Abnormal sterol metabolism in holoprosencephaly
Holoprosencephaly (HPE) is the most common structural malformation of the developing forebrain in humans. The HPE phenotype is extremely variable and the etiology is heterogeneous. Among a variety of embryological toxins that can induce HPE, inhibitors, and other pertubations of cholesterol biosynth...
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
26. Januar 2010
|
| In: |
American journal of medical genetics. Part C, Seminars in medical genetics
Year: 2010, Jahrgang: 154C, Heft: 1, Pages: 102-108 |
| ISSN: | 1552-4876 |
| DOI: | 10.1002/ajmg.c.30243 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ajmg.c.30243 Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.30243 |
| Verfasserangaben: | Dorothea Haas and Maximilian Muenke |
MARC
| LEADER | 00000caa a2200000 c 4500 | ||
|---|---|---|---|
| 001 | 1847680003 | ||
| 003 | DE-627 | ||
| 005 | 20230710131222.0 | ||
| 007 | cr uuu---uuuuu | ||
| 008 | 230607s2010 xx |||||o 00| ||eng c | ||
| 024 | 7 | |a 10.1002/ajmg.c.30243 |2 doi | |
| 035 | |a (DE-627)1847680003 | ||
| 035 | |a (DE-599)KXP1847680003 | ||
| 035 | |a (OCoLC)1389794218 | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rda | ||
| 041 | |a eng | ||
| 084 | |a 33 |2 sdnb | ||
| 100 | 1 | |a Haas, Dorothea |d 1965- |e VerfasserIn |0 (DE-588)1038104505 |0 (DE-627)756671280 |0 (DE-576)392125196 |4 aut | |
| 245 | 1 | 0 | |a Abnormal sterol metabolism in holoprosencephaly |c Dorothea Haas and Maximilian Muenke |
| 264 | 1 | |c 26. Januar 2010 | |
| 300 | |a 7 | ||
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a Computermedien |b c |2 rdamedia | ||
| 338 | |a Online-Ressource |b cr |2 rdacarrier | ||
| 500 | |a Gesehen am 07.06.2023 | ||
| 520 | |a Holoprosencephaly (HPE) is the most common structural malformation of the developing forebrain in humans. The HPE phenotype is extremely variable and the etiology is heterogeneous. Among a variety of embryological toxins that can induce HPE, inhibitors, and other pertubations of cholesterol biosynthesis have been shown to be important factors, most likely because cholesterol is required in the Sonic hedgehog signaling cascade. Decreased levels of maternal cholesterol during pregnancy increase the risk for preterm delivery, but they are not associated with congenital malformations. However, if the fetus is affected by an inborn error of endogenous cholesterol synthesis, a reduction of maternal cholesterol concentration and cholesterol transport over the placenta aggravates the phenotypic expression. Exposure to lipophilic statins in early pregnancy may be associated with a substantial risk for structural CNS defects. © 2010 Wiley-Liss, Inc. | ||
| 650 | 4 | |a cholesterol biosynthesis | |
| 650 | 4 | |a cholesterol precursors | |
| 650 | 4 | |a holoprosencephaly | |
| 650 | 4 | |a Shh signaling | |
| 650 | 4 | |a Smith-Lemli-Opitz syndrome | |
| 700 | 1 | |a Muenke, Maximilian |e VerfasserIn |0 (DE-588)1292270918 |0 (DE-627)184767996X |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t American journal of medical genetics. Part C, Seminars in medical genetics |d Hoboken, NJ : Wiley-Liss, 2003 |g 154C(2010), 1, Seite 102-108 |h Online-Ressource |w (DE-627)386577870 |w (DE-600)2143867-5 |w (DE-576)114425035 |x 1552-4876 |7 nnas |a Abnormal sterol metabolism in holoprosencephaly |
| 773 | 1 | 8 | |g volume:154C |g year:2010 |g number:1 |g pages:102-108 |g extent:7 |a Abnormal sterol metabolism in holoprosencephaly |
| 856 | 4 | 0 | |u https://doi.org/10.1002/ajmg.c.30243 |x Verlag |x Resolving-System |z lizenzpflichtig |3 Volltext |
| 856 | 4 | 0 | |u https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.30243 |x Verlag |z lizenzpflichtig |3 Volltext |
| 951 | |a AR | ||
| 992 | |a 20230607 | ||
| 993 | |a Article | ||
| 994 | |a 2010 | ||
| 998 | |g 1038104505 |a Haas, Dorothea |m 1038104505:Haas, Dorothea |d 910000 |d 910500 |e 910000PH1038104505 |e 910500PH1038104505 |k 0/910000/ |k 1/910000/910500/ |p 1 |x j | ||
| 999 | |a KXP-PPN1847680003 |e 4330122537 | ||
| BIB | |a Y | ||
| SER | |a journal | ||
| JSO | |a {"note":["Gesehen am 07.06.2023"],"origin":[{"dateIssuedKey":"2010","dateIssuedDisp":"26. Januar 2010"}],"relHost":[{"disp":"Abnormal sterol metabolism in holoprosencephalyAmerican journal of medical genetics. Part C, Seminars in medical genetics","language":["eng"],"titleAlt":[{"title":"American journal of medical genetics / C"},{"title":"Seminars in medical genetics"}],"type":{"media":"Online-Ressource","bibl":"periodical"},"part":{"pages":"102-108","text":"154C(2010), 1, Seite 102-108","issue":"1","year":"2010","volume":"154C","extent":"7"},"title":[{"title_sort":"American journal of medical genetics","title":"American journal of medical genetics","partname":"Seminars in medical genetics"}],"recId":"386577870","id":{"eki":["386577870"],"issn":["1552-4876"],"doi":["10.1002/(ISSN)1552-4876"],"zdb":["2143867-5"]},"pubHistory":["117C.2003 - 154C.2010; 157.2011 -"],"origin":[{"dateIssuedKey":"2003","publisherPlace":"Hoboken, NJ","dateIssuedDisp":"2003-","publisher":"Wiley-Liss"}],"note":["Gesehen am 19.05.11"],"physDesc":[{"extent":"Online-Ressource"}]}],"person":[{"given":"Dorothea","family":"Haas","display":"Haas, Dorothea","role":"aut"},{"display":"Muenke, Maximilian","role":"aut","family":"Muenke","given":"Maximilian"}],"title":[{"title_sort":"Abnormal sterol metabolism in holoprosencephaly","title":"Abnormal sterol metabolism in holoprosencephaly"}],"physDesc":[{"extent":"7 S."}],"recId":"1847680003","type":{"bibl":"article-journal","media":"Online-Ressource"},"name":{"displayForm":["Dorothea Haas and Maximilian Muenke"]},"language":["eng"],"id":{"doi":["10.1002/ajmg.c.30243"],"eki":["1847680003"]}} | ||
| SRT | |a HAASDOROTHABNORMALST2620 | ||