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Items: 1 to 20 of 101

1.

Medicinal signalling cells: they work, so use them.

Caplan AI.

Nature. 2019 Feb;566(7742):39. doi: 10.1038/d41586-019-00490-6. No abstract available.

PMID:
30723355
2.

Japan should put the brakes on stem-cell sales.

[No authors listed]

Nature. 2019 Jan;565(7741):535-536. doi: 10.1038/d41586-019-00332-5. No abstract available.

PMID:
30700883
3.

Meckel-Gruber syndrome: prevalence from a hospital-based study in Oman.

Sawardekar KP.

J Matern Fetal Neonatal Med. 2016 Nov;29(22):3696-8. doi: 10.3109/14767058.2016.1141883. Epub 2016 Feb 26. No abstract available.

PMID:
26788898
4.

Re: Meckel-Gruber syndrome: prevalence from a hospital based in Oman.

Al-Belushi M, Al Ibrahim A, Ahmed M, Ahmed B, Khenyab N, Konje JC.

J Matern Fetal Neonatal Med. 2016 Nov;29(22):3695. doi: 10.3109/14767058.2016.1141475. Epub 2016 Feb 26. No abstract available.

PMID:
26762791
5.

Clinical utility gene card for: Meckel syndrome.

Salonen R, Kestilä M, Bergmann C.

Eur J Hum Genet. 2011 Jul;19(7). doi: 10.1038/ejhg.2010.255. Epub 2011 Feb 2. No abstract available.

6.

A rare case of Meckel-Gruber syndrome.

Chiriac DV, Hogea LM, Bredicean AC, Rednic R, Nussbaum LA, Hogea GB, Grigoraş ML.

Rom J Morphol Embryol. 2017;58(3):1023-1027.

7.

Meckel-Gruber syndrome and the role of primary cilia in kidney, skeleton, and central nervous system development.

Barker AR, Thomas R, Dawe HR.

Organogenesis. 2014 Jan 1;10(1):96-107. doi: 10.4161/org.27375. Epub 2013 Dec 9. Review.

8.

Clinical utility gene card for: Meckel syndrome - update 2016.

Bergmann C, Frank V, Salonen R.

Eur J Hum Genet. 2016 Aug;24(8). doi: 10.1038/ejhg.2016.33. Epub 2016 Apr 20. No abstract available.

9.

[Meckel Gruber syndrome: about a rare case].

Itchimouh S, Khabtou K, Mahdaoui S, Boufettal H, Samouh N.

Pan Afr Med J. 2016 Sep 29;25:43. doi: 10.11604/pamj.2016.25.43.9696. eCollection 2016. French.

10.

An unusual case of Meckel-Gruber syndrome (MKS) associated with visceroatrial heterotaxy and facial anomalies.

Yuksel MA, Mammadov Z, Sofiyeva N, Alici Davutoglu E, Temel Yuksel I, Madazli R.

J Obstet Gynaecol. 2016 May;36(4):524-5. doi: 10.3109/01443615.2015.1110123. Epub 2016 Mar 16. No abstract available.

PMID:
26982535
11.

Fetal autopsy of Meckel Gruber syndrome -a case report.

Bolineni C, Nagamuthu EA, Neelala N.

Fetal Pediatr Pathol. 2013 Oct;32(5):387-93. doi: 10.3109/15513815.2013.768741. Epub 2013 Feb 27.

PMID:
23445452
12.

Meckel-Gruber syndrome: ultrasonographic and fetal autopsy correlation.

Khurana S, Saini V, Wadhwa V, Kaur H.

J Ultrasound. 2017 Jan 4;20(2):167-170. doi: 10.1007/s40477-016-0231-4. eCollection 2017 Jun.

13.

Disruption of a ciliary B9 protein complex causes Meckel syndrome.

Dowdle WE, Robinson JF, Kneist A, Sirerol-Piquer MS, Frints SG, Corbit KC, Zaghloul NA, van Lijnschoten G, Mulders L, Verver DE, Zerres K, Reed RR, Attié-Bitach T, Johnson CA, García-Verdugo JM, Katsanis N, Bergmann C, Reiter JF.

Am J Hum Genet. 2011 Jul 15;89(1):94-110. doi: 10.1016/j.ajhg.2011.06.003. Erratum in: Am J Hum Genet. 2011 Oct 7;89(4):589. Zaghloul, Norran A [corrected to Zaghloul, Norann A].

14.

Variable expressivity of ciliopathy neurological phenotypes that encompass Meckel-Gruber syndrome and Joubert syndrome is caused by complex de-regulated ciliogenesis, Shh and Wnt signalling defects.

Abdelhamed ZA, Wheway G, Szymanska K, Natarajan S, Toomes C, Inglehearn C, Johnson CA.

Hum Mol Genet. 2013 Apr 1;22(7):1358-72. doi: 10.1093/hmg/dds546. Epub 2013 Jan 2.

15.

Meckel-Gruber Syndrome with unilateral renal agenesis.

Uysal F, Uysal A.

J Coll Physicians Surg Pak. 2015 Apr;25 Suppl 1:S56-7. doi: 04.2015/JCPSP.S56S57.

PMID:
25933467
16.

The Ciliopathy Protein CC2D2A Associates with NINL and Functions in RAB8-MICAL3-Regulated Vesicle Trafficking.

Bachmann-Gagescu R, Dona M, Hetterschijt L, Tonnaer E, Peters T, de Vrieze E, Mans DA, van Beersum SE, Phelps IG, Arts HH, Keunen JE, Ueffing M, Roepman R, Boldt K, Doherty D, Moens CB, Neuhauss SC, Kremer H, van Wijk E.

PLoS Genet. 2015 Oct 20;11(10):e1005575. doi: 10.1371/journal.pgen.1005575. eCollection 2015 Oct.

17.

Meckel-Gruber syndrome (dysencephalia splanchnocystica).

Shetty BP, Alva N, Patil S, Shetty R.

J Contemp Dent Pract. 2012 Sep 1;13(5):713-5.

PMID:
23250180
18.

Aberrant Wnt signalling and cellular over-proliferation in a novel mouse model of Meckel-Gruber syndrome.

Wheway G, Abdelhamed Z, Natarajan S, Toomes C, Inglehearn C, Johnson CA.

Dev Biol. 2013 May 1;377(1):55-66. doi: 10.1016/j.ydbio.2013.02.015. Epub 2013 Feb 27.

19.

A review of Meckel-Gruber syndrome--incidence and outcome in the state of Qatar.

Al-Belushi M, Al Ibrahim A, Ahmed M, Ahmed B, Khenyab N, Konje JC.

J Matern Fetal Neonatal Med. 2016;29(12):2013-6. doi: 10.3109/14767058.2015.1072162. Epub 2015 Aug 26.

PMID:
26333300
20.

Meckel syndrome with Caroli disease and choledochal cysts.

Venkatachala S, Sivaraman A.

Fetal Pediatr Pathol. 2011;30(5):350-4. doi: 10.3109/15513815.2011.587499. Epub 2011 Aug 15.

PMID:
21843058

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