Understanding the Role of the SMN Complex Component GEMIN5 and Its Functional Relationship with Demethylase KDM6B in the Flunarizine-Mediated Neuroprotection of Motor Neuron Disease Spinal Muscular Atrophy.

SMN1 KDM6B

Limb alterations in brachypodism mice due to mutations in a new member of the TGF beta-superfamily.

PAX1 GDF6

A dual-activity topoisomerase complex regulates mRNA translation and turnover.

DPH2 ARHGEF19 LATS2 KDM6B SRCAP PLEKHO2 RNF43

The Hippo Pathway Kinases LATS1/2 Suppress Cancer Immunity.

LATS2 TICAM1

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.

LMTK3 SRCAP

Genome-wide association study of pancreatic cancer in Japanese population.

FOXQ1 RNF43

The contribution of de novo coding mutations to autism spectrum disorder.

KDM6B SRCAP

High-throughput analyses of hnRNP H1 dissects its multi-functional aspect.

ARHGEF19 OAZ1 LMTK3 PRR34 CARNS1 NOL3

Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico.

PAX1 GDF6

NANOG initiates epiblast fate through the coordination of pluripotency genes expression.

FOXQ1 LATS2

LINC01547

156

ADAM19

671

C16orf54

16

CARNS1

516

DPH2

366

RAB44

381

CAPN15

896

ARHGEF19

101

LATS2

461

KDM6B

26

KIAA1614

41

LMTK3

496

PDZD3

96

KCNH4

916

OAZ1

61

MACF1

36

ACP2

336

PAX1

506

DMRTC2

316

LINC00304

36

MFSD13A

446

C4orf19

71

PSMF1

176

FOXQ1

296

GDF6

171

PRR34

6

RNF43

691

SMN1

226

NOL3

106

SRCAP

1986

TICAM1

621

TICAM1

626

PLEKHO2

376