.; Hancock, Mark A. «Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism». Molecular Genetics and Metabolism, 107, 3, 11-2012, pàg. 352–362. DOI: 10.1016/j.ymgme.2012.07.001. ISSN: 1096-7206. PMID: 22832074.
Li, Zhu; Gouda, Harsha; Pillay, Shubhadra; Yaw, Madeline; Ruetz, Markus «The human B12 trafficking chaperones: CblA, ATR, CblC and CblD». Methods in Enzymology, 668, 2022, pàg. 137–156. DOI: 10.1016/bs.mie.2021.12.009. ISSN: 1557-7988. PMC: 9418966. PMID: 35589192.

orpha.net (Global: 3,537^th place; Catalan: 4,222^nd place)

RESERVADOS, INSERM US14-- TODOS LOS DERECHOS. «Orphanet: Acidemia metilmalónica con homocistinuria tipo cblD» (en castellà). [Consulta: 26 octubre 2023].

sciencedirect.com (Global: 149^th place; Catalan: 111^th place)

Mah, Wayne; Deme, Justin C.; Watkins, David; Fung, Stephen; Janer, Alexandre «Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B12 metabolism». Molecular Genetics and Metabolism, 108, 2, 2-2013, pàg. 112–118. DOI: 10.1016/j.ymgme.2012.11.284. ISSN: 1096-7192.

uzh.ch (Global: 3,633^rd place; Catalan: 6,235^th place)

zora.uzh.ch

Jusufi, Jehona ; Suormala, Terttu ; Burda, Patricie ; Fowler, Brian ; Froese, D Sean ; Baumgartner, Matthias R «Characterization of functional domains of the cblD (MMADHC) gene product». Journal of inherited metabolic disease, 2014, pàg. 1. DOI: 10.1007/s10545-014-9709-4. PMID: 24722857.
McCorvie, Thomas J ; Ferreira, Douglas ; Yue, Wyatt W ; Froese, D Sean «The complex machinery of human cobalamin metabolism». Journal of inherited metabolic disease, 2023, pàg. 1-2.
McCorvie, Thomas J ; Ferreira, Douglas ; Yue, Wyatt W ; Froese, D Sean «The complex machinery of human cobalamin metabolism». Journal of inherited metabolic disease, 2023, pàg. 4 - 6. DOI: 10.1002/jimd.12593. PMID: 36680553.

wikidata.org (Global: 43^rd place; Catalan: 170^th place)

«Malalties que s'associen genèticament amb MMADHC, vegeu/editeu les referències a wikidata».

worldcat.org (Global: 5^th place; Catalan: 5^th place)

Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene identification for the cblD defect of vitamin B12 metabolism». The New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 1533-4406. PMID: 18385497.
Yamada, Kazuhiro; Gherasim, Carmen; Banerjee, Ruma; Koutmos, Markos «Structure of Human B12 Trafficking Protein CblD Reveals Molecular Mimicry and Identifies a New Subfamily of Nitro-FMN Reductases». The Journal of Biological Chemistry, 290, 49, 12-2015, pàg. 29155–29166. DOI: 10.1074/jbc.M115.682435. ISSN: 0021-9258. PMC: 4705922. PMID: 26364851.
Mah, Wayne; Deme, Justin C.; Watkins, David; Fung, Stephen; Janer, Alexandre «Subcellular location of MMACHC and MMADHC, two human proteins central to intracellular vitamin B12 metabolism». Molecular Genetics and Metabolism, 108, 2, 2-2013, pàg. 112–118. DOI: 10.1016/j.ymgme.2012.11.284. ISSN: 1096-7192.
Deme, Justin C.; Miousse, Isabelle R.; Plesa, Maria; Kim, Jaeseung C.; Hancock, Mark A. «Structural features of recombinant MMADHC isoforms and their interactions with MMACHC, proteins of mammalian vitamin B12 metabolism». Molecular Genetics and Metabolism, 107, 3, 11-2012, pàg. 352–362. DOI: 10.1016/j.ymgme.2012.07.001. ISSN: 1096-7206. PMID: 22832074.
Fettelschoss, Victoria; Burda, Patricie; Sagné, Corinne; Coelho, David; De Laet, Corinne «Clinical or ATPase domain mutations in ABCD4 disrupt the interaction between the vitamin B12-trafficking proteins ABCD4 and LMBD1». The Journal of Biological Chemistry, 292, 28, 14-07-2017, pàg. 11980–11991. DOI: 10.1074/jbc.M117.784819. ISSN: 0021-9258. PMC: 5512089. PMID: 28572511.
Li, Zhu; Gouda, Harsha; Pillay, Shubhadra; Yaw, Madeline; Ruetz, Markus «The human B12 trafficking chaperones: CblA, ATR, CblC and CblD». Methods in Enzymology, 668, 2022, pàg. 137–156. DOI: 10.1016/bs.mie.2021.12.009. ISSN: 1557-7988. PMC: 9418966. PMID: 35589192.
Coelho, David; Suormala, Terttu; Stucki, Martin; Lerner-Ellis, Jordan P.; Rosenblatt, David S. «Gene Identification for the cblD Defect of Vitamin B 12 Metabolism» (en anglès). New England Journal of Medicine, 358, 14, 4-2008, pàg. 1454–1464. DOI: 10.1056/NEJMoa072200. ISSN: 0028-4793.
Baumgartner, Matthias R.; Hörster, Friederike; Dionisi-Vici, Carlo; Haliloglu, Goknur; Karall, Daniela «Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia». Orphanet Journal of Rare Diseases, 9, 1, 9-2014, pàg. 130. DOI: 10.1186/s13023-014-0130-8. ISSN: 1750-1172. PMC: PMC4180313. PMID: 25205257.

MMADHC (Catalan Wikipedia)

doi.org (Global: 2nd place; Catalan: 6th place)

dx.doi.org

doi.org

ensembl.org (Global: 1,626th place; Catalan: 8,169th place)

May2017.archive.ensembl.org

ivami.com (Global: low place; Catalan: low place)

nejm.org (Global: 2,374th place; Catalan: 2,440th place)

nih.gov (Global: 4th place; Catalan: 7th place)