Anosmin-1 contributes to brain brain development. Loss-of-function mutations of KAL1 results in Kallmann syndrome with delayed puberty and anosmia. There is, however, little comprehension of its role in the microenvironment in vivo. Combined, these data suggest that anosmin-1 can facilitate " Kallmann syndrom
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
Abstract: Kallmann Syndrome is a heritable disorder characterized by congenital anosmia, hypogonadot...
AbstractThe anosmin-1 protein family regulates cell migration, axon guidance, and branching, by mech...
Infertility and inability to smell are the phenotypical features of Kallmann's syndrome (KS), a gene...
X-linked Kallmann's syndrome, a disease characterised by anosmia (a consequence of hypoplastic/absen...
AbstractThree new studies into the function of human anosmin-1 and related proteins in C. elegans an...
AbstractThe physiological role of anosmin-1, defective in the X chromosome-linked form of Kallmann s...
The protein anosmin-1, coded by the KAL1 gene responsible for the X-linked form of Kallmann syndrome...
Kallmann's syndrome (KS) is characterised by the association of anosmia (a loss of sense of smell) a...
Kallmann syndrome (KS) consists of congenital, isolated, idio-pathic hypogonadotropic hypogonadism (...
92 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2008.The X chromosome-linked form o...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
Abstract: Kallmann Syndrome is a heritable disorder characterized by congenital anosmia, hypogonadot...
AbstractThe anosmin-1 protein family regulates cell migration, axon guidance, and branching, by mech...
Infertility and inability to smell are the phenotypical features of Kallmann's syndrome (KS), a gene...
X-linked Kallmann's syndrome, a disease characterised by anosmia (a consequence of hypoplastic/absen...
AbstractThree new studies into the function of human anosmin-1 and related proteins in C. elegans an...
AbstractThe physiological role of anosmin-1, defective in the X chromosome-linked form of Kallmann s...
The protein anosmin-1, coded by the KAL1 gene responsible for the X-linked form of Kallmann syndrome...
Kallmann's syndrome (KS) is characterised by the association of anosmia (a loss of sense of smell) a...
Kallmann syndrome (KS) consists of congenital, isolated, idio-pathic hypogonadotropic hypogonadism (...
92 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2008.The X chromosome-linked form o...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
International audienceKallmann syndrome (KS) combines hypogonadotropic hypogonadism and anosmia. Ano...
Abstract: Kallmann Syndrome is a heritable disorder characterized by congenital anosmia, hypogonadot...
AbstractThe anosmin-1 protein family regulates cell migration, axon guidance, and branching, by mech...