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101. Author Correction: Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

103. Somatic Ras/Raf/MAPK Variants Enriched in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy

104. Macrolides selectively inhibit mutant KCNJ5 potassium channels that cause aldosterone-producing adenoma

105. Isolated polycystic liver disease genes define effectors of polycystin-1 function

109. Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

110. A Novel Missense Mutation in ERCC8 Co-Segregates with Cerebellar Ataxia in a Consanguineous Pakistani Family

111. Supplement to: Genetic drivers of kidney defects in the DiGeorge syndrome.

113. Advillin acts upstream of phospholipase C ε1 in steroid-resistant nephrotic syndrome

115. Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

116. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

121. Mutation spectrum of congenital heart disease in a consanguineous Turkish population

122. Genome-Wide De Novo Variants in Congenital Heart Disease Are Not Associated With Maternal Diabetes or Obesity

123. Centers for Mendelian Genomics: A decade of facilitating gene discovery

125. Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration

126. Landscape of somatic single-nucleotide and copy-number mutations in uterine serous carcinoma

127. A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations via Dysregulation of Retinoic Acid Signaling

128. Mutations in sphingosine-1-phosphate lyase cause nephrosis with ichthyosis and adrenal insufficiency

129. Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

130. A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury

132. KANK deficiency leads to podocyte dysfunction and nephrotic syndrome

133. Genomic landscape of cutaneous T cell lymphoma

134. Exome sequencing identifies recurrent mutations in NF1 and RASopathy genes in sun-exposed melanomas

135. Mutations of the SLIT2–ROBO2 pathway genes SLIT2 and SRGAP1 confer risk for congenital anomalies of the kidney and urinary tract

138. Whole exome sequencing identifies potential candidate genes for spina bifida derived from mouse models

139. The Genomic and Phenotypic Landscape of Ichthyosis

140. Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk

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