Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Mutations in STARD8 (DLC3) may cause 46,XY gonadal dysgenesis
CONCLUSION: Based on these and previous results, it is reasonable to include STARD8 in gene panels for 46,XY gonadal dysgenesis.PMID:38447543 | DOI:10.1159/000537877 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - March 6, 2024 Category: Genetics & Stem Cells Authors: Dmytro Sirokha Alexey Rayevsky Olexandra Gorodna Vitalii Kalynovskyi Nataliya Zelinska Oksana Samson Krystyna Kwiatkowska Serge Nef Jadwiga Jaruzelska Kamila Kusz-Zamelczyk Ludmila Livshits Source Type: research

Rare case of Turner syndrome patient with metastatic dysgerminoma and no Y-chromosomal material with pathogenic variants found in KIT and MTOR
CONCLUSION: Females with TS can develop metastatic dysgerminoma even in the absence of Y-chromosomal material. This questions the current understanding of Y-chromosomal material being essential for the malignant transformation of a gonadoblastoma in the dysgenetic gonad.PMID:38281483 | DOI:10.1159/000536236 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - January 28, 2024 Category: Genetics & Stem Cells Authors: Camilla Mains Balle Christine Gaasdal Kassentoft Jolinda Iris van Heusden Michael Knudsen Line Raaby Claus H øjbjerg Gravholt Source Type: research

Rare case of Turner syndrome patient with metastatic dysgerminoma and no Y-chromosomal material with pathogenic variants found in KIT and MTOR
CONCLUSION: Females with TS can develop metastatic dysgerminoma even in the absence of Y-chromosomal material. This questions the current understanding of Y-chromosomal material being essential for the malignant transformation of a gonadoblastoma in the dysgenetic gonad.PMID:38281483 | DOI:10.1159/000536236 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - January 28, 2024 Category: Genetics & Stem Cells Authors: Camilla Mains Balle Christine Gaasdal Kassentoft Jolinda Iris van Heusden Michael Knudsen Line Raaby Claus H øjbjerg Gravholt Source Type: research

Rare case of Turner syndrome patient with metastatic dysgerminoma and no Y-chromosomal material with pathogenic variants found in KIT and MTOR
CONCLUSION: Females with TS can develop metastatic dysgerminoma even in the absence of Y-chromosomal material. This questions the current understanding of Y-chromosomal material being essential for the malignant transformation of a gonadoblastoma in the dysgenetic gonad.PMID:38281483 | DOI:10.1159/000536236 (Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation)
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - January 28, 2024 Category: Genetics & Stem Cells Authors: Camilla Mains Balle Christine Gaasdal Kassentoft Jolinda Iris van Heusden Michael Knudsen Line Raaby Claus H øjbjerg Gravholt Source Type: research