Cargando…

AB188. Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4

BACKGROUND: Ring chromosomes are often associated with spermatogenetic failure. However, the mechanism is poorly understood. We here reported a single man with severe oligospermia and a ring chromosome 4 with a microdeletion at 4p16.3. METHODS: Synapsis (asSCP3), recombination (as MLH1) and transcri...

Descripción completa

Detalles Bibliográficos
Autores principales:	Yao, Qi, Wang, Liu, Yao, Bing, Gao, Hongliu, Li, Weiwei, Xia, Xinyi, Shi, Qinghua, Cui, Yingxia
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	AME Publishing Company 2014
Materias:	Abstract Publication Basic Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4708340/ http://dx.doi.org/10.3978/j.issn.2223-4683.2014.s188

Ejemplares similares

Meiotic prophase I defects in an oligospermic man with Wolf-Hirschhorn syndrome with ring chromosome 4
por: Yao, Qi, et al.
Publicado: (2014)

Phenotypic Variations in Wolf-Hirschhorn Syndrome
por: Sukarova-Angelovska, E, et al.
Publicado: (2014)

Wolf–Hirschhorn (4p-) syndrome with West syndrome
por: Motoi, Hirotaka, et al.
Publicado: (2016)

Airway Management in a Patient with Wolf-Hirschhorn Syndrome
por: Gamble, John F., et al.
Publicado: (2016)

Mitochondrial defects potentiate seizure development in Wolf-Hirschhorn syndrome
Publicado: (2014)

Early Postnatal Seizures in a Neonate with Wolf–Hirschhorn Syndrome
por: Go, Hayato, et al.
Publicado: (2016)

A case for cannabidiol in Wolf–Hirschhorn syndrome seizure management
por: Ho, Karen S., et al.
Publicado: (2016)

Prenatal sonographic findings in confirmed cases of Wolf-Hirschhorn syndrome
por: Simonini, Corinna, et al.
Publicado: (2022)

Phospho-Regulation of Meiotic Prophase
por: Kar, Funda M., et al.
Publicado: (2021)

Growth charts for Wolf-Hirschhorn syndrome (0–4 years of age)
por: Antonius, T., et al.
Publicado: (2007)

Wolf–Hirschhorn syndrome: A case demonstrated by a cytogenetic study
por: Pokale, Yamini S., et al.
Publicado: (2012)

Inflammatory Myofibroblastic Bladder Tumor in a Patient with Wolf-Hirschhorn Syndrome
por: Marte, Antonio, et al.
Publicado: (2013)

Oral Manifestations of Wolf-Hirschhorn Syndrome: Genotype-Phenotype Correlation Analysis
por: Limeres, Jacobo, et al.
Publicado: (2020)

Nonossified cervical vertebrae in Wolf-Hirschhorn Syndrome: A case report
por: Hong, You Mi, et al.
Publicado: (2019)

Anesthetic considerations for an adult with Wolf-Hirschhorn syndrome - A case report -
por: Kim, Hye-Jin, et al.
Publicado: (2020)

Features of the Wolf-Hirschhorn Syndrome (WHS) from Infant to Young Teenager
por: Popescu, D.E., et al.
Publicado: (2023)

Chromosome Organization in Early Meiotic Prophase
por: Grey, Corinne, et al.
Publicado: (2021)

Genotype-Phenotype Characterization of Wolf-Hirschhorn Syndrome Confirmed by FISH: Case Reports
por: Sheth, F., et al.
Publicado: (2012)

Cytogenomic Integrative Network Analysis of the Critical Region Associated with Wolf-Hirschhorn Syndrome
por: Corrêa, Thiago, et al.
Publicado: (2018)

Diabetes Mellitus Secondary to Acute Pancreatitis in a Child with Wolf-Hirschhorn Syndrome
por: Deeb, Asma
Publicado: (2017)

Coping with Wolf-Hirschhorn syndrome: quality of life and psychosocial features of family carers
por: Berrocoso, Sarah, et al.
Publicado: (2020)

Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review
por: Tang, Feng, et al.
Publicado: (2023)

Wolf–Hirschhorn Syndrome Candidate 1 (whsc1) Functions as a Tumor Suppressor by Governing Cell Differentiation
por: Yu, Chuan, et al.
Publicado: (2017)

De novo truncating variant in NSD2gene leading to atypical Wolf-Hirschhorn syndrome phenotype
por: Jiang, Yanrui, et al.
Publicado: (2019)

Regulation of Meiotic Prophase One in Mammalian Oocytes
por: Wang, Xiaoyi, et al.
Publicado: (2021)

Meiotic Cohesin Promotes Pairing of Nonhomologous Centromeres in Early Meiotic Prophase
por: Bardhan, Amit, et al.
Publicado: (2010)

Auditory hair cell defects as potential cause for sensorineural deafness in Wolf-Hirschhorn syndrome
por: Ahmed, Mohi, et al.
Publicado: (2015)

Anesthetic considerations for a pediatric patient with Wolf-Hirschhorn syndrome: a case report
por: Tsukamoto, Masanori, et al.
Publicado: (2017)

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review
por: Gavril, Eva-Cristiana, et al.
Publicado: (2021)

Clinical and genetic characterization of ten Egyptian patients with Wolf–Hirschhorn syndrome and review of literature
por: Mekkawy, Mona K., et al.
Publicado: (2020)

Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing
Publicado: (1996)

Meiotic cohesins modulate chromosome compaction during meiotic prophase in fission yeast
por: Ding, Da-Qiao, et al.
Publicado: (2006)

THE FINE STRUCTURE OF CHROMOSOMES IN THE MEIOTIC PROPHASE OF VERTEBRATE SPERMATOCYTES
por: Fawcett, Don W.
Publicado: (1956)

DNA-DEPENDENT FORMATION OF THE SYNAPTINEMAL COMPLEX AT MEIOTIC PROPHASE
por: Roth, Thomas F., et al.
Publicado: (1967)

Meioc maintains an extended meiotic prophase I in mice
por: Soh, Y. Q. Shirleen, et al.
Publicado: (2017)

Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot deformity
por: Aslan, Halil, et al.
Publicado: (2003)

The Many Faces of Xenopus: Xenopus laevis as a Model System to Study Wolf–Hirschhorn Syndrome
por: Lasser, Micaela, et al.
Publicado: (2019)

Single port laparoscopic splenectomy for wandering spleen with splenomegaly in a patient with Wolf-Hirschhorn syndrome
por: Zorron, Ricardo, et al.
Publicado: (2017)

UHRF1-repressed 5’-hydroxymethylcytosine is essential for the male meiotic prophase I
por: Pan, Hongjie, et al.
Publicado: (2020)

Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes
por: Malvestiti, Francesca, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_07bv1qodank761v17k80f7qff8