scholarly journals A molecular genetic study of the variations in metabolic function during schistosome development

1995 ◽  
Vol 90 (2) ◽  
pp. 281-284 ◽  
Author(s):  
Patrick J. Skelly ◽  
Charles B. Shoemaker
Keyword(s):  
Genetic Study ◽  
Molecular Genetic ◽  
Metabolic Function ◽  
Molecular Genetic Study

Dedifferentiated endometrial carcinomas with neuroendocrine features: a clinicopathologic, immunohistochemical, and molecular genetic study

2018 ◽  
Vol 72 ◽  
pp. 100-106 ◽  
Author(s):  
Iñigo Espinosa ◽  
Antonio De Leo ◽  
Emanuela D'Angelo ◽  
Juan M. Rosa-Rosa ◽  
Marina Corominas ◽  
...  
Keyword(s):  
Genetic Study ◽  
Molecular Genetic ◽  
Molecular Genetic Study ◽  
Endometrial Carcinomas

scholarly journals Erratum: Malignant Peripheral Nerve Sheath Tumors with t(X;18). A Pathologic and Molecular Genetic Study

2000 ◽  
Vol 13 (12) ◽  
pp. 1336-1346 ◽  
Author(s):  
Maureen J O'Sullivan ◽  
Michael Kyriakos ◽  
Xiaopei Zhu ◽  
Mark R Wick ◽  
Paul E Swanson ◽  
...  
Keyword(s):  
Peripheral Nerve ◽  
Genetic Study ◽  
Molecular Genetic ◽  
Molecular Genetic Study ◽  
Nerve Sheath Tumors ◽  
Peripheral Nerve Sheath Tumors ◽  
Nerve Sheath

A case of megalencephalic leukoencephalopathy with subcortical cysts (van der Knaap disease): molecular genetic study

2003 ◽  
Vol 25 (5) ◽  
pp. 362-366 ◽  
Author(s):  
Harumi Saijo ◽  
Harumi Nakayama ◽  
Takanori Ezoe ◽  
Katsuhito Araki ◽  
Sui Sone ◽  
...  
Keyword(s):  
Genetic Study ◽  
Molecular Genetic ◽  
Molecular Genetic Study ◽  
Subcortical Cysts

scholarly journals A Molecular-Genetic Study of the Arabidopsis Toc75 Gene Family

2005 ◽  
Vol 138 (2) ◽  
pp. 715-733 ◽  
Author(s):  
Amy Baldwin ◽  
Anthony Wardle ◽  
Ramesh Patel ◽  
Penny Dudley ◽  
Soon Ki Park ◽  
...  
Keyword(s):  
Gene Family ◽  
Genetic Study ◽  
Molecular Genetic ◽  
Molecular Genetic Study

Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases

2018 ◽  
Vol 32 (3) ◽  
pp. 423-434 ◽  
Author(s):  
Alyaa Al-Ibraheemi ◽  
Andrew L. Folpe ◽  
Antonio R. Perez-Atayde ◽  
Kyle Perry ◽  
Jakob Hofvander ◽  
...  
Keyword(s):  
Tyrosine Kinase ◽  
Receptor Tyrosine Kinase ◽  
Genetic Study ◽  
Molecular Genetic ◽  
Kinase Signaling ◽  
Molecular Genetic Study ◽  
Tyrosine Kinase Signaling

scholarly journals Clinical and molecular genetic study of 12 Italian families with autosomal recessive Stargardt disease

2012 ◽  
Vol 11 (4) ◽  
pp. 4342-4350 ◽  
Author(s):  
M. Oldani ◽  
S. Marchi ◽  
A. Giani ◽  
S. Cecchin ◽  
E. Rigoni ◽  
...  
Keyword(s):  
Genetic Study ◽  
Autosomal Recessive ◽  
Molecular Genetic ◽  
Stargardt Disease ◽  
Molecular Genetic Study

scholarly journals WT1 gene mutation in exone 7 in boy with disturbance of the sex formation and the bilateral nephroblastoma

2020 ◽  
Vol 64 (6) ◽  
pp. 94-97
Author(s):  
N. R. Akramov ◽  
I. V. Osipova ◽  
A. M. Zakirova ◽  
E. I. Khaertdinov ◽  
E. L. Rashitova
Keyword(s):  
Gene Mutation ◽  
Genetic Study ◽  
Molecular Genetic ◽  
Lower Pole ◽  
Molecular Genetic Study ◽  
Metachronous Tumor ◽  
The Right ◽  
Surgical Operations ◽  
I Gene ◽  
Final Operation

The case of observing a patient with WT1 gene mutation in exone 7 with bilateral Wilms metachronous tumor, disturbance of the sex formation in the form of scrotal hypospadias and bilateral abdominal cryptorchidism, without nephropathy, is presented. The child underwent surgical operations: left-sided nephrectomy, resection of the lower pole of the right kidney, bilateral orchiopexy and two-stage hypospadias correction. 7 years after the start of treatment and 3 years after the final operation, the condition of the child was estimated as satisfactory. The presented case by the results of the molecular genetic study has no previously described analogues and requires further observation.

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