1,105 results on '"Glaser, B."'
Search Results
152. Noyau caudé et traitement temporel dans le syndrome vélocardiofacial (22q11)
153. Amount-dependent isotopic fractionation during compound-specific isotope analysis
154. ChemInform Abstract: Chemistry of Boron. Part 217. (2 + 2) Cycloaddition Reactions of 9- Fluorenylidene(tetramethylpiperidino)borane with Carbonyl and Thiocarbonyl Compounds.
155. Age- and puberty-dependent association between IQ score in early childhood and depressive symptoms in adolescence
156. Organic matter quality of a forest soil subjected to repeated drying and different re-wetting intensities
157. Ameliorating physical and chemical properties of highly weathered soils in the tropics with charcoal: A review
158. d13C of individual lignin phenols in a postglacial lake deposit in Nepal: A reassessment of the vegetation/climate reconstruction based on bulk-d13C
159. Bestimmung substanzspezifischer d13C-Verhältnisse in Ligninphenolen mittels Gaschromatographie-Verbrennungs-Isotopenmassenspektrometrie (GC-C-IRMS)
160. Ameliorating physical and chemical properties of highly weathered soils in the tropics with charcoal: A review
161. Uptake of intact amino acids by plants depends on soil amino acid concentrations
162. Fluxes and <sup>13</sup>C isotopic composition of dissolved carbon and pathways of methanogenesis in a fen soil exposed to experimental drought
163. Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation
164. Fluxes and 13C isotopic composition of dissolved carbon and pathways of methanogenesis in a fen soil exposed to experimental drought
165. O25 Les nouveaux gènes associés au diabète de type 2 : impact dans des populations non européennes et mesure de leurs effets combinés
166. 235 – Cortical thickness in 22q11 deletion syndrome: Alterations in affected children and evolution into adulthood
167. Disturbed cortical gyrification in 22q11 deletion syndrome: Potential cues to the etiology of brain malformations in the syndrome
168. Source monitoring for actions in adolescents with 22q11.2 deletion syndrome (22q11DS)
169. Structural changes to the fusiform gyrus: A cerebral marker for social impairments in 22q11.2 deletion syndrome?
170. A through G
171. Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism
172. Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome
173. Alkylphenols in sediments of the Atlantic Rainforest south-west of São Paulo, Brazil
174. Idiotype protein vaccination in combination with adjuvant cytokines in patients with multiple myeloma - evaluation of T-cell responses by different read-out systems
175. INFLUENCE OF MONOCYTE CHEMOATTRACTANT PROTEIN-1 (MCP-1) AND ITS RECEPTOR CCR2 ON PANCREATIC AND PULMONARY DAMAGE IN EXPERIMENTAL ACUTE PANCREATITIS
176. Black carbon in a temperate mixed-grass savanna
177. A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers
178. Clear-cutting of a Norway spruce stand: implications for controls on the dynamics of dissolved organic matter in the forest floor
179. Surface exposure dating using in situ cosmogenic 10Be
180. Self-management of oral anticoagulation: long-term results
181. Short-term effects of dairy slurry amendment on carbon sequestration and enzyme activities in a temperate grassland
182. Ausonius: Cupid Crucified
183. Response to Mastrototaro and Gross
184. Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.
185. Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes
186. CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers
187. Hyperinsulinism of Infancy: The Regulated Release of Insulin by KATP Channel--Independent Pathways
188. Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.
189. Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators.
190. Genetics of neonatal hyperinsulinism
191. Soviet and Chinese Strategic Perceptions in Peacetime and Wartime.
192. Transposition of SRY into the ancestral pseudoautosomal region creates a new pseudoautosomal boundary in a progenitor of simian primates [In Process Citation]
193. Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
194. Sulfate Transport Is Not Impaired in Pendred Syndrome Thyrocytes
195. Soviet and Chinese Strategic Perceptions in Peacetime and Wartime.
196. Isolation and characterization of the human PAX4 gene.
197. Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
198. Genetic Heterogeneity in Familial Hyperinsulinism
199. Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.
200. Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews.
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