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A novel homozygous DOCK8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK8 deficiency patient

Journal of the European Academy of Dermatology and Venereology, 2017-11, Vol.31 (11), p.e504-e505

2017

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Effect of gestational subclinical hypothyroidism on early neurodevelopment of offspring

Journal of perinatology, 2015-09, Vol.35 (9), p.678-682

2015

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Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome

Andrologia, 2012-05, Vol.44 (s1), p.523-529

2012

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A novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters

The journal of clinical endocrinology and metabolism, 1998-06, Vol.83 (6), p.2091-2098

1998

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The identification of 5α-reductase-2 and 17β-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred

The journal of clinical endocrinology and metabolism, 1998-02, Vol.83 (2), p.560-569

1998

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EFFECTS OF LEUKAEMIA INHIBITORY FACTOR ON EMBRYO IMPLANTATION IN THE MOUSE

Cytokine (Philadelphia, Pa.), 2000-11, Vol.12 (11), p.1676-1682

2000

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Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genes

Clinical and experimental dermatology, 2014-03, Vol.39 (2), p.225-227

2014

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A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred

The journal of clinical endocrinology and metabolism, 1999-05, Vol.84 (5), p.1590-1594

1999

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Effects of Stubble Management on Soil Fertility and Crop Yield of Rainfed Area in Western Loess Plateau, China

Applied and Environmental Soil Science, 2012, Vol.2012 (2012), p.101-109

2012

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5 alpha-reductase-2 gene mutations in the Dominican Republic

The journal of clinical endocrinology and metabolism, 1996-05, Vol.81 (5), p.1730-1735

1996

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Dihydrotestosterone regulation of semen in male pseudohermaphrodites with 5α-reductase-2 deficiency

The journal of clinical endocrinology and metabolism, 1994-08, Vol.79 (2), p.409-414

1994

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The biochemical and phenotypic characterization of females homozygous for 5α-reductase-2 deficiency

The journal of clinical endocrinology and metabolism, 1995-11, Vol.80 (11), p.3160-3167

1995

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The androgen control of sebum production. Studies of subjects with dihydrotestosterone deficiency and complete androgen insensitivity

The journal of clinical endocrinology and metabolism, 1993-02, Vol.76 (2), p.524-528

1993

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Immunogenicity of polyepitope libraries assembled by epitope shuffling: an approach to the development of chimeric gene vaccination against malaria

Vaccine, 2004-11, Vol.23 (2), p.267-277

2004

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Association of HLA-DRB1 alleles with keloids in Chinese Han individuals

Tissue antigens, 2010-10, Vol.76 (4), p.276-281

2010

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Mutations in CYP11B1 gene: Phenotype-genotype correlations

American journal of medical genetics, 2003-10, Vol.122A (3), p.193-200

2003

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Metal Element Doping Graphene for the Oxygen Electrode: A Density Functional Calculation

International journal of electrochemical science, 2019-01, Vol.14 (1), p.598-605

2019

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Central opioid modulation of fetal cardiovascular function: role of mu- and delta-receptors

American journal of physiology. Regulatory, integrative and comparative physiology, 1990-06, Vol.258 (6), p.1453-R1458

1990

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Paternity by Intrauterine Insemination with Sperm from a Man with 5α-Reductase-2 Deficiency

The New England journal of medicine, 1997-04, Vol.336 (14), p.994-998

1997

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Cervical spondylotic myelopathy treated by anterior multilevel decompression and fusion: follow-up report of 214 cases

Clinical orthopaedics and related research, 1987-08, Vol.221 (221), p.161-164

1987

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A novel homozygous DOCK 8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK 8 deficiency patient

Journal of the European Academy of Dermatology and Venereology, 2017-11, Vol.31 (11)

2017

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Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome: Characterisation of an androgen receptor mutation

Andrologia, 2012-05, Vol.44, p.523-529

2012

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Evaluation of the risk factors of depressive disorders comorbid with obstructive sleep apnea

Neuropsychiatric disease and treatment, 2017-01, Vol.13, p.155-159

2017

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Remodeling of the Intestine during Metamorphosis of Xenopus laevis

Proceedings of the National Academy of Sciences - PNAS, 2005-03, Vol.102 (10), p.3720-3725

2005

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Expression of type II iodothyronine deiodinase marks the time that a tissue responds to thyroid hormone-induced metamorphosis in Xenopus laevis

Developmental biology, 2004-02, Vol.266 (1), p.87-95

2004

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A novel homozygous DOCK8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK8 deficiency patient

Effect of gestational subclinical hypothyroidism on early neurodevelopment of offspring

Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome

A novel mutation of the human luteinizing hormone receptor in 46XY and 46XX sisters

The identification of 5α-reductase-2 and 17β-hydroxysteroid dehydrogenase-3 gene defects in male pseudohermaphrodites from a Turkish kindred

EFFECTS OF LEUKAEMIA INHIBITORY FACTOR ON EMBRYO IMPLANTATION IN THE MOUSE

Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genes

A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred

Effects of Stubble Management on Soil Fertility and Crop Yield of Rainfed Area in Western Loess Plateau, China

5 alpha-reductase-2 gene mutations in the Dominican Republic

Dihydrotestosterone regulation of semen in male pseudohermaphrodites with 5α-reductase-2 deficiency

The biochemical and phenotypic characterization of females homozygous for 5α-reductase-2 deficiency

The androgen control of sebum production. Studies of subjects with dihydrotestosterone deficiency and complete androgen insensitivity

Immunogenicity of polyepitope libraries assembled by epitope shuffling: an approach to the development of chimeric gene vaccination against malaria

Association of HLA-DRB1 alleles with keloids in Chinese Han individuals

Mutations in CYP11B1 gene: Phenotype-genotype correlations

Metal Element Doping Graphene for the Oxygen Electrode: A Density Functional Calculation

Central opioid modulation of fetal cardiovascular function: role of mu- and delta-receptors

Paternity by Intrauterine Insemination with Sperm from a Man with 5α-Reductase-2 Deficiency

Cervical spondylotic myelopathy treated by anterior multilevel decompression and fusion: follow-up report of 214 cases

A novel homozygous DOCK 8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK 8 deficiency patient

Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome: Characterisation of an androgen receptor mutation

Evaluation of the risk factors of depressive disorders comorbid with obstructive sleep apnea

Remodeling of the Intestine during Metamorphosis of Xenopus laevis

Expression of type II iodothyronine deiodinase marks the time that a tissue responds to thyroid hormone-induced metamorphosis in Xenopus laevis

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