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Items: 13

1.

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.

Fuchs H, Sabrautzki S, Przemeck GK, Leuchtenberger S, Lorenz-Depiereux B, Becker L, Rathkolb B, Horsch M, Garrett L, Östereicher MA, Hans W, Abe K, Sagawa N, Rozman J, Vargas-Panesso IL, Sandholzer M, Lisse TS, Adler T, Aguilar-Pimentel JA, Calzada-Wack J, Ehrhard N, Elvert R, Gau C, Hölter SM, Micklich K, Moreth K, Prehn C, Puk O, Racz I, Stoeger C, Vernaleken A, Michel D, Diener S, Wieland T, Adamski J, Bekeredjian R, Busch DH, Favor J, Graw J, Klingenspor M, Lengger C, Maier H, Neff F, Ollert M, Stoeger T, Yildirim AÖ, Strom TM, Zimmer A, Wolf E, Wurst W, Klopstock T, Beckers J, Gailus-Durner V, Hrabé de Angelis M.

G3 (Bethesda). 2016 Dec 7;6(12):4035-4046. doi: 10.1534/g3.116.033670.

2.

Mammalian axoneme central pair complex proteins: Broader roles revealed by gene knockout phenotypes.

Teves ME, Nagarkatti-Gude DR, Zhang Z, Strauss JF 3rd.

Cytoskeleton (Hoboken). 2016 Jan;73(1):3-22. doi: 10.1002/cm.21271. Review.

3.

Spag17 deficiency results in skeletal malformations and bone abnormalities.

Teves ME, Sundaresan G, Cohen DJ, Hyzy SL, Kajan I, Maczis M, Zhang Z, Costanzo RM, Zweit J, Schwartz Z, Boyan BD, Strauss JF 3rd.

PLoS One. 2015 May 27;10(5):e0125936. doi: 10.1371/journal.pone.0125936. eCollection 2015.

4.

Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita.

Ravenscroft G, Nolent F, Rajagopalan S, Meireles AM, Paavola KJ, Gaillard D, Alanio E, Buckland M, Arbuckle S, Krivanek M, Maluenda J, Pannell S, Gooding R, Ong RW, Allcock RJ, Carvalho ED, Carvalho MD, Kok F, Talbot WS, Melki J, Laing NG.

Am J Hum Genet. 2015 Jun 4;96(6):955-61. doi: 10.1016/j.ajhg.2015.04.014. Epub 2015 May 21.

5.

Genome-wide interrogation of longitudinal FEV1 in children with asthma.

Wu K, Gamazon ER, Im HK, Geeleher P, White SR, Solway J, Clemmer GL, Weiss ST, Tantisira KG, Cox NJ, Ratain MJ, Huang RS.

Am J Respir Crit Care Med. 2014 Sep 15;190(6):619-27. doi: 10.1164/rccm.201403-0460OC.

6.

Whole-genome sequencing of Berkshire (European native pig) provides insights into its origin and domestication.

Li M, Tian S, Yeung CK, Meng X, Tang Q, Niu L, Wang X, Jin L, Ma J, Long K, Zhou C, Cao Y, Zhu L, Bai L, Tang G, Gu Y, Jiang A, Li X, Li R.

Sci Rep. 2014 Apr 14;4:4678. doi: 10.1038/srep04678.

7.

The evolution of lineage-specific regulatory activities in the human embryonic limb.

Cotney J, Leng J, Yin J, Reilly SK, DeMare LE, Emera D, Ayoub AE, Rakic P, Noonan JP.

Cell. 2013 Jul 3;154(1):185-96. doi: 10.1016/j.cell.2013.05.056.

8.

Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.

Grafodatskaya D, Chung BH, Butcher DT, Turinsky AL, Goodman SJ, Choufani S, Chen YA, Lou Y, Zhao C, Rajendram R, Abidi FE, Skinner C, Stavropoulos J, Bondy CA, Hamilton J, Wodak S, Scherer SW, Schwartz CE, Weksberg R.

BMC Med Genomics. 2013 Jan 28;6:1. doi: 10.1186/1755-8794-6-1.

9.

The Developmental Basis of Quantitative Craniofacial Variation in Humans and Mice.

Martínez-Abadías N, Mitteroecker P, Parsons TE, Esparza M, Sjøvold T, Rolian C, Richtsmeier JT, Hallgrímsson B.

Evol Biol. 2012 Dec;39(4):554-567. Epub 2012 Nov 20.

10.

Model-specific tests on variance heterogeneity for detection of potentially interacting genetic loci.

Hothorn LA, Libiger O, Gerhard D.

BMC Genet. 2012 Jul 18;13:59. doi: 10.1186/1471-2156-13-59.

11.

The postnatal role of Sox9 in cartilage.

Henry SP, Liang S, Akdemir KC, de Crombrugghe B.

J Bone Miner Res. 2012 Dec;27(12):2511-25. doi: 10.1002/jbmr.1696.

12.

Adult height variants affect birth length and growth rate in children.

Paternoster L, Howe LD, Tilling K, Weedon MN, Freathy RM, Frayling TM, Kemp JP, Smith GD, Timpson NJ, Ring SM, Evans DM, Lawlor DA.

Hum Mol Genet. 2011 Oct 15;20(20):4069-75. doi: 10.1093/hmg/ddr309. Epub 2011 Jul 14.

13.

The orphan adhesion-GPCR GPR126 is required for embryonic development in the mouse.

Waller-Evans H, Prömel S, Langenhan T, Dixon J, Zahn D, Colledge WH, Doran J, Carlton MB, Davies B, Aparicio SA, Grosse J, Russ AP.

PLoS One. 2010 Nov 18;5(11):e14047. doi: 10.1371/journal.pone.0014047.

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