704 results on '"Moser, Markus"'
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202. Leukocyte Adhesion Deficiency-III: When Leukocytes Cannot Stop
203. The ARF-Like GTPase ARFRP1 Is Essential for Lipid Droplet Growth and Is Involved in the Regulation of Lipolysis
204. The Fibronectin RGD Motif Is Required for Multiple Angiogenic Events During Early Embryonic Development
205. Ultrastructural cartilage abnormalities in MIA/CD-RAP-deficient mice
206. Kindlin-3 is required for β2 integrin–mediated leukocyte adhesion to endothelial cells
207. Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation
208. Two biochemically distinct and tissue-specific twinfilin isoforms are generated from the mouse Twf2 gene by alternative promoter usage
209. Loss of Kindlin-1 Causes Skin Atrophy and Lethal Neonatal Intestinal Epithelial Dysfunction
210. Comparative expression analysis of the murine palladin isoforms
211. Targeted disruption of the mouse Csrp2gene encoding the cysteine- and glycine-rich LIM domain protein CRP2 result in subtle alteration of cardiac ultrastructure
212. SILAC Mouse for Quantitative Proteomics Uncovers Kindlin-3 as an Essential Factor for Red Blood Cell Function
213. Das Projekt Hochwassergefahrenkarten in Baden-Württemberg
214. Hydraulische Berechnungen der Hochwassergefahrenkarten
215. Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) and Proteome Quantitation of Mouse Embryonic Stem Cells to a Depth of 5,111 Proteins
216. Redundant function of the heparan sulfate 6‐O‐endosulfatases Sulf1 and Sulf2 during skeletal development
217. Targeted disruption ofSlc2a8(GLUT8) reduces motility and mitochondrial potential of spermatozoa
218. Effect of Apolipoprotein M on High Density Lipoprotein Metabolism and Atherosclerosis in Low Density Lipoprotein Receptor Knock-out Mice
219. Disruption of the latent transforming growth factor-β binding protein-1 gene causes alteration in facial structure and influences TGF-β bioavailability
220. Loss of talin1 in platelets abrogates integrin activation, platelet aggregation, and thrombus formation in vitro and in vivo
221. REVISION OF THE TYPE MATERIAL AND NOMENCLATURE OF MASTODONSAURUS GIGANTEUS (JAEGER) (TEMNOSPONDYLI) FROM THE MIDDLE TRIASSIC OF GERMANY
222. Cloning, expression and characterization of the murine orthologue of SBF2, the gene mutated in Charcot-Marie-Tooth disease type 4B2
223. Regulation of integrin α10 expression in chondrocytes by the transcription factors AP-2ε and Ets-1
224. Consequences of loss of PINCH2 expression in mice
225. Mutations in SIL1 cause Marinesco-Sjögren syndrome, a cerebellar ataxia with cataract and myopathy
226. PINCH1 regulates cell-matrix and cell-cell adhesions, cell polarity and cell survival during the peri-implantation stage
227. A mouse model for cystic biliary dysgenesis in autosomal recessive polycystic kidney disease (ARPKD)
228. Loss of Swiss Cheese/Neuropathy Target Esterase Activity Causes Disruption of Phosphatidylcholine Homeostasis and Neuronal and Glial Death in AdultDrosophila
229. Bone Morphogenic Proteins Are Overexpressed in Malignant Melanoma and Promote Cell Invasion and Migration
230. Impaired Channel Targeting and Retinal Degeneration in Mice Lacking the Cyclic Nucleotide-Gated Channel Subunit CNGB1
231. PKHD1mutations in autosomal recessive polycystic kidney disease (ARPKD)
232. PKHD1mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)
233. Placental Failure and Impaired Vasculogenesis Result in Embryonic Lethality for Neuropathy Target Esterase-Deficient Mice
234. GLUT1 mRNA and Protein Expression in Ovarian Borderline Tumors and Cancer
235. Identification and embryonic expression of a new AP-2 transcription factor, AP-2?
236. GLUT1 Messenger RNA and Protein Induction Relates to the Malignant Transformation of Cervical Cancer
237. PINCH2 is a new five LIM domain protein, homologous to PINCHand localized to focal adhesions☆
238. Terminal Renal Failure in Mice Lacking Transcription Factor AP-2β
239. The murine latent transforming growth factor-β binding protein (Ltbp-1) is alternatively spliced, and maps to a region syntenic to human chromosome 2p21–22
240. Specific Expression and Regulation of the New Melanoma Inhibitory Activity-related Gene MIA2 in Hepatocytes
241. Spectrum of Mutations in the Gene for Autosomal Recessive Polycystic Kidney Disease (ARPKD/PKHD1)
242. Identification and Characterization of Pkhd1, the Mouse Orthologue of the Human ARPKD Gene
243. Validation of a luminescence immunoassay for the detection of PrPSc in brain homogenate
244. Ultrastructural Cartilage Abnormalities in MIA/CD-RAP-Deficient Mice
245. LIM-domain protein cysteine- and glycine-rich protein 2 (CRP2) is a novel marker of hepatic stellate cells and binding partner of the protein inhibitor of activated STAT1
246. Neurocan Is Dispensable for Brain Development
247. Induction of AP-2α Expression by Adenoviral Infection Involves Inactivation of the AP-2rep Transcriptional Corepressor CtBP1
248. Regulatory roles of AP-2 transcription factors in vertebrate development, apoptosis and cell-cycle control
249. The Basic Helix-Loop-Helix Transcription Factors Myogenin and Id2 Mediate Specific Induction of Caveolin-3 Gene Expression during Embryonic Development
250. Molecular cloning and characterization of a human metalloprotease disintegrin— a novel marker for dendritic cell differentiation
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