Results 141 to 150 of about 2,722 (177)

Large-scale mouse mutagenesis identifies novel genes affecting vertebral anatomy. [PDF]

Mamm Genome
Ibarra-Soria X, Webb E, Mulley JF.
europepmc   +1 more source

Fibrillin gene family and its role in plant growth, development, and abiotic stress. [PDF]

Front Plant Sci
El-Sappah AH, Li J, Yan K, Zhu C, Huang Q, Zhu Y, Chen Y, El-Tarabily KA, AbuQamar SF.   +8 more
europepmc   +1 more source

Transcriptomic signatures in Gaucher disease subtypes: A systems biology perspective. [PDF]

Mol Genet Metab Rep
Elahimanesh M, Ganjali R, Najafi M.
europepmc   +1 more source

Elucidating Regulatory Mechanisms of Genes Involved in Pathobiology of Sjögren's Disease: Immunostimulation Using a Cell Culture Model. [PDF]

Int J Mol Sci
Kepple DD, Thornburg TE, Beckman MF, Bahrani Mougeot F, Mougeot JC.   +4 more
europepmc   +1 more source

Whole -genome survival analysis of 144 286 people from the UK Biobank identifies novel loci associated with blood pressure. [PDF]

J Hypertens
Saluja S, Darlay R, Lennon R, Keavney BD, Cordell HJ.   +4 more
europepmc   +1 more source

The Biomechanics of Fibrillin Microfibrils: Lessons from the Ciliary Zonule. [PDF]

Cells
Rathaur P, Rodriguez J, Kuchtey J, Insignares S, Jones WB, Kuchtey RW, Bassnett S.   +6 more
europepmc   +1 more source

Identification of 16 novel Alzheimer's disease loci using multi-ancestry meta-analyses. [PDF]

Alzheimers Dement
Willett JDS, Waqas M, Choi Y, Ngai T, Mullin K, Tanzi RE, Prokopenko D.   +6 more
europepmc   +1 more source

Pathway-Centric Comparative Molecular Profiling of Sézary Syndrome and Primary Cutaneous CD8⁺ Aggressive Epidermotropic Cytotoxic T-Cell Lymphoma via Conversational Artificial Intelligence. [PDF]

Cancers (Basel)
Diaz FC, Waldrup B, Carranza FG, Manjarrez S, Velazquez-Villarreal E.   +4 more
europepmc   +1 more source

TheFBN2gene: new mutations, locus-specific database (Universal Mutation DatabaseFBN2), and genotype-phenotype correlations [PDF]

Human Mutation, 2009
International audienceCongenital contractural arachnodactyly (CCA) is an extremely rare disease, due to mutations in the FBN2 gene encoding fibrillin-2. Another member of the fibrillin family, the FBN1 gene, is involved in a broad phenotypic continuum of
Christoph Marschall, Dalîl Hamroun, Cheryl L Maslen   +2 more
exaly   +6 more sources