Suggested Topics within your search.
Showing 2,561 - 2,580 results of 11,391 for search '"genetics"', query time: 0.07s Refine Results
  1. 2561
    Transcriptomic Response of Arabidopsis thaliana to Pseudomonas syringae Infection: An In Silico Approach

    Transcriptomic Response of Arabidopsis thaliana to Pseudomonas syringae Infection: An In Silico Approach by Amir Ghaffar Shahriari, Mohamad Hamed Ghodoum Parizipour, Yaser Biniaz, Aminallah Tahmasebi, Fatemeh Gholizadeh

    Published 2024-09-01
    “…Journal of Genetic Resources…”
    Get full text
    Article
    Save to List
    Saved in:
  2. 2562
    LAMA2 Congenital Muscle Dystrophy: A Novel Pathogenic Mutation in Bulgarian Patient

    LAMA2 Congenital Muscle Dystrophy: A Novel Pathogenic Mutation in Bulgarian Patient by Ivanka Dimova, Ivo Kremensky

    Published 2018-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  3. 2563
    Persistent Mosaicism for 12p Duplication/Triplication Chromosome Structural Abnormality in Peripheral Blood

    Persistent Mosaicism for 12p Duplication/Triplication Chromosome Structural Abnormality in Peripheral Blood by Amy L. Shackelford, Laura K. Conlin, Marybeth Hummel, Nancy B. Spinner, Sharon L. Wenger

    Published 2013-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  4. 2564
    Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation

    Rare Manifestation of a c.290 C>T, p.Gly97Glu VCP Mutation by Nivedita U. Jerath, Cameron D. Crockett, Steven A. Moore, Michael E. Shy, Conrad C. Weihl, Tsui-Fen Chou, Tiffany Grider, Michael A. Gonzalez, Stephan Zuchner, Andrea Swenson

    Published 2015-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  5. 2565
    De Novo Interstitial Microdeletion at 1q32.1 in a 10-Year-Old Boy with Developmental Delay and Dysmorphism

    De Novo Interstitial Microdeletion at 1q32.1 in a 10-Year-Old Boy with Developmental Delay and Dysmorphism by Jennifer Carter, Melinda Zombor, Adrienn Máté, László Sztriha, Jonathan J. Waters

    Published 2016-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  6. 2566
    Effect of Black Cumin on the Expression of Genes Related to Lipid Metabolism in Adipose Tissue: A Mouse Model Study

    Effect of Black Cumin on the Expression of Genes Related to Lipid Metabolism in Adipose Tissue: A Mouse Model Study by Roya Maleki, Ali Ahadi, Hoda Ayat

    Published 2024-02-01
    “…Journal of Genetic Resources…”
    Get full text
    Article
    Save to List
    Saved in:
  7. 2567
    Hepatocellular Carcinoma in a 24-Year-Old Female with Beckwith–Wiedemann Syndrome: A Case Report and Review of the Literature

    Hepatocellular Carcinoma in a 24-Year-Old Female with Beckwith–Wiedemann Syndrome: A Case Report and Review of the Literature by Carolyn G. Ahlers, Quoc-Huy Trinh, Martin Montenovo

    Published 2020-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  8. 2568
    Molecular Detection and Determination of Phylogenetic Position of Watermelon Chlorotic Stunt Virus Khouzestan Isolate Based on Coat Protein Gene

    Molecular Detection and Determination of Phylogenetic Position of Watermelon Chlorotic Stunt Virus Khouzestan Isolate Based on Coat Protein Gene by Samira Pakbaz, Zahra Jelavi, Ehsan Hasanvand, Hossein Mirzaei Najafgholi

    Published 2024-02-01
    “…Journal of Genetic Resources…”
    Get full text
    Article
    Save to List
    Saved in:
  9. 2569
    Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature

    Ring Chromosome 4 in a Child with Multiple Congenital Abnormalities: A Case Report and Review of the Literature by C. S. Paththinige, N. D. Sirisena, U. G. I. U. Kariyawasam, L. P. C. Saman Kumara, V. H. W. Dissanayake

    Published 2016-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  10. 2570
    Deciphering the Regulatory Network of Some Key Drought-responsive Genes and microRNAs in Canola

    Deciphering the Regulatory Network of Some Key Drought-responsive Genes and microRNAs in Canola by Maryam Pasandideh Arjmand, Naser Farrokhi, Habibollah Samizadeh Lahiji, Mohammad Mohsenzadeh Golfazani

    Published 2024-02-01
    “…Journal of Genetic Resources…”
    Get full text
    Article
    Save to List
    Saved in:
  11. 2571
    Goldenhar Syndrome with Dextrocardia and Right Pulmonary Hypoplasia: An Unusual Association

    Goldenhar Syndrome with Dextrocardia and Right Pulmonary Hypoplasia: An Unusual Association by Nagendra Chaudhary, Sandeep Shrestha, Hemant Kumar Halwai

    Published 2017-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  12. 2572
    A Neonatal Patient Diagnosed with a COL4A1 Mutation Presenting with Hemorrhagic Infarction and Severe Jaundice

    A Neonatal Patient Diagnosed with a COL4A1 Mutation Presenting with Hemorrhagic Infarction and Severe Jaundice by Akihiro Kirimura, Hajime Yasuhara, Soshi Hachisuka, Kumiko Takagi, Reiko Ebisu, Ayako Ohgitani, Hideki Minowa

    Published 2022-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  13. 2573
    Prenatal Identification and Molecular Characterization of Two Simultaneous De Novo Interstitial Duplications of Chromosomal Regions 7p22.1p21.1 and 15q24.1

    Prenatal Identification and Molecular Characterization of Two Simultaneous De Novo Interstitial Duplications of Chromosomal Regions 7p22.1p21.1 and 15q24.1 by Sabrina C. Burn, Kali Swift, Maria Palmquist

    Published 2018-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  14. 2574
    Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3)

    Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3) by Norma Elena de León Ojeda, Michel Soriano-Torres, Mercedes J. Cabrera, Dunia Bárbara Benítez Ramos

    Published 2012-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  15. 2575
    Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome

    Genital Abnormalities and Growth Retardation as Early Signs of Dilated Cardiomyopathy with Ataxia Syndrome by Kyriaki Papadopoulou-Legbelou, Maria Ntoumpara, Maria Kavga, Eleni P. Kotanidou, Ioannis Papoulidis, Assimina Galli-Tsinopoulou, Maria Fotoulaki

    Published 2024-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  16. 2576
    Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma

    Cytogenomic Characterization of Giant Ring or Rod Marker Chromosome in Four Cases of Well-Differentiated and Dedifferentiated Liposarcoma by Hongyan Chai, Fang Xu, Autumn DiAdamo, Brittany Grommisch, Huanzhi Mao, Peining Li

    Published 2022-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  17. 2577
    Premature Moustache As Presenting Symptom of Nonclassic Congenital Adrenal Hyperplasia due to 2 Uncommon Mutations of the CYP21A2 Gene

    Premature Moustache As Presenting Symptom of Nonclassic Congenital Adrenal Hyperplasia due to 2 Uncommon Mutations of the CYP21A2 Gene by Guy Massa, Philippe Gillis, Marianne Schwartz

    Published 2011-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  18. 2578
    Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report)

    Novel Homozygous TTI2 Variant Causing Autosomal Recessive Syndromic Intellectual Disability and Primary Microcephaly from Pakistan: A Case Report (Exome Report) by Zul Qarnain, Fatima Khan, Fizza Akbar, Salman Kirmani

    Published 2022-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  19. 2579
    Multifactorial Origin of Exertional Rhabdomyolysis, Recurrent Hematuria, and Episodic Pain in a Service Member with Sickle Cell Trait

    Multifactorial Origin of Exertional Rhabdomyolysis, Recurrent Hematuria, and Episodic Pain in a Service Member with Sickle Cell Trait by Nyamkhishig Sambuughin, Mingqiang Ren, John F. Capacchione, Ognoon Mungunsukh, Kevin Chuang, Iren Horkayne-Szakaly, Francis G. O’Connor, Patricia A. Deuster

    Published 2018-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:
  20. 2580
    A De Novo Missense MYLK Variant Leading to Nonsyndromic Thoracic Aortic Aneurysm and Dissection Identified by Segregation Analysis

    A De Novo Missense MYLK Variant Leading to Nonsyndromic Thoracic Aortic Aneurysm and Dissection Identified by Segregation Analysis by Daigo Nishijo, Hiroki Yagi, Nana Akiyama, Norifumi Takeda, Masahiko Ando, Haruo Yamauchi, Norihiko Takeda, Issei Komuro

    Published 2024-01-01
    “…Case Reports in Genetics…”
    Get full text
    Article
    Save to List
    Saved in:

Search Tools: