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KAL1 wt Allele
Known as:
KALIG-1
, KMS
, HHA
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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…
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National Institutes of Health
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Related topics
Related topics
11 relations
ANOS1 gene
Cell Adhesion
Cell Movement
Homo sapiens
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2005
Highly Cited
2005
Kallmann syndrome: 14 novel mutations in KAL1 and FGFR1 (KAL2)
J. Albuisson
,
Chistophe Pêcheux
,
+11 authors
C. Dodé
Human mutation
2005
Corpus ID: 27321801
Kallmann syndrome (KAL) combines hypogonadotropic hypogonadism and anosmia. Hypogonadism is due to Gonadotropin Releasing Hormone…
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Highly Cited
2005
Highly Cited
2005
Modulation of multiply scattered coherent light by ultrasonic pulses: an analytical model.
S. Sakadzic
,
Lihong V. Wang
Physical review. E, Statistical, nonlinear, and…
2005
Corpus ID: 34377153
We present an analytical solution for the acousto-optical modulation of multiply scattered light in a medium irradiated with a…
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Review
2003
Review
2003
Genetic disorders of human congenital anomalies of the kidney and urinary tract (CAKUT)
K. Nakanishi
,
N. Yoshikawa
Pediatrics international : official journal of…
2003
Corpus ID: 21151354
Congenital abnormalities of the kidney and urinary tract, CAKUT are common in humans, occurring at a frequency of approximately 1…
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Highly Cited
2001
Highly Cited
2001
Idiopathic gonadotrophin deficiency: genetic questions addressed through phenotypic characterization*
R. Quinton
,
V. Duke
,
+10 authors
P. Bouloux
Clinical endocrinology
2001
Corpus ID: 10368223
OBJECTIVE The association of idiopathic hypogonadotrophic hypogonadism (IHH) with congenital olfactory deficit defines Kallmann's…
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Highly Cited
2001
Highly Cited
2001
The importance of autosomal genes in Kallmann syndrome: genotype-phenotype correlations and neuroendocrine characteristics.
L. M. Oliveira
,
S. Seminara
,
+7 authors
M. Vallejo
The Journal of clinical endocrinology and…
2001
Corpus ID: 30817970
Kallmann syndrome (KS) consists of congenital, isolated, idiopathic hypogonadotropic hypogonadism (IHH) and anosmia. The gene…
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Review
1996
Review
1996
The neuroradiology of Kallmann's syndrome: a genotypic and phenotypic analysis.
R. Quinton
,
V. Duke
,
+8 authors
P. Bouloux
The Journal of clinical endocrinology and…
1996
Corpus ID: 24483626
A detailed neurological investigation of patients with Kallmann's syndrome (KS) has been performed in an attempt to relate…
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Highly Cited
1995
Highly Cited
1995
KAL, a gene mutated in Kallmann's syndrome, is expressed in the first trimester of human development
V. Duke
,
P. Winyard
,
P. Thorogood
,
P. Soothill
,
P. Bouloux
,
A. Woolf
Molecular and Cellular Endocrinology
1995
Corpus ID: 7147769
Highly Cited
1994
Highly Cited
1994
Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo.
B. Lutz
,
S. Kuratani
,
+5 authors
G. Eichele
Human molecular genetics
1994
Corpus ID: 8972268
Kallmann syndrome is an inherited disorder characterized by an abnormality in olfactory system development. The gene for the X…
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Highly Cited
1993
Highly Cited
1993
Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome.
J. Hardelin
,
J. Levilliers
,
+5 authors
C. Petit
Human molecular genetics
1993
Corpus ID: 25088306
Kallmann syndrome represents the association of hypogonadotropic hypogonadism with anosmia. Three modes of transmission, X…
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Highly Cited
1989
Highly Cited
1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.
A. Ballabio
,
B. Bardoni
,
+7 authors
M. Fraccaro
Proceedings of the National Academy of Sciences…
1989
Corpus ID: 6973830
Mendelian inherited disorders due to deletions of adjacent genes on a chromosome have been described as "contiguous gene…
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