KAL1 wt Allele

Known as: KALIG-1, KMS, HHA 
Human KAL1 wild-type allele is located in the vicinity of Xp22.32 and is approximately 203 kb in length. This allele, which encodes anosmin-1 protein… (More)

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Topic mentions per year

1983-2017
051019832017

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Highly Cited
2006
Highly Cited
2006
DNA copy number changes represent molecular fingerprints of solid tumors and are as such relevant for better understanding of… (More)
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2004
2004
X-linked Kallmann's syndrome (KS) is a genetic disease characterized by anosmia and hypogonadism due to impairment in the… (More)
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2002
2002
As our knowledge of the molecular mechanisms underlying idiopathic hypogonadotropic hypogonadism (IHH) expands, it becomes… (More)
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2001
2001
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene… (More)
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2001
2001
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's… (More)
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Highly Cited
2000
Highly Cited
2000
Polymorphisms in CC chemokine receptor 5 (CCR5), the major coreceptor of human immunodeficiency virus 1 (HIV-1) and simian… (More)
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1996
1996
The KAL gene is responsible for the X-chromosome linked form of Kallmann's syndrome in humans. Upon transfection of CHO cells… (More)
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1993
1993
Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. Three modes of transmission, X… (More)
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1992
1992
The gene for the X-linked Kallmann syndrome (KAL), a developmental disorder characterized by hypogonadotropic hypogonadism and… (More)
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Highly Cited
1991
Highly Cited
1991
Kallmann syndrome associates hypogonadotropic hypogonadism and anosmia and is probably due to a defect in the embryonic migration… (More)
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