תוצאות חיפוש - Yangzhu Du
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Loss-of-function mutations in the human <i>GLI2</i> gene are associated with pituitary anomalies and holoprosencephaly-like features מאת Erich Roessler, Yangzhu Du, José L. Mullor, Esther Casas, William Allen, Gabriele Gillessen‐Kaesbach, Elizabeth Roeder, Jeffrey E. Ming, Ariel Ruiz i Altaba, Maximilian Muenke
יצא לאור 2003Artigo -
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The Tabby phenotype is caused by mutation in a mouse homologue of the<i>EDA</i>gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenou... מאת Anand K. Srivastava, Johanna Pispa, Andrew J. Hartung, Yangzhu Du, Sini Ezer, Ted Jenks, Tokihiko Shimada, Maija Pekkanen, Marja L. Mikkola, Minoru S.H. Ko, Irma Thesleff, Juha Kere, David Schlessinger
יצא לאור 1997Artigo
כלי חיפוש:
נושאים קשורים
Biology
Gene
Genetics
Endocrinology
Phenotype
Adipokine
Anovulation
Candidate gene
Cell biology
Central nervous system
Complementary DNA
Diabetes mellitus
Exon
Fetus
Forebrain
GLI2
GLI3
Gene isoform
Genetic association
Genotype
Holoprosencephaly
Homeobox
Hypopituitarism
Insulin resistance
Internal medicine
Loss function
Medicine
Molecular biology
Mutation
Obesity