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HOXA10 mutations in congenital absence of uterus and vagina

Fertility and sterility, 2008-02, Vol.89 (2), p.325-330

2008

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Predicting Overall Survival in Patients With Metastatic Melanoma on Antiangiogenic Therapy and RECIST Stable Disease on Initial Posttherapy Images Using CT Texture Analysis

American journal of roentgenology (1976), 2015-09, Vol.205 (3), p.W283-W293

2015

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CCN5, a secreted protein, localizes to the nucleus

Journal of cell communication and signaling, 2010-06, Vol.4 (2), p.91-98

2010

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Metastatic melanoma: lactate dehydrogenase levels and CT imaging findings of tumor devascularization allow accurate prediction of survival in patients treated with bevacizumab

Radiology, 2014-02, Vol.270 (2), p.425-434

2014

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Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone β-Subunit Gene

The New England journal of medicine, 1997-08, Vol.337 (9), p.607-611

1997

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Covalent genomic DNA modification patterns revealed by denaturing gradient gel blots

Gene, 2007-04, Vol.391 (1), p.45-52

2007

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CCN5 Expression in mammals. II. Adult rodent tissues

Journal of cell communication and signaling, 2007-09, Vol.1 (2), p.145-158

2007

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CCN5 expression in mammals : I. Embryonic and fetal tissues of mouse and human

Journal of cell communication and signaling, 2007-09, Vol.1 (2), p.127-143

2007

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Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina

American journal of medical genetics, 2003-07, Vol.120A (1), p.72-76

2003

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Characterization and mutation analysis of the human FORMIN-2 ( FMN2) gene in women with unexplained infertility

Fertility and sterility, 2005-05, Vol.83 (5), p.1363-1371

2005

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Dominant transmission of imperforate hymen

Fertility and sterility, 2000-12, Vol.74 (6), p.1241-1244

2000

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Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism

Fertility and sterility, 1997-12, Vol.68 (6), p.1079-1085

1997

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Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene

Human mutation, 1998, Vol.12 (6), p.393-402

1998

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Using the Climate Assessment Tool (CAT) in U.S. EPA BASINS integrated modeling system to assess watershed vulnerability to climate change

Water science and technology, 2007-01, Vol.56 (8), p.49-56

2007

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CCN5 expression in mammals

Journal of cell communication and signaling, 2007-09, Vol.1 (2), p.127-143

2007

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Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: Outcomes of surrogate pregnancies

Fertility and sterility, 1997-02, Vol.67 (2), p.387-389

1997

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Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone beta-Subunit Gene

Obstetrical & gynecological survey, 1998-02, Vol.53 (2), p.85-87

1998

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Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct

American journal of obstetrics and gynecology, 1998-09, Vol.179 (3), p.597-603

1998

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Analysis of the WNT-4 gene in women with congenital absence of the uterus and vagina

Fertility and sterility, 2002-09, Vol.78, p.S169-S170

2002

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Characterization of the human FORMIN2 (FMN2) gene

Fertility and sterility, 2003-09, Vol.80, p.252-253

2003

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Role for anti-Müllerian hormone in congenital absence of the uterus and vagina

American journal of medical genetics, 2001-01, Vol.98 (2), p.129-136

2001

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Detection of DNA sequence polymorphisms in human genomic DNA by using denaturing gradient gel blots

American journal of human genetics, 1992-02, Vol.50 (2), p.331-346

GRAY, M. R

1992

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Methylation-dependent melting polymorphisms in genomic fragments of deoxyribonucleic acid

American journal of obstetrics and gynecology, 2000-04, Vol.182 (4), p.785-793

2000

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Rapid identification of deoxyribonucleic acid sequence differences in cytochrome P-450 21-hydroxylase (CYP21) genes with denaturing gradient gel blots

American journal of obstetrics and gynecology, 1992, Vol.166 (1), p.184-191

1992

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Gonadotropin-releasing hormone-associated peptide gene sequences in women with hyperprolactinemia

Fertility and sterility, 1992-11, Vol.58 (5), p.908-913

1992

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HOXA10 mutations in congenital absence of uterus and vagina

Predicting Overall Survival in Patients With Metastatic Melanoma on Antiangiogenic Therapy and RECIST Stable Disease on Initial Posttherapy Images Using CT Texture Analysis

CCN5, a secreted protein, localizes to the nucleus

Metastatic melanoma: lactate dehydrogenase levels and CT imaging findings of tumor devascularization allow accurate prediction of survival in patients treated with bevacizumab

Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone β-Subunit Gene

Covalent genomic DNA modification patterns revealed by denaturing gradient gel blots

CCN5 Expression in mammals. II. Adult rodent tissues

CCN5 expression in mammals : I. Embryonic and fetal tissues of mouse and human

Analysis of cystic fibrosis transmembrane conductance regulator gene mutations in patients with congenital absence of the uterus and vagina

Characterization and mutation analysis of the human FORMIN-2 ( FMN2) gene in women with unexplained infertility

Dominant transmission of imperforate hymen

Mutation analysis of the gonadotropin-releasing hormone receptor gene in idiopathic hypogonadotropic hypogonadism

Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene

Using the Climate Assessment Tool (CAT) in U.S. EPA BASINS integrated modeling system to assess watershed vulnerability to climate change

CCN5 expression in mammals

Congenital absence of the uterus and vagina is not commonly transmitted as a dominant genetic trait: Outcomes of surrogate pregnancies

Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone beta-Subunit Gene

Further evidence that the WT1 gene does not have a role in the development of the derivatives of the müllerian duct

Analysis of the WNT-4 gene in women with congenital absence of the uterus and vagina

Characterization of the human FORMIN2 (FMN2) gene

Role for anti-Müllerian hormone in congenital absence of the uterus and vagina

Detection of DNA sequence polymorphisms in human genomic DNA by using denaturing gradient gel blots

Methylation-dependent melting polymorphisms in genomic fragments of deoxyribonucleic acid

Rapid identification of deoxyribonucleic acid sequence differences in cytochrome P-450 21-hydroxylase (CYP21) genes with denaturing gradient gel blots

Gonadotropin-releasing hormone-associated peptide gene sequences in women with hyperprolactinemia

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